Treatment Paradigms for Advanced Non-Small Cell Lung Cancer at Academic Medical Centers: Involvement in Clinical Trial Endpoint Design

被引:14
作者
Aggarwal, Charu [1 ]
Borghaei, Hossein [2 ]
机构
[1] Hosp Univ Penn, Abramson Canc Ctr, Div Hematol Oncol, 3400 Spruce St, Philadelphia, PA 19104 USA
[2] Fox Chase Canc Ctr, Dept Med Oncol, 7701 Burholme Ave, Philadelphia, PA 19111 USA
关键词
Carcinoma; Non-small cell lung cancer; Antineoplastic agents; Surrogate endpoint; Food and Drug Administration drug approval; PROGRESSION-FREE SURVIVAL; PHASE-III TRIAL; DRUG-ADMINISTRATION APPROVAL; CISPLATIN PLUS GEMCITABINE; 1ST-LINE THERAPY; OPEN-LABEL; AFATINIB; CHEMOTHERAPY; DOCETAXEL; ERLOTINIB;
D O I
10.1634/theoncologist.2016-0345
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Based on the positive results of various clinical trials, treatment options for non-small cell lung cancer (NSCLC) have expanded greatly over the last 25 years. While regulatory approvals of chemotherapeutic agents for NSCLC have largely been based on improvements in overall survival, recent approvals of many targeted agents for NSCLC (afatinib, crizotinib, ceritinib, osimertinib) have been based on surrogate endpoints such as progression-free survival and objective response. As such, selection of appropriate clinical endpoints for examining the efficacy of investigational agents for NSCLC is of vital importance in clinical trial design. This review provides an overview of clinical trial endpoints previously utilized for approved agents for NSCLC and highlights the key efficacy results for these trials. Trends for more recent approvals in NSCLC, including those for the immunotherapeutic agents nivolumab and pembrolizumab, are also discussed. The results of a correlative analysis of endpoints from 18 clinical trials that supported approvals of investigational agents in clinical trials for NSCLC are also presented.
引用
收藏
页码:700 / 708
页数:9
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