The eligibility of advanced non-small-cell lung cancer patients for targeted therapy clinical trials

被引:17
|
作者
Clarey, J. [2 ]
Kao, S. C. [1 ,2 ]
Clarke, S. J. [2 ,3 ]
Vardy, J. [1 ,2 ]
机构
[1] Concord Repatriat Gen Hosp, Dept Med Oncol, Sydney, NSW, Australia
[2] Univ Sydney, Fac Med, Sydney, NSW 2006, Australia
[3] Royal N Shore Hosp, Dept Med Oncol, Sydney, NSW, Australia
基金
英国医学研究理事会;
关键词
clinical trial; lung cancer; targeted therapy; PHASE-III TRIAL; CHEMOTHERAPY; COMBINATION; BEVACIZUMAB; GEMCITABINE; CISPLATIN; CARBOPLATIN; PACLITAXEL; GEFITINIB; SURVIVAL;
D O I
10.1093/annonc/mdr443
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The selection criteria for phase III trials are often stringent. We aimed to determine how many advanced non-small-cell lung cancer (NSCLC) patients would have been eligible for phase III targeted therapy trials and the proportion receiving anticancer treatment. From March 2007 to May 2008, all advanced NSCLC patients presented at our lung cancer multidisciplinary team meeting were included to assess eligibility for the targeted therapy trials: ECOG-4599, AVAiL, FLEX, TALENT, INTACT-1, INTACT-2, ESCAPE, NEXUS and MONET1. Medical records were examined to determine treatment utilisation and overall survival. A total of 62 patients were registered: 63% male; median age 71 years; 61% stage IIIB disease. Percentages that met criteria were: ECOG-4599 31%, AVAiL 24%, FLEX 69%, TALENT 27%, INTACT-1 50%, INTACT-2 42%, ESCAPE 39%, NEXUS 63% and MONET1 34%. Common reasons for ineligibility were insufficient life expectancy, poor performance status, abnormal bloods, proteinuria and associated cancer problems. Systemic therapies were received by 66% of patients and median survival was 10.3 months. Only 24%-69% were eligible for targeted therapy trials but 66% received anticancer treatment. Clinical trials in patients with advanced NSCLC need to be more representative of the majority of patients.
引用
收藏
页码:1229 / 1233
页数:5
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