Irinotecan plus Fluorouracil and Leucovorin for Metastatic Colorectal Cancer
Leonard B. Saltz, M.D., John V. Cox, D.O., Charles Blanke, M.D., Lee S. Rosen, M.D., Louis Fehrenbacher, M.D., Malcolm J. Moore, M.D., Jean A. Maroun, M.D., Stephen P. Ackland, M.B., B.S., Paula K. Locker, M.S., Nicoletta Pirotta, M.S., Gary L. Elfring, M.S., Langdon L. Miller, M.D., for The Irinotecan Study Group
Background The combination of fluorouracil and leucovorin hasuntil recently been standard therapy for metastatic colorectalcancer. Irinotecan prolongs survival in patients with colorectalcancer that is refractory to treatment with fluorouracil andleucovorin. In a multicenter trial, we compared a combinationof irinotecan, fluorouracil, and leucovorin with bolus dosesof fluorouracil and leucovorin as first-line therapy for metastaticcolorectal cancer. A third group of patients received irinotecanalone.
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 mgper square meter as an intravenous bolus) and leucovorin (20mg per square meter as an intravenous bolus) daily for fiveconsecutive days every four weeks; or irinotecan alone (125mg per square meter intravenously) weekly for four weeks everysix weeks. End points included progression-free survival andoverall survival.
Results Of 683 patients, 231 were assigned to receive irinotecan,fluorouracil, and leucovorin; 226 to receive fluorouracil andleucovorin; and 226 to receive irinotecan alone. In an intention-to-treatanalysis, as compared with treatment with fluorouracil and leucovorin,treatment with irinotecan, fluorouracil, and leucovorin resultedin significantly longer progression-free survival (median, 7.0vs. 4.3 months; P=0.004), a higher rate of confirmed response(39 percent vs. 21 percent, P<0.001), and longer overallsurvival (median, 14.8 vs. 12.6 months; P=0.04). Results foririnotecan alone were similar to those for fluorouracil andleucovorin. Grade 3 (severe) diarrhea was more common duringtreatment with irinotecan, fluorouracil, and leucovorin thanduring treatment with fluorouracil and leucovorin, but the incidenceof grade 4 (life-threatening) diarrhea was similar in the twogroups (<8 percent). Grade 3 or 4 mucositis, grade 4 neutropenia,and neutropenic fever were less frequent during treatment withirinotecan, fluorouracil, and leucovorin. Adding irinotecanto the regimen of fluorouracil and leucovorin did not compromisethe quality of life.
Conclusions Weekly treatment with irinotecan plus fluorouraciland leucovorin is superior to a widely used regimen of fluorouraciland leucovorin for metastatic colorectal cancer in terms ofprogression-free survival and overall survival.
Source Information
From Memorial Sloan-Kettering Cancer Center, New York (L.B.S.); U.S. Oncology, Dallas (J.V.C.); the Vanderbilt Cancer Center, Nashville (C.B.); UCLA Medical Center, Los Angeles (L.S.R.); Kaiser Permanente Medical Center, Vallejo, Calif. (L.F.); Princess Margaret Hospital, Toronto (M.J.M.); Ottawa Regional Cancer Center, Ottawa, Ont., Canada (J.A.M.); Newcastle Mater Misericordiae Hospital, Waratah, N.S.W., Australia (S.P.A.); and Pharmacia Corporation, Peapack, N.J. (P.K.L., N.P., G.L.E., L.L.M.).
Address reprint requests to Dr. Saltz at the Gastrointestinal Oncology Service, Memorial Sloan-Kettering Cancer Center, 1275 York Ave., New York, NY 10021.
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