Do all patients with advanced non-small-cell lung cancer benefit from cisplatin-based combination therapy?

被引:58
作者
Soria, JC [1 ]
Brisgand, D [1 ]
Le Chevalier, T [1 ]
机构
[1] Inst Gustave Roussy, Dept Med, F-94805 Villejuif, France
关键词
chemotherapy; multivariate analysis; non-small-cell lung cancer; performance status; prognostic factor;
D O I
10.1023/A:1013574413217
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Platinum-based chemotherapy has been shown to be effective in improving survival and quality of life in advanced non-small-cell lung cancer (NSCLC) patients. The objective of this study was to identify patients more likely to benefit from chemotherapy in order to avoid the indiscriminate treatment of all patients. Patients and methods: A multivariate analysis of survival was performed using the database of the European randomized phase III trial that compared vinorelbine (navelbine(R)) (NVB), vinorelbine-cisplatin (NVB-P) and vindesine-cisplatin (VDS-P) in 612 patients with inoperable NSCLC (stage III or IV). Interactions between treatment and the prognostic factors singled out by the Cox procedure were specifically tested. Results: The performance status (PS) was the only significant interaction among the selected prognostic factors and treatment. Subgroup analysis showed that the advantage obtained with NVB-P predominantly concerned PS 0-1 patients, whose median survival lasted 43 weeks (95% confidence interval (95% CI): 39-50 weeks) with a one-year survival rate of 38% (95% CI: 31%-46%) versus 36 weeks (95% CI: 30-40 weeks) and 34% (95% CI: 27%-42%) for NVB alone, and 33 weeks (95% CI: 30-39 weeks) and 29% (95% CI: 22%-36%) for VDS-P. In sharp contrast, survival in PS 2 patients was similar (median 18 weeks) (NVB-P 95% CI: 11-34 weeks; NVB 95% CI: 11-35 weeks; VDS-P 95% CI: 14-32 weeks) whatever the treatment. Conclusion: PS 2 patients with advanced NSCLC might not benefit from cisplatin combination therapy.
引用
收藏
页码:1667 / 1670
页数:4
相关论文
共 23 条
[1]   SURVIVAL DETERMINANTS IN EXTENSIVE-STAGE NON-SMALL-CELL LUNG-CANCER - THE SOUTHWEST-ONCOLOGY-GROUP EXPERIENCE [J].
ALBAIN, KS ;
CROWLEY, JJ ;
LEBLANC, M ;
LIVINGSTON, RB .
JOURNAL OF CLINICAL ONCOLOGY, 1991, 9 (09) :1618-1626
[2]  
ALBERTI W, 1995, BRIT MED J, V311, P899
[3]   CISPLATIN CYCLOPHOSPHAMIDE MITOMYCIN COMBINATION CHEMOTHERAPY WITH SUPPORTIVE CARE VERSUS SUPPORTIVE CARE ALONE FOR TREATMENT OF METASTATIC NON-SMALL-CELL LUNG-CANCER [J].
CARTEI, G ;
CARTEI, F ;
CANTONE, A ;
CAUSARANO, D ;
GENCO, G ;
TOBALDIN, A ;
INTERLANDI, G ;
GIRALDI, T .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1993, 85 (10) :794-800
[4]  
CORMIER Y, 1982, CANCER, V50, P845, DOI 10.1002/1097-0142(19820901)50:5<845::AID-CNCR2820500507>3.0.CO
[5]  
2-S
[6]  
ENGAN T, 1990, ACTA ONCOL, V29, P151
[7]   THE VALUE OF TUMOR-MARKERS IN LUNG-CANCER [J].
GOMM, SA ;
KEEVIL, BG ;
THATCHER, N ;
HASLETON, PS ;
SWINDELL, RS .
BRITISH JOURNAL OF CANCER, 1988, 58 (06) :797-804
[8]  
Gridelli C, 1999, JNCI-J NATL CANCER I, V91, P66
[9]  
Gridelli C, 1997, EUR J CANCER, V33, P392, DOI 10.1016/S0959-8049(97)89011-9
[10]   PRETREATMENT PROGNOSTIC FACTORS IN PATIENTS WITH STAGE-III NON-SMALL-CELL LUNG-CANCER TREATED WITH HYPERFRACTIONATED RADIATION-THERAPY WITH OR WITHOUT CONCURRENT CHEMOTHERAPY [J].
JEREMIC, B ;
SHIBAMOTO, Y .
LUNG CANCER, 1995, 13 (01) :21-30