Shortened irradiation scheme, continuous infusion of 5-fluorouracil and fractionation of mitomycin C in locally advanced anal carcinomas.: Results of a phase II study of the European Organization for Research and Treatment of Cancer.: Radiotherapy and Gastrointestinal Cooperative Groups

被引:62
作者
Bosset, JF [1 ]
Roelofsen, F
Morgan, DAL
Budach, V
Coucke, P
Jager, JJ
Van der Steen-Banasik, E
Trivière, N
Stüben, G
Puyraveau, M
Mercier, M
机构
[1] Besancon Univ Hosp, Dept Radiotherapy, Besancon, France
[2] Univ Essen Gesamthsch Klinikum, Klin Allgemein & Visceralchirurg, D-4300 Essen, Germany
[3] City Hosp, Dept Clin Oncol, Nottingham NG5 1PB, England
[4] Charite Hosp, Klin Strahlentherapie, Berlin, Germany
[5] CHU Vaudois, Dept Radiotherapie Oncol, CH-1011 Lausanne, Switzerland
[6] Radiotherapeut Inst Limburg, Heerlen, Netherlands
[7] Arnhems Radiotherapy Inst, Dept Radiotherapy, Arnhem, Netherlands
[8] Inst Jules Bordet, Dept Radiotherapy, B-1000 Brussels, Belgium
[9] Univ Essen Gesamthsch Klinikum, Strahlenklin, D-4300 Essen, Germany
关键词
chemoradiotherapy; anal cancer; accelerated treatment; phase II clinical trial;
D O I
10.1016/S0959-8049(02)00377-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The European Organization for Research and Treatment of Cancer (EORTC) 22861 randomised trial established that combined radiochemotherapy is the standard treatment for locally advanced anal cancer. This EORTC phase II study (#22953) tests the feasibility of reducing the gap between sequences to 2 weeks, to deliver Mitomycin C (MMC) in each radiotherapy sequence and 5-FU continuously during the treatment. The first sequence consisted of 36 Gy over 4 weeks. 5-FU 200 mg/m(2)/days 1-26, MMC 10 mg/m(2)/day 1 gap 16 days. Then a second sequence of 23.4 Gy over 17 days, 5-FU 200 mg/m(2)/days 1-17 and, MMC 10 mg/m(2)/day 1 was given. 43 patients with a World Health Organization (WHO) status of 0 (n = 27) or 1 (n = 16) and with T2-T4, N0-3 tumours were included. Compliance with the planned treatment, doses and duration was 93%. The complete response rate was 90.7%. Grade 3 toxicities of 28, 12 and 2% were observed for skin, diarrhoea and haematological toxicities, respectively. The 3-year estimated rates for trials 22861 and 22953 are: 68 and 88% for local control; 72 and 81% for colostomy-free interval, 62 and 84% for severe late toxicity-free interval, and 70 and 81% for survival, respectively. The 22953 scheme is feasible and the results are promising. This is now considered as the new standard scheme by the EORTC. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:45 / 51
页数:7
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