Irinotecan plus fluorouracil and leucovorin for metastatic colorectal cancer.

被引:2436
|
作者
Saltz, LB
Cox, JV
Blanke, C
Rosen, LS
Fehrenbacher, L
Moore, MJ
Maroun, JA
Ackland, SP
Locker, PK
Pirotta, N
Elfring, GL
Miller, LL
机构
[1] Mem Sloan Kettering Canc Ctr, Gastroenterol Oncol Serv, New York, NY 10021 USA
[2] US Oncol, Dallas, TX USA
[3] Vanderbilt Canc Ctr, Nashville, TN USA
[4] Univ Calif Los Angeles, Med Ctr, Los Angeles, CA 90024 USA
[5] Kaiser Permanente Med Ctr, Vallejo, CA USA
[6] Princess Margaret Hosp, Toronto, ON M4X 1K9, Canada
[7] Ottawa Reg Canc Ctr, Ottawa, ON K1Y 4K7, Canada
[8] Newcastle Mater Misericordiae Hosp, Waratah, NSW, Australia
[9] Pharmacia Corp, Peapack, NJ USA
来源
NEW ENGLAND JOURNAL OF MEDICINE | 2000年 / 343卷 / 13期
关键词
D O I
10.1056/NEJM200009283431302
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: The combination of fluorouracil and leucovorin has until recently been standard therapy for metastatic colorectal cancer. Irinotecan prolongs survival in patients with colorectal cancer that is refractory to treatment with fluorouracil and leucovorin. In a multicenter trial, we compared a combination of irinotecan, fluorouracil, and leucovorin with bolus doses of fluorouracil and leucovorin as first-line therapy for metastatic colorectal cancer. A third group of patients received irinotecan alone. Methods: Patients were randomly assigned to receive irinotecan (125 mg per square meter of body-surface area intravenously), fluorouracil (500 mg per square meter as an intravenous bolus), and leucovorin (20 mg per square meter as an intravenous bolus) weekly for four weeks every six weeks; fluorouracil (425 mg per square meter as an intravenous bolus) and leucovorin (20 mg per square meter as an intravenous bolus) daily for five consecutive days every four weeks; or irinotecan alone (125 mg per square meter intravenously) weekly for four weeks every six weeks. End points included progression-free survival and overall survival. Results: Of 683 patients, 231 were assigned to receive irinotecan, fluorouracil, and leucovorin; 226 to receive fluorouracil and leucovorin; and 226 to receive irinotecan alone. In an intention-to-treat analysis, as compared with treatment with fluorouracil and leucovorin, treatment with irinotecan, fluorouracil, and leucovorin resulted in significantly longer progression-free survival (median, 7.0 vs. 4.3 months; P = 0.004), a higher rate of confirmed response (39 percent vs. 21 percent, P<0.001), and longer overall survival (median, 14.8 vs. 12.6 months; P = 0.04). Results for irinotecan alone were similar to those for fluorouracil and leucovorin. Grade 3 (severe) diarrhea was more common during treatment with irinotecan, fluorouracil, and leucovorin than during treatment with fluorouracil and leucovorin, but the incidence of grade 4 (life-threatening) diarrhea was similar in the two groups (<8 percent). Grade 3 or 4 mucositis, grade 4 neutropenia, and neutropenic fever were less frequent during treatment with irinotecan, fluorouracil, and leucovorin. Adding irinotecan to the regimen of fluorouracil and leucovorin did not compromise the quality of life. Conclusions: Weekly treatment with irinotecan plus fluorouracil and leucovorin is superior to a widely used regimen of fluorouracil and leucovorin for metastatic colorectal cancer in terms of progression-free survival and overall survival. (N Engl J Med 2000;343:905-14.) (C) 2000, Massachusetts Medical Society.
引用
收藏
页码:905 / 914
页数:10
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