Survival impact of chemotherapy in patients with colorectal metastases confined to the liver: A re-analysis of 1458 non-operable patients randomised in 22 trials and 4 meta-analyses

被引:42
作者
Thirion, P
Wolmark, N
Haddad, E
Buyse, M
Piedbois, P [1 ]
机构
[1] Hop Henri Mondor, Dept Oncol, F-94010 Creteil, France
[2] Inst Human Oncol, Dept Surg, Pittsburgh, PA USA
[3] Int Inst Drug Dev, Brussels, Belgium
关键词
advanced colorectal cancer; chemotherapy; meta-analysis; non-operable metastases confined to the liver;
D O I
10.1023/A:1008365511961
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Metastases confined to the liver is a frequent situation in patients with advanced colorectal cancer. For non-operable patients, 5-FU-based chemotherapy is often proposed but the importance of the choice of first line 5-FU regimen remains debatable. Design: In four previously performed meta-analyses, our group had compared bolus intravenous fluoropyrimidines (bolus FU group) with experimental fluoropyrimidines (experimental FU group), consisting of 5-FU plus leucovorin, 5-FU plus methotrexate, continuous infusion 5-FU, or hepatic-artery infusion FUDR. We re-analysed this data set to focus on 1458 patients with non-operable colorectal metastases confined to the liver, randomised in 22 trials. All analyses were stratified by trial and used individual patient data. Results: Median survival times were 11.3 months in the bolus FU group (95% CI: 10.5-12.0 months) compared to 12.7 months in the experimental FU group (95% CI: 12.0-13.1 months). This difference, although clinically small, was statistically significant, with an overall survival hazard ratio of 0.88 (95% CI: 0.79-0.99, P = 0.037). In a multivariate analysis, performance status was the only significant predictor of survival (P < 10(-4)), whereas the statistical significance of allocated treatment was borderline (P = 0.058). Conclusions: The outcome of patient with non-operable colorectal metastases confined to the liver is poor, and mainly driven by their initial performance status. Experimental chemotherapy schedules yield a small improvement in their overall survival, indicating the importance of the choice of first-line chemotherapy.
引用
收藏
页码:1317 / 1320
页数:4
相关论文
共 28 条
[11]  
GRIFFITH KD, 1990, SURGERY, V107, P101
[12]   SURVIVAL IN PATIENTS WITH LARGE-BOWEL CANCER - A POPULATION-BASED INVESTIGATION FROM THE MELBOURNE COLORECTAL-CANCER STUDY [J].
KUNE, GA ;
KUNE, S ;
FIELD, B ;
WHITE, R ;
BROUGH, W ;
SCHELLENBERGER, R ;
WATSON, LF .
DISEASES OF THE COLON & RECTUM, 1990, 33 (11) :938-946
[13]   Trends in mortality from cancer in the European Union, 1955-94 [J].
Levi, F ;
Lucchini, F ;
La Vecchia, C ;
Negri, E .
LANCET, 1999, 354 (9180) :742-743
[14]   Toxicity of fluorouracil in patients with advanced colorectal cancer:: Effect of administration schedule and prognostic factors [J].
Lévy, E ;
Piedbois, P ;
Buyse, M ;
Pignon, JP ;
Rougier, P ;
Ryan, L ;
Hansen, R ;
Zee, B ;
Weinerman, B ;
Pater, J ;
Leichman, C ;
Macdonald, J ;
Benedetti, J ;
Lokich, J ;
Fryer, J ;
Brufman, G ;
Isacson, R ;
Laplanche, A ;
Quinaux, E ;
Thirion, P ;
Ryan, L ;
Hansen, R ;
Harrington, D ;
McFadden, E ;
Ribble, A ;
Jacobson, R ;
Zee, B ;
Weinerman, B ;
Pater, J ;
Leichman, C ;
Macdonald, J ;
Benedetti, J ;
Lokich, J ;
Fryer, J ;
Pignon, JP ;
Laplanche, A ;
Luboinski, M ;
Rougier, P ;
Brufman, G ;
Isacson, R ;
Vaitkevicius, V ;
Piedbois, P ;
Le Bourgeois, JP ;
Piedbois, Y ;
Gauthier, E ;
Lévy, E ;
Thirion, P ;
Durand-Zalenski, I ;
Buyse, M ;
Quinaux, E .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (11) :3537-3541
[15]  
Nordlinger B, 1996, CANCER, V77, P1254, DOI 10.1002/(SICI)1097-0142(19960401)77:7<1254::AID-CNCR5>3.3.CO
[16]  
2-R
[17]  
NORDLINGER B, 1992, TREATMENT HEPATIC ME, P129, DOI DOI 10.1007/978-3-642-51873-7_12
[18]  
PENNA C, 1998, MANAGEMENT COLORECTA, P103
[19]   DESIGN AND ANALYSIS OF RANDOMIZED CLINICAL-TRIALS REQUIRING PROLONGED OBSERVATION OF EACH PATIENT .2. ANALYSIS AND EXAMPLES [J].
PETO, R ;
PIKE, MC ;
ARMITAGE, P ;
BRESLOW, NE ;
COX, DR ;
HOWARD, SV ;
MANTEL, N ;
MCPHERSON, K ;
PETO, J ;
SMITH, PG .
BRITISH JOURNAL OF CANCER, 1977, 35 (01) :1-39
[20]  
PIEDBOIS P, 1994, J CLIN ONCOL, V12, P960