Pooled Safety and Efficacy Analysis Examining the Effect of Performance Status on Outcomes in Nine First-Line Treatment Trials Using Individual Data From Patients With Metastatic Colorectal Cancer

被引:155
作者
Sargent, Daniel J. [1 ]
Koehne, Claus Henning
Sanoff, Hanna Kelly
Bot, Brian M.
Seymour, Matthew T.
de Gramont, Aimery
Porschen, Ranier
Saltz, Leonard B.
Rougier, Philippe
Tournigand, Christopher
Douillard, Jean-Yves
Stephens, Richard J.
Grothey, Axel
Goldberg, Richard M.
机构
[1] Mayo Clin, Rochester, MN 55905 USA
关键词
COMBINATION CHEMOTHERAPY; PHASE-III; FOLINIC ACID; FLUOROURACIL; OXALIPLATIN; IRINOTECAN; LEUCOVORIN; CAPECITABINE; CARCINOMA; SURVIVAL;
D O I
10.1200/JCO.2008.20.2879
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Performance status (PS) is a prognostic factor in patients with metastatic colorectal cancer. Clinical trials typically enroll less than 10% of patients with a PS of 2 (PS2); thus, the benefit of systemic chemotherapy in PS2 patients is uncertain. Patients and Methods Individual data from 6,286 patients (509 PS2 patients) from nine clinical trials were used to compare treatment efficacy by PS. Progression-free survival (PFS), grade >= 3 adverse events, 60-day all-cause mortality, overall survival (OS), and response rate (RR) were explored in the full set of nine trials and in the five trials comparing first-line monotherapy with combination therapy. Results Compared with patients with PS of 0 or 1, PS2 patients had significantly higher rates of grade >= 3 nausea (8.5% v 16.4%, respectively; P < .0001) and vomiting (7.6% v 11.9%, respectively; P = .006) and 60-day all-cause mortality (2.8% v 12.0%, respectively; P < .0001). PS2 was prognostic for PFS (hazard ratio [HR] = 1.52; P < .0001; median PFS, 7.6 months for PS 0 or 1 v 4.9 months for PS2), OS (HR = 2.18; P < .0001; median OS, 17.3 months for PS 0 or 1 v 8.5 months for PS2), and RR (odds ratio = 0.61; P < .0001; 43.8% for PS 0 or 1 v 32.0% for PS2). The relative benefit and toxicity of experimental versus control treatment and monotherapy versus combination therapy were not different in PS 0 or 1 patients versus PS2 patients. Conclusion In clinical trials, PS2 patients derive similar benefit from superior treatment as patients with PS of 0 to 1 but with an increased risk of toxicities and 12% 60-day mortality. Although current treatment provides benefit, new approaches are required to approach 1-year median survival for PS2 patients. J Clin Oncol 27: 1948-1955. (C) 2009 by American Society of Clinical Oncology
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收藏
页码:1948 / 1955
页数:8
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