Outcomes after radiation therapy with concurrent weekly platinum-based chemotherapy or every-3-4-week 5-fluorouracil-containing regimens for squamous cell carcinoma of the vulva

被引:30
作者
Mak, Raymond H. [1 ]
Halasz, Lia M. [1 ]
Tanaka, Cynthia K. [2 ,3 ]
Ancukiewicz, Marek [3 ,4 ]
Schultz, Delray J. [5 ]
Russell, Anthony H. [3 ,4 ]
Viswanathan, Akila N. [2 ,3 ]
机构
[1] Harvard Radiat Oncol Program, Boston, MA USA
[2] Dana Farber Brigham & Womens Canc Ctr, Dept Radiat Oncol, Boston, MA USA
[3] Harvard Univ, Sch Med, Boston, MA USA
[4] Massachusetts Gen Hosp, Dept Radiat Oncol, Boston, MA 02114 USA
[5] Millersville Univ Pennsylvania, Dept Math, Millersville, PA 17551 USA
关键词
Chemotherapy; Radiotherapy; Squamous cell carcinoma; Vulvar cancer; LOCALLY ADVANCED-CARCINOMA; GYNECOLOGIC-ONCOLOGY-GROUP; ADVANCED CERVICAL-CANCER; PELVIC NODE RESECTION; PREOPERATIVE CHEMORADIATION; MITOMYCIN-C; RADICAL SURGERY; RADIOTHERAPY; CISPLATIN; TRIAL;
D O I
10.1016/j.ygyno.2010.09.004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective. To compare outcomes in patients with squamous cell carcinoma (SCC) of the vulva treated with radiation (RT) and concurrent weekly platinum-based or every-3-4-week regimens containing 5-fluorouracil (5-FU). Methods. Records of 44 patients with vulvar SCC treated with concurrent chemotherapy and radiation (chemoRT) from 1988 to 2008 were reviewed. Rates of disease-free survival (DFS), overall survival (OS), locoregional recurrence (LRR), and distant metastases (DM) were estimated using the Kaplan-Meier method. Results. The median age was 63 years (range, 44-90), 84.1% of patients had ECOG performance status 0-1, and patients had FIGO Stage II (n = 6), III (n = 31), or IVA (n = 7) disease. Patients were treated preoperatively (n = 10), postoperatively (n = 10), or without surgery (n = 24). The median RT dose to the vulva was 50.2 Gray (range, 22-75). Concurrent chemotherapy regimens included weekly platinum (n = 16) or every 3-4 week regimens with 5-FU as the backbone (n = 28). With a median follow-up of 31.5 months, there was no significant difference in 2-year OS (74.5% vs. 70.0%; p = 0.65), DFS (61.9% vs. 56.0%; p = 0.85), LRR (31.3% vs. 32.9%; p = 0.93), or DM (6.3% vs. 10.6%; p = 0.81) between the weekly platinum and every-3-4-week 5-FU regimens. Twenty patients (45.4%) recurred: 16 LRR, 2 DM, and 2 with both. The clinical and pathologic complete response rates were 58.8% (20/34), and 53.8% (14/26), respectively. There was a higher proportion of grade 3 or higher acute non-skin toxicities in patients receiving every-3-4-week 5-RI (46.1% vs. 13.3%; p = 0.07), but more grade 3 or higher skin toxicity in patients receiving weekly platinum (62.5% vs. 32.0%; p = 0.01). Conclusion. OS, response rates, and recurrence rates were not significantly different after RT with concurrent weekly platinum-based versus every-3-4-week regimens containing 5-FU for vulvar SCC. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:101 / 107
页数:7
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