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Postprogression Survival in Patients With Advanced Non-Small-Cell Lung Cancer Who Receive Second-Line or Third-Line Chemotherapy
被引:36
|作者:
Hayashi, Hidetoshi
[1
]
Okamoto, Isamu
[1
]
Taguri, Masataka
[2
]
Morita, Satoshi
[2
]
Nakagawa, Kazuhiko
[1
]
机构:
[1] Kinki Univ, Fac Med, Dept Med Oncol, Osakasayama, Japan
[2] Yokohama City Univ, Med Ctr, Dept Biostat & Epidemiol, Yokohama, Kanagawa 232, Japan
关键词:
Overall survival;
Phase III trial;
Progression-free survival;
Subsequent chemotherapy;
RANDOMIZED PHASE-III;
PROGRESSION-FREE SURVIVAL;
CLINICAL-TRIALS;
PROGNOSTIC-FACTORS;
DOCETAXEL;
METAANALYSIS;
CARBOPLATIN;
CISPLATIN;
GEFITINIB;
NSCLC;
D O I:
10.1016/j.cllc.2012.09.006
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
The effect of subsequent chemotherapy on overall survival (OS) has the potential to result in underestimation of the efficacy of an experimental treatment in clinical trials for advanced non-small-cell lung cancer (NSCLC). In this study, we investigated postprogression survival (PPS), defined as overall survival (OS) minus progression-free survival (PFS), in the second-line setting. PPS was highly associated with OS, and the induction rate for subsequent chemotherapy was associated with the duration of PPS. Our findings indicate that a beneficial effect of treatment on OS in patients with advanced NSCLC can be skewed by the effects of subsequent therapies in the second-line or third-line setting. Background: The increased availability of active agents has improved overall survival (OS) in patients with advanced non-small-cell lung cancer (NSCLC). We previously showed that postprogression survival (PPS) is highly associated with OS in the first-line setting, but little is known about PPS in the salvage setting. In this study, we analyzed PPS in phase III trials in the second-line or third-line setting. Patients and Methods: A literature search identified 18 trials for previously treated patients with advanced NSCLC. We partitioned OS into progression-free survival (PFS) and PPS and evaluated the association between OS and either PFS or PPS. Correlation analysis to examine whether a treatment benefit for PFS carried over to OS was performed by calculation of incremental gains in OS and PFS at the trial level. Results: The average median PPS was longer than the average median PFS (5.4 and 2.6 months, respectively). The induction rate for subsequent chemotherapy after second-line or third-line treatment was related to the duration of PPS in linear regression analysis (r(2) = 0.4813). Median OS was highly associated with median PPS but not with PFS (r = 0.94 and 0.51, respectively), and only a weak association between the treatment benefits for PFS and OS was detected (r = 0.29). Conclusions: Treatment benefit for OS in patients with advanced NSCLC can be skewed by the effects of subsequent therapies in the second-line or third-line setting. Whether PFS or OS is the more appropriate endpoint for trials in the salvage setting should be considered. Clinical Lung Cancer, Vol. 14, No. 3, 261-6 (C) 2013 Elsevier Inc. All rights reserved.
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页码:261 / 266
页数:6
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