Patient motivations surrounding participation in phase I and phase II clinical trials of cancer chemotherapy

被引:105
|
作者
Nurgat, ZA
Craig, W
Campbell, NC
Bissett, JD
Cassidy, J
Nicolson, MC
机构
[1] Univ Aberdeen, Sch Med, Foresterhill Hlth Ctr, Dept Gen Practice & Primary Care, Aberdeen AB25 2AY, Scotland
[2] Aberdeen Royal Infirm, Dept Clin Oncol, ANCHOR Unit, Aberdeen AB25 2ZN, Scotland
[3] Univ Glasgow, Western Infirm, Beatson Oncol Ctr, Glasgow G11 6NT, Lanark, Scotland
[4] Aberdeen Royal Infirm, Dept Med Oncol, ANCHOR Unit, Aberdeen AB25 2ZN, Scotland
[5] Aberdeen Royal Infirm, Dept Pharm, Aberdeen AB25 2ZN, Scotland
[6] Aberdeen Royal Infirm, Dept Gen Surg, Aberdeen AB25 2ZN, Scotland
关键词
informed consent; phase I/II cancer clinical trials; patient motivations;
D O I
10.1038/sj.bjc.6602423
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Successful advances in the treatment of advanced malignant diseases rely on recruitment of patients into clinical trials of novel agents. However, there is a genuine concern for the welfare of individual patients. The aim of this study was to examine motives of patients entering early clinical trials of novel cancer therapies. Questionnaire survey with both open- and close-ended questions. The patients were surveyed after they had given informed consent and before or during the first cycle of treatment. In all, 38 phase I/II trial patients participated and completed the survey. Obtaining possible health benefit was listed by 89% as being a 'very important' factor in their decision to participate, with only 17% giving reasons of helping future cancer patients and treatment. Other items cited as a 'very important' motivating factor were 'trust in the doctor' (66%), 'being treated by the latest treatment available' (66%), 'better standard of care and closer follow-up' (61%), and 'closer monitoring of patients in trials' (58%). Only 47% patients indicated that someone had explained to them about any 'reasonable' alternatives to the trial. In total, 71% strongly agreed that 'surviving for as long time as possible was the most important thing (for them)'. Nearly all (97%) indicated that they knew the purpose of the trial and had enough time to consider participation in the trial (100%). In this survey, most patients entering phase I and II clinical trials felt they understood the purpose of the research and had given truly informed consent. Despite this, most patients participated in the hope of therapeutic benefit, although this is known to be a rare outcome in this patient subset. Trialists should be aware, and take account of the expectations that participants place in trial drugs.
引用
收藏
页码:1001 / 1005
页数:5
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