Overall Response Rate, Progression-Free Survival, and Overall Survival With Targeted and Standard Therapies in Advanced Non-Small-Cell Lung Cancer: US Food and Drug Administration Trial-Level and Patient-Level Analyses

被引:175
作者
Blumenthal, Gideon M. [1 ]
Karuri, Stella W. [1 ]
Zhang, Hui [1 ]
Zhang, Lijun [1 ]
Khozin, Sean [1 ]
Kazandjian, Dickran [1 ]
Tang, Shenghui [1 ]
Sridhara, Rajeshwari [1 ]
Keegan, Patricia [1 ]
Pazdur, Richard [1 ]
机构
[1] US FDA, Ctr Drug Evaluat & Res, Off Hematol & Oncol Prod, White Oak, MD USA
关键词
PHASE-III TRIAL; 1ST-LINE TREATMENT; END-POINTS; TUMOR SIZE; OPEN-LABEL; APPROVAL; CHEMOTHERAPY; MULTICENTER; DOCETAXEL; BEVACIZUMAB;
D O I
10.1200/JCO.2014.59.0489
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose To conduct analyses exploring trial-level and patient-level associations between overall response rate (ORR), progression-free survival (PFS), and overall survival (OS) in advanced non-small-cell lung cancer (NSCLC) trials. Methods We identified 14 trials (N = 12,567) submitted to US Food and Drug Administration since 2003 of treatments for advanced NSCLC. Only randomized, active-controlled trials with more than 150 patients were included. Associations between trial-level PFS hazard ratio (HR), OS HR, and ORR odds ratio were analyzed using a weighted linear regression model. Patient-level responder analyses comparing PFS and OS between patients with and without an objective response were performed using pooled data from all studies. Results In the trial-level analysis, the association between PFS and ORR was strong (R-2 = 0.89; 95% CI, 0.80 to 0.98). There was no association between OS and ORR (R-2 = 0.09; 95% CI, 0 to 0.33) and OS and PFS (R-2 = 0.08; 95% CI, 0 to 0.31). In the patient-level responder analyses, patients who achieved a response had better PFS and OS compared with nonresponders (PFS: HR, 0.40; 95% CI, 0.38 to 0.42; OS: HR, 0.40; 95% CI, 0.38 to 0.43). Conclusion On a trial level, there is a strong association between ORR and PFS. An association between ORR and OS and between PFS and OS was not established, possibly because of cross-over and longer survival after progression in the targeted therapy and first-line trials. The patient-level analysis showed that responders have a better PFS and OS compared with nonresponders. A therapy in advanced NSCLC with a large magnitude of effect on ORR may have a large PFS effect. (C) 2015 by American Society of Clinical Oncology
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收藏
页码:1008 / +
页数:8
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