The effectiveness of dual-phase 18F-FDG PET/CT in the detection of epithelial ovarian carcinoma: a pilot study.

From March 2009 to February 2011, we enrolled 20 consecutive patients presenting ovarian masses with diffuse peritoneal infiltration identified on abdomen–pelvis CT or pelvic MRI scans at Guro Hospital, Korea University. Each patient underwent conventional diagnostic work-up, including physical examination, pelvic ultrasound, and abdomen–pelvis CT or pelvic MRI. In all patients, images on CT or MRI suggested either benign or malignant masses with similar probability, making differential diagnosis difficult. To further confirm the characteristics of the masses, dual-phase 18 F-FDG-PET/CT examinations were then performed in all patients. Patients who were pregnant, had a history of other types of cancers, or had liver cirrhosis, renal failure, or cardiovascular disease were excluded. All suspicious lesions were confirmed histopathologically by surgical exploration. The study protocol was approved by the Institutional Review Board for Research on Human Subjects at the Guro Hospital, Korea University, and written informed consent was obtained from all patients. All patients fasted for at least 6 h to maintain serum glucose level of <140 mg/dL before examination. One hour after intravenous injection of 555 MBq of 18 F-FDG, each patient was scanned from the cerebellum to the pelvis using a PET/CT scanner (Gemini Time of Flight PET/CT, Philips, Amsterdam, the Netherlands). An additional delayed scan of the same area was taken 2 h after the 18 F-FDG injection using the same scanner. Neither muscle relaxant nor contrast agent was administered. All images were interpreted and analyzed by 2 experienced nuclear medicine physicians with all available clinical information. PET images were analyzed on a dedicated workstation (Extended Brilliance Workspace 3.5 with PET/CT viewer for automated image registration, Philips, Amsterdam, the Netherlands). After image reconstruction, regions of interest were accurately placed over the lesion visualized on the PET images. All regions of interest were quantitatively evaluated using the standardized uptake value (SUV). The maximum SUV was calculated using the following formula: SUV = tissue concentration × injected dose ‒ 1 × body weight ‒ 1 For quantitative analysis of the uptake of the lesion, a region of interest was placed over the area of maximum activity within the lesion, and the maximum SUV (SUV max ) was calculated from the measured tissue concentration at 1 h (SUV max1 ) and 2 h (SUV max2 ). The retention index (RI) was calculated by subtracting the SUV max 1 from the SUV max 2 and dividing by SUV max 1 . The diagnostic accuracy of 18 F-FDG-PET/CT in differentiating benign from malignant lesions was determined based on the histopathological findings. Numerical data such as age, parity, and body mass index were expressed as median (range). Mean percentage changes between SUV max1 and SUV max2 in both malignant and benign lesions were calculated, and were compared using the two-tailed Student’s t -test. Individual receiver-operating characteristic (ROC) curves of SUV max1 , SUV max2 , and RI were analyzed to determine their clinical significance in differentiating benign from malignant lesions. Pairwise comparisons of their performances were conducted using the Hanley and McNeil method. A P value of <0.05 was considered statistically significant. All statistical analyses were conducted using MedCalc Software for Windows (Version 11.6.0, MedCalc Software bvba, Ostend, Belgium).

Baseline characteristics of the enrolled patients are summarized in Table  1 . Of the 20 patients, 13 were histopathologically diagnosed with primary epithelial ovarian cancers; 8 serous, 3 mucinous, and 2 endometrioid. The remaining 7 had non-cancerous lesions such as pelvic tuberculosis (3 patients), endometriosis (3 patients), and PID (1 patient). The median size of ovarian masses in 13 patients with primary epithelial ovarian cancers was 9.5 cm (range, 4–20), whereas the median size of ovarian masses in 7 patients with non-cancerous lesions was 3 cm (range, 1–7). In addition, all 20 patients showed diffuse peritoneal infiltration, such as peritoneal nodularity, omental or mesenteric infiltration, suggesting peritoneal carcinomatosis. Preoperative findings on CT or MRI scans in 13 patients with primary epithelial ovarian cancers mostly suggested malignancy as the first differential diagnosis, but other conditions could not be excluded using these scans, such as borderline ovarian malignancy, benign ovarian tumors, or soft tissue masses. In contrast, CT or MRI findings in 7 patients with benign lesions strongly suggested malignancies, but the possibilities of benign inflammatory lesions could not be completely excluded. Baseline characteristics of patients BMI = body mass index, SUV = standardized uptake value, RI = retention index, PID = pelvic inflammatory disease. Data are presented as median (range) or mean ± SD. The mean percentage changes between SUV max1 and SUV max2 in malignant and benign lesions were 2.6 ± 1.4 and 0.6 ± 0.4, respectively, indicating that SUV max was significantly increased in malignant compared to benign lesions ( P  = 0.014). The PET/CT images taken 1 and 2 h after 18 F-FDG injection in a patient with ovarian cancer and peritoneal carcinomatosis and in a patient with pelvic tuberculosis are presented in Figure  1 . SUV max1 was 11.5 and 10.1 in a patient with ovarian cancer and a patient with pelvic tuberculosis, respectively. However, SUV max2 increased to 13.6 in the patient with ovarian cancer, whereas it decreased to 10.0 in the patient with pelvic tuberculosis. The results of the ROC analysis of SUV max1 are shown in Figure  2 . The area under the curve (AUC) of SUV max1 was 0.753 ( P  = 0.063, 95% confidence interval [CI] = 0.512–0.915), indicating that was not a useful parameter in differentiating benign from malignant lesions. When the SUV max1 cutoff value was set at 3.2, the sensitivity and specificity were 100% and 57.1%, respectively. The results of the ROC analysis of SUV max2 are shown in Figure  3 . In contrast, the AUC of SUV max2 was 0.835 ( P  = 0.001, 95% CI = 0.604–0.961), showing that the clinical usefulness of SUV max2 in differentiating benign from malignant lesions was statistically significant. When the SUV max2 cutoff value was set at 3.9, the sensitivity and specificity were 100% and 57.1%, respectively. Figure  4 shows the results of the ROC curve analysis of RI. The AUC was 0.901 ( P  < 0.001, 95% CI = 0.684–0.988), showing the greatest significance among the 3 parameters (SUV max1 , SUV max2 , and RI). When the RI cutoff value was set at 16.67, the sensitivity and specificity were 92.3% and 71.4%, respectively. The PET/CT images taken 1 h and 2 h after 18 F-FDG injection in a patient with ovarian cancer with peritoneal carcinomatosis (a) and pelvic tuberculosis (b). (a) Whole body MIP image (upper). Axial image showed that FDG uptake at 2 h was significantly increased than FDG uptake at 1 h (lower) (b) Whole body MIP image (upper). Axial image showed almost no change of FDG uptake between at 2 h and at 1 h (lower). MIP = multiple intensity projection. Receiver operating curve analysis of standardized uptake value (SUV) max1 . The sensitivity and specificity were calculated when the SUV max1 cutoff value was set at 3.2. Receiver operating curve analysis of standardized uptake value (SUV) max2 . The sensitivity and specificity were calculated when the SUV max2 cutoff value was set at 3.9. Receiver operating curve analysis of retention index. The sensitivity and specificity were calculated when the retention index cutoff value was set at 16.67. Pairwise comparison of the ROC curves was performed to compare the clinical utility of the 3 parameters in differentiating benign from malignant lesions. The AUC of SUV max2 was significantly higher than that of SUV max1 ( P  = 0.032). The AUC of RI was higher than both those of SUV max1 and SUV max2 , but the differences obtained were not statistically significant.

The authors declare that they have no competing interests.

SK and JHH devised the study and supervised the data collection. JKL and JHH performed wrote the manuscript. KAS and KJM contributed to the discussions and collected the data and performed the analyses. All authors contributed to the discussions. All authors read and approved the final manuscript.

Epithelial ovarian cancer is the leading cause of death among all other gynecological malignancies. The symptoms of this cancer are usually nonspecific, and most women are diagnosed at advanced stages. Therefore, early detection and characterization is crucial in patients who present with an adnexal mass for prompt surgical intervention and for improving survival. However, characterization of adnexal masses is often challenging to clinicians because both benign and malignant adnexal masses have overlapping imaging features [ 1 ]. To date, no strategies have proved to be effective in screening and early diagnosis of ovarian cancer [ 2 ]. Numerous imaging modalities, including computed tomography (CT) and magnetic resonance imaging (MRI), have been proposed as useful adjuncts to conventional ultrasound for the detection of ovarian cancer. However, despite having higher sensitivity and specificity than ultrasound, preoperative diagnosis using CT or MRI is often indeterminate [ 3 , 4 ]. Until recently, most series have used 18 F-fluorodeoxyglucose-positron emission tomography/CT ( 18 F-FDG-PET/CT) to detect recurrence or distant metastasis [ 5 - 8 ]. In contrast, only a few studies have demonstrated the effectiveness of 18 F-FDG-PET/CT in detecting primary ovarian cancer [ 9 , 10 ]. Despite high diagnostic value in identifying primary ovarian cancer, some pitfalls exist. False-positive results have been reported in patients with pelvic inflammatory disease (PID), tubo-ovarian abscess, and endometriosis [ 11 , 12 ], and false-negative results have been reported in patients with borderline tumors and early stage ovarian cancer [ 13 ]. To overcome this problem, acquisition of delayed images has been suggested. A previous study has demonstrated that 18 F-FDG uptake continues to rise for several hours after the injection of the radiotracer in various malignancies [ 14 ]. This dual-time acquisition procedure has proved to be valuable in differentiating benign from malignant lesions in some solid tumors [ 15 - 19 ]. However, it has not been validated in patients with ovarian cancers. The aim of our study is to establish the potential role of dual-phase 18 F-FDG PET/CT for improving diagnostic accuracy of ovarian cancers.

The purpose of this study was to evaluate the value of dual-phase 18 F-FDG-PET/CT in differentiating benign from malignant lesions in patients with indeterminate adnexal masses. We demonstrated that SUV max2 measured from images obtained from delayed phase scanning have a pivotal role when preoperative diagnosis is indeterminate. To the best of our knowledge, this is the first study to evaluate the clinical effectiveness of dual-phase 18 F-FDG-PET/CT in the initial diagnosis of suspected malignant adnexal masses. Although 18 F-FDG-PET/CT is a useful tool in differentiating benign from malignant lesions, it cannot be used for specifically determining malignant lesions. Some infectious or inflammatory lesions can also cause high 18 F-FDG uptake [ 20 ]. For example, Chen et al. [ 21 ] reported a patient with an adnexal mass referred for 18 F-FDG-PET/CT scan owing to elevated tumor marker levels. The 18 F-FDG-PET/CT scan showed multiple hypermetabolic foci in the peritoneum that mimicked peritoneal carcinomatosis. However, peritoneal tuberculosis was confirmed later. In our study, 3 out of 7 benign lesions were due to pelvic tuberculosis and mimicked peritoneal carcinomatosis. Conversely, most advanced stage ovarian cancers show peritoneal metastasis, and such peritoneal lesions often cause confusion during diagnosis because images obtained for these cancers are similar to those obtained for benign inflammatory conditions involving the gross peritoneal surface, as seen in our series. Generally, whole-body 18 F-FDG-PET/CT examination is performed 1 h after the administration of 18 F-FDG. This seems to be ideal taking into account the half-life of the radiotracer, which is 110 min [ 17 ]. However, many different acquisition protocols have been proposed to overcome the aforementioned false-negative or false-positive results obtained with 18 F-FDG-PET/CT. Saito et al. [ 15 ] used a protocol involving early-phase and delayed-phase scans (1 h and 2 h after 18 F-FDG administration) in 48 consecutive patients with intraductal papillary mucinous neoplasia of the pancreas. In this study, SUV max increased further in the delayed phase imaging in 92.3% patients with malignant pancreatic neoplasia, and only 60.0% of those with benign pancreatic neoplasia. This result is consistent with that of ours, in which SUV max increased significantly in delayed phase PET/CT in malignant but not benign lesions. Cheng et al. performed dual-phase 18 F-FDG-PET/CT in 35 patients with equivocal infiltrative hepatic lesions on abdominal CT or MRI scans [ 16 ]. In contrast to our study, the authors observed that SUV max was significantly higher in infiltrative hepatic malignancies than in benign lesions in both early (5.9 ± 5.0 versus 3.9 ± 1.7, respectively) and delayed images (6.8 ± 10.2 versus 4.1 ± 3.9, respectively). Thus, early phase SUV max of benign and malignant lesions were significantly different. In our study, only the AUC of SUV max2 was statistically significant in differentiating benign from malignant lesions. This might be attributed to either a different time point (45 min) for the early phase 18 F-FDG-PET/CT examination or organ-specific characteristics. Caprio et al. evaluated the performance of dual-phase 18 F-FDG-PET/CT in 48 patients suspected with breast lesions [ 17 ]. In their study, dual-time point acquisition of 18 F-FDG-PET/CT displayed an accuracy of 85% for lesions with a SUV max  ≥ 2.5, with sensitivity and specificity values of 81% and 100% compared with 63% and 100%, respectively, for the single-time point acquisition. In our study, the sensitivity and specificity of the SUV max2 were 100% and 57.1%, respectively, with a SUV max2  > 3.9. The relatively small number of patients and the different time point of the (3 h) in delayed phase 18 F-FDG-PET/CT examination might account for the differences in sensitivity and specificity. Yang et al. investigated whether adding delayed phase imaging can improve diagnostic ability of 18 F-FDG-PET in evaluating solitary pulmonary nodules [ 18 ]. In their study, combined early and delayed phase scans of 28 patients showed correct diagnosis of the 3 malignant lesions with an initial SUV < 2.5. Despite minor differences in the study design and results compared to those of our study, the abovementioned studies confirmed the clinical usefulness of dual-phase PET/CT in differentiating benign from malignant lesions. The major limitations of the current study include the small number of patients. Although patients were prospectively enrolled at the beginning of this study, selection bias could have been introduced. In other words, the clinicians’ attitudes to dual-phase PET/CT might affect the referral of patients. Second, this study was performed in a single institution. Differences in image acquisition and interpretation might influence the study results. Therefore, an additional large-scale, prospective study is necessary to check if our findings have an impact on future clinical practice. In addition, cost-effectiveness analysis should also be conducted. Despite these limitations, the findings of the present study provide useful information for the management of patients with equivocal adnexal masses; the sensitivities of both MRI and single-phase 18 F-FDG-PET/CT for detecting ovarian cancer have reported to be similar [ 22 , 23 ]. Hence, if differential diagnosis of an adnexal mass is indeterminate by MRI, then probably the usefulness of single-phase 18 F-FDG-PET/CT are also limited. Dual-phase 18 F-FDG-PET/CT may be a better procedure in resolving this ambiguity. Accurate preoperative assessment could help clinicians perform prompt debulking surgery in patients with “true positive” ovarian cancers, and avoid unnecessary surgery in patients with benign conditions.

SUV max2 obtained from dual-phase 18 F-FDG-PET/CT is a useful parameter in differentiating benign from malignant lesions in patients with indeterminate adnexal masses. Further studies with larger patient populations are warranted.

FDG-PET/CT: Fluorodeoxyglucose positron emission tomography / computed tomography; SUV: The standardized uptake value; SUVmax: The maximum standardized uptake value; AUCs: The areas under the receiver operating characteristic curves; CI: Confidence interval; CT: Computed tomography; MRI: Magnetic resonance imaging; PID: Pelvic inflammatory disease; RI: Retention index.