Postoperative adjuvant gemcitabine and concurrent radiation after curative resection of pancreatic head carcinoma: A phase II study

被引:27
作者
Van Laethem, JL
Demols, A
Gay, F
Closon, MT
Collette, M
Polus, M
Houbiers, G
Gastelblum, P
Gelin, M
Van Houtte, P
Closset, J
机构
[1] Free Univ Brussels, Hop Erasme, Medsurg Dept Gastroenterol, B-1070 Brussels, Belgium
[2] CHU Sart Tilman, Dept Med Oncol & Radiotherapy, B-4000 Liege, Belgium
[3] Ctr Hosp Bois Abbaye, Seraing, Belgium
[4] Inst Jules Bordet, Dept Radiotherapy, B-1000 Brussels, Belgium
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2003年 / 56卷 / 04期
关键词
gemcitabine; radiation; adjuvant; pancreatic adenocarcinoma;
D O I
10.1016/S0360-3016(03)00164-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: The addition of radiation to adjuvant 5-fluorouracil for the treatment of pancreatic cancer has not yet shown any definite benefit. Gemcitabine (GEM) has potential activity in advanced pancreatic cancer and is a powerful radiosensitizer. We evaluated the feasibility of postoperative administration of GEM alone, followed by concurrent GEM and irradiation (RT) after curative resection for pancreatic adenocarcinoma. Methods and Materials: GEM 1000 mg/m(2) on Days 1 and 8 every 21 days for three courses was given within 8 weeks after surgery and was followed by GEM 300 mg/m(2) weekly +40 Gy in a split course. Twenty-two patients (median age 59 years, range 39-74, Performance Status 0-1) with Stage II and III curatively resected pancreatic head adenocarcinoma were included. Results: For GEM alone, all patients received the three planned courses, with dose reductions in 7 (32%) of 22 patients. All patients, except two, completed full chemoradiation; one received only 20 Gy because of both World Health Organization Grade 4 vomiting and thrombopenia and the other stopped RT after 32 Gy because of early disease progression. No reduction in GEM during RT was necessary; no toxic death was noted; and World Health Organization Grade 3-4 hematologic and nonhematologic toxicities occurred in 8 (36%) and 7 (nausea, vomiting) (32%) of 22 patients respectively. No late toxicity developed. After a median follow-up of 15 months, 11 patients were alive, and 2 patients had died of causes unrelated to their disease or toxicity, The median disease-free survival and overall survival was 6 and 15 months, respectively. Conclusion: This adjuvant regimen was well tolerated and can be easily administered after curative surgery for pancreatic cancer. Its intensification with continuous RT is currently being investigated. (C) 2003 Elsevier Inc.
引用
收藏
页码:974 / 980
页数:7
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