Robot-Assisted vs. Laparoscopic Radical Prostatectomy for Immediate- and High-Risk Localized Prostate Cancer: A Propensity-Score Matched Analysis

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Robot-assisted radical prostatectomy showed a lower risk of complications and better functional outcomes for high-risk prostate cancer compared to laparoscopic radical prostatectomy, without compromising cancer control.

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This retrospective propensity-score matched analysis compared robot-assisted radical prostatectomy (RARP) versus laparoscopic radical prostatectomy (LRP) in 232 men with immediate- and high-risk localized prostate cancer treated between 2016 and 2019, using 1:1 matching to reduce baseline confounding. After matching, 85 RARP cases were compared with 85 LRP cases, with preoperative variable differences becoming insignificant, and no open conversion was required in either group. RARP had a significantly shorter operative time and a lower risk of ≤ Grade II complications, while transfusion, estimated blood loss, pathologic T3 disease, positive surgical margins, specimen Gleason score, and hospital stay were similar; functional outcomes showed tendencies toward better urinary continence at catheter removal, 6 months, and last follow-up, and better erectile function at 6 months and last follow-up, without a significant difference in biochemical recurrence-free survival. A key limitation is that this is a preprint and retrospective design with a median follow-up of about 29 vs 23 months, which may limit inference about longer-term oncologic outcomes. The paper does not explicitly discuss endometriosis or adenomyosis; it was included in the corpus via a keyword match in the upstream search index.

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Abstract

Background: To evaluate the functional and oncological efficacy of robot-assisted radical prostatectomy (RARP) and laparoscopic radical prostatectomy (LRP) for immediate- and high-risk localized prostate cancer (PCa). Methods 232 patients bearing immediate- and high-risk localized PCa between January 2016 and October 2019 were enrolled according to the inclusion criteria. The perioperative, functional and oncological outcomes were compared between the RARP and LRP groups after applying the propensity-score matching (PM) (1:1) method, which were employed to attenuate the impact of the potential baseline confounders. Results In all, except for 10 patients without a suitable pair, the remaining patients in the LRP group were successfully matched to 85 patients in the RARP arm. All differences in preoperative variables turned to be insignificant after PM. Within the matched cohort, no open conversion was required in both groups. The RARP group was corrected with a significantly shorter mean operative time than the LRP group ( p  < 0.001). Patients in the RARP arm were also at a lower risk of ≤ Grade II complications than those in the LRP group ( p  = 0.036). Meanwhile, the proportions of transfusion and ≥ Grade II complications in the RARP group were similar to that in the LRP group ( p  = 0.192 and p  = 1.000, respectively). No significant differences regarding the mean estimated blood loss, rates of pT3 disease and positive surgical margin, median specimen Gleason score and hospital stay length existed between the two groups. RARP vs. LRP tended to a significantly higher percentage of urinary continence at the removal of catheter ( p  = 0.031), postoperative 6 months ( p  = 0.043), and last follow-up ( p  = 0.046). Significant differences were also found between the RARP and LRP arms in erectile function at postoperative 6 months and last follow-up ( p  = 0.013 and p  = 0.009, respectively). The statistical comparability between the two groups was observed in biochemical recurrence-free survival ( p  = 0.228). Conclusions For surgically managing immediate- and high-risk localized PCa, RARP tended to a lower risk of ≤ Grade II complications and superior functional preservation without cancer control being compromised when comparing with LRP.
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Robot-Assisted vs. Laparoscopic Radical Prostatectomy for Immediate- and High-Risk Localized Prostate Cancer: A Propensity-Score Matched Analysis | Research Square window.SnipcartSettings = { analytics: { enabled: false } }; (function() { var accessVector = localStorage.getItem('access_vector') || ''; window.dataLayer = window.dataLayer || []; if (accessVector) { window.dataLayer.push({ user: { profile: { profileInfo: { snid: accessVector } } } }); } })(); (function(w,d,s,l,i){w[l]=w[l]||[];w[l].push({'gtm.start':new Date().getTime(),event:'gtm.js'});var f=d.getElementsByTagName(s)[0],j=d.createElement(s),dl=l!='dataLayer'?'&l='+l:'';j.async=true;j.src='https://www.googletagmanager.com/gtm.js?id='+i+dl;f.parentNode.insertBefore(j,f);})(window,document,'script','dataLayer','GTM-K279D39R'); Browse Preprints In Review Journals COVID-19 Preprints AJE Video Bytes Research Tools Research Promotion AJE Professional Editing AJE Rubriq About Preprint Platform In Review Editorial Policies Our Team Advisory Board Help Center Sign In Submit a Preprint Cite Share Download PDF Research Robot-Assisted vs. Laparoscopic Radical Prostatectomy for Immediate- and High-Risk Localized Prostate Cancer: A Propensity-Score Matched Analysis Deng Wen, Zhang Cheng, Jiang Hao, Li Yulei, Liu Xiaoqiang, Chen Luyao, and 5 more This is a preprint; it has not been peer reviewed by a journal. https://doi.org/ 10.21203/rs.3.rs-442704/v1 This work is licensed under a CC BY 4.0 License Status: Posted Version 1 posted You are reading this latest preprint version Abstract Background To evaluate the functional and oncological efficacy of robot-assisted radical prostatectomy (RARP) and laparoscopic radical prostatectomy (LRP) for immediate- and high-risk localized prostate cancer (PCa). Methods 232 patients bearing immediate- and high-risk localized PCa between January 2016 and October 2019 were enrolled according to the inclusion criteria. The perioperative, functional and oncological outcomes were compared between the RARP and LRP groups after applying the propensity-score matching (PM) (1:1) method, which were employed to attenuate the impact of the potential baseline confounders. Results In all, except for 10 patients without a suitable pair, the remaining patients in the LRP group were successfully matched to 85 patients in the RARP arm. All differences in preoperative variables turned to be insignificant after PM. Within the matched cohort, no open conversion was required in both groups. The RARP group was corrected with a significantly shorter mean operative time than the LRP group ( p < 0.001). Patients in the RARP arm were also at a lower risk of ≤ Grade II complications than those in the LRP group ( p = 0.036). Meanwhile, the proportions of transfusion and ≥ Grade II complications in the RARP group were similar to that in the LRP group ( p = 0.192 and p = 1.000, respectively). No significant differences regarding the mean estimated blood loss, rates of pT3 disease and positive surgical margin, median specimen Gleason score and hospital stay length existed between the two groups. RARP vs. LRP tended to a significantly higher percentage of urinary continence at the removal of catheter ( p = 0.031), postoperative 6 months ( p = 0.043), and last follow-up ( p = 0.046). Significant differences were also found between the RARP and LRP arms in erectile function at postoperative 6 months and last follow-up ( p = 0.013 and p = 0.009, respectively). The statistical comparability between the two groups was observed in biochemical recurrence-free survival ( p = 0.228). Conclusions For surgically managing immediate- and high-risk localized PCa, RARP tended to a lower risk of ≤ Grade II complications and superior functional preservation without cancer control being compromised when comparing with LRP. Cancer Biology Oncology radical prostatectomy robot laparoscopic immediate-risk high-risk prostate cancer. Figures Figure 1 Figure 2 Background Prostate cancer (PCa), the second most common cancer and the fifth dominating cause of cancer-specific mortality among men around the world ( 1 ), is increasingly been discovered due to the widespread diffusion of prostate specific antigen (PSA) screening, markedly the localized ones ( 2 , 3 ). Given the slowly evolving nature of localized prostate tumors, it is of great significance to distinguish PCa destined to cause clinical symptoms or metastases from more clinically indolent PCa that is highly unlikely to impact survival to reduce overtreatment in patients with PCa without compromising opportunities for cure. The D'Amico risk classifications proposed on the basis of clinical and pathological characteristics including the clinical stage, PSA, and biopsy Gleason score have been widely endorsed worldwide ( 3 ). The role of radical prostatectomy (RP) in managing D'Amico low-risk PCa is in doubt due to the similar survival benefit of patients with low-risk localized PCa following immediate radical treatment and active surveillance and RP-related harms to quality of life ( 3 – 5 ), whilst RP has a tendency towards a better survival benefit over watchful waiting for immediate-risk localized PCa ( 4 , 6 , 7 ) and 10-year PCa-specific survival rates after RP coupled with node dissection were generally over 90% and remarkably consistent across all large studies focusing on high-risk PCa ( 8 ). In 2020, surgery is not recommended in those patients with low-grade, low-volume Gleason 6 PCa in consideration of the little clinical benefit and considerable adverse effects following surgery, while RP is considered appropriate for men with intermediate- and high-risk disease ( 9 ). With the superiority of surgical robots in three-dimensional magnified vision of the surgical field, improved dexterity, and higher precision during the surgical procedure, robot-assisted RP (RARP) is considered as a great evolution of minimally invasive surgery to reduce the difficulty associated with complex laparoscopic surgery ( 10 ) and has been widely disseminated for localized PCa since 2001 ( 11 ). However, thus far, whether the advantages of RARP over laparoscopic RP (LRP) mentioned above could translate into superior functional preservation and oncological control was still inconclusive due to the scarcity of high-level evidence comparing RARP and LRP for localized PCa ( 10 , 12 ). There are only three randomized controlled trials (RCTs) concentrating on comparing RARP and LRP for localized PCa with different endpoints over the short-term study periods ( 13 – 15 ), which is far from reaching a convincing consensus about the controversy. What’s worse, no study focusing on comparing RARP and LRP for patients with immediate- and high-risk localized PCa has been reported yet, while the cogent evidence comparing the efficacy and safety of RARP and LRP for immediate- and high-risk localized PCa is of great clinical importance. To close this gap of cogent evidence concerning the functional and oncological efficacy of RARP and LRP for immediate- and high-risk localized PCa, we designed this first analysis comparing RARP and LRP for immediate- and high-risk localized PCa in an attempt to document differences in the perioperative, functional and oncological outcomes obtained after the two techniques in a retrospective fashion. Methods Having obtained the approval of the Ethnic Committee of the First Affiliated Hospital of Nanchang University, we meticulously reviewed our prospectively maintained database to retrospectively gather all the demographic, clinical, and pathologic information of patients harbouring localized PCa between January 2016 and October 2019. All patients with PCa were screened and incorporated into the final analysis on the grounds of the following eligibility criteria: ( 1 ) total serum PSA ≥ 10 ng/mL or Gleason score ≥ 7 or localized T2b or T2c stage; ( 2 ) patients undergoing RARP or LRP for localized PCa; ( 3 ) no evidence of clinical positive lymph nodes or clinical T3-4 stage. Only when the case simultaneously satisfied all these inclusion criteria were the men included, whilst the others were excluded from our study. On the basis of inclusion criteria described above, included in the final analysis were 232 patients, of whom 137 and 95 patients were divided by surgical approaches into the RARP and LRP arms, respectively, and none of them had a history of abdominal surgery. Prostate magnetic resonance imaging and bone scintigraphy were routinely performed in all patients before surgeries. All surgeries were conducted with the anterior approach by three highly experienced hands (Fu B, Wang GX, and Sun T). Prior to this study initiation, each of these three surgeons had performed more than 300 LRPs and 100 RARPs as an operator or a trainee. The patients’ assignment was usually at the discretion of these four highly experienced surgeons according to tumor and patient characteristics. The written informed consent was acquired from each patient in both groups. The anterior approach to RARP was done according to the techniques established by Menon et al. ( 16 ), while the anterior approach to LRP was completed following the surgical steps described by Touijer et al. ( 17 ). Pelvic lymph node dissection (PLND) was routinely done in all high-risk patients and those immediate-risk cases with a preoperative estimated risk exceeding 5% in nodal involvement, while the nodal dissection could be omitted at a low risk of missing positive nodes in other immediate-risk men. A standardized extended PLND (ePLND) template with the upper margin being the common iliac artery was closely observed when performing all these lymph node dissections. Nerve sparing was preoperatively proposed according to clinical features and intraoperatively modified based on evidence of bundle invasion. Baseline demographics and clinical elements (age, body mass index [BMI], diabetes mellitus, hypertension, American Society of Anesthesiologists [ASA] score, preoperative total PSA, preoperative erectile function quantified in accordance with the International Index of Erectile Function [IIEF]-5 score ( 18 ), and risk stratification assessed with D'Amico risk classifications ( 3 )) and preoperative tumor characteristics (clinical TNM stage, biopsy Gleason score, and prostate volume calculated by the virtue of transrectal ultrasound) were extracted from the database. Data with regard to perioperative outcomes (operative time [OT], estimated blood loss [EBL], ePLND, nerve sparing procedure, open conversion, transfusion, postoperative hospital stay, and postoperative complications evaluated with Clavien-Dindo classification ( 19 )) and pathologic results (pathological T stage, specimen Gleason score, positive surgical margin [PSM] which were defined as tumor extending to the inked-surface of prostate specimen, and positive lymph node) was also retrieved from our database. Information about postoperative complications could also be collected via chart reviews or face-to-face and telephone interviews. The median postoperative follow-up length for the RARP and LRP groups was 29 and 23 months, respectively. Postoperative follow-up was regularly arranged every 3 months within the first year after surgery and every 6 months since the second year after surgery for each patient. Each case routinely underwent postoperative PSA tests every 3 months to monitor biochemical recurrence (BCR), which was considered as the occurrence after prostatectomy that two consecutive rising serum PSA measured on two separate occasions was 0.2 ng/mL or greater. UC was defined by the use of ≤ one dry pad over the 24-hour period. The total PSA level and erectile function score were reported at postoperative 6 months and last follow-up, while the rate of UC recovery were presented at the removal of catheter, postoperative 6 months, and last follow-up. Propensity-score matching (PM) method was employed to impose restrictions on significant differences in preoperative clinical and tumor characteristics. The propensity score was calculated with non-parsimonious multivariate logistic regression on the basis of all preoperative variables, namely, age, BMI, diabetes mellitus, hypertension, ASA score, preoperative total PSA, preoperative IIEF-5 score, clinical TNM stage, biopsy Gleason score, and prostate volume. Finally, except for 10 patients missing an appropriate pair, all the remaining cases in the LRP arm were successfully matched to 85 patients in the RARP group using a 1:1 ratio with the nearest neighbour pairing method. All differences before and after PM in preoperative elements were analyzed between the RARP and LRP arms with the independent t-test or the Pearson chi-squared test being utilized. All non-normally distributed continuous variables were presented as median and interquartile range and compared using the Wilcoxon rank-sum test, whilst those in a normally distributed fashion were presented as mean and standard deviation and analyzed with the independent t-test. All categorical variables were presented as proportion and percentages and calculated with the Pearson chi-squared test or the Fisher’s exact test being used. The Kaplan–Meier method was employed to estimate BCR-free survival probabilities and the proportions of postoperative return to UC with the log-rank test. All statistical analyses were conducted on STATA version 12.0 (STATA corp., College Station, TX), and the statistical significance was defined a two-sided p value of < 0.05. Results All preoperative information concerning the clinical and tumor characteristics before and after PM was detailedly described in Table 1 . In all, 232 patients with primary immediate- and high-risk localized PCa in line with the inclusion criteria, comprising 137 RARPs and 95 LRPs, were enrolled in this analysis over the study period being reviewed. Before the PM, the RARP group was significantly corrected with a lower mean age (65.4 vs. 68.0 years, p = 0.010), higher mean BMI (23.2 vs. 22.2 kg/m 2 , p = 0.044), smaller mean prostate volume (38.4 vs. 43.9 mL, p = 0.001), higher median preoperative IIEF-5 score (17 vs. 15, p = 0.011), and lower median biopsy Gleason score (6 vs. 7, p = 0.020) than the LRP group, while no significant differences in other preoperative variables existed between the two arms. All these significant differences in preoperative variables disappeared within the well-balanced matched cohorts after applying the PM method (Table 1 ). Table 1 Preoperative characteristics by surgery type before and after propensity score matching. Variable Before propensity score matching After propensity score matching RARP ( n = 137) LRP ( n = 95) p value RARP ( n = 85) LRP ( n = 85) p value Age, years, mean (SD) 65.4 (7.3) 68.0 (7.3) 0.010 65.5 (7.3) 67.2 (7.2) 0.138 BMI, kg/m2, mean (SD) 23.2 (3.5) 22.2 (3.8) 0.044 23.1 (3.6) 22.7 (3.8) 0.482 Diabetes mellitus (yes), n (%) 17 (13.4%) 15 (15.8%) 0.614 12 (14.1%) 14 (16.5%) 0.670 Hypertension (yes), n (%) 33 (26.0%) 23 (24.2%) 0.763 22 (25.9%) 20 (23.5%) 0.722 ASA score (≥ 3), n (%) 7 (5.5%) 7 (7.4%) 0.573 4 (4.7%) 5 (5.9%) 1.000 Preoperative total PSA, ng/mL, mean (SD) 25.7 (25.5) 26.6 (26.9) 0.795 27.5 (27.9) 26.6 (28.1) 0.834 Prostate volume, mL, mean (SD) 38.4 (10.6) 43.9 (13.0) 0.001 39.7 (10.8) 42.8 (13.0) 0.093 Preoperative IIEF-5 score, median (IQR) 17 (14, 19) 15 (13, 18) 0.011 18 (14.3, 19) 16 (13, 18.75) 0.113 cTNM stage, n (%) 0.365 0.385 T1-T2a 52 (41.0%) 48 (50.5%) 37 (43.5%) 46 (54.1%) T2b 46 (36.2%) 29 (30.5%) 31 (36.5%) 25 (29.4%) T2c 29 (22.8%) 18 (19.0%) 17 (20.0%) 14 (16.5%) Biopsy Gleason score, median (IQR) 6 (5, 8) 7 (6, 8) 0.020 7 (5.75, 8) 7 (6, 8) 0.214 High risk ┿ , n (%) 62 (45.3%) 53 (55.8%) 0.115 43 (50.6%) 46 (54.1%) 0.645 SD: standard deviation; BMI: body mass index; ASA: American Society of Anesthesiologists; IIEF: International Index of Erectile Function; IQR: inter-quartile range. ┿ according to the D'Amico risk classifications Table 2 delineated the perioperative and pathological outcomes in detail. Within the matched settings, no surgery was converted to an open approach in either arm. Patients in the RARP group had a significantly shorter mean OT than those in the LRP group (146.0 vs. 167.9 min, p < 0.001), but no significant difference in the mean EBL was found between the two groups (152.6 vs. 166.4 mL, p = 0.200). 55 (64.7%) and 50 (58.8%) cases underwent ePLND in the RARP and LRP groups, respectively ( p = 0.430), while nerve sparing technique was more frequently completed in patients undergoing RARP than those with LRP (48.2% vs. 32.9%, p = 0.042). There were no significant differences in the probability of transfusion and > Grade II postoperative complications between the two groups ( p = 0.192 and p = 1.000, respectively). The distributions of pathologic T2 and T3 disease were comparable among the RARP and LRP groups ( p = 0.345), and the comparability between the two groups remained with regard to the median specimen Gleason score and hospital stay length ( p = 0.179 and p = 0.563, respectively). The occurrence rates of PSM and positive lymph node were also statistically similar between the RARP and LRP arms ( p = 0.260 and p = 0.501, respectively). However, patients in the LRP group had a tendency towards a higher incidence of ≤ Grade II complications than those in the RARP group ( p = 0.036). Table 2 Perioperative outcomes for RARP and LRP after propensity score matching. Variable RARP ( n = 85) LRP ( n = 85) p value Operative time, min, mean (SD) 146.0 (40.4) 167.9 (34.2) < 0.001 Estimated blood loss, mL, mean (SD) 152.6 (60.5) 166.4 (78.2) 0.200 ePLND, n (%) 55 (64.7%) 50 (58.8%) 0.430 Nerve sparing procedures, n (%) 41 (48.2%) 28 (32.9%) 0.042 Open conversion, n (%) 0 (0%) 0 (0%) - Transfusion, n (%) 3 (3.5%) 7 (8.2%) 0.192 Postoperative pathology Pathological T stage, n (%) 0.345 pT2 49 (57.6%) 55 (64.7%) pT3 36 (42.4%) 30 (35.3%) Specimen Gleason score, median (IQR) 7 (5.5, 8) 7 (6, 8) 0.179 Positive surgical margin, n (%) 15 (17.6%) 21 (24.7%) 0.260 Positive lymph nodes, n (%) 13 (15.3%) 10 (11.8%) 0.501 Postoperative complications, n (%) 8 (9.4%) 18 (21.2%) 0.033 ≤ Grade II complications 6 (7.1%) 15 (17.6%) 0.036 > Grade II complications 2 (2.4%) 3 (3.5%) 1.000 Hospital stay, days, median (IQR) 14 (14, 15) 15 (14, 15) 0.563 ePLND: extended pelvic lymph nodes dissection; SD: standard deviation; IQR: inter-quartile range. Within the matched cohort, median follow-up durations after RARP and LRP were 29 and 23 months, respectively. As shown in Table 3 , no significant differences were detected between the two groups in terms of the mean total serum PSA at postoperative 6 months and last follow-up ( p = 546 and p = 0.688, respectively). The appearances of BCR have happened in 8 and 11 patients following RARP and LRP, respectively, over the periods covered by the follow-ups. The likelihoods of BCR-free survivals of immediate- and high-risk patients following RARP and LRP were also statistically similar after matching ( p = 0.228) (Figure. 1). Table 3 Postoperative outcomes for RARP and LRP after propensity score matching. Variable RARP ( n = 85) LRP ( n = 85) p value Oncology: postoperative total PSA, ng/mL Postoperative 6 months, mean (SD) 0.053 (0.062) 0.047 (0.078) 0.546 Last follow-up, mean (SD) 0.218 (0.955) 0.280 (1.021) 0.688 Urinary continence Continent on removal of catheter, n (%) 33 (38.8%) 20 (23.5%) 0.031 Continent at 6 months, n (%) 66 (77.6%) 54 (63.5%) 0.043 Continent at last follow-up, n (%) 80 (94.1%) 72 (84.7%) 0.046 Erectile function IIEF-5 score at postoperative 6 month, median (IQR) 14 (12, 16) 12 (11, 15) 0.013 IIEF-5 score at last follow-up, median (IQR) 14 (11, 16) 12 (11, 14) 0.009 PSA: prostate specific antigen; SD: standard deviation; IIEF: International Index of Erectile Function; IQR: inter-quartile range. The Foley catheter was routinely removed at postoperative 2 weeks regardless of the surgical approach. As described in Table 3 , the proportions of patients reporting UC recovery at the moment of removing catheter (38.8% vs. 23.5%, p = 0.031), postoperative 6 months (77.6% vs. 63.5%, p = 0.043), and last follow-up (94.1% vs. 84.7%, p = 0.046) in the RARP group were significantly higher than that in the LRP group. Intriguingly, the difference in postoperative UC recovery obtained following RARP and LRP was gradually alleviated and close to be out of statistical significance. The patients in the RARP group achieved a significantly higher cumulative proportion of postoperative return to UC than those following LRP ( p = 0.011) (Figure. 2). As presented in Table 3 , within the matched cohort, significant differences were also revealed between the RARP and LRP groups with respect to the median IIEF-5 score at postoperative 6 months and last follow-up ( p = 0.013 and p = 0.009, respectively), exhibiting the superiority of RARP over LRP in erectile functional protection for men with immediate- and high-risk PCa. Discussion Given the limited overall survival benefits and considerable adverse events after RP for D'Amico low-risk PCa, the role of RP in managing D'Amico low-risk PCa remains highly contentious ( 3 , 4 ). While RP for D'Amico immediate- and high-risk PCa could achieve favorable survival benefits from preventing further metastatic seeding of potentially lethal clones of PCa cells ( 9 ). In 2020, RP is widely perceived as appropriate for men with intermediate-risk and high-risk PCa rather than those bearing D'Amico low-risk PCa ( 9 ). Although RARP has been widely diffused for surgically handling localized PCa, the paucity of high-level evidence still triggers the controversy on the impacts of RARP and LRP on oncological and functional outcomes obtained after surgery. What’s worse, there has been no study which was immersed in comparing RARP and LRP for intermediate-risk and high-risk PCa up to now, while the cogent evidence concerning the functional and oncological efficacy of RARP and LRP for immediate- and high-risk localized PCa is of great clinical importance. In this content, we designed this retrospective study which is the first one comparing RARP and LRP for immediate- and high-risk PCa. To eliminate the influences of any significant differences in any preoperative factors and selection bias, we rigorously utilized the PM method to guarantee the similarity in all preoperative parameters between the two groups. Within the well-balanced matched cohort, our results revealed the superiority of RARP in functional preservation coupled with fewer postoperative ≤ Grade II complications than LRP without cancer control being compromised for managing immediate- and high-risk PCa. As regards the extended mean OT in the LRP group, this significant difference may be attributable to the fact that the robotic platform facilitates suturing, one of the most challenging procedures during the standard laparoscopic approach ( 20 ), and this advantage is even more obvious when comparing RARP and LRP for the immediate- and high-risk patients enrolled in our analysis. As to the similar mean EBL and transfusion rates following RARP and LRP, the similarity can be explained by the counterbalance between the contributing factors including the better visualization, improved dexterity, and higher precision to minimize bleeding during RARP and unfavorable factors leading to EBL including more ePLNDs and nerve sparing procedures done in the RARP group. Both Johnson et al. ( 21 ) and Papachristos et al. ( 22 ) also achieved similar outcomes regarding EBL and OT after RARP and LRP to ours, in spite of the drastic variation of mean EBL and OT offered from different medical centers. The variation could be easily interpreted when taking the surgeons’ experience and patients’ and tumors’ characteristics into account. Although both LRP and RARP are minimally invasive, the better visualization and higher precision offered by the robotic platform could help in further reducing the operative invasiveness and the hazard of organ injures ( 20 , 21 ), which may translate into the significantly lower proportion of overall and ≤ Grade II postoperative complications after RARP in our analysis. However, these advantages mentioned above may be restricted by the higher rate of ePLNDs underwent in the RARP group which was associated with the occurrences of symptomatic lymphocele, the most frequent > Grade II complication in our study, thus resulting in similar rates of > Grade II postoperative complications. The comparability of the incidence rates of postoperative > Grade II complications between the two groups in our analysis was consistent with those reported in the contemporary series ( 14 , 20 – 24 ) comparing RARP and LRP, demonstrating the similar operative safety of RARP and LRP for immediate- and high-risk PCa in experienced hands. Surgical approach to RP should be tempered with critical significance of cancer control, especially when managing immediate- and high-risk PCa. Consistent with the results reported in published analyses ( 13 , 14 , 25 ), no significant difference in PSM rate was discovered in our study comparing RARP (17.6%) and LRP (24.7%) for immediate- and high-risk PCa. Evaluated BMI and large prostate volume were considered as the independent predictors of PSMs in men with organ-confined PCa ( 26 ), and cumulative evidences revealed that margin status following RP was related to surgical experience ( 26 , 27 ). Fortunately, all these influencing elements were under stringent control with PM method being employed in this single-center analysis, thus greatly contributing to the similarity in PSM rates after RARP and LRP. Of note, compared with the 15% mean rate of PSMs in RARP series including more than 100 cases ( 26 ), 17.6% rate of PSMs acquired after RARP in our analysis was relatively high even in highly experienced hands when removing immediate- and high-risk PCa, coordinating the caution that the more extensive the cancer, the higher the possibility of positive margins ( 26 ). Although PSMs in RP specimens were in consistent correction with an enhanced risk of PSA relapse ( 28 , 29 ), the long-term impacts of PSMs on more robust clinical endpoints of the disease is variable and mostly depends on other variables, such as Gleason score, pathologic stage, and preoperative PSA ( 16 , 30 ). Intriguingly, most of these decisive factors including Gleason score and preoperative PSA were the basis of D'Amico risk classifications, namely, the clinical endpoints, such as clinical recurrence rates, largely relied on preoperative baseline characteristics rather than PSMs after RP. In alignment with other series ( 14 , 25 ) comparing RARP and LRP, the similarity in the BCR-free survivals obtained after RARP and LRP was still existing, corroborating the equivalent potency of the two procedures in cancer control even when managing immediate- and high-risk PCa. The aims of RP are to completely eradicate localized PCa whilst, whenever possible, preserves UC and erectile function, namely, a trifecta outcome ( 4 ). Urinary incontinence after RP is one of the most adverse events that negatively impact patients’ quality of life ( 20 , 31 ). Multiple pathophysiologic mechanisms contribute to the emergence of post-prostatectomy incontinence (PPI). In addition to the biological/preoperative parameters encompassing the patient age at time of surgery, pre-existing lower urinary tract symptoms, high BMI, and abnormal bladder function, the impairments of the integrity of anatomic supporting structures and neural components during the RP procedure appear to be crucial contributing factors to the development of PPI ( 31 , 32 ). In our analysis, preoperative/biological parameters are comparable between the RARP and LRP groups with PM method being applied, but the robotic platforms allowed better preservation of membranous urethra and nerve branches and reconstruction of bladder neck, thus supporting the higher UC probability after RARP over the whole follow-up period. In the prospective randomized controlled study reported by Porpiglia et al. ( 25 ), UC rate after RARP was also significantly higher than that after LRP for localized PCa over the 5-year follow-up period. Our results also corroborated the outcomes obtained in the first multicenter, randomized, patient-blinded controlled trial (LAP-01) ( 14 ) which demonstrated the improved postoperative return to UC of RARP over LRP. The advantage of robotic platforms in better surgical vision and higher precision for preserving the neurovascular structures could be greatly responsible for the superior erectile function recovery after RARP than that obtained after LRP. Notably, several limitations should be taken into consideration when interpreting our conclusions. Structural shortages in data collection were inevitable in a retrospective setting of our analysis. The study population, although well-balanced between the two groups, is relatively small. The long-term oncological survivals and functional recoveries could not be further evaluated over the relatively limited follow-up lengths. Certain complications may be undervalued, especially ≤ Grade II complications, in spite of the elaborative investigation of medical records and telephone interview. Despite these limitations, our study is the first one designed to assess the perioperative, functional, and oncological outcomes acquired after RARP and LRP for localized immediate- and high-risk PCa up to now, and our conclusions are drew and strengthened on the basis of the comparability of all perioperative elements between the two arms and rigorous methodology. Conclusions For surgically managing immediate- and high-risk localized PCa, RARP tended to a lower risk of ≤ Grade II complications and superior functional preservation without cancer control being compromised when comparing with LRP. Our present conclusions need to be confirmed further on the basis of prospectively randomized trials with large sample sizes and sufficiently long follow-ups. Abbreviations RARP robot-assisted radical prostatectomy; RP:radical prostatectomy; LRP laparoscopic radical prostatectomy; PCa:prostate cancer; PPI post-prostatectomy incontinence; PSA:prostate specific antigen; PM propensity-score matching; RCT:randomized controlled trial; PLND Pelvic lymph node dissection; BMI:body mass index; ASA American Society of Anesthesiologists; OT:operative time; IIEF International Index of Erectile Function; EBL:estimated blood loss; PSM positive surgical margin; UC:urinary continence; BCR biochemical recurrence. Declarations Ethics approval and consent to participate Not applicable. Consent for publication Not applicable. Availability of data and materials The datasets used and/or analysed during the current study are available from the corresponding author on reasonable request. Competing interests The authors declare that they have no competing interests. Funding Not applicable. Authors' contributions All the authors contributed in the preparation of this work. DW, ZC, JH and LYL were drafted and revised the article, DW, LXQ and CLY were responsible for the theme, final editing, and preparation of the manuscript for submission, LWP, ZXC, ST, WGX and FB critically revised the manuscript. All authors read and approved the final manuscript. Acknowledgements Not applicable. Author details 1 Department of Urology, the First Affiliated Hospital of Nanchang University, Yongwai street 17, Nanchang City, Jiangxi Province, China, 2 Jiangxi Institute of Urology, Yongwai street 17, Nanchang City, Jiangxi Province, China. References Bray F, Ferlay J, Soerjomataram I, Siegel RL, Torre LA, Jemal A. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA: a cancer journal for clinicians. 2018 Nov;68(6):394–424. Ilic D, Djulbegovic M, Jung JH, Hwang EC, Zhou Q, Cleves A, et al. Prostate cancer screening with prostate-specific antigen (PSA) test: a systematic review and meta-analysis. BMJ (Clinical research ed). 2018 Sep 5;362:k3519. Moschini M, Carroll PR, Eggener SE, Epstein JI, Graefen M, Montironi R, et al. Low-risk Prostate Cancer: Identification, Management, and Outcomes. European urology. 2017 Aug;72(2):238 – 49. Mottet N, van den Bergh RCN, Briers E, Van den Broeck T, Cumberbatch MG, De Santis M, et al. EAU-EANM-ESTRO-ESUR-SIOG Guidelines on Prostate Cancer-2020 Update. Part 1: Screening, Diagnosis, and Local Treatment with Curative Intent. European urology. 2021 Feb;79(2):243–62. Tienza A, Akin Y, Rassweiler J, Gözen AS. A match-pair analysis of continence in intermediate and high-risk prostate cancer patients after robot-assisted radical prostatectomy: the role of urine loss ratio and predictive analysis. Prostate international. 2018 Sep;6(3):94–8. Bill-Axelson A, Holmberg L, Garmo H, Rider JR, Taari K, Busch C, et al. Radical prostatectomy or watchful waiting in early prostate cancer. The New England journal of medicine. 2014 Mar 6;370(10):932 – 42. Wilt TJ, Jones KM, Barry MJ, Andriole GL, Culkin D, Wheeler T, et al. Follow-up of Prostatectomy versus Observation for Early Prostate Cancer. The New England journal of medicine. 2017 Jul 13;377(2):132–42. Chang AJ, Autio KA, Roach M 3rd, Scher HI. High-risk prostate cancer-classification and therapy. Nature reviews Clinical oncology. 2014 Jun;11(6):308–23. Costello AJ. Considering the role of radical prostatectomy in 21st century prostate cancer care. Nature reviews Urology. 2020 Mar;17(3):177–88. Okegawa T, Omura S, Samejima M, Ninomiya N, Taguchi S, Nakamura Y, et al. Laparoscopic radical prostatectomy versus robot-assisted radical prostatectomy: comparison of oncological outcomes at a single center. Prostate international. 2020 Mar;8(1):16–21. Coughlin GD, Yaxley JW, Chambers SK, Occhipinti S, Samaratunga H, Zajdlewicz L, et al. Robot-assisted laparoscopic prostatectomy versus open radical retropubic prostatectomy: 24-month outcomes from a randomised controlled study. The Lancet Oncology. 2018 Aug;19(8):1051–60. Nossiter J, Sujenthiran A, Charman SC, Cathcart PJ, Aggarwal A, Payne H, et al. Robot-assisted radical prostatectomy vs laparoscopic and open retropubic radical prostatectomy: functional outcomes 18 months after diagnosis from a national cohort study in England. British journal of cancer. 2018 Feb 20;118(4):489–94. Asimakopoulos AD, Pereira Fraga CT, Annino F, Pasqualetti P, Calado AA, Mugnier C. Randomized comparison between laparoscopic and robot-assisted nerve-sparing radical prostatectomy. J Sex Med. 2011 May;8(5):1503–12. Stolzenburg JU, Holze S, Neuhaus P, Kyriazis I, Do HM, Dietel A, et al. Robotic-assisted Versus Laparoscopic Surgery: Outcomes from the First Multicentre, Randomised, Patient-blinded Controlled Trial in Radical Prostatectomy (LAP-01). European urology. 2021 Feb 8. Porpiglia F, Morra I, Lucci Chiarissi M, Manfredi M, Mele F, Grande S, et al. Randomised controlled trial comparing laparoscopic and robot-assisted radical prostatectomy. European urology. 2013 Apr;63(4):606–14. Umari P, Eden C, Cahill D, Rizzo M, Eden D, Sooriakumaran P. Retzius-Sparing versus Standard Robot-Assisted Radical Prostatectomy: A Comparative Prospective Study of Nearly 500 Patients. The Journal of urology. 2021 Mar;205(3):780–90. Touijer AK, Guillonneau B. Laparoscopic radical prostatectomy. Urologic oncology. 2004 Mar-Apr;22(2):133-8. Rosen RC, Riley A, Wagner G, Osterloh IH, Kirkpatrick J, Mishra A. The international index of erectile function (IIEF): a multidimensional scale for assessment of erectile dysfunction. Urology. 1997 Jun;49(6):822–30. Dindo D, Demartines N, Clavien PA. Classification of surgical complications: a new proposal with evaluation in a cohort of 6336 patients and results of a survey. Annals of surgery. 2004 Aug;240(2):205–13. Carbonara U, Srinath M, Crocerossa F, Ferro M, Cantiello F, Lucarelli G, et al. Robot-assisted radical prostatectomy versus standard laparoscopic radical prostatectomy: an evidence-based analysis of comparative outcomes. World journal of urology. 2021 Apr 11. Johnson I, Ottosson F, Diep LM, Berg RE, Hoff JR, Wessel N, et al. Switching from laparoscopic radical prostatectomy to robot assisted laparoscopic prostatectomy: comparing oncological outcomes and complications. Scandinavian journal of urology. 2018 Apr;52(2):116–21. Papachristos A, Basto M, Te Marvelde L, Moon D. Laparoscopic versus robotic-assisted radical prostatectomy: an Australian single-surgeon series. ANZ J Surg. 2015 Mar;85(3):154–8. Hakimi AA, Blitstein J, Feder M, Shapiro E, Ghavamian R. Direct comparison of surgical and functional outcomes of robotic-assisted versus pure laparoscopic radical prostatectomy: single-surgeon experience. Urology. 2009 Jan;73(1):119–23. Menon M, Shrivastava A, Tewari A, Sarle R, Hemal A, Peabody JO, et al. Laparoscopic and robot assisted radical prostatectomy: establishment of a structured program and preliminary analysis of outcomes. The Journal of urology. 2002 Sep;168(3):945–9. Porpiglia F, Fiori C, Bertolo R, Manfredi M, Mele F, Checcucci E, et al. Five-year Outcomes for a Prospective Randomised Controlled Trial Comparing Laparoscopic and Robot-assisted Radical Prostatectomy. European urology focus. 2018 Jan;4(1):80–6. Yossepowitch O, Briganti A, Eastham JA, Epstein J, Graefen M, Montironi R, et al. Positive surgical margins after radical prostatectomy: a systematic review and contemporary update. European urology. 2014 Feb;65(2):303–13. Bravi CA, Tin A, Vertosick E, Mazzone E, Martini A, Dell'Oglio P, et al. The Impact of Experience on the Risk of Surgical Margins and Biochemical Recurrence after Robot-Assisted Radical Prostatectomy: A Learning Curve Study. The Journal of urology. 2019 Jul;202(1):108–13. Jo JK, Hong SK, Byun SS, Zargar H, Autorino R, Lee SE. Positive surgical margin in robot-assisted radical prostatectomy: correlation with pathology findings and risk of biochemical recurrence. Minerva urologica e nefrologica = The Italian journal of urology and nephrology. 2017 Oct;69(5):493–500. Zhang L, Wu B, Zha Z, Zhao H, Jiang Y, Yuan J. Positive surgical margin is associated with biochemical recurrence risk following radical prostatectomy: a meta-analysis from high-quality retrospective cohort studies. World journal of surgical oncology. 2018 Jul 3;16(1):124. Checcucci E, Veccia A, Fiori C, Amparore D, Manfredi M, Di Dio M, et al. Retzius-sparing robot-assisted radical prostatectomy vs the standard approach: a systematic review and analysis of comparative outcomes. BJU Int. 2020 Jan;125(1):8–16. Asimakopoulos AD, Topazio L, De Angelis M, Agrò EF, Pastore AL, Fuschi A, et al. Retzius-sparing versus standard robot-assisted radical prostatectomy: a prospective randomized comparison on immediate continence rates. Surgical endoscopy. 2019 Jul;33(7):2187–96. Heesakkers J, Farag F, Bauer RM, Sandhu J, De Ridder D, Stenzl A. Pathophysiology and Contributing Factors in Postprostatectomy Incontinence: A Review. European urology. 2017 Jun;71(6):936–44. Cite Share Download PDF Status: Posted Version 1 posted You are reading this latest preprint version Research Square lets you share your work early, gain feedback from the community, and start making changes to your manuscript prior to peer review in a journal. As a division of Research Square Company, we’re committed to making research communication faster, fairer, and more useful. We do this by developing innovative software and high quality services for the global research community. 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Also discoverable on Platform About Our Team In Review Editorial Policies Advisory Board Help Center Resources Author Services Accessibility API Access RSS feed Manage Cookie Preferences © Research Square 2026 | ISSN 2693-5015 (online) Privacy Policy Terms of Service Do Not Sell My Personal Information {"props":{"pageProps":{"initialData":{"identity":"rs-442704","acceptedTermsAndConditions":true,"allowDirectSubmit":true,"archivedVersions":[],"articleType":"Research","associatedPublications":[],"authors":[{"id":25197297,"identity":"ffd27d9d-d17c-4434-8027-54fc9d2bcddc","order_by":0,"name":"Deng Wen","email":"","orcid":"","institution":"First Affiliated Hospital of Nanchang University","correspondingAuthor":false,"submittingAuthor":false,"prefix":"","firstName":"Deng","middleName":"","lastName":"Wen","suffix":""},{"id":25197298,"identity":"b7afd323-f740-4044-b5d8-fa0a8cdde8b7","order_by":1,"name":"Zhang Cheng","email":"","orcid":"","institution":"First Affiliated Hospital of Nanchang University","correspondingAuthor":false,"submittingAuthor":false,"prefix":"","firstName":"Zhang","middleName":"","lastName":"Cheng","suffix":""},{"id":25197299,"identity":"6a82a619-d1d5-44a6-8f6b-6896fdd488df","order_by":2,"name":"Jiang Hao","email":"","orcid":"","institution":"First Affiliated Hospital of Nanchang University","correspondingAuthor":false,"submittingAuthor":false,"prefix":"","firstName":"Jiang","middleName":"","lastName":"Hao","suffix":""},{"id":25197300,"identity":"eecabc62-b6cd-4213-aab2-45064ddd2e64","order_by":3,"name":"Li Yulei","email":"","orcid":"","institution":"First Affiliated Hospital of Nanchang University","correspondingAuthor":false,"submittingAuthor":false,"prefix":"","firstName":"Li","middleName":"","lastName":"Yulei","suffix":""},{"id":25197301,"identity":"56b357b0-c61d-4c58-866f-d2e9ca003c23","order_by":4,"name":"Liu Xiaoqiang","email":"","orcid":"","institution":"First Affiliated Hospital of Nanchang University","correspondingAuthor":false,"submittingAuthor":false,"prefix":"","firstName":"Liu","middleName":"","lastName":"Xiaoqiang","suffix":""},{"id":25197302,"identity":"1f3b8723-6db3-4094-b586-43e1955499f2","order_by":5,"name":"Chen Luyao","email":"","orcid":"","institution":"First Affiliated Hospital of Nanchang University","correspondingAuthor":false,"submittingAuthor":false,"prefix":"","firstName":"Chen","middleName":"","lastName":"Luyao","suffix":""},{"id":25197303,"identity":"69cda187-4e51-4fe8-aea3-50a456317cbd","order_by":6,"name":"Liu Weipeng","email":"","orcid":"","institution":"First Affiliated Hospital of Nanchang University","correspondingAuthor":false,"submittingAuthor":false,"prefix":"","firstName":"Liu","middleName":"","lastName":"Weipeng","suffix":""},{"id":25197304,"identity":"d60777aa-71f8-4e0d-811f-34bbbc3dc41b","order_by":7,"name":"Zhou Xiaochen","email":"","orcid":"","institution":"First Affiliated Hospital of Nanchang University","correspondingAuthor":false,"submittingAuthor":false,"prefix":"","firstName":"Zhou","middleName":"","lastName":"Xiaochen","suffix":""},{"id":25197305,"identity":"1dec6203-38ab-4533-8871-9a40323f2eba","order_by":8,"name":"Sun Ting","email":"","orcid":"","institution":"First Affiliated Hospital of Nanchang University","correspondingAuthor":false,"submittingAuthor":false,"prefix":"","firstName":"Sun","middleName":"","lastName":"Ting","suffix":""},{"id":25197306,"identity":"01def46a-d620-4029-b6e6-3613ba3b1ca6","order_by":9,"name":"Wang Gongxian","email":"","orcid":"","institution":"First Affiliated Hospital of Nanchang University","correspondingAuthor":false,"submittingAuthor":false,"prefix":"","firstName":"Wang","middleName":"","lastName":"Gongxian","suffix":""},{"id":25197307,"identity":"bdca6ec4-c5af-4384-9c42-20722dc18a3d","order_by":10,"name":"Bin Fu","email":"data:image/png;base64,iVBORw0KGgoAAAANSUhEUgAAAZAAAAAyAQMAAABI0h/eAAAABlBMVEX///8AAABVwtN+AAAACXBIWXMAAA7EAAAOxAGVKw4bAAAAqElEQVRIiWNgGAWjYJCCzwwGDHJs7O0HiNbBOBuoxZiP50wCKVoYGBLnSTgYEKfe4Pbhg80FBXfS2yQYEhh+VGwjQsu5tMTmGQbPctukGw8w9py5TYSWMzzmj3kMDue2yRxIYGZsI06LYTNQSzqbRIIBaVoSiNcieYYN5JfDhm3AQD5IlF/4zjADQ+zPYXn59vaDD35UEKEFBRwgUf0oGAWjYBSMAlwAAM1XO23AOr/ZAAAAAElFTkSuQmCC","orcid":"","institution":"First Affiliated Hospital of Nanchang University","correspondingAuthor":true,"submittingAuthor":false,"prefix":"","firstName":"Bin","middleName":"","lastName":"Fu","suffix":""}],"badges":[],"createdAt":"2021-04-20 10:43:18","currentVersionCode":1,"declarations":"","doi":"10.21203/rs.3.rs-442704/v1","doiUrl":"https://doi.org/10.21203/rs.3.rs-442704/v1","draftVersion":[],"editorialEvents":[],"editorialNote":"","failedWorkflow":false,"files":[{"id":8935751,"identity":"a0f6ac2a-5d3c-41c0-a900-669b07ee330c","added_by":"auto","created_at":"2021-05-07 20:46:27","extension":"png","order_by":1,"title":"Figure 1","display":"","copyAsset":false,"role":"figure","size":17292,"visible":true,"origin":"","legend":"Kaplan–Meier curves showing biochemical recurrence‑free survival for patients undergoing robot-assisted and laparoscopic radical prostatectomy over the follow-up durations.","description":"","filename":"Figure1.png","url":"https://assets-eu.researchsquare.com/files/rs-442704/v1/319e2ab2476cb262e04ffcda.png"},{"id":8935700,"identity":"cea2532b-b54e-4046-a59e-f8cff76ea50e","added_by":"auto","created_at":"2021-05-07 20:43:27","extension":"png","order_by":2,"title":"Figure 2","display":"","copyAsset":false,"role":"figure","size":17218,"visible":true,"origin":"","legend":"Kaplan–Meier curves showing the proportion of urinary continence (UC) in patients undergoing robot-assisted and laparoscopic radical prostatectomy over the follow-up durations. UC was defined as requiring no pad or preventively using one dry pad per day.","description":"","filename":"Figure2.png","url":"https://assets-eu.researchsquare.com/files/rs-442704/v1/8ca86feb95643c2dc56a287c.png"},{"id":13691461,"identity":"a668a6f8-b20b-48e7-b89a-2a21b7dc4860","added_by":"auto","created_at":"2021-09-17 12:38:50","extension":"pdf","order_by":0,"title":"","display":"","copyAsset":false,"role":"manuscript-pdf","size":336668,"visible":true,"origin":"","legend":"","description":"","filename":"manuscript.pdf","url":"https://assets-eu.researchsquare.com/files/rs-442704/v1/b9355b19-3780-438d-91bb-85ed6bbaba51.pdf"}],"financialInterests":"","formattedTitle":"\u003cp\u003eRobot-Assisted vs. Laparoscopic Radical Prostatectomy for Immediate- and High-Risk Localized Prostate Cancer: A Propensity-Score Matched Analysis\u003c/p\u003e","fulltext":[{"header":"Background","content":" \u003cp\u003eProstate cancer (PCa), the second most common cancer and the fifth dominating cause of cancer-specific mortality among men around the world (\u003cspan citationid=\"CR1\" class=\"CitationRef\"\u003e1\u003c/span\u003e), is increasingly been discovered due to the widespread diffusion of prostate specific antigen (PSA) screening, markedly the localized ones (\u003cspan citationid=\"CR2\" class=\"CitationRef\"\u003e2\u003c/span\u003e, \u003cspan citationid=\"CR3\" class=\"CitationRef\"\u003e3\u003c/span\u003e). Given the slowly evolving nature of localized prostate tumors, it is of great significance to distinguish PCa destined to cause clinical symptoms or metastases from more clinically indolent PCa that is highly unlikely to impact survival to reduce overtreatment in patients with PCa without compromising opportunities for cure. The D'Amico risk classifications proposed on the basis of clinical and pathological characteristics including the clinical stage, PSA, and biopsy Gleason score have been widely endorsed worldwide (\u003cspan citationid=\"CR3\" class=\"CitationRef\"\u003e3\u003c/span\u003e). The role of radical prostatectomy (RP) in managing D'Amico low-risk PCa is in doubt due to the similar survival benefit of patients with low-risk localized PCa following immediate radical treatment and active surveillance and RP-related harms to quality of life (\u003cspan additionalcitationids=\"CR4\" citationid=\"CR3\" class=\"CitationRef\"\u003e3\u003c/span\u003e\u0026ndash;\u003cspan citationid=\"CR5\" class=\"CitationRef\"\u003e5\u003c/span\u003e), whilst RP has a tendency towards a better survival benefit over watchful waiting for immediate-risk localized PCa (\u003cspan citationid=\"CR4\" class=\"CitationRef\"\u003e4\u003c/span\u003e, \u003cspan citationid=\"CR6\" class=\"CitationRef\"\u003e6\u003c/span\u003e, \u003cspan citationid=\"CR7\" class=\"CitationRef\"\u003e7\u003c/span\u003e) and 10-year PCa-specific survival rates after RP coupled with node dissection were generally over 90% and remarkably consistent across all large studies focusing on high-risk PCa (\u003cspan citationid=\"CR8\" class=\"CitationRef\"\u003e8\u003c/span\u003e). In 2020, surgery is not recommended in those patients with low-grade, low-volume Gleason 6 PCa in consideration of the little clinical benefit and considerable adverse effects following surgery, while RP is considered appropriate for men with intermediate- and high-risk disease (\u003cspan citationid=\"CR9\" class=\"CitationRef\"\u003e9\u003c/span\u003e).\u003c/p\u003e \u003cp\u003eWith the superiority of surgical robots in three-dimensional magnified vision of the surgical field, improved dexterity, and higher precision during the surgical procedure, robot-assisted RP (RARP) is considered as a great evolution of minimally invasive surgery to reduce the difficulty associated with complex laparoscopic surgery (\u003cspan citationid=\"CR10\" class=\"CitationRef\"\u003e10\u003c/span\u003e) and has been widely disseminated for localized PCa since 2001 (\u003cspan citationid=\"CR11\" class=\"CitationRef\"\u003e11\u003c/span\u003e). However, thus far, whether the advantages of RARP over laparoscopic RP (LRP) mentioned above could translate into superior functional preservation and oncological control was still inconclusive due to the scarcity of high-level evidence comparing RARP and LRP for localized PCa (\u003cspan citationid=\"CR10\" class=\"CitationRef\"\u003e10\u003c/span\u003e, \u003cspan citationid=\"CR12\" class=\"CitationRef\"\u003e12\u003c/span\u003e). There are only three randomized controlled trials (RCTs) concentrating on comparing RARP and LRP for localized PCa with different endpoints over the short-term study periods (\u003cspan additionalcitationids=\"CR14\" citationid=\"CR13\" class=\"CitationRef\"\u003e13\u003c/span\u003e\u0026ndash;\u003cspan citationid=\"CR15\" class=\"CitationRef\"\u003e15\u003c/span\u003e), which is far from reaching a convincing consensus about the controversy. What\u0026rsquo;s worse, no study focusing on comparing RARP and LRP for patients with immediate- and high-risk localized PCa has been reported yet, while the cogent evidence comparing the efficacy and safety of RARP and LRP for immediate- and high-risk localized PCa is of great clinical importance.\u003c/p\u003e \u003cp\u003eTo close this gap of cogent evidence concerning the functional and oncological efficacy of RARP and LRP for immediate- and high-risk localized PCa, we designed this first analysis comparing RARP and LRP for immediate- and high-risk localized PCa in an attempt to document differences in the perioperative, functional and oncological outcomes obtained after the two techniques in a retrospective fashion.\u003c/p\u003e "},{"header":"Methods","content":" \u003cp\u003e Having obtained the approval of the Ethnic Committee of the First Affiliated Hospital of Nanchang University, we meticulously reviewed our prospectively maintained database to retrospectively gather all the demographic, clinical, and pathologic information of patients harbouring localized PCa between January 2016 and October 2019. All patients with PCa were screened and incorporated into the final analysis on the grounds of the following eligibility criteria: (\u003cspan citationid=\"CR1\" class=\"CitationRef\"\u003e1\u003c/span\u003e) total serum PSA\u0026thinsp;\u0026ge;\u0026thinsp;10 ng/mL or Gleason score\u0026thinsp;\u0026ge;\u0026thinsp;7 or localized T2b or T2c stage; (\u003cspan citationid=\"CR2\" class=\"CitationRef\"\u003e2\u003c/span\u003e) patients undergoing RARP or LRP for localized PCa; (\u003cspan citationid=\"CR3\" class=\"CitationRef\"\u003e3\u003c/span\u003e) no evidence of clinical positive lymph nodes or clinical T3-4 stage. Only when the case simultaneously satisfied all these inclusion criteria were the men included, whilst the others were excluded from our study. On the basis of inclusion criteria described above, included in the final analysis were 232 patients, of whom 137 and 95 patients were divided by surgical approaches into the RARP and LRP arms, respectively, and none of them had a history of abdominal surgery. Prostate magnetic resonance imaging and bone scintigraphy were routinely performed in all patients before surgeries.\u003c/p\u003e \u003cp\u003eAll surgeries were conducted with the anterior approach by three highly experienced hands (Fu B, Wang GX, and Sun T). Prior to this study initiation, each of these three surgeons had performed more than 300 LRPs and 100 RARPs as an operator or a trainee. The patients\u0026rsquo; assignment was usually at the discretion of these four highly experienced surgeons according to tumor and patient characteristics. The written informed consent was acquired from each patient in both groups. The anterior approach to RARP was done according to the techniques established by Menon et al. (\u003cspan citationid=\"CR16\" class=\"CitationRef\"\u003e16\u003c/span\u003e), while the anterior approach to LRP was completed following the surgical steps described by Touijer et al. (\u003cspan citationid=\"CR17\" class=\"CitationRef\"\u003e17\u003c/span\u003e). Pelvic lymph node dissection (PLND) was routinely done in all high-risk patients and those immediate-risk cases with a preoperative estimated risk exceeding 5% in nodal involvement, while the nodal dissection could be omitted at a low risk of missing positive nodes in other immediate-risk men. A standardized extended PLND (ePLND) template with the upper margin being the common iliac artery was closely observed when performing all these lymph node dissections. Nerve sparing was preoperatively proposed according to clinical features and intraoperatively modified based on evidence of bundle invasion.\u003c/p\u003e \u003cp\u003eBaseline demographics and clinical elements (age, body mass index [BMI], diabetes mellitus, hypertension, American Society of Anesthesiologists [ASA] score, preoperative total PSA, preoperative erectile function quantified in accordance with the International Index of Erectile Function [IIEF]-5 score (\u003cspan citationid=\"CR18\" class=\"CitationRef\"\u003e18\u003c/span\u003e), and risk stratification assessed with D'Amico risk classifications (\u003cspan citationid=\"CR3\" class=\"CitationRef\"\u003e3\u003c/span\u003e)) and preoperative tumor characteristics (clinical TNM stage, biopsy Gleason score, and prostate volume calculated by the virtue of transrectal ultrasound) were extracted from the database.\u003c/p\u003e \u003cp\u003eData with regard to perioperative outcomes (operative time [OT], estimated blood loss [EBL], ePLND, nerve sparing procedure, open conversion, transfusion, postoperative hospital stay, and postoperative complications evaluated with Clavien-Dindo classification (\u003cspan citationid=\"CR19\" class=\"CitationRef\"\u003e19\u003c/span\u003e)) and pathologic results (pathological T stage, specimen Gleason score, positive surgical margin [PSM] which were defined as tumor extending to the inked-surface of prostate specimen, and positive lymph node) was also retrieved from our database. Information about postoperative complications could also be collected via chart reviews or face-to-face and telephone interviews.\u003c/p\u003e \u003cp\u003eThe median postoperative follow-up length for the RARP and LRP groups was 29 and 23 months, respectively. Postoperative follow-up was regularly arranged every 3 months within the first year after surgery and every 6 months since the second year after surgery for each patient. Each case routinely underwent postoperative PSA tests every 3 months to monitor biochemical recurrence (BCR), which was considered as the occurrence after prostatectomy that two consecutive rising serum PSA measured on two separate occasions was 0.2 ng/mL or greater. UC was defined by the use of \u0026le;\u0026thinsp;one dry pad over the 24-hour period. The total PSA level and erectile function score were reported at postoperative 6 months and last follow-up, while the rate of UC recovery were presented at the removal of catheter, postoperative 6 months, and last follow-up.\u003c/p\u003e \u003cp\u003ePropensity-score matching (PM) method was employed to impose restrictions on significant differences in preoperative clinical and tumor characteristics. The propensity score was calculated with non-parsimonious multivariate logistic regression on the basis of all preoperative variables, namely, age, BMI, diabetes mellitus, hypertension, ASA score, preoperative total PSA, preoperative IIEF-5 score, clinical TNM stage, biopsy Gleason score, and prostate volume. Finally, except for 10 patients missing an appropriate pair, all the remaining cases in the LRP arm were successfully matched to 85 patients in the RARP group using a 1:1 ratio with the nearest neighbour pairing method. All differences before and after PM in preoperative elements were analyzed between the RARP and LRP arms with the independent t-test or the Pearson chi-squared test being utilized.\u003c/p\u003e \u003cp\u003eAll non-normally distributed continuous variables were presented as median and interquartile range and compared using the Wilcoxon rank-sum test, whilst those in a normally distributed fashion were presented as mean and standard deviation and analyzed with the independent t-test. All categorical variables were presented as proportion and percentages and calculated with the Pearson chi-squared test or the Fisher\u0026rsquo;s exact test being used. The Kaplan\u0026ndash;Meier method was employed to estimate BCR-free survival probabilities and the proportions of postoperative return to UC with the log-rank test. All statistical analyses were conducted on STATA version 12.0 (STATA corp., College Station, TX), and the statistical significance was defined a two-sided \u003cem\u003ep\u003c/em\u003e value of \u0026lt;\u0026thinsp;0.05.\u003c/p\u003e "},{"header":"Results","content":"\u003cp\u003eAll preoperative information concerning the clinical and tumor characteristics before and after PM was detailedly described in Table\u0026nbsp;\u003cspan class=\"InternalRef\"\u003e1\u003c/span\u003e. In all, 232 patients with primary immediate- and high-risk localized PCa in line with the inclusion criteria, comprising 137 RARPs and 95 LRPs, were enrolled in this analysis over the study period being reviewed. Before the PM, the RARP group was significantly corrected with a lower mean age (65.4 vs. 68.0 years, \u003cem\u003ep\u003c/em\u003e\u0026thinsp;=\u0026thinsp;0.010), higher mean BMI (23.2 vs. 22.2 kg/m\u003csup\u003e2\u003c/sup\u003e, \u003cem\u003ep\u003c/em\u003e\u0026thinsp;=\u0026thinsp;0.044), smaller mean prostate volume (38.4 vs. 43.9 mL, \u003cem\u003ep\u003c/em\u003e\u0026thinsp;=\u0026thinsp;0.001), higher median preoperative IIEF-5 score (17 vs. 15, \u003cem\u003ep\u003c/em\u003e\u0026thinsp;=\u0026thinsp;0.011), and lower median biopsy Gleason score (6 vs. 7, \u003cem\u003ep\u003c/em\u003e\u0026thinsp;=\u0026thinsp;0.020) than the LRP group, while no significant differences in other preoperative variables existed between the two arms. All these significant differences in preoperative variables disappeared within the well-balanced matched cohorts after applying the PM method (Table\u0026nbsp;\u003cspan class=\"InternalRef\"\u003e1\u003c/span\u003e).\u003c/p\u003e\n\u003cdiv class=\"gridtable\"\u003e\n\u003ctable id=\"Tab1\" border=\"1\"\u003e\u003ccaption\u003e\n\u003cdiv class=\"CaptionNumber\"\u003eTable 1\u003c/div\u003e\n\u003cdiv class=\"CaptionContent\"\u003e\n\u003cp\u003ePreoperative characteristics by surgery type before and after propensity score matching.\u003c/p\u003e\n\u003c/div\u003e\n\u003c/caption\u003e\n\u003cthead\u003e\n\u003ctr\u003e\n\u003cth rowspan=\"2\" align=\"left\"\u003e\n\u003cp\u003eVariable\u003c/p\u003e\n\u003c/th\u003e\n\u003cth colspan=\"3\" align=\"left\"\u003e\n\u003cp\u003eBefore propensity score matching\u003c/p\u003e\n\u003c/th\u003e\n\u003cth colspan=\"3\" align=\"left\"\u003e\n\u003cp\u003eAfter propensity score matching\u003c/p\u003e\n\u003c/th\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003cth align=\"left\"\u003e\n\u003cp\u003eRARP (\u003cem\u003en\u003c/em\u003e\u0026thinsp;=\u0026thinsp;137)\u003c/p\u003e\n\u003c/th\u003e\n\u003cth align=\"left\"\u003e\n\u003cp\u003eLRP (\u003cem\u003en\u003c/em\u003e\u0026thinsp;=\u0026thinsp;95)\u003c/p\u003e\n\u003c/th\u003e\n\u003cth align=\"left\"\u003e\n\u003cp\u003e\u003cem\u003ep\u003c/em\u003e value\u003c/p\u003e\n\u003c/th\u003e\n\u003cth align=\"left\"\u003e\n\u003cp\u003eRARP (\u003cem\u003en\u003c/em\u003e\u0026thinsp;=\u0026thinsp;85)\u003c/p\u003e\n\u003c/th\u003e\n\u003cth align=\"left\"\u003e\n\u003cp\u003eLRP (\u003cem\u003en\u003c/em\u003e\u0026thinsp;=\u0026thinsp;85)\u003c/p\u003e\n\u003c/th\u003e\n\u003cth align=\"left\"\u003e\n\u003cp\u003e\u003cem\u003ep\u003c/em\u003e value\u003c/p\u003e\n\u003c/th\u003e\n\u003c/tr\u003e\n\u003c/thead\u003e\n\u003ctbody\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003eAge, years, mean (SD)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e65.4 (7.3)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e68.0 (7.3)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.010\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e65.5 (7.3)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e67.2 (7.2)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.138\u003c/p\u003e\n\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003eBMI, kg/m2, mean (SD)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e23.2 (3.5)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e22.2 (3.8)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.044\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e23.1 (3.6)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e22.7 (3.8)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.482\u003c/p\u003e\n\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003eDiabetes mellitus (yes), n (%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e17 (13.4%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e15 (15.8%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.614\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e12 (14.1%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e14 (16.5%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.670\u003c/p\u003e\n\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003eHypertension (yes), n (%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e33 (26.0%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e23 (24.2%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.763\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e22 (25.9%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e20 (23.5%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.722\u003c/p\u003e\n\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003eASA score (\u0026ge;\u0026thinsp;3), n (%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e7 (5.5%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e7 (7.4%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.573\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e4 (4.7%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e5 (5.9%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e1.000\u003c/p\u003e\n\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003ePreoperative total PSA, ng/mL, mean (SD)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e25.7 (25.5)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e26.6 (26.9)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.795\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e27.5 (27.9)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e26.6 (28.1)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.834\u003c/p\u003e\n\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003eProstate volume, mL, mean (SD)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e38.4 (10.6)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e43.9 (13.0)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.001\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e39.7 (10.8)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e42.8 (13.0)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.093\u003c/p\u003e\n\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003ePreoperative IIEF-5 score, median (IQR)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e17 (14, 19)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e15 (13, 18)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.011\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e18 (14.3, 19)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e16 (13, 18.75)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.113\u003c/p\u003e\n\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003ecTNM stage, n (%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\u0026nbsp;\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\u0026nbsp;\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.365\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\u0026nbsp;\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\u0026nbsp;\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.385\u003c/p\u003e\n\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003eT1-T2a\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e52 (41.0%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e48 (50.5%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\u0026nbsp;\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e37 (43.5%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e46 (54.1%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\u0026nbsp;\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003eT2b\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e46 (36.2%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e29 (30.5%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\u0026nbsp;\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e31 (36.5%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e25 (29.4%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\u0026nbsp;\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003eT2c\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e29 (22.8%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e18 (19.0%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\u0026nbsp;\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e17 (20.0%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e14 (16.5%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\u0026nbsp;\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003eBiopsy Gleason score, median (IQR)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e6 (5, 8)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e7 (6, 8)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.020\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e7 (5.75, 8)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e7 (6, 8)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.214\u003c/p\u003e\n\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003eHigh risk \u003csup\u003e┿\u003c/sup\u003e, n (%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e62 (45.3%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e53 (55.8%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.115\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e43 (50.6%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e46 (54.1%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.645\u003c/p\u003e\n\u003c/td\u003e\n\u003c/tr\u003e\n\u003c/tbody\u003e\n\u003c/table\u003e\n\u003cp\u003eSD: standard deviation; BMI: body mass index; ASA: American Society of Anesthesiologists; IIEF: International Index of Erectile Function; IQR: inter-quartile range.\u003c/p\u003e\n\u003cp\u003e\u003csup\u003e┿\u003c/sup\u003e according to the D'Amico risk classifications\u003c/p\u003e\n\u003c/div\u003e\n\u003cp\u003eTable\u0026nbsp;\u003cspan class=\"InternalRef\"\u003e2\u003c/span\u003e delineated the perioperative and pathological outcomes in detail. Within the matched settings, no surgery was converted to an open approach in either arm. Patients in the RARP group had a significantly shorter mean OT than those in the LRP group (146.0 vs. 167.9 min, \u003cem\u003ep\u003c/em\u003e\u0026thinsp;\u0026lt;\u0026thinsp;0.001), but no significant difference in the mean EBL was found between the two groups (152.6 vs. 166.4 mL, \u003cem\u003ep\u003c/em\u003e\u0026thinsp;=\u0026thinsp;0.200). 55 (64.7%) and 50 (58.8%) cases underwent ePLND in the RARP and LRP groups, respectively (\u003cem\u003ep\u003c/em\u003e\u0026thinsp;=\u0026thinsp;0.430), while nerve sparing technique was more frequently completed in patients undergoing RARP than those with LRP (48.2% vs. 32.9%, \u003cem\u003ep\u003c/em\u003e\u0026thinsp;=\u0026thinsp;0.042). There were no significant differences in the probability of transfusion and \u0026gt;\u0026thinsp;Grade II postoperative complications between the two groups (\u003cem\u003ep\u003c/em\u003e\u0026thinsp;=\u0026thinsp;0.192 and \u003cem\u003ep\u003c/em\u003e\u0026thinsp;=\u0026thinsp;1.000, respectively). The distributions of pathologic T2 and T3 disease were comparable among the RARP and LRP groups (\u003cem\u003ep\u003c/em\u003e\u0026thinsp;=\u0026thinsp;0.345), and the comparability between the two groups remained with regard to the median specimen Gleason score and hospital stay length (\u003cem\u003ep\u003c/em\u003e\u0026thinsp;=\u0026thinsp;0.179 and \u003cem\u003ep\u003c/em\u003e\u0026thinsp;=\u0026thinsp;0.563, respectively). The occurrence rates of PSM and positive lymph node were also statistically similar between the RARP and LRP arms (\u003cem\u003ep\u003c/em\u003e\u0026thinsp;=\u0026thinsp;0.260 and \u003cem\u003ep\u003c/em\u003e\u0026thinsp;=\u0026thinsp;0.501, respectively). However, patients in the LRP group had a tendency towards a higher incidence of \u0026le;\u0026thinsp;Grade II complications than those in the RARP group (\u003cem\u003ep\u003c/em\u003e\u0026thinsp;=\u0026thinsp;0.036).\u003c/p\u003e\n\u003cdiv class=\"gridtable\"\u003e\n\u003ctable id=\"Tab2\" border=\"1\"\u003e\u003ccaption\u003e\n\u003cdiv class=\"CaptionNumber\"\u003eTable 2\u003c/div\u003e\n\u003cdiv class=\"CaptionContent\"\u003e\n\u003cp\u003ePerioperative outcomes for RARP and LRP after propensity score matching.\u003c/p\u003e\n\u003c/div\u003e\n\u003c/caption\u003e\n\u003cthead\u003e\n\u003ctr\u003e\n\u003cth align=\"left\"\u003e\n\u003cp\u003eVariable\u003c/p\u003e\n\u003c/th\u003e\n\u003cth align=\"left\"\u003e\n\u003cp\u003eRARP (\u003cem\u003en\u003c/em\u003e\u0026thinsp;=\u0026thinsp;85)\u003c/p\u003e\n\u003c/th\u003e\n\u003cth align=\"left\"\u003e\n\u003cp\u003eLRP (\u003cem\u003en\u003c/em\u003e\u0026thinsp;=\u0026thinsp;85)\u003c/p\u003e\n\u003c/th\u003e\n\u003cth align=\"left\"\u003e\n\u003cp\u003e\u003cem\u003ep\u003c/em\u003e value\u003c/p\u003e\n\u003c/th\u003e\n\u003c/tr\u003e\n\u003c/thead\u003e\n\u003ctbody\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003eOperative time, min, mean (SD)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e146.0 (40.4)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e167.9 (34.2)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e\u0026lt;\u0026thinsp;0.001\u003c/p\u003e\n\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003eEstimated blood loss, mL, mean (SD)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e152.6 (60.5)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e166.4 (78.2)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.200\u003c/p\u003e\n\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003eePLND, n (%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e55 (64.7%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e50 (58.8%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.430\u003c/p\u003e\n\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003eNerve sparing procedures, n (%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e41 (48.2%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e28 (32.9%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.042\u003c/p\u003e\n\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003eOpen conversion, n (%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0 (0%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0 (0%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e-\u003c/p\u003e\n\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003eTransfusion, n (%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e3 (3.5%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e7 (8.2%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.192\u003c/p\u003e\n\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003ePostoperative pathology\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\u0026nbsp;\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\u0026nbsp;\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\u0026nbsp;\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003ePathological T stage, n (%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\u0026nbsp;\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\u0026nbsp;\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.345\u003c/p\u003e\n\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003epT2\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e49 (57.6%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e55 (64.7%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\u0026nbsp;\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003epT3\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e36 (42.4%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e30 (35.3%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\u0026nbsp;\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003eSpecimen Gleason score, median (IQR)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e7 (5.5, 8)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e7 (6, 8)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.179\u003c/p\u003e\n\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003ePositive surgical margin, n (%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e15 (17.6%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e21 (24.7%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.260\u003c/p\u003e\n\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003ePositive lymph nodes, n (%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e13 (15.3%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e10 (11.8%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.501\u003c/p\u003e\n\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003ePostoperative complications, n (%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e8 (9.4%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e18 (21.2%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.033\u003c/p\u003e\n\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e\u0026le; Grade II complications\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e6 (7.1%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e15 (17.6%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.036\u003c/p\u003e\n\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e\u0026gt; Grade II complications\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e2 (2.4%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e3 (3.5%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e1.000\u003c/p\u003e\n\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003eHospital stay, days, median (IQR)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e14 (14, 15)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e15 (14, 15)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.563\u003c/p\u003e\n\u003c/td\u003e\n\u003c/tr\u003e\n\u003c/tbody\u003e\n\u003c/table\u003e\n\u003cp\u003eePLND: extended pelvic lymph nodes dissection; SD: standard deviation; IQR: inter-quartile range.\u003c/p\u003e\n\u003c/div\u003e\n\u003cp\u003eWithin the matched cohort, median follow-up durations after RARP and LRP were 29 and 23 months, respectively. As shown in Table\u0026nbsp;\u003cspan class=\"InternalRef\"\u003e3\u003c/span\u003e, no significant differences were detected between the two groups in terms of the mean total serum PSA at postoperative 6 months and last follow-up (\u003cem\u003ep\u003c/em\u003e\u0026thinsp;=\u0026thinsp;546 and \u003cem\u003ep\u003c/em\u003e\u0026thinsp;=\u0026thinsp;0.688, respectively). The appearances of BCR have happened in 8 and 11 patients following RARP and LRP, respectively, over the periods covered by the follow-ups. The likelihoods of BCR-free survivals of immediate- and high-risk patients following RARP and LRP were also statistically similar after matching (\u003cem\u003ep\u003c/em\u003e\u0026thinsp;=\u0026thinsp;0.228) (Figure. 1).\u003c/p\u003e\n\u003cdiv class=\"gridtable\"\u003e\n\u003ctable id=\"Tab3\" border=\"1\"\u003e\u003ccaption\u003e\n\u003cdiv class=\"CaptionNumber\"\u003eTable 3\u003c/div\u003e\n\u003cdiv class=\"CaptionContent\"\u003e\n\u003cp\u003ePostoperative outcomes for RARP and LRP after propensity score matching.\u003c/p\u003e\n\u003c/div\u003e\n\u003c/caption\u003e\n\u003cthead\u003e\n\u003ctr\u003e\n\u003cth align=\"left\"\u003e\n\u003cp\u003eVariable\u003c/p\u003e\n\u003c/th\u003e\n\u003cth align=\"left\"\u003e\n\u003cp\u003eRARP (\u003cem\u003en\u003c/em\u003e\u0026thinsp;=\u0026thinsp;85)\u003c/p\u003e\n\u003c/th\u003e\n\u003cth align=\"left\"\u003e\n\u003cp\u003eLRP (\u003cem\u003en\u003c/em\u003e\u0026thinsp;=\u0026thinsp;85)\u003c/p\u003e\n\u003c/th\u003e\n\u003cth align=\"left\"\u003e\n\u003cp\u003e\u003cem\u003ep\u003c/em\u003e value\u003c/p\u003e\n\u003c/th\u003e\n\u003c/tr\u003e\n\u003c/thead\u003e\n\u003ctbody\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003eOncology: postoperative total PSA, ng/mL\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\u0026nbsp;\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\u0026nbsp;\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\u0026nbsp;\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003ePostoperative 6 months, mean (SD)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.053 (0.062)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.047 (0.078)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.546\u003c/p\u003e\n\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003eLast follow-up, mean (SD)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.218 (0.955)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.280 (1.021)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.688\u003c/p\u003e\n\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003eUrinary continence\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\u0026nbsp;\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\u0026nbsp;\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\u0026nbsp;\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003eContinent on removal of catheter, n (%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e33 (38.8%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e20 (23.5%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.031\u003c/p\u003e\n\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003eContinent at 6 months, n (%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e66 (77.6%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e54 (63.5%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.043\u003c/p\u003e\n\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003eContinent at last follow-up, n (%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e80 (94.1%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e72 (84.7%)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.046\u003c/p\u003e\n\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003eErectile function\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\u0026nbsp;\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\u0026nbsp;\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\u0026nbsp;\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003eIIEF-5 score at postoperative 6 month, median (IQR)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e14 (12, 16)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e12 (11, 15)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.013\u003c/p\u003e\n\u003c/td\u003e\n\u003c/tr\u003e\n\u003ctr\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003eIIEF-5 score at last follow-up, median (IQR)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e14 (11, 16)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e12 (11, 14)\u003c/p\u003e\n\u003c/td\u003e\n\u003ctd align=\"left\"\u003e\n\u003cp\u003e0.009\u003c/p\u003e\n\u003c/td\u003e\n\u003c/tr\u003e\n\u003c/tbody\u003e\n\u003c/table\u003e\n\u003cp\u003ePSA: prostate specific antigen; SD: standard deviation; IIEF: International Index of Erectile Function; IQR: inter-quartile range.\u003c/p\u003e\n\u003c/div\u003e\n\u003cp\u003eThe Foley catheter was routinely removed at postoperative 2 weeks regardless of the surgical approach. As described in Table\u0026nbsp;\u003cspan class=\"InternalRef\"\u003e3\u003c/span\u003e, the proportions of patients reporting UC recovery at the moment of removing catheter (38.8% vs. 23.5%, \u003cem\u003ep\u003c/em\u003e\u0026thinsp;=\u0026thinsp;0.031), postoperative 6 months (77.6% vs. 63.5%, \u003cem\u003ep\u003c/em\u003e\u0026thinsp;=\u0026thinsp;0.043), and last follow-up (94.1% vs. 84.7%, \u003cem\u003ep\u003c/em\u003e\u0026thinsp;=\u0026thinsp;0.046) in the RARP group were significantly higher than that in the LRP group. Intriguingly, the difference in postoperative UC recovery obtained following RARP and LRP was gradually alleviated and close to be out of statistical significance. The patients in the RARP group achieved a significantly higher cumulative proportion of postoperative return to UC than those following LRP (\u003cem\u003ep\u003c/em\u003e\u0026thinsp;=\u0026thinsp;0.011) (Figure. 2).\u003c/p\u003e\n\u003cp\u003eAs presented in Table\u0026nbsp;\u003cspan class=\"InternalRef\"\u003e3\u003c/span\u003e, within the matched cohort, significant differences were also revealed between the RARP and LRP groups with respect to the median IIEF-5 score at postoperative 6 months and last follow-up (\u003cem\u003ep\u003c/em\u003e\u0026thinsp;=\u0026thinsp;0.013 and \u003cem\u003ep\u003c/em\u003e\u0026thinsp;=\u0026thinsp;0.009, respectively), exhibiting the superiority of RARP over LRP in erectile functional protection for men with immediate- and high-risk PCa.\u003c/p\u003e"},{"header":"Discussion","content":" \u003cp\u003eGiven the limited overall survival benefits and considerable adverse events after RP for D'Amico low-risk PCa, the role of RP in managing D'Amico low-risk PCa remains highly contentious (\u003cspan citationid=\"CR3\" class=\"CitationRef\"\u003e3\u003c/span\u003e, \u003cspan citationid=\"CR4\" class=\"CitationRef\"\u003e4\u003c/span\u003e). While RP for D'Amico immediate- and high-risk PCa could achieve favorable survival benefits from preventing further metastatic seeding of potentially lethal clones of PCa cells (\u003cspan citationid=\"CR9\" class=\"CitationRef\"\u003e9\u003c/span\u003e). In 2020, RP is widely perceived as appropriate for men with intermediate-risk and high-risk PCa rather than those bearing D'Amico low-risk PCa (\u003cspan citationid=\"CR9\" class=\"CitationRef\"\u003e9\u003c/span\u003e). Although RARP has been widely diffused for surgically handling localized PCa, the paucity of high-level evidence still triggers the controversy on the impacts of RARP and LRP on oncological and functional outcomes obtained after surgery. What\u0026rsquo;s worse, there has been no study which was immersed in comparing RARP and LRP for intermediate-risk and high-risk PCa up to now, while the cogent evidence concerning the functional and oncological efficacy of RARP and LRP for immediate- and high-risk localized PCa is of great clinical importance.\u003c/p\u003e \u003cp\u003eIn this content, we designed this retrospective study which is the first one comparing RARP and LRP for immediate- and high-risk PCa. To eliminate the influences of any significant differences in any preoperative factors and selection bias, we rigorously utilized the PM method to guarantee the similarity in all preoperative parameters between the two groups. Within the well-balanced matched cohort, our results revealed the superiority of RARP in functional preservation coupled with fewer postoperative\u0026thinsp;\u0026le;\u0026thinsp;Grade II complications than LRP without cancer control being compromised for managing immediate- and high-risk PCa.\u003c/p\u003e \u003cp\u003eAs regards the extended mean OT in the LRP group, this significant difference may be attributable to the fact that the robotic platform facilitates suturing, one of the most challenging procedures during the standard laparoscopic approach (\u003cspan citationid=\"CR20\" class=\"CitationRef\"\u003e20\u003c/span\u003e), and this advantage is even more obvious when comparing RARP and LRP for the immediate- and high-risk patients enrolled in our analysis. As to the similar mean EBL and transfusion rates following RARP and LRP, the similarity can be explained by the counterbalance between the contributing factors including the better visualization, improved dexterity, and higher precision to minimize bleeding during RARP and unfavorable factors leading to EBL including more ePLNDs and nerve sparing procedures done in the RARP group. Both Johnson et al. (\u003cspan citationid=\"CR21\" class=\"CitationRef\"\u003e21\u003c/span\u003e) and Papachristos et al. (\u003cspan citationid=\"CR22\" class=\"CitationRef\"\u003e22\u003c/span\u003e) also achieved similar outcomes regarding EBL and OT after RARP and LRP to ours, in spite of the drastic variation of mean EBL and OT offered from different medical centers. The variation could be easily interpreted when taking the surgeons\u0026rsquo; experience and patients\u0026rsquo; and tumors\u0026rsquo; characteristics into account.\u003c/p\u003e \u003cp\u003eAlthough both LRP and RARP are minimally invasive, the better visualization and higher precision offered by the robotic platform could help in further reducing the operative invasiveness and the hazard of organ injures (\u003cspan citationid=\"CR20\" class=\"CitationRef\"\u003e20\u003c/span\u003e, \u003cspan citationid=\"CR21\" class=\"CitationRef\"\u003e21\u003c/span\u003e), which may translate into the significantly lower proportion of overall and \u0026le;\u0026thinsp;Grade II postoperative complications after RARP in our analysis. However, these advantages mentioned above may be restricted by the higher rate of ePLNDs underwent in the RARP group which was associated with the occurrences of symptomatic lymphocele, the most frequent\u0026thinsp;\u0026gt;\u0026thinsp;Grade II complication in our study, thus resulting in similar rates of \u0026gt;\u0026thinsp;Grade II postoperative complications. The comparability of the incidence rates of postoperative\u0026thinsp;\u0026gt;\u0026thinsp;Grade II complications between the two groups in our analysis was consistent with those reported in the contemporary series (\u003cspan citationid=\"CR14\" class=\"CitationRef\"\u003e14\u003c/span\u003e, \u003cspan additionalcitationids=\"CR21 CR22 CR23\" citationid=\"CR20\" class=\"CitationRef\"\u003e20\u003c/span\u003e\u0026ndash;\u003cspan citationid=\"CR24\" class=\"CitationRef\"\u003e24\u003c/span\u003e) comparing RARP and LRP, demonstrating the similar operative safety of RARP and LRP for immediate- and high-risk PCa in experienced hands.\u003c/p\u003e \u003cp\u003eSurgical approach to RP should be tempered with critical significance of cancer control, especially when managing immediate- and high-risk PCa. Consistent with the results reported in published analyses (\u003cspan citationid=\"CR13\" class=\"CitationRef\"\u003e13\u003c/span\u003e, \u003cspan citationid=\"CR14\" class=\"CitationRef\"\u003e14\u003c/span\u003e, \u003cspan citationid=\"CR25\" class=\"CitationRef\"\u003e25\u003c/span\u003e), no significant difference in PSM rate was discovered in our study comparing RARP (17.6%) and LRP (24.7%) for immediate- and high-risk PCa. Evaluated BMI and large prostate volume were considered as the independent predictors of PSMs in men with organ-confined PCa (\u003cspan citationid=\"CR26\" class=\"CitationRef\"\u003e26\u003c/span\u003e), and cumulative evidences revealed that margin status following RP was related to surgical experience (\u003cspan citationid=\"CR26\" class=\"CitationRef\"\u003e26\u003c/span\u003e, \u003cspan citationid=\"CR27\" class=\"CitationRef\"\u003e27\u003c/span\u003e). Fortunately, all these influencing elements were under stringent control with PM method being employed in this single-center analysis, thus greatly contributing to the similarity in PSM rates after RARP and LRP. Of note, compared with the 15% mean rate of PSMs in RARP series including more than 100 cases (\u003cspan citationid=\"CR26\" class=\"CitationRef\"\u003e26\u003c/span\u003e), 17.6% rate of PSMs acquired after RARP in our analysis was relatively high even in highly experienced hands when removing immediate- and high-risk PCa, coordinating the caution that the more extensive the cancer, the higher the possibility of positive margins (\u003cspan citationid=\"CR26\" class=\"CitationRef\"\u003e26\u003c/span\u003e). Although PSMs in RP specimens were in consistent correction with an enhanced risk of PSA relapse (\u003cspan citationid=\"CR28\" class=\"CitationRef\"\u003e28\u003c/span\u003e, \u003cspan citationid=\"CR29\" class=\"CitationRef\"\u003e29\u003c/span\u003e), the long-term impacts of PSMs on more robust clinical endpoints of the disease is variable and mostly depends on other variables, such as Gleason score, pathologic stage, and preoperative PSA (\u003cspan citationid=\"CR16\" class=\"CitationRef\"\u003e16\u003c/span\u003e, \u003cspan citationid=\"CR30\" class=\"CitationRef\"\u003e30\u003c/span\u003e). Intriguingly, most of these decisive factors including Gleason score and preoperative PSA were the basis of D'Amico risk classifications, namely, the clinical endpoints, such as clinical recurrence rates, largely relied on preoperative baseline characteristics rather than PSMs after RP. In alignment with other series (\u003cspan citationid=\"CR14\" class=\"CitationRef\"\u003e14\u003c/span\u003e, \u003cspan citationid=\"CR25\" class=\"CitationRef\"\u003e25\u003c/span\u003e) comparing RARP and LRP, the similarity in the BCR-free survivals obtained after RARP and LRP was still existing, corroborating the equivalent potency of the two procedures in cancer control even when managing immediate- and high-risk PCa.\u003c/p\u003e \u003cp\u003eThe aims of RP are to completely eradicate localized PCa whilst, whenever possible, preserves UC and erectile function, namely, a trifecta outcome (\u003cspan citationid=\"CR4\" class=\"CitationRef\"\u003e4\u003c/span\u003e). Urinary incontinence after RP is one of the most adverse events that negatively impact patients\u0026rsquo; quality of life (\u003cspan citationid=\"CR20\" class=\"CitationRef\"\u003e20\u003c/span\u003e, \u003cspan citationid=\"CR31\" class=\"CitationRef\"\u003e31\u003c/span\u003e). Multiple pathophysiologic mechanisms contribute to the emergence of post-prostatectomy incontinence (PPI). In addition to the biological/preoperative parameters encompassing the patient age at time of surgery, pre-existing lower urinary tract symptoms, high BMI, and abnormal bladder function, the impairments of the integrity of anatomic supporting structures and neural components during the RP procedure appear to be crucial contributing factors to the development of PPI (\u003cspan citationid=\"CR31\" class=\"CitationRef\"\u003e31\u003c/span\u003e, \u003cspan citationid=\"CR32\" class=\"CitationRef\"\u003e32\u003c/span\u003e). In our analysis, preoperative/biological parameters are comparable between the RARP and LRP groups with PM method being applied, but the robotic platforms allowed better preservation of membranous urethra and nerve branches and reconstruction of bladder neck, thus supporting the higher UC probability after RARP over the whole follow-up period. In the prospective randomized controlled study reported by Porpiglia et al. (\u003cspan citationid=\"CR25\" class=\"CitationRef\"\u003e25\u003c/span\u003e), UC rate after RARP was also significantly higher than that after LRP for localized PCa over the 5-year follow-up period. Our results also corroborated the outcomes obtained in the first multicenter, randomized, patient-blinded controlled trial (LAP-01) (\u003cspan citationid=\"CR14\" class=\"CitationRef\"\u003e14\u003c/span\u003e) which demonstrated the improved postoperative return to UC of RARP over LRP. The advantage of robotic platforms in better surgical vision and higher precision for preserving the neurovascular structures could be greatly responsible for the superior erectile function recovery after RARP than that obtained after LRP.\u003c/p\u003e \u003cp\u003eNotably, several limitations should be taken into consideration when interpreting our conclusions. Structural shortages in data collection were inevitable in a retrospective setting of our analysis. The study population, although well-balanced between the two groups, is relatively small. The long-term oncological survivals and functional recoveries could not be further evaluated over the relatively limited follow-up lengths. Certain complications may be undervalued, especially\u0026thinsp;\u0026le;\u0026thinsp;Grade II complications, in spite of the elaborative investigation of medical records and telephone interview.\u003c/p\u003e \u003cp\u003eDespite these limitations, our study is the first one designed to assess the perioperative, functional, and oncological outcomes acquired after RARP and LRP for localized immediate- and high-risk PCa up to now, and our conclusions are drew and strengthened on the basis of the comparability of all perioperative elements between the two arms and rigorous methodology.\u003c/p\u003e "},{"header":"Conclusions","content":" \u003cp\u003eFor surgically managing immediate- and high-risk localized PCa, RARP tended to a lower risk of \u0026le;\u0026thinsp;Grade II complications and superior functional preservation without cancer control being compromised when comparing with LRP. Our present conclusions need to be confirmed further on the basis of prospectively randomized trials with large sample sizes and sufficiently long follow-ups.\u003c/p\u003e "},{"header":"Abbreviations","content":"\u003cp\u003eRARP robot-assisted radical prostatectomy;\u003c/p\u003e\n\u003cp\u003eRP:radical prostatectomy;\u003c/p\u003e\n\u003cp\u003eLRP laparoscopic radical prostatectomy;\u003c/p\u003e\n\u003cp\u003ePCa:prostate cancer;\u003c/p\u003e\n\u003cp\u003ePPI post-prostatectomy incontinence;\u003c/p\u003e\n\u003cp\u003ePSA:prostate specific antigen;\u003c/p\u003e\n\u003cp\u003ePM propensity-score matching;\u003c/p\u003e\n\u003cp\u003eRCT:randomized controlled trial;\u003c/p\u003e\n\u003cp\u003ePLND Pelvic lymph node dissection;\u003c/p\u003e\n\u003cp\u003eBMI:body mass index;\u003c/p\u003e\n\u003cp\u003eASA American Society of Anesthesiologists;\u003c/p\u003e\n\u003cp\u003eOT:operative time;\u003c/p\u003e\n\u003cp\u003eIIEF International Index of Erectile Function;\u003c/p\u003e\n\u003cp\u003eEBL:estimated blood loss;\u003c/p\u003e\n\u003cp\u003ePSM positive surgical margin;\u003c/p\u003e\n\u003cp\u003eUC:urinary continence;\u003c/p\u003e\n\u003cp\u003eBCR biochemical recurrence.\u003c/p\u003e"},{"header":"Declarations","content":"\u003cp\u003e\u003cstrong\u003eEthics approval and consent to participate\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eNot applicable.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eConsent for publication\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eNot applicable.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eAvailability of data and materials\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eThe datasets used and/or analysed during the current study are available from the corresponding author on reasonable request.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eCompeting interests\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eThe authors declare that they have no competing interests.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eFunding\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eNot applicable.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eAuthors' contributions\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eAll the authors contributed in the preparation of this work. DW, ZC, JH and LYL were drafted and revised the article, DW, LXQ and CLY were responsible for the theme, final editing, and preparation of the manuscript for submission, LWP, ZXC, ST, WGX and FB critically revised the manuscript. All authors read and approved the final manuscript.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eAcknowledgements\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003eNot applicable.\u003c/p\u003e\n\u003cp\u003e\u003cstrong\u003eAuthor details\u003c/strong\u003e\u003c/p\u003e\n\u003cp\u003e\u003csup\u003e1\u003c/sup\u003e Department of Urology, the First Affiliated Hospital of Nanchang University, Yongwai street 17, Nanchang City, Jiangxi Province, China, \u003csup\u003e2\u003c/sup\u003e Jiangxi Institute of Urology, Yongwai street 17, Nanchang City, Jiangxi Province, China.\u003c/p\u003e"},{"header":"References","content":"\u003col\u003e\u003cli\u003e\u003cspan\u003eBray F, Ferlay J, Soerjomataram I, Siegel RL, Torre LA, Jemal A. 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Positive surgical margins after radical prostatectomy: a systematic review and contemporary update. European urology. 2014 Feb;65(2):303\u0026ndash;13.\u003c/span\u003e\u003c/li\u003e \u003cli\u003e\u003cspan\u003eBravi CA, Tin A, Vertosick E, Mazzone E, Martini A, Dell'Oglio P, et al. The Impact of Experience on the Risk of Surgical Margins and Biochemical Recurrence after Robot-Assisted Radical Prostatectomy: A Learning Curve Study. The Journal of urology. 2019 Jul;202(1):108\u0026ndash;13.\u003c/span\u003e\u003c/li\u003e \u003cli\u003e\u003cspan\u003eJo JK, Hong SK, Byun SS, Zargar H, Autorino R, Lee SE. Positive surgical margin in robot-assisted radical prostatectomy: correlation with pathology findings and risk of biochemical recurrence. Minerva urologica e nefrologica = The Italian journal of urology and nephrology. 2017 Oct;69(5):493\u0026ndash;500.\u003c/span\u003e\u003c/li\u003e \u003cli\u003e\u003cspan\u003eZhang L, Wu B, Zha Z, Zhao H, Jiang Y, Yuan J. Positive surgical margin is associated with biochemical recurrence risk following radical prostatectomy: a meta-analysis from high-quality retrospective cohort studies. World journal of surgical oncology. 2018 Jul 3;16(1):124.\u003c/span\u003e\u003c/li\u003e \u003cli\u003e\u003cspan\u003eCheccucci E, Veccia A, Fiori C, Amparore D, Manfredi M, Di Dio M, et al. Retzius-sparing robot-assisted radical prostatectomy vs the standard approach: a systematic review and analysis of comparative outcomes. BJU Int. 2020 Jan;125(1):8\u0026ndash;16.\u003c/span\u003e\u003c/li\u003e \u003cli\u003e\u003cspan\u003eAsimakopoulos AD, Topazio L, De Angelis M, Agr\u0026ograve; EF, Pastore AL, Fuschi A, et al. Retzius-sparing versus standard robot-assisted radical prostatectomy: a prospective randomized comparison on immediate continence rates. Surgical endoscopy. 2019 Jul;33(7):2187\u0026ndash;96.\u003c/span\u003e\u003c/li\u003e \u003cli\u003e\u003cspan\u003eHeesakkers J, Farag F, Bauer RM, Sandhu J, De Ridder D, Stenzl A. Pathophysiology and Contributing Factors in Postprostatectomy Incontinence: A Review. European urology. 2017 Jun;71(6):936\u0026ndash;44.\u003c/span\u003e\u003c/li\u003e\u003c/ol\u003e"}],"fulltextSource":"","fullText":"","funders":[],"hasAdminPriorityOnWorkflow":false,"hasManuscriptDocX":true,"hasOptedInToPreprint":true,"hasPassedJournalQc":"","hasAnyPriority":false,"hideJournal":true,"highlight":"","institution":"","isAcceptedByJournal":false,"isAuthorSuppliedPdf":false,"isDeskRejected":"","isHiddenFromSearch":false,"isInQc":false,"isInWorkflow":false,"isPdf":false,"isPdfUpToDate":true,"isWithdrawnOrRetracted":false,"journal":{"display":true,"email":"[email protected]","identity":"researchsquare","isNatureJournal":false,"hasQc":true,"allowDirectSubmit":true,"externalIdentity":"","sideBox":"","snPcode":"","submissionUrl":"/submission","title":"Research Square","twitterHandle":"researchsquare","acdcEnabled":true,"dfaEnabled":false,"editorialSystem":"","reportingPortfolio":"","inReviewEnabled":false,"inReviewRevisionsEnabled":true},"keywords":"radical prostatectomy, robot, laparoscopic, immediate-risk, high-risk, prostate cancer.","lastPublishedDoi":"10.21203/rs.3.rs-442704/v1","lastPublishedDoiUrl":"https://doi.org/10.21203/rs.3.rs-442704/v1","license":{"name":"CC BY 4.0","url":"https://creativecommons.org/licenses/by/4.0/"},"manuscriptAbstract":"\u003ch2\u003eBackground\u003c/h2\u003e \u003cp\u003eTo evaluate the functional and oncological efficacy of robot-assisted radical prostatectomy (RARP) and laparoscopic radical prostatectomy (LRP) for immediate- and high-risk localized prostate cancer (PCa).\u003c/p\u003e\u003ch2\u003eMethods\u003c/h2\u003e \u003cp\u003e232 patients bearing immediate- and high-risk localized PCa between January 2016 and October 2019 were enrolled according to the inclusion criteria. The perioperative, functional and oncological outcomes were compared between the RARP and LRP groups after applying the propensity-score matching (PM) (1:1) method, which were employed to attenuate the impact of the potential baseline confounders.\u003c/p\u003e\u003ch2\u003eResults\u003c/h2\u003e \u003cp\u003eIn all, except for 10 patients without a suitable pair, the remaining patients in the LRP group were successfully matched to 85 patients in the RARP arm. All differences in preoperative variables turned to be insignificant after PM. Within the matched cohort, no open conversion was required in both groups. The RARP group was corrected with a significantly shorter mean operative time than the LRP group (\u003cem\u003ep\u003c/em\u003e\u0026thinsp;\u0026lt;\u0026thinsp;0.001). Patients in the RARP arm were also at a lower risk of \u0026le;\u0026thinsp;Grade II complications than those in the LRP group (\u003cem\u003ep\u003c/em\u003e\u0026thinsp;=\u0026thinsp;0.036). Meanwhile, the proportions of transfusion and \u0026ge;\u0026thinsp;Grade II complications in the RARP group were similar to that in the LRP group (\u003cem\u003ep\u003c/em\u003e\u0026thinsp;=\u0026thinsp;0.192 and \u003cem\u003ep\u003c/em\u003e\u0026thinsp;=\u0026thinsp;1.000, respectively). No significant differences regarding the mean estimated blood loss, rates of pT3 disease and positive surgical margin, median specimen Gleason score and hospital stay length existed between the two groups. RARP vs. LRP tended to a significantly higher percentage of urinary continence at the removal of catheter (\u003cem\u003ep\u003c/em\u003e\u0026thinsp;=\u0026thinsp;0.031), postoperative 6 months (\u003cem\u003ep\u003c/em\u003e\u0026thinsp;=\u0026thinsp;0.043), and last follow-up (\u003cem\u003ep\u003c/em\u003e\u0026thinsp;=\u0026thinsp;0.046). Significant differences were also found between the RARP and LRP arms in erectile function at postoperative 6 months and last follow-up (\u003cem\u003ep\u003c/em\u003e\u0026thinsp;=\u0026thinsp;0.013 and \u003cem\u003ep\u003c/em\u003e\u0026thinsp;=\u0026thinsp;0.009, respectively). The statistical comparability between the two groups was observed in biochemical recurrence-free survival (\u003cem\u003ep\u003c/em\u003e\u0026thinsp;=\u0026thinsp;0.228).\u003c/p\u003e\u003ch2\u003eConclusions\u003c/h2\u003e \u003cp\u003eFor surgically managing immediate- and high-risk localized PCa, RARP tended to a lower risk of \u0026le;\u0026thinsp;Grade II complications and superior functional preservation without cancer control being compromised when comparing with LRP.\u003c/p\u003e","manuscriptTitle":"Robot-Assisted vs. Laparoscopic Radical Prostatectomy for Immediate- and High-Risk Localized Prostate Cancer: A Propensity-Score Matched Analysis","msid":"","msnumber":"","nonDraftVersions":[{"code":1,"date":"2021-05-07 20:43:25","doi":"10.21203/rs.3.rs-442704/v1","editorialEvents":[{"type":"communityComments","content":0}],"status":"published","journal":{"display":true,"email":"[email protected]","identity":"researchsquare","isNatureJournal":false,"hasQc":true,"allowDirectSubmit":true,"externalIdentity":"","sideBox":"","snPcode":"","submissionUrl":"/submission","title":"Research Square","twitterHandle":"researchsquare","acdcEnabled":true,"dfaEnabled":false,"editorialSystem":"","reportingPortfolio":"","inReviewEnabled":false,"inReviewRevisionsEnabled":true}}],"origin":"","ownerIdentity":"712d54a1-eeed-4c14-994c-a088d1d5716d","owner":[],"postedDate":"May 7th, 2021","published":true,"recentEditorialEvents":[],"rejectedJournal":[],"revision":"","amendment":"","status":"posted","subjectAreas":[{"id":4154672,"name":"Cancer Biology"},{"id":4154673,"name":"Oncology"}],"tags":[],"updatedAt":"2021-05-07T20:43:26+00:00","versionOfRecord":[],"versionCreatedAt":"2021-05-07 20:43:25","video":"","vorDoi":"","vorDoiUrl":"","workflowStages":[]},"version":"v1","identity":"rs-442704","journalConfig":"researchsquare"},"__N_SSP":true},"page":"/article/[identity]/[[...version]]","query":{"redirect":"/article/rs-442704","identity":"rs-442704","version":["v1"]},"buildId":"cBFmMYwuxLRRLfASyISRj","isFallback":false,"isExperimentalCompile":false,"dynamicIds":[84888],"gssp":true,"scriptLoader":[]}

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