EORTC Early Clinical Studies Group early phase II trial of S-I in patients with advanced or metastatic colorectal cancer

被引:71
作者
Van den Brande, J
Schöffski, P
Schellens, JHM
Roth, AD
Duffaud, F
Weigang-Köhler, K
Reinke, F
Wanders, J
de Boer, RF
Vermorken, JB
Fumoleau, P
机构
[1] Univ Hosp, Dept Med Oncol, B-2650 Edegem, Belgium
[2] Hannover Med Sch, Dept Haematol & Oncol, D-30625 Hannover, Germany
[3] Netherlands Canc Inst, Antoni Van Leeuwenhoek Ziekenhuis, NL-1066 CX Amsterdam, Netherlands
[4] Geneva Univ Hosp, Dept Surg, CH-1211 Geneva, Switzerland
[5] CHU Timone, Med Oncol Unit, F-13385 Marseille 5, France
[6] Klin Nurnberg, D-90419 Nurnberg, Germany
[7] NDDO Oncol, NL-1081 JD Amsterdam, Netherlands
[8] Ctr Rene Gauducheau, Dept Med Oncol, F-44805 St Herblain, France
关键词
colorectal cancer; fluoropyrimidines; oral; phase II; S-I; FIRST-LINE TREATMENT; FLUOROURACIL PLUS LEUCOVORIN; ADVANCED GASTRIC-CANCER; INTRAVENOUS FLUOROURACIL; ANTITUMOR-ACTIVITY; ORAL FLUOROURACIL; LIVER METASTASES; S-1; 5-FLUOROURACIL; OXALIPLATIN;
D O I
10.1038/sj.bjc.6600781
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cancer of the colon and rectum is one of the most frequent malignancies both in the US and Europe. Standard palliative therapy is based on 5-fluorouracil/folinic acid combinations, with or without oxaliplatin or irinotecan, given intravenously, Oral medication has the advantage of greater patient convenience and acceptance and potential cost savings. S-1 is a new oral fluorinated pyrimidine derivative. In a nonrandomised phase II study, patients with advanced/metastatc colorectal cancer were treated with S-1 at 40 mg m(-2) b.i.d. for 28 consecutive days, repeated every 5 weeks, but by amendment the dose was reduced to 35 mg m-2 during the study because of a higher than expected number of severe adverse drug reactions. In total 47 patients with colorectal cancer were included. In the 37 evaluable patients there were nine partial responses (24%), 17 stable diseases (46%) and II patients had progressive disease (30%). Diarrhoea occurred frequently and was often severe: in the 40 and 35 mg m(-2) group, respectively, 38 and 35% of the patients experienced grade 3-4 diarrhoea. The other toxicites were limited and manageable. S-1 is active in advanced colorectal cancer, but in order to establish a safer dose the drug should be subject to further investigations. (C) 2003 Cancer Research UK.
引用
收藏
页码:648 / 653
页数:6
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