Division of Medical Oncology & Hematology, Department of Medicine, Princess Margaret Cancer Centre, University of Toronto, Toronto, ON, Canada.
Department of Medical Oncology, Institute of Oncology Ljubljana, Ljubljana, Slovenia.
Cancer Med. 2020 Nov;9(21):7888-7895. doi: 10.1002/cam4.3390. Epub 2020 Sep 4.
BACKGROUND: Anti-cancer drugs are approved typically on the basis of efficacy and safety as evaluated in phase III randomized trials (RCTs). Health-related quality of life (HRQoL) is a direct measure of patient benefit, but is under-reported. Here we explore associations with reporting of HRQoL data in phase III RCTs in common solid tumors. METHODS: We searched ClinicalTrials.gov to identify phase III RCTs evaluating new drugs in adults with advanced cancers that completed accrual between January 2005 and October 2016. Data on HRQoL, safety, and tolerability comprising treatment-related death, treatment discontinuation and commonly reported grade 3 or 4 adverse events (AEs) were extracted. Associations between these measures and reporting of HRQoL data were explored using logistic regression. RESULTS: Of 377 phase III RCTs identified initially, 143 studies were analysed and comprised 55% positive trials and 90% industry sponsored trials. HRQoL was listed as an endpoint in 59% trials; and of these, only 65% reported HRQoL data. There were higher odds of reporting HRQoL data for positive trials (OR 2.05, P = .04) and trials published in journals with higher impact factor (OR 1.35, P = .01). Reporting of HRQoL was not associated with treatment-related death (OR 1.25, P = .40) or treatment discontinuation (OR 1.12, P = .61), but was positively associated with dyspnea and dermatological adverse events. CONCLUSIONS: HRQoL is reported in only two-thirds of RCTs that describe collecting such data. Reporting of HRQoL is associated with positive trial outcome and higher journal impact factor, but not associated with overall safety and tolerability of anti-cancer drugs.
背景:抗癌药物通常是基于 III 期随机对照试验(RCT)中评估的疗效和安全性而获得批准的。健康相关生活质量(HRQoL)是衡量患者受益的直接指标,但报告不足。在这里,我们探讨了 III 期 RCT 中常见实体瘤报告 HRQoL 数据的相关性。
方法:我们在 ClinicalTrials.gov 上搜索了评估新药物在成人晚期癌症中的 III 期 RCT,这些 RCT 于 2005 年 1 月至 2016 年 10 月期间完成了入组。提取了包括治疗相关死亡、治疗中止以及常见报告的 3 或 4 级不良事件(AE)的 HRQoL、安全性和耐受性数据。使用逻辑回归探讨了这些措施与 HRQoL 数据报告之间的关系。
结果:最初确定了 377 项 III 期 RCT,其中 143 项研究进行了分析,包括 55%的阳性试验和 90%的行业赞助试验。HRQoL 在 59%的试验中被列为终点;其中,只有 65%报告了 HRQoL 数据。阳性试验(OR 2.05,P=0.04)和发表在影响因子较高的期刊上的试验(OR 1.35,P=0.01)报告 HRQoL 数据的可能性更高。HRQoL 的报告与治疗相关死亡(OR 1.25,P=0.40)或治疗中止(OR 1.12,P=0.61)无关,但与呼吸困难和皮肤病学不良事件呈正相关。
结论:只有三分之二的描述收集此类数据的 RCT 报告了 HRQoL。HRQoL 的报告与阳性试验结果和更高的期刊影响因子相关,但与抗癌药物的总体安全性和耐受性无关。
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