Factors predicting for efficacy of oxaliplatin in combination with 5-fluorouracil (5-FU)±folinic acid (FA) in a compassionate-use cohort of 370 5-FU-resistant advanced colorectal cancer (CRC) patients

被引:7
作者
Bensmaïne, MA
de Gramont, A
Brienza, S
Marty, M
Lévi, F
Ducreux, M
François, E
Gamelin, E
Bleiberg, H
Bleuzen, P
Simon, J
Cvitkovic, E [1 ]
机构
[1] Cvitkov & Associates, Le Kremlin Bicetre, France
[2] Hop St Antoine, Serv Med Interne Oncol, F-75571 Paris, France
[3] Debiopharm, Charenton Le Pont, France
[4] Hop St Louis, Med Oncol Serv, Paris, France
[5] Hop Paul Brousse, Serv Cancerol, Villejuif, France
[6] Inst Gustave Roussy, Dept Med, Villejuif, France
[7] Ctr Antoine Lacassagne, Oncopharmacol Unit, F-06054 Nice, France
[8] Ctr Paul Papin, Dept Oncol Med & Oncopharmacol, Angers, France
[9] Inst Jules Bordet, Dept Gastroenterol, B-1000 Brussels, Belgium
关键词
clinical resistance; multivariate analysis; salvage chemotherapy;
D O I
10.1016/S0959-8049(00)00305-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Univariate and multivariate analyses were performed on data from 370 5-fluorouracil (5-FU)-resistant advanced colorectal cancer patients treated with oxaliplatin (Eloxatin(R))/5-FU+/-folinic acid (FA) to identify prognostic factors for oxaliplatin-based treatment. The response rate was 14.6% (95% confidence interval (CT): 11.0-18.2%), median time to progression was 4.3 months (95% CI, 3.9-4.7), and median overall survival 9.7 months (95% CT: 8.5-10.8). Multivariate analysis indicated <2 prior chemotherapy regimens, bi-weekly treatment administration schedule (versus tri-weekly) and continuous chronomodulated delivery (CCM) as significantly associated (P < 0.05) with a higher overall response rate. Performance status (PS) <2, having only one involved organ, biweekly schedule and CCM were associated (P<0.05) with a longer time to progression. Good PS, one involved organ, low alkaline phosphatase (AP) serum levels, bi-weekly schedule and CGM were significantly correlated with longer overall survival, while confirming the efficacy of oxaliplatin/5-FU+/-FA in this indication. (C) 2000 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:2335 / 2343
页数:9
相关论文
共 38 条
[1]  
ANDRE T, 1997, P AN M AM SOC CLIN, V16, P270
[2]  
[Anonymous], 1989, Analysis of binary data
[3]   Phase II trial of oxaliplatin as first-line chemotherapy in metastatic colorectal cancer patients [J].
Bécouarn, Y ;
Ychou, M ;
Ducreux, M ;
Borel, C ;
Bertheault-Cvitkovic, F ;
Seitz, JF ;
Nasca, S ;
Nguyen, TD ;
Paillot, B ;
Raoul, JL ;
Duffour, J ;
Fandi, A ;
Dupont-André, G ;
Rougier, P .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (08) :2739-2744
[4]  
BEHRENS BC, 1989, P AN M AM SOC CLIN, V8, P126
[5]   Biweekly intensified ambulatory chronomodulated chemotherapy with oxaliplatin, fluorouracil, and leucovorin in patients with metastatic colorectal cancer [J].
BertheaultCvitkovic, F ;
Jami, A ;
Ithzaki, M ;
Brummer, PD ;
Brienza, S ;
Adam, R ;
Kunstlinger, F ;
Bismuth, H ;
Misset, JL ;
Levi, F .
JOURNAL OF CLINICAL ONCOLOGY, 1996, 14 (11) :2950-2958
[6]   CANCER STATISTICS, 1992 [J].
BORING, CC ;
SQUIRES, TS ;
TONG, T .
CA-A CANCER JOURNAL FOR CLINICIANS, 1992, 42 (01) :19-38
[7]  
COX DR, 1972, J R STAT SOC B, V34, P187
[8]   Oxaliplatin with high-dose leucovorin and 5-fluorouracil 48 hour continuous infusion in pretreated metastatic colorectal cancer [J].
deGramont, A ;
Vignoud, J ;
Tournigand, C ;
Louvet, C ;
Andre, T ;
Varette, C ;
Raymond, E ;
Moreau, S ;
LeBail, N ;
Krulik, M .
EUROPEAN JOURNAL OF CANCER, 1997, 33 (02) :214-219
[9]   CONTINUOUS-INFUSION 5-FLUOROURACIL IN METASTATIC COLORECTAL-CANCER PATIENTS PRETREATED WITH BOLUS 5-FLUOROURACIL - CLINICAL-EVIDENCE OF INCOMPLETE CROSS-RESISTANCE [J].
FALCONE, A ;
CIANCI, C ;
PFANNER, E ;
BERTUCCELLI, M ;
BRUNETTI, I ;
MUTTINI, MP ;
DARGENIO, F ;
RICCI, S ;
CONTE, PF .
ANNALS OF ONCOLOGY, 1994, 5 (03) :291-291
[10]  
GARUFI C, 1995, P AN M AM SOC CLIN, V14, P192