Preoperative intensity-modulated radiotherapy and chemotherapy for locally advanced vulvar carcinoma

被引:45
|
作者
Beriwal, Sushil [1 ]
Coon, Devin [1 ]
Heron, Dwight E. [1 ]
Kelley, Joseph L. [2 ]
Edwards, Robert P. [2 ]
Sukumvanich, Paniti [2 ]
Zorn, Kristin K. [2 ]
Krivak, Thomas C. [2 ]
机构
[1] Univ Pittsburgh, Inst Canc, Dept Radiat Oncol, Pittsburgh, PA USA
[2] Univ Pittsburgh, Inst Canc, Div Gynecol Oncol, Pittsburgh, PA USA
关键词
IMRT; chemoradiation; vulva;
D O I
10.1016/j.ygyno.2007.10.026
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective. Intensity-modulated radiation therapy (IMRT) is a rapidly maturing technology that allows delivery of radiation dose in a more conformal manner by varying the radiation beams spatially or temporally. The purpose of the study was to assess the clinical outcome in patients with locally-advanced vulvar cancers treated using preoperative chemotherapy with IMRT. Methods. Eighteen patients with stage II-IVA cancer were treated with a modified GOG schema using 5-fluorouracil (5-FU) and cisplatin with twice-daily (BID) IMRT during the first and last weeks of treatment. Surgery was planned for 6-8 weeks post-treatment. Results. The median follow-up time was 22 months (2-60 months). Fourteen patients had surgery performed with Pathological complete response (pCR) in 9 (64%) patients and partial response (pPR) in 5 patients. There were no recurrences in the 9 patients who achieved pCR whereas 315 with pPR had local recurrence (p=0.027). Four patients did not have surgery: one patient died a week after treatment while 2 of the remaining 3 patients had local recurrences. Acute desquamative skin reactions in the vulva and perineum were seen in all patients. Three of the 14 patients who had surgery had prolonged wound complications requiring debridement. No patients had radiation-related acute or late toxicity of grade =3. The 2-year cause specific and overall survivals were 75% and 70% respectively. Conclusion. Preoperative chemotherapy and IMRT were well tolerated with good clinical response and early clinical outcome. Pathological complete response predicts better outcomes. Prospective clinical trials with sufficient patient numbers and follow-up are needed to determine the true impact of IMRT in these patients. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:291 / 295
页数:5
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