Jairath V, Zou G, Parker C E, MacDonald J K, Mosli M H, AlAmeel T, Al Beshir M, AlMadi M, Al-Taweel T, Atkinson N S S, Biswas S, Chapman T P, Dulai P S, Glaire M A, Hoekman D, Kherad O, Koutsoumpas A, Minas E, Restellini S, Samaan M A, Khanna R, Levesque B G, D'Haens G, Sandborn W J, Feagan B G
London, ON, Canada.
Oxford, UK.
Aliment Pharmacol Ther. 2017 Apr;45(8):1021-1042. doi: 10.1111/apt.13973. Epub 2017 Feb 5.
Minimising placebo response is essential for drug development.
To conduct a meta-analysis to determine placebo response and remission rates in trials and identify the factors affecting these rates.
MEDLINE, EMBASE and CENTRAL were searched from inception to April 2014 for placebo-controlled trials of pharmacological interventions for Crohn's disease. Placebo response and remission rates for induction and maintenance trials were pooled by random-effects and mixed-effects meta-regression models to evaluate effects of study-level characteristics on these rates.
In 100 studies containing 67 induction and 40 maintenance phases and 7638 participants, pooled placebo remission and response rates for induction trials were 18% [95% confidence interval (CI) 16-21%] and 28% (95% CI 24-32%), respectively. Corresponding values for maintenance trials were 32% (95% CI 25-39%) and 26% (95% CI 19-35%), respectively. For remission, trials enrolling patients with more severe disease activity, longer disease duration and more study centres were associated with lower placebo rates, whereas more study visits and longer study duration was associated with higher placebo rates. For response, findings were opposite such that trials enrolling patients with less severe disease activity and longer study duration were associated with lower placebo rates. Placebo rates varied by drug class and route of administration, with the highest placebo response rates observed for biologics.
Placebo rates vary according to whether trials are designed for induction or maintenance and the factors influencing them differ for the endpoints of remission and response. These findings have important implications for clinical trial design in Crohn's disease.
将安慰剂反应降至最低对药物研发至关重要。
进行一项荟萃分析,以确定试验中的安慰剂反应和缓解率,并识别影响这些率的因素。
检索MEDLINE、EMBASE和CENTRAL数据库,从建库至2014年4月,查找针对克罗恩病的药物干预安慰剂对照试验。通过随机效应和混合效应荟萃回归模型汇总诱导试验和维持试验的安慰剂反应率和缓解率,以评估研究水平特征对这些率的影响。
在100项研究中,包含67个诱导期和40个维持期,共7638名参与者,诱导试验的汇总安慰剂缓解率和反应率分别为18%[95%置信区间(CI)16 - 21%]和28%(95%CI 24 - 32%)。维持试验的相应值分别为32%(95%CI 25 - 39%)和26%(95%CI 19 - 35%)。对于缓解,纳入疾病活动度更严重、病程更长且研究中心更多的患者的试验,其安慰剂率较低,而研究访视次数更多和研究持续时间更长与较高的安慰剂率相关。对于反应,结果相反,即纳入疾病活动度较轻且研究持续时间更长的患者的试验,其安慰剂率较低。安慰剂率因药物类别和给药途径而异,生物制剂的安慰剂反应率最高。
安慰剂率因试验是设计用于诱导还是维持而有所不同,影响缓解和反应终点的因素也不同。这些发现对克罗恩病的临床试验设计具有重要意义。