Factors associated with survival after relapse in patients with low-risk endometrial cancer treated with surgery alone / 부인종양

OBJECTIVE: To determine factors influencing overall survival following recurrence (OSFR) in women with low-risk endometrial cancer (EC) treated with surgery alone. METHODS: A multicenter, retrospective department database review was performed to identify patients with recurrent “low-risk EC” (patients having less than 50% myometrial invasion [MMI] with grade 1 or 2 endometrioid EC) at 10 gynecologic oncology centers in Turkey. Demographic, clinicopathological, and survival data were collected. RESULTS: We identified 67 patients who developed recurrence of their EC after initially being diagnosed and treated for low-risk EC. For the entire study cohort, the median time to recurrence (TTR) was 23 months (95% confidence interval [CI]=11.5–34.5; standard error [SE]=5.8) and the median OSFR was 59 months (95% CI=12.7–105.2; SE=23.5). We observed 32 (47.8%) isolated vaginal recurrences, 6 (9%) nodal failures, 19 (28.4%) peritoneal failures, and 10 (14.9%) hematogenous disseminations. Overall, 45 relapses (67.2%) were loco-regional whereas 22 (32.8%) were extrapelvic. According to the Gynecologic Oncology Group (GOG) Trial-99, 7 (10.4%) out of 67 women with recurrent low-risk EC were qualified as high-intermediate risk (HIR). The 5-year OSFR rate was significantly higher for patients with TTR ≥36 months compared to those with TTR <36 months (74.3% compared to 33%, p=0.001). On multivariate analysis for OSFR, TTR <36 months (hazard ratio [HR]=8.46; 95% CI=1.65–43.36; p=0.010) and presence of HIR criteria (HR=4.62; 95% CI=1.69–12.58; p=0.003) were significant predictors. CONCLUSION: Low-risk EC patients recurring earlier than 36 months and those carrying HIR criteria seem more likely to succumb to their tumors after recurrence.

Prognostic factors and treatment outcomes in surgically-staged non-invasive uterine clear cell carcinoma: a Turkish Gynecologic Oncology Group study / 부인종양

OBJECTIVE: To assess the prognosis of surgically-staged non-invasive uterine clear cell carcinoma (UCCC), and to determine the role of adjuvant therapy. METHODS: A multicenter, retrospective department database review was performed to identify patients with UCCC who underwent surgical treatment between 1997 and 2016 at 8 Gynecologic Oncology Centers. Demographic, clinicopathological, and survival data were collected. RESULTS: A total of 232 women with UCCC were identified. Of these, 53 (22.8%) had surgically-staged non-invasive UCCC. Twelve patients (22.6%) were upstaged at surgical assessment, including a 5.6% rate of lymphatic dissemination (3/53). Of those, 1 had stage IIIA, 1 had stage IIIC1, 1 had stage IIIC2, and 9 had stage IVB disease. Of the 9 women with stage IVB disease, 5 had isolated omental involvement indicating omentum as the most common metastatic site. UCCC limited only to the endometrium with no extra-uterine disease was confirmed in 41 women (73.3%) after surgical staging. Of those, 13 women (32%) were observed without adjuvant treatment whereas 28 patients (68%) underwent adjuvant therapy. The 5-year disease-free survival rates for patients with and without adjuvant treatment were 100.0% vs. 74.1%, respectively (p=0.060). CONCLUSION: Extra-uterine disease may occur in the absence of myometrial invasion (MMI), therefore comprehensive surgical staging including omentectomy should be the standard of care for women with UCCC regardless of the depth of MMI. Larger cohorts are needed in order to clarify the necessity of adjuvant treatment for women with UCCC truly confined to the endometrium.

Detection of high risk human papilloma viruses [HR-HPV] in endocervical scrapes from women with abnormal cytology in a Turkish university hospital

To assess the utility of a commercial PCR based HPV test for evaluating patients before colposcopy and colposcopic biopsy sampling in a Turkish hospital and to compare its efficacy with histology in preventing unnecessary colposcopic biopsy sampling. Case control study. Akdeniz University, Faculty of Medicine, Antalya, Turkey. One hundred and seventy-four women with abnormal Pap smear results [40 with high-grade squamous intraepithelial lesions [HSIL] and 134 with low-grade squamous intraepithelial lesions [LSIL] and 34 women with normal cytologic test results were included. Papanicolaou stainings and high risk HPV DNA [HR-HPV DNA] detections were done for all endocervical scrape specimens. Colposcopic evaluation and endocervical sampling were done for 52 patients. Papanicolaou stainings, HR-HPV DNA detections and histologic examination from endocervical samplings were evaluated. Human beta-globin was not detected in 40 samples. All of the 13 samples from patients with HR-HPV DNA positivity and HSIL were diagnosed as CIN2+ lesions [100%], whereas 23.2% [4/17] of patients with HR-HPV DNA negativity and HSIL were found to have CIN2+ lesions. HR-HPV DNA test, which also amplifies a genomic fragment as an internal control, seems to be a good screening tool. Besides the benefit of an early diagnosis of cervical cancer, HR-HPV DNA assay may also lead to a marked decrease in unnecessary invasive cervical samplings