Biweekly intensified ambulatory chronomodulated chemotherapy with oxaliplatin, fluorouracil, and leucovorin in patients with metastatic colorectal cancer

被引:142
作者
BertheaultCvitkovic, F
Jami, A
Ithzaki, M
Brummer, PD
Brienza, S
Adam, R
Kunstlinger, F
Bismuth, H
Misset, JL
Levi, F
机构
[1] HOP PAUL BROUSSE, LAB RYTHMES BIOL & CHRONOTHERAPEUT, INST CANC & IMMUNOGENET, F-94807 VILLEJUIF, FRANCE
[2] HOP PAUL BROUSSE, CTR HEPATOBILIAIRE, F-94807 VILLEJUIF, FRANCE
[3] HOP PAUL BROUSSE, CTR CHRONOTHERAPIE, SERV MALAD SANGUNIES IMMUNITAIRES & TUMORALES, F-94807 VILLEJUIF, FRANCE
关键词
D O I
10.1200/JCO.1996.14.11.2950
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: This study sought to determine the feasibility and antitumor efficacy of an intensified three-drug chronomodulated regimen with maximum delivery at 4:00 AM for fluorouracil (5-FU)-leucovorin (folinic acid [FA]) and at 4:00 PM for oxaliplatin (I-OHP). Patients and Methods: Fifty patients with metastatic coloretal cancer were enrolled in the trial. The first treatment course consisted of daily administration of 5-FU (700 mg/m(2)/d), FA (300 mg/m(2)/d), and L-OHP (25 mg/m(2)/d) for 4 days with a multichannel programmable pump. Courses were repeated every 14 days, with 5-FU escalation by 100 mg/m(2)/d if toxicity was less than grade 2. Results: World Health Organization (WHO)-modified grade 3 or 4 diarrhea (40% of patients and 7% of courses) or stomatitis (28% of patients and 4% of courses) or grade 2 cumulative peripheral sensitive neuropathy (28% of patients) were dose-limiting, Median 5-FU and L-OHP dose-intensities (DIs), were increased by 32% and 18%, respectively, as compared with our previous 5 days on-16 days off schedule, The overall objective response rate was 48% (95% confidence limits [CL], 34% to 62%), being 40% (24% to 57%) in 37 previously treated patients and 69% (48% to 90%) in 13 chemotherapy-naive patients, A 5-FU DI >1,400 mg/m(2)/wk over four courses was associated with a near doubling of the response rate, Residual metastases were surgically removed in 13 patients (26%). Median progression-free survival and survival durations were 9.3 months (95% CL, 6.6 to 11.2) and 17.8 months (95% CL, 14.1 to 21.4), respectively. Conclusion: This highly effective fully ambulatory outpatient regimen deserves further testing in randomised trials both in chemotherapy-naive patients and before surgery to remove metastases. (C) 1996 American Society of Clinical Oncology.
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页码:2950 / 2958
页数:9
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