Leucovorin and fluorouracil with or without oxaliplatin as first-line treatment in advanced colorectal cancer

被引:3109
作者
de Gramont, A
Figer, A
Seymour, M
Homerin, M
Hmissi, A
Cassidy, J
Boni, C
Cortes-Funes, H
Cervantes, A
Freyer, G
Papamichael, D
Le Bail, N
Louvet, C
Hendler, D
de Braud, F
Wilson, C
Morvan, F
Bonetti, A
机构
[1] Hop St Antoine, Serv Med Interne Oncol, F-75571 Paris 12, France
[2] Debiopharm, Charenton Le Pont, France
[3] Ctr Hosp Lyon Sud, Med Oncol Serv, Pierre Benite, France
[4] Ctr Hosp Rene Dubos, Pontoise, France
[5] Belinson Med Ctr, Inst Oncol, Petah Tiqwa, Israel
[6] Univ Leeds, Imperial Canc Res Fund, Canc Med Res Unit, Leeds, W Yorkshire, England
[7] Univ Aberdeen, Dept Med & Therapeut, Aberdeen, Peoples R China
[8] St Bartholomews Hosp, Dept Med Oncol, London, England
[9] Addenbrookes Natl Hlth Serv Trust, Cambridge, England
[10] Arcispedale S Maria Nuova, Med Oncol Serv, Reggio Emilia, Italy
[11] Inst Europe Oncol, Milan, Italy
[12] Osped Verona, Div Oncol Med Azienda, Med Oncol Serv, Clin Oncol Ctr, Verona, Italy
[13] Hosp 12 Octubre, Serv Oncol, Madrid, Spain
[14] Hosp Clin Univ, Serv Oncohematol, Valencia, Spain
关键词
D O I
10.1200/JCO.2000.18.16.2938
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: In a previous study of treatment for advanced colorectal cancer, the LV5FU2 regimen, comprising leucovorin (LV) plus bolus and infusional fluorouracil (5FU) every 2 weeks, was superior to the standard North Central Cancer Treatment Group/Mayo Clinic 5-day bolus 5FU/LV regimen. This phase III study investigated the effect of combining oxaliplatin with LV5FU2, with progression-free survival as the primary end point. Patients and Methods: Four hundred twenty previously untreated patients with measurable disease were randomized to receive a 2-hour infusion of LV (200 mg/m(2)/d) followed by a 5FU bolus (400 mg/m(2)/d) and 22-hour infusion (600 mg/m(2)/d) for 2 consecutive days every 2 weeks, either alone or together with oxaliplatin 85 mg/m(2) as a 2-hour infusion on day 1. Results: Patients allocated to oxaliplatin plus LV5FU2 had significantly longer progression-free survival (median, 9.0 v 6.2 months; P = .0003) and better response rate (50.7% v 22.3%; P = .0001) when compared with the control arm. The improvement in overall survival did not reach significance (median, 16.2 v 14.7 months; P = .12). LV5FU2 plus oxaliplatin gave higher frequencies of National Cancer Institute common toxicity criteria grade 3/4 neutropenia (41.7% v 5.3% of patients), grade 3/4 diarrhea (11.9% v 5.3%), and grade 3 neurosensory toxicity (18.2% v 0%), but this did not result in impairment of quality of life (QoL). Survival without disease progression or deterioration in global health status was longer in patients allocated to oxaliplatin treatment (P = .004). Conclusion: The LV5FU2-oxaliplatin combination seems beneficial as first-line therapy in advanced colorectal cancer, demonstrating a prolonged progression-free survival with acceptable tolerability and maintenance of QoL. (C) 2000 by American Society of Clinical Oncology.
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收藏
页码:2938 / 2947
页数:10
相关论文
共 44 条
[1]  
AARANSON NK, 1993, J NATL CANCER I, V85, P365
[2]  
*AM CANC SOC, 1995, CANC FACTS FIG 1995
[3]   Bimonthly high-dose leucovorin, 5-fluorouracil infusion and oxaliplatin (FOLFOX3) for metastatic colorectal cancer resistant to the same leucovorin and 5-fluorouracil regimen [J].
André, T ;
Louvet, C ;
Raymond, E ;
Tournigand, C ;
de Gramont, A .
ANNALS OF ONCOLOGY, 1998, 9 (11) :1251-1253
[4]   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
[5]   Modulation of high-dose infusional fluorouracil by low-dose methotrexate in patients with advanced or metastatic colorectal cancer: Final results of a randomized European Organization for Research and Treatment of Cancer Study [J].
Blijham, G ;
Wagener, T ;
Wils, J ;
deGreve, J ;
Buset, M ;
Bleiberg, H ;
Lacave, A ;
Dalmark, M ;
Selleslag, J ;
Collette, L ;
Sahmoud, T .
JOURNAL OF CLINICAL ONCOLOGY, 1996, 14 (08) :2266-2273
[6]  
CARMICHAEL J, 1999, P AN M AM SOC CLIN, V18, pA264
[7]  
COX DR, 1972, J R STAT SOC B, V34, P187
[8]  
COX J, 1999, P AN M AM SOC CLIN, V18, pS265
[9]   Final results of a randomised trial comparing 'Tomudex'(R) (raltitrexed) with 5-fluorouracil plus leucovorin in advanced colorectal cancer [J].
Cunningham, D ;
Zalcberg, JR ;
Rath, U ;
Oliver, I ;
vanCutsem, E ;
Svensson, C ;
Seitz, JF ;
Harper, P ;
Kerr, D ;
PerezManga, G .
ANNALS OF ONCOLOGY, 1996, 7 (09) :961-965
[10]   Randomised trial of irinotecan plus supportive care versus supportive care alone after fluorouracil failure for patients with metastatic colorectal cancer [J].
Cunningham, D ;
Pyrhönen, S ;
James, RD ;
Punt, CJA ;
Hickish, TF ;
Heikkila, R ;
Johannesen, TB ;
Starkhammar, H ;
Topham, CA ;
Awad, L ;
Jacques, C ;
Herait, P .
LANCET, 1998, 352 (9138) :1413-1418