Adjuvant vaginal cuff brachytherapy for high-risk, early stage endometrial cancer

作者:Eldredge Hindy Harriet Belding*; Eastwick Gary; Anne Pramila Rani; Rosenblum Norman G; Schilder Russell J; Chalian Raffi; Zibelli Allison M; Kim Christine H; Den Robert
来源:Journal of Contemporary Brachytherapy, 2014, 6(3): 262-270.
DOI:10.5114/jcb.2014.45031

摘要

Purpose: To report outcomes following adjuvant high-dose-rate vaginal brachytherapy (VET) with or without chemotherapy for high-intermediate risk (HIR) and high-risk, early stage endometrial cancer as defined in Gynecologic Oncology Group trial 0249. %26lt;br%26gt;Material and methods: From May 2000 to January 2014, 68 women with HIR and high-risk endometrial cancer underwent surgical staging followed by VBT. Median VBT dose was 21 Gy delivered in three fractions prescribed to 0.5 cm depth. Paclitaxel 175 mg/m(2) and carboplatin area under the curve 6 was administered every 21 days in sequence with VBT. Actuarial survival estimates were calculated using the Kaplan-Meier method. %26lt;br%26gt;Results: Patient demographics included a median age of 66 years (range: 36-91) and stages IA (49%), IB (38%), and II (13%), respectively. Thirty-one (46%) patients had HIR disease with endometrioid histology, and 33 (48%) patients had serous or clear cell histology. Thirty-seven (54%) patients received a median 3 cycles (range: 3-6) of chemotherapy in addition to VBT, and 65 patients (96%) completed all prescribed therapy. During a median follow up of 33.1 months (range: 4.0-161.7), four patients have recurred, including one vaginal recurrence. The 3-year estimates of vaginal, pelvic, and distant recurrences were 1.9%, 2.4%, and 9.1%, respectively. The 3-year rates of disease-free and overall survival were 87.7% and 93.9%, respectively. %26lt;br%26gt;Conclusions: Early outcomes with adjuvant VBT with or without chemotherapy demonstrate high rates of vaginal and pelvic control for women with HIR disease. Early vaginal and pelvic relapses in high-risk patients suggest that pelvic external beam radiotherapy is warranted in this subgroup, but additional data from large phase III trials is warranted.

  • 出版日期2014-9