Paclitaxel-based chemoradiotherapy in the treatment of patients with operable esophageal cancer

被引:43
作者
Kelsey, Chris R.
Chino, Junzo P.
Willett, Christopher G.
Clough, Robert W.
Hurwitz, Herbert I.
Morse, Michael A.
Bendell, Johanna C.
D'Amico, Thomas A.
Czito, Brian G.
机构
[1] Duke Univ, Med Ctr, Dept Radiat Oncol, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Dept Internal Med, Div Med Oncol & Transplantat, Durham, NC 27710 USA
[3] Duke Univ, Med Ctr, Dept Gen Surg, Durham, NC 27710 USA
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2007年 / 69卷 / 03期
关键词
esophageal cancer; paclitaxel; neoadjuvant; chemoradiation; pathologic response;
D O I
10.1016/j.ijrobp.2007.03.035
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To compare a neoadjuvant regimen of cisplatin/5-fluorouracil (5-FU) and concurrent radiation therapy (RT) with paclitaxel-based regimens and RT in the management of operable esophageal (EC)/gastroesophageal junction (GEJ) cancer. Methods and Materials: All patients receiving neoadjuvant chemotherapy (CT) and RT for EC/GEJ cancer at Duke University between January 1995 and December 2004 were included. Clinical end points were compared for patients receiving paclitaxel-based regimens (TAX) vs. alternative regimens (non-TAX). Local control (LC), disease-free survival (DFS), and overall survival (OS) were estimated using the Kaplan-Meier method. Chi-square analysis was performed to test the effect of TAX on pathologic complete response (pCR) rates and toxicity. Results: A total of 109 patients received CT-RT followed by esophagectomy (95 M; 14 F). Median RT dose was 45 Gy (range, 36-66 Gy). The TAX and non-TAX groups comprised 47% and 53% of patients, respectively. Most (83%) TAX patients received three drug regimens including platinum and a fluoropyrimidine. In the non-TAX group, 89% of the patients received cisplatin and 5-FU. The remainder received 5-FU or capecitabine alone. Grade 3-4 toxicity occurred in 41% of patients receiving TAX vs. 24% of those receiving non-TAX (p =0.19). Overall pCR rate was 39% (39% with TAX vs. 40% with non-TAX,p = 0.9). Overall LC, DFS, and OS at 3 years were 80%, 34%, and 37%, respectively. At 3 years, there were no differences in LC (75% vs. 85%, p = 0.33) or OS (37% vs. 37 %, p = 0.32) between TAX and non-TAX groups. Conclusions: In this large experience, paclitaxel-containing regimens did not improve pCR rates or clinical end points compared to non-paclitaxel-containing regimens. (C) 2007 Elsevier Inc.
引用
收藏
页码:770 / 776
页数:7
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