Reproductive outcomes in women with advanced endometriosis in fresh versus frozen embryo transfer cycles

In: Middle East Fertility Society Journal · 2024 · vol. 29(1) · doi:10.1186/s43043-024-00200-x · W4401419365
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This study found that women with advanced endometriosis had significantly higher implantation and ongoing pregnancy rates in frozen embryo transfer cycles compared to fresh embryo transfer cycles.

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This retrospective cohort study compared reproductive outcomes between fresh embryo transfer and freeze-all with deferred day-5 embryo transfer in women aged 18–37 with laparoscopically diagnosed advanced (r-ASRM stage III/IV) endometriosis undergoing ICSI in two IVF centers in Alexandria, Egypt (2018–2021). After matching baseline characteristics across 211 eligible participants, clinical pregnancy, implantation, and ongoing pregnancy rates were significantly higher in the frozen embryo transfer group, while miscarriage was numerically higher after fresh transfer without statistical significance (20.9% vs 9.2%, p=0.072). The authors’ main limitation is that the design is retrospective, relying on existing medical records. This paper is centrally about endometriosis — it directly evaluates whether freeze-all versus fresh embryo transfer is associated with differences in implantation and ongoing pregnancy rates specifically in women with advanced endometriosis.

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Abstract

Abstract Background ART in women with endometriosis is associated with poor quality of the retrieved oocytes and lower fertilization and pregnancy rates, reflecting that endometriosis may influence fertility by altering the quality of both the oocyte and embryo quality and also by impairing the endometrial receptivity. On comparing endometriosis-affected patients to healthy counterparts, many differences were demonstrated at the endometrial level. Thus, choosing the appropriate method of embryo transfer is of utmost importance, particularly for patients with advanced endometriosis. Objective The aim of the present study was to compare the reproductive outcomes between fresh and frozen embryo transfer cycles in women with advanced endometriosis. Material and methods A retrospective cohort study was conducted in the period from January 2018 until December 2021 for patients recruited from two IVF centers, Alexandria, Egypt. Careful review of paper and electronic medical records of infertile women (primary, relative, or secondary infertility) aged 18–37 years who were diagnosed with advanced endometriosis by means of laparoscopy and were scheduled for ICSI followed by either fresh embryo transfer (group I) or freeze-all embryos and deferred embryo transfer (group II) of day 5 embryo(s) was included in the study. Results Two-hundred and eleven women were eligible and included in the study. Women in each study group were matched regarding baseline characteristics. Clinical pregnancy, implantation, and ongoing pregnancy rates were statistically significantly higher in the group of frozen embryo transfer ( p < 0.001). Miscarriage rate was found to be higher in the group of fresh transfer compared to FET group but without a statistical significance (20.9% vs 9.2%, p = 0.072). Conclusion In women with advanced endometriosis, freeze-all policy seems to be associated with better implantation, ongoing pregnancy rates.
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Abstract

Background ART in women with endometriosis is associated with poor quality of the retrieved oocytes and lower fertilization and pregnancy rates, reflecting that endometriosis may influence fertility by altering the quality of both the oocyte and embryo quality and also by impairing the endometrial receptivity. On comparing endometri- osis-affected patients to healthy counterparts, many differences were demonstrated at the endometrial level. Thus, choosing the appropriate method of embryo transfer is of utmost importance, particularly for patients with advanced endometriosis.

Objective

The aim of the present study was to compare the reproductive outcomes between fresh and frozen embryo transfer cycles in women with advanced endometriosis.

Material and methods

A retrospective cohort study was conducted in the period from January 2018 until Decem- ber 2021 for patients recruited from two IVF centers, Alexandria, Egypt. Careful review of paper and electronic medical records of infertile women (primary, relative, or secondary infertility) aged 18–37 years who were diagnosed with advanced endometriosis by means of laparoscopy and were scheduled for ICSI followed by either fresh embryo transfer (group I) or freeze-all embryos and deferred embryo transfer (group II) of day 5 embryo(s) was included in the study.

Results

Two-hundred and eleven women were eligible and included in the study. Women in each study group were matched regarding baseline characteristics. Clinical pregnancy, implantation, and ongoing pregnancy rates were sta- tistically significantly higher in the group of frozen embryo transfer (p < 0.001). Miscarriage rate was found to be higher in the group of fresh transfer compared to FET group but without a statistical significance (20.9% vs 9.2%, p = 0.072).

Conclusion

In women with advanced endometriosis, freeze-all policy seems to be associated with better implanta- tion, ongoing pregnancy rates.

Keywords

Endometriosis, Freeze all, Frozen embryo transfer, Ongoing pregnancy rate

Introduction

Endometriosis is defined as a disease characterized by the presence of endometrium resembling epithelium and/or stroma outside the endometrium and myome - trium, usually in association with an inflammatory pro - cess [1]. It roughly affects 10% (approximately 190 million women worldwide) of girls and women of reproductive age globally. Open Access © The Author(s) 2024. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. Middle East Fertility Society Journal *Correspondence: Ahmed Shoukry [email protected] 1 Obstetrics and Gynecology, Department of Obstetrics and Gynecology, Faculty of Medicine, Alexandria University, Alexandria, Egypt 2 Obstetrics and Gynecology, Alexandria University Hospitals, Alexandria, Egypt Page 2 of 8Shoukry et al. Middle East Fertility Society Journal (2024) 29:41 Endometriosis-infertility relationship has been a point of debate for decades. The fecundity ranges from 15 to 20% per month in normal couples and declines with age. Patients with endometriosis have a decreased monthly fecundity of about 0.2–1% each month [2, 3]. Moreover, endometriosis is associated with decline in the live birth rate (LBR) [4]. Although ART remain the most effective treatment modality for infertile women with endometrio- sis, it still yields poor outcomes as ART could not over - come all the substantial effects of endometriosis [5, 6]. Endometriosis-affected women have declined pregnancy and implantation rates in comparison to women without endometriosis [7]. It was noticed that endometriosis has undesirable effect on the pregnancy, miscarriage, and live birth rates. It was found that ART outcomes, as the quality of the retrieved oocytes and fertilization rate, are negatively influenced by the existence of endometriosis, reflect - ing that endometriosis influence fertility by altering the quality of both the oocyte and embryo quality and by impairing the endometrial receptivity [6]. On comparing endometriosis-affected patients to healthy counterparts, many differences were demonstrated at the endometrial level [8], which define the decline in the receptivity of the endometrium. Thus, choosing the appropriate method of embryo transfer is of utmost importance, particularly for patients with advanced endometriosis. In the view of the impact of the supraphysiological level of hormones associated with stimulation in fresh embryo transfer on the uterine environment during early peri- implantation, it was demonstrated that flowing of blood in the endometrium and sub-endometrium is reduced in stimulated cycles in comparison to natural cycles as evaluated by three-dimensional power Doppler ultra - sonography [9]. Furthermore, histopathologic alterations of the stimulated endometrium were reported, and this includes advancement in the maturation of the endome - trium [10] and premature development of channel sys - tems in the nucleolus [11]. On the other hand, in frozen embryo transfer (FET) cycles, endometrial growth can be more controlled than in fresh cycles [12]. Based on that, the use of frozen embryos avoided the supraphysiological hormone level found during ovarian hyperstimulation in in vitro fertili - zation (IVF)/ICSI with fresh embryo transfer, which leads to an unfavorable environment for implantation and has been found to have detrimental effects on the endome - trial receptivity, irrespective of the amount of retrieved oocytes or levels of progesterone (P) [13–16]. Therefore, the aim of the present study was to com - pare the reproductive outcomes between fresh and fro - zen embryo transfer cycles in women with advanced endometriosis. Study design and setting A retrospective cohort study was conducted in the period from January 2018 until December 2021 for patients recruited from two IVF centers (Agial Fertility Center & Dar-Elkhosoba Center), Alexandria, Egypt.

Materials and methods

Careful review of paper and electronic medical records of infertile women (primary, relative, or secondary infertility) aged 18–37 years who were diagnosed with advanced endometriosis, stage III/IV r-ASRM clas - sification [17], by means of laparoscopy and were scheduled for intracytoplasmic sperm injection (ICSI) followed by either fresh embryo transfer or freeze- all embryos and deferred embryo transfer of day 5 embryo(s) was included in the study. Couples with abnormal semen analysis of the male partner, recurrent implantation failure in previous ICSI trials, and women with uterine lesions such as fibroids, adenomyosis, polypi, uterine septum, and women with no available follow up data were excluded from the study. The study protocol was approved from the Eth - ics Committee of Faculty of Medicine, Alexandria University. Ovarian stimulation All the women enrolled in the study underwent con - trolled ovarian stimulation via the fixed GnRH antago - nist protocol. Before ovarian stimulation, women were pretreated with combined oral contraceptive pills for 2–3 weeks. On day 2 of the menstrual cycle (stimula - tion day 1), patients received a fixed daily dose of recom - binant FSH or combination of rec-FSH and human menopausal gonadotropins. Starting on day 5 of stimu - lation, patients underwent monitoring with transvaginal ultrasound and serial assessment of estradiol every 2–3 days as required. A daily subcutaneous dose of 0.25 mg of GnRH antagonist cetrorelix was initiated on day 6 of ovarian stimulation and continued up to the day of trig - ger administration. When at least three follicles reached 17 mm in diameter, final oocyte maturation was trig - gered using 10,000 IU of human chorionic gonadotropin (hCG). Ovum pickup (OPU) was performed 35–36 h of hCG administration. Mature oocytes were inseminated by means of intracytoplasmic sperm injection and cul - tured to blastocyst stage. Group I: Women who underwent fresh embryo transfer (ET) Combined vaginal suppositories (400 mg twice daily) and intramuscular progesterone in oil (50 mg once daily) Page 3 of 8 Shoukry et al. Middle East Fertility Society Journal (2024) 29:41 injections were started on day of OPU, and ET was per - formed 5 days after P administration. Group II: Women who underwent frozen embryo transfer after endometrial preparation through artificial or programmed cycle After vitrification of the available embryos, in the sub - sequent cycle, women underwent ovarian suppression by combined pills for 2–3 weeks, and then endometrial preparation was achieved with a daily dose of 8 mg of estradiol valerate for at least 12–14 days. When endome - trium thickness was at least 8 mm and E2 level reached at least 200 pg/dl, progesterone as vaginal suppositories (400 mg twice daily) and intramuscular in oil (50 mg once daily) injection was administered, and ET of thawed embryos was performed after 5 days of P therapy. Outcome variables The primary outcome of the study was the ongoing pregnancy rate (OPR) defined as pregnancy progressed beyond 14 weeks’ gestation. Secondary outcomes include the following: implantation rate, defined as the num - ber of intrauterine gestational sacs observed by trans - vaginal ultrasound divided by the number of transferred embryos; clinical pregnancy rate (CPR), calculated by considering clinical pregnancy and determined by the visualization of a viable gestational sac within the uter - ine cavity by ultrasound 3–4 weeks after embryo transfer; and miscarriage rate, defined as the number of cases who aborted (after a confirmed clinical pregnancy) divided by the total number of pregnant cases. Statistical analysis Data were fed to the computer and analyzed using IBM SPSS software package version 20.0. (Armonk, NY: IBM Corp.). Qualitative data were described using number and percent. The Kolmogorov-Smirnov test was used to verify the normality of distribution. Quantitative data were described using range (minimum and maximum), mean, standard deviation, median, and interquartile range (IQR). Significance of the obtained results was judged at the 5% level. The used tests were chi-square test for categorical variables, to compare between different groups; Student t-test for normally distributed quantita - tive variables, to compare between two studied groups; and Mann-Whitney test for abnormally distributed quantitative variables, to compare between two studied groups.

Results

Over the 4-year study period, there were 237 women with advanced endometriosis who underwent either fresh or frozen embryo transfer cycles; out of them, 211 women were eligible and included in the study, and Fig.  1 dem- onstrates the flow chart of the study. The study included 211 patients divided into two groups as follows: Group I includes 103 patients who underwent fresh embryo transfer, and Group II includes 108 patients who under - went frozen embryo transfer. Regarding the baseline characteristics of both groups (Table 1), patients in the two study groups were matched regarding mean age, infertility duration, type of infertil - ity (primary or secondary), body mass index, and AMH level. Fig. 1 Study flowchart Page 4 of 8Shoukry et al. Middle East Fertility Society Journal (2024) 29:41 Table 2 shows that the number of retrieved oocytes, MII (metaphase II) oocyte number, and the number of available blastocysts for transfer on day 5 were sig - nificantly higher in the group of frozen embryo transfer (p < 0.001). As shown in Table  3, the number of embryos trans - ferred was either a single embryo or two embryos, and there was no statistical significant difference between the two groups (p 0.473); for the quality of the embryos transferred that were either high-quality embryos alone or low -quality embryos alone or both of them together, both groups showed no statistically significant difference (p 0.325). The clinical pregnancy rate was significantly higher in the frozen embryo transfer group than the fresh group (82 patients (75.9%) vs 46 patients (44.7%) (p < 0.001)); again, the FET group showed a significantly higher Table 1 Comparison between the two studied groups according to the baseline characteristics Baseline characteristics Fresh ET (n = 103) Frozen ET (n = 108) Test of sig P Mean age (years) 31.22 ± 4.94 30.87 ± 4.45 t = 0.546 0.586 Median infertility duration (IQR) years 4.0 (3.0–7.0) 4.25 (3.0–8.0) U = 5266.50 0.502 Mean BMI (kg/m2) 25.83 ± 3.26 25.01 ± 3.04 t = 1.903 0.058 Infertility type No % No % χ2 = 3.987 0.136 Primary 76 73.8 71 65.7 Secondary 17 16.5 16 14.8 Relative 10 9.7 21 19.4 Mean AMH 1.91 ± 1.11 2.21 ± 1.31 t = 1.813 0.071 AFC U = 5064.5 0.258 Mean 7.74 ± 2.93 8.18 ± 2.96 Median (IQR) 7.0 (6.0–10.0) 8.0 (6.0–10.0) Chocolate cyst before OI χ2 = 0.021 0.884 Absent 87 (84.5%) 92 (85.2%) Present 16 (15.5%) 16 (14.8%) Table 2 Comparison between the two groups regarding the number of oocyte retrieved, mature oocytes, and available embryos number at day 5 * : statistically significant  Fresh (n = 103) Frozen (n = 108) U p Oocyte retrieved Min.–max 2.0–10.0 3.0–12.0 3710.5* < 0.001* Mean ± SD 5.29 ± 2.08 6.56 ± 1.93 Median (IQR) 5.0 (4.0–7.0) 6.0 (6.0–8.0) MII oocytes Min.–max 1.0–7.0 2.0–9.0 3546.5* < 0.001* Mean ± SD 3.78 ± 1.62 4.87 ± 1.46 Median (IQR) 4.0 (2.0–5.0) 5.0 (4.0–6.0) Embryo no. on day 5 Min.–max 1.0–5.0 1.0–7.0 3612.0* < 0.001* Mean ± SD 2.55 ± 0.96 3.22 ± 1.06 Median (IQR) 2.0 (2.0–3.0) 3.0 (2.0–4.0) Table 3 Comparison between the two studied groups according to the embryos transferred Embryos transferred Fresh ET (n = 103) Frozen ET (n = 108) χ2 P No % No % Number Single embryo 47 45.6 44 40.7 0.514 0.473 Two embryos 56 54.4 64 59.3 Quality Low 26 25.2 22 20.4 2.246 0.325 High 73 70.9 77 71.3 High + low 4 3.9 9 8.3 Page 5 of 8 Shoukry et al. Middle East Fertility Society Journal (2024) 29:41 implantation rate in comparison to the fresh group as illustrated in Table 4 (30.8% vs 54.1% (p < 0.001)). Out of the 128 pregnant females in the study, 3 preg - nant patients dropped out from the fresh group, and 6 pregnant patients dropped out from the frozen group; those 9 patients were excluded from our statistical

Results

while estimating the miscarriage rate. The mis - carriage rate was higher in the fresh ET group than in the frozen ET group; however, the difference did not reach statistical significance (9 (20.9%) vs 7 (9.2%) (p = 0.072). As for the primary outcome of the study, the ongo - ing pregnancy rate, out of the 211 patients included in our study, there was no available data for 9 pregnant patients, 3 patients in group 1, and 6 patients in group 2; those 9 patients were excluded from our statistical analysis while estimating the ongoing pregnancy rate. Sixty-nine patients in the frozen embryo transfer group (69/102 = 67.6%) continued their pregnancy beyond 14 weeks, while 33 patients (34/100 = 34%) of the fresh embryo transfer group continued their pregnancy beyond 14 weeks, and the OPR was significantly higher in the frozen embryo transfer group (p < 0.001) (Table 5). Furthermore, a subgroup analysis was performed to compare the pregnancy rates between women who underwent single embryo transfer (SET) and those to whom two embryos were transferred (Table  6). It was observed that the clinical and ongoing pregnancy rates in women who underwent SET and who have under - went double embryo transfer are not significantly dif - ferent (in the group of fresh ET, the group of FET, and for the total sample).

Discussion

The present study showed that OPR in women with advanced endometriosis is significantly higher in the group of frozen embryo transfer compared to the fresh embryo transfer group (67.6% vs. 34%, respectively). Regarding the secondary outcomes, there was a statisti - cally significant higher implantation and clinical preg - nancy rates also in the frozen embryo transfer group. To the best of our knowledge, only few studies have addressed the issue of freeze-all policy in women with advanced endometriosis. In agreement with the findings of the current study, Wu et  al. [18] conducted a retrospective study that Table 4 Comparison between the two studied groups according clinical pregnancy and implantation rates * : statistically significant  Fresh ET (n = 103) Frozen ET (n = 108) χ2 p No % No % Clinical pregnancy rate 46 44.7 82 75.9 21.597* < 0.001* Number of GS seen by TVU (after 3–5 weeks) 49 93 < 0.001* Number of transferred embryos 159 172 Implantation rate 30.8% 54.1% Table 5 Comparison between the two studied groups according to the ongoing pregnancy * : statistically significant Fresh ET Frozen ET χ2 p No. (%) No. (%) Ongoing pregnancy (n = 100) (n = 102) 22.876* < 0.001* 34 (34.0%) 69 (67.6%) Table 6 Relation between numbers of embryos transferred with clinical and ongoing pregnancy rates a Not available cases were excluded Number χ2 p 1 2 Clinical pregnancy rate Fresh (n = 103) (n = 47) (n = 56) Negative 30 (63.8%) 27 (48.2%) 2.521 0.112 Positive 17 (36.2%) 29 (51.8%) Frozen (n = 108) (n = 44) (n = 64) Negative 9 (20.5%) 17 (26.6%) 0.532 0.466 Positive 35 (79.5%) 47 (73.4%) Total (n = 211) (n = 91) (n = 120) Negative 39 (42.9%) 44 (36.7%) 0.831 0.362 Positive 52 (57.1%) 76 (63.3%) Ongoing pregnancy rate Fresh (n = 100)a (n = 47) (n = 53) Negative/miscarriage 35 (74.5%) 31 (58.5%) 2.834 0.092 Positive 12 (25.5%) 22 (41.5%) Frozen (n = 102)a (n = 43) (n = 59) Negative/miscarriage 14 (32.6%) 19 (32.2%) 0.001 0.970 Positive 29 (67.4%) 40 (67.8%) Total (n = 202)a (n = 90) (n = 112) Negative/miscarriage 49 (54.4%) 50 (44.6%) 1.918 0.166 Positive 41 (45.6%) 62 (55.4%) Page 6 of 8Shoukry et al. Middle East Fertility Society Journal (2024) 29:41 encompassed 1651 women with advanced stages of endo- metriosis performing ICSI. After matching, 506 women and 255 women were eligible in the freeze-all group and the fresh group, respectively. In their matched cohort study, the implantation, CPR, and LBR were significantly higher in the FET group in comparison to the fresh groups. Those results coincide with the current study in all perspectives except for the LBR as it was not included in the outcomes for the study. However, the present study differs from Wu et  al., where in their study the development of the embryo was accessed on day 3, and the embryos selected to be trans - ferred were high-quality cleavage-stage embryos only (at least six blastomeres with ≤ 20% fragmentation based on the Cummins’ criteria). In the fresh embryo transfer group, patients were arranged for a day 3 fresh embryo transfer and vitrification of the extra embryos. For the FET  group,  vitrification on day 3 of the entire cohort of good quality embryos. While in the present study, embryo development was assessed on day 5, and patients performing fresh transfer were scheduled for a day-5 ET, while in the frozen group, the embryos were vitri - fied on day 5, and embryo transfer was not exclusively for high-quality embryos, but in some cases, average or low-quality embryos were transferred either alone or in combination with a high-quality embryo. Again, the results of the present study coincided with a matched cohort prospective study conducted by Bour - don et al. [19], and they compared the results of FET to fresh ET in women having endometriosis, where the FET group involved 135 women and the fresh group involved 424 matched women. CPR was of higher significance toward the FET group in comparison to the fresh group; also, the ongoing pregnancy rate showed greater statisti - cal significance in the FET group (34.8%) in comparison to the fresh-ET group (17.8%) (p = 0.005), and the live birth rate as well was of higher significance in FET in comparison to fresh embryo transfer group. Another interesting study conducted by Mohamed et  al. [20] is a retrospective, database-searched cohort study. The study included two groups: the first group had freshly transferred embryos, while the second group per - formed frozen embryo transfer. The primary outcome for the study was the live birth rate, while the secondary out- comes included the clinical pregnancy rate and the mis - carriage rate. Out of the total number of cases, 415 (5.7%) had infertility attributed to endometriosis, in whom fro - zen ET cycles were associated with a relatively similar clinical pregnancy rate and live birth rate, in comparison to the clinical pregnancy rate and live birth rate of fresh ET cycles, showing no significant difference. Neverthe - less, the study of Mohamed et al. differs from the present study as they considered other causes of infertility rather than endometriosis alone as a sole factor of infertility, and it also concluded that there was no significant differ - ence between FET over the fresh ET in cases of endome - triosis concerning CPR (18.2 vs. 20.2%, respectively) and LBR (16.9% vs. 15.5%, respectively). In accordance, a recent systematic review and meta- analysis conducted by Chang et al. [21] aimed at evaluat - ing if FET has the ability to reimpose optimal receptivity targeting better ART results in patients with endometrio- sis. A total of six studies with moderate methodological quality were included in the meta-analysis. Three-thou - sand and ten patients with endometriosis who under - went ICSI were included in the studies: 1777 performed FET, and 1233 performed fresh ET. LBR was significantly higher in the FET group in comparison to the fresh group. Although that CPR was similar between the two study groups, there was a significantly higher miscarriage rate in the fresh group. The endometrium of endometriosis-affected women is different from that of healthy, unaffected women [8], which could be the main reason for the decline in endo - metrial receptivity quality. Thus, it is crucial to select the right embryo transfer technique, particularly for women who have severe endometriosis. The effects of ovarian stimulation in fresh ET cycles on the early peri-implan - tation uterine milieu have been documented in a number of studies, and three-dimensional power Doppler ultra - sonography measurements have revealed that stimulated cycles have reduced endometrial and subendometrial blood flow in comparison to normal cycles [9]. Further - more, certain pathologic alterations of the stimulated endometrium have been verified, such as the progression of endometrial maturation [10], as well as the early estab- lishment of nucleolar channel systems [11]. Additionally, a number of researchers have demon - strated that during fresh embryo transfer cycles, there are abnormalities in the transcriptional activity of genes related to endometrial receptivity [22–24]. The altera - tions indicated above are linked to the hyperestrogenic environment created during fresh IVF, which might sub - sequently hinder early embryonic adhesion [18, 25] and, consequently, the embryos’ capacity to implant. It follows that the current study’s findings regarding implantation, clinical pregnancy, and ongoing pregnancy are better in FET cycles. Our study has the advantage of being one of the few studies that addressed the role of FET in endometriosis- affected women and was conducted for a fair number of patients; moreover, this study focused on advanced endometriosis being the sole factor of infertility in the studied patients, excluding any other infertility-related factors; however, the main study limitation was being a retrospective analysis depending on the availability of Page 7 of 8 Shoukry et al. Middle East Fertility Society Journal (2024) 29:41 complete medical records, and the follow-up stopped at 14 weeks of gestation.

Conclusions

The findings of the present study suggest that frozen embryo transfer policy in cases of advanced endometrio - sis would result in better reproductive outcomes in com - parison to fresh embryo transfer in terms of clinical and ongoing pregnancy rates. Further, randomized controlled studies are needed for confirmation of such findings. Abbreviations ART Assisted reproductive technologies LBR Live birth rate FET Frozen embryo transfer ASRM American Society of Reproductive Medicine CPR Clinical pregnancy rate OPR Ongoing pregnancy rate IVF In vitro fertilization ICSI Intracytoplasmic sperm injection GnRH Gonadotropin-releasing hormone AMH Anti-Mullerian hormone

Acknowledgements

Not applicable. Authors’ contributions HA and AS were the main authors responsible of the research and writing the paper. MK was responsible for the data collection, and WEG was responsible for reviewing and revising the paper. All authors read and approved the final manuscript. Funding The authors received no external funds. Availability of data and materials The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request. Declarations Ethical approval and consent to participate The study protocol was approved by the ethical committee of the Faculty of Medicine, Alexandria University, Egypt. No informed consent was required due to the retrospective design of the study. Consent for publication Not applicable. Competing interests The authors declare that they have no competing interests. Received: 27 April 2024 Accepted: 4 August 2024

References

1. Zegers-Hochschild F, Adamson GD, Dyer S, Racowsky C, De Mouzon J, Sokol R, Cooke ID (2017) The international glossary on infertility and fertil- ity care, 2017. Hum Reprod 32(9):1786–1801 2. Navot D, Drews MR, Bergh PA, Guzman I, Karstaedt A, Scott RT Jr, Hofmann GE (1994) Age-related decline in female fertility is not due to diminished capacity of the uterus to sustain embryo implantation. Fertil Steril 61(1):97–101 3. Hughes EG, Fedorkow DM, Collins JA (1993) A quantitative overview of controlled trials in endometriosis-associated infertility. Fertil Steril 59(5):963–970 4. Collins JA, Burrows EA, Willan AR (1995) The prognosis for live birth among untreated infertile couples. Fertil Steril 64(1):22–28 5. Somigliana E, Vigano P , Benaglia L, Busnelli A, Berlanda N, Vercellini P (2017) Management of endometriosis in the infertile patient. Semin Reprod Med 35(1):31–37 6. Barnhart K, Dunsmoor-Su R, Coutifaris C (2002) Effect of endometriosis on in vitro fertilization. Fertil Steril 77(6):1148–1155 7. Pellicer A, Oliveira N, Ruiz A, Remohí J, Simón C (1995) Exploring the mechanism (s) of endometriosis-related infertility: an analysis of embryo development and implantation in assisted reproduction. Hum Reprod 10(suppl_2):91–97 8. SHARPE-TIMMS, K. L. (2001) Endometrial anomalies in women with endometriosis. Ann N Y Acad Sci 943(1):131–147 9. Ng EHY, Chan CCW, Tang OS, Yeung WSB, Ho PC (2004) Comparison of endometrial and subendometrial blood flow measured by three- dimensional power Doppler ultrasound between stimulated and natural cycles in the same patients. Hum Reprod 19(10):2385–2390 10. Kolibianakis E, Bourgain C, Albano C, Osmanagaoglu K, Smitz J, Van Steirteghem A, Devroey P (2002) Effect of ovarian stimulation with recombinant follicle-stimulating hormone, gonadotropin releas- ing hormone antagonists, and human chorionic gonadotropin on endometrial maturation on the day of oocyte pick-up. Fertil Steril 78(5):1025–1029 11. Zapantis G, Szmyga M, Rybak E, Meier U (2013) Premature formation of nucleolar channel systems indicates advanced endometrial matura- tion following controlled ovarian hyperstimulation. Hum Reprod 28(12):3292–3300 12. Basirat Z, Rad HA, Esmailzadeh S, Jorsaraei SGA, Hajian-Tilaki K, Pasha H, Ghofrani F (2016) Comparison of pregnancy rate between fresh embryo transfers and frozen-thawed embryo transfers following ICSI treatment. Int J Reprod Biomed 14(1):39 13. Shapiro BS, Daneshmand ST, Garner FC, Aguirre M, Hudson C, Thomas S (2011) Evidence of impaired endometrial receptivity after ovar - ian stimulation for in vitro fertilization: a prospective randomized trial comparing fresh and frozen–thawed embryo transfer in normal responders. Fertil Steril 96(2):344–348 14. Singh N, Lata K, Naha M, Malhotra N, Tiwari A, Vanamail P (2014) Effect of endometriosis on implantation rates when compared to tubal factor in fresh non donor in vitro fertilization cycles. J Hum Reprod Sci 7(2):143–147 15. Simon C, Domínguez F, Valbuena D, Pellicer A (2003) The role of estrogen in uterine receptivity and blastocyst implantation. Trends Endocrinol Metab 14(5):197–199 16. Kao L, Germeyer A, Tulac S, Lobo S, Yang J, Taylor R, Giudice L (2003) Expression profiling of endometrium from women with endometriosis reveals candidate genes for disease-based implantation failure and infertility. Endocrinology 144(7):2870–2881 17. Canis M, Donnez JG, Guzick DS, Halme JK, Rock JA, Schenken RS, Ver - non MW (1997) Revised American Society for reproductive medicine classification of endometriosis. Fertil Steril 67(5):817–821 18. Wu J, Yang X, Huang J, Kuang Y, Wang Y (2019) Fertility and neona- tal outcomes of freeze-all vs. fresh embryo transfer in women with advanced endometriosis. Front Endocrinol. 10:770 19. Bourdon M, Santulli P , Maignien C, Gayet V, Pocate-Cheriet K, Marcellin L, Chapron C (2018) The deferred embryo transfer strategy improves cumulative pregnancy rates in endometriosis-related infertility: a retrospective matched cohort study. PLoS One 13(4):e0194800 20. Mohamed AM, Chouliaras S, Jones CJ, Nardo LG (2011) Live birth rate in fresh and frozen embryo transfer cycles in women with endometriosis. Eur J Obstet Gynecol Reprod Biol 156(2):177–180 21. Chang Y, Shen M, Wang S, Li X, Duan H (2022) Association of embryo transfer type with infertility in endometriosis: a systematic review and meta-analysis. J Assist Reprod Genet 39(5):1033–1043 22. Mirkin S, Nikas G, Hsiu J-G, Díaz J, Oehninger S (2004) Gene expression profiles and structural/functional features of the peri-implantation endometrium in natural and gonadotropin-stimulated cycles. J Clin Endocrinol Metab 89(11):5742–5752 Page 8 of 8Shoukry et al. Middle East Fertility Society Journal (2024) 29:41 23. Horcajadas JA, Riesewijk A, Polman J, van Os R, Pellicer A, Mosselman S, Simón C (2004) Effect of controlled ovarian hyperstimulation in IVF on endometrial gene expression profiles. Mol Hum Reprod 11(3):195–205 24. Haouzi D, Assou S, Mahmoud K, Tondeur S, Rème T, Hedon B, Hamamah S (2009) Gene expression profile of human endometrial receptivity: com- parison between natural and stimulated cycles for the same patients. Hum Reprod 24(6):1436–1445 25. Valbuena D, Martin J, de Pablo JL, Remohı́, J., Pellicer, A., & Simón, C. (2001) Increasing levels of estradiol are deleterious to embryonic implan- tation because they directly affect the embryo. Fertil Steril 76(5):962–968 Publisher’s Note Springer Nature remains neutral with regard to jurisdictional claims in pub- lished maps and institutional affiliations.

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