Preoperative hyperfractionated accelerated radiotherapy (HART) and concomitant CPT-11 in locally advanced rectal carcinoma: A phase I study

被引:14
作者
Voelter, V
Stupp, R [1 ]
Matter, M
Gillet, M
Bouzourene, H
Leyvraz, S
Coucke, P
机构
[1] CHU Vaudois, Univ Hosp, Multidisciplinary Oncol Ctr, CH-1011 Lausanne, Switzerland
[2] CHU Vaudois, Univ Hosp, Dept Surg, CH-1011 Lausanne, Switzerland
[3] CHU Vaudois, Univ Hosp, Dept Pathol, CH-1011 Lausanne, Switzerland
[4] CHU Vaudois, Univ Hosp, Dept Radiooncol, CH-1011 Lausanne, Switzerland
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2003年 / 56卷 / 05期
关键词
peoperative radiochemotherapy; CPT-11; hyperfractionated radiotherapy; rectal cancer;
D O I
10.1016/S0360-3016(03)00326-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Patients with locally advanced rectal carcinoma are at risk for both local recurrence and distant metastases. We demonstrated the efficacy of preoperative hyperfractionated accelerated radiotherapy (HART). In this Phase I trial, we aimed at introducing chemotherapy early in the treatment course with both intrinsic antitumor activity and a radiosensitizer effect. Methods and Materials: Twenty-eight patients (19 males; median age 63, range 28-75) with advanced rectal carcinoma (cT3: 24; cT4: 4; cN+: 12; M1: 5) were enrolled, including 8 patients treated at the maximally tolerated dose. Escalating doses of CPT-11 (30-105 mg/m(2)/week) were given on Days 1, 8, and 15, and concomitant HART (41.6 Gy, 1.6 Gy bid X 13 days) started on Day 8. Surgery was to be performed within 1 week after the end of radiochemotherapy. Results: Twenty-six patients completed all preoperative radiochemotherapy as scheduled; all patients underwent surgery. Dose-limiting toxicity was diarrhea Grade 3 occurring at dose level 6 (105 mg/m(2)). Hematotoxicity was mild, with only 1 patient experiencing Grade 3 neutropenia. Postoperative complications (30 days) occurred in 7 patients, with an anastomotic leak rate of 22%. Conclusions: The recommended Phase II dose of CPT-11 in this setting is 90 mg/m(2)/week. Further Phase II exploration at this dose is warranted. (C) 2003 Elsevier Inc.
引用
收藏
页码:1288 / 1294
页数:7
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