Marie Curie Palliative Care Research Department, University College London, London, UK.
Department of Statistical Science, University College London, London, UK.
BMJ Support Palliat Care. 2020 Dec;10(4):385-394. doi: 10.1136/bmjspcare-2019-002163. Epub 2020 Feb 11.
Cancer-related fatigue (CRF) is one of the most distressing symptoms experienced by patients. There is no gold standard treatment, although multiple drugs have been tested with little evidence of efficacy. Randomised controlled trials (RCTs) of these drugs have commented on the existence or size of the placebo response (PR). The objective of this systematic review was to establish the magnitude of the PR in RCTs of drugs to relieve CRF and to identify contributing factors.
RCTs were included in which the objective was to treat CRF. A meta-analysis was conducted using the standardised mean change (SMC) between baseline and final measurement in the placebo group. To explore factors that may be associated with the PR (eg, population or drug), a meta-regression was undertaken. Risk of bias was assessed using the revised Cochrane tool.
From 3916 citations, 30 relevant RCTs were identified. All had limitations that increased their risk of bias. The pooled SMC in reduction in fatigue status in placebo groups was -0.23 (95% confidence intervals -0.42 to -0.04). None of the variables analysed in the meta-regression were statistically significant related to PR.
There is some evidence, based on trials with small samples, that the PR in trials testing drugs for CRF is non-trivial in size and statistically significant. We recommend that researchers planning drug studies in CRF should consider implementing alternative trial designs to better account for PR and decrease impact on the study results.
癌症相关疲劳(CRF)是患者最痛苦的症状之一。虽然已经测试了多种药物,但没有金标准治疗方法,而且几乎没有证据表明这些药物有效。这些药物的随机对照试验(RCT)已经评论了安慰剂反应(PR)的存在或大小。本系统评价的目的是确定治疗 CRF 的药物的 RCT 中 PR 的幅度,并确定促成因素。
纳入了以治疗 CRF 为目的的 RCT。使用安慰剂组在基线和最终测量之间的标准化平均变化(SMC)进行荟萃分析。为了探索可能与 PR 相关的因素(例如人群或药物),进行了荟萃回归分析。使用修订后的 Cochrane 工具评估偏倚风险。
从 3916 条引文,确定了 30 项相关 RCT。所有 RCT 都存在增加偏倚风险的局限性。安慰剂组疲劳状态降低的汇总 SMC 为-0.23(95%置信区间-0.42 至-0.04)。荟萃回归分析中分析的变量均与 PR 无统计学显著相关。
基于小样本试验,有一些证据表明,CRF 药物试验中的 PR 大小不小且具有统计学意义。我们建议计划在 CRF 中进行药物研究的研究人员应考虑实施替代试验设计,以更好地考虑 PR 并减少对研究结果的影响。