Ludovic Trinquart, Justine Jacot, Sarah C. Conner, and Raphaël Porcher, Institut National de la Santé et de la Recherche Médicale U1153; Ludovic Trinquart and Raphaël Porcher, Université Paris Descartes; and Assistance Publique-Hôpitaux de Paris; and Ludovic Trinquart, Cochrane France, Paris, France.
J Clin Oncol. 2016 May 20;34(15):1813-9. doi: 10.1200/JCO.2015.64.2488. Epub 2016 Feb 16.
We aimed to compare empirically the treatment effects measured by the hazard ratio (HR) and by the difference (and ratio) of restricted mean survival times (RMST) in oncology randomized trials.
We selected oncology randomized controlled trials from five leading journals during the last 6 months of 2014. We reconstructed individual patient data for one time-to-event outcome from each trial, preferably the primary outcome. We reanalyzed each trial and compared the treatment effect estimated by the HR with that by the difference (and ratio) of RMST. We estimated an average ratio of the HR to the ratio of RMST; an average ratio less than one indicates more optimistic assessments with HRs.
We analyzed 54 randomized controlled trials totaling 33,212 patients. The selected outcome was overall survival in 21 (39%) trials. There was evidence of nonproportionality of hazards in 13 (24%) trials. The HR and RMST-based measures were in agreement regarding the statistical significance of the effect, except in one case. The median HR was 0.84 (Q1 to Q3 range, 0.67 to 0.97) and the median difference in RMST was 1.12 months (range, 0.22 to 2.75 months). The average ratio of the HR to the ratio of RMST was 1.11 (95% CI, 1.07 to 1.15), with substantial between-trial variability (I(2) = 86%). Results were consistent by outcome type (overall survival v other outcomes) and whether the proportional hazard assumption held or not.
On average, the HR provided significantly larger treatment effect estimates than the ratio of RMST. The HR may seem large when the absolute effect is small. RMST-based measures should be routinely reported in randomized trials with time-to-event outcomes.
我们旨在比较肿瘤学随机试验中风险比(HR)和受限平均生存时间(RMST)差值(和比值)测量的治疗效果。
我们从 2014 年最后 6 个月的 5 种主要期刊中选择了肿瘤学随机对照试验。我们从每个试验中重新构建了一个生存时间结局的个体患者数据,最好是主要结局。我们重新分析了每个试验,并比较了 HR 和 RMST 差值(和比值)估计的治疗效果。我们估计了 HR 与 RMST 比值的平均比值;平均比值小于 1 表明 HR 评估更为乐观。
我们分析了 54 项随机对照试验,共 33212 名患者。选择的结局是 21 项(39%)试验的总生存。13 项(24%)试验存在危险比例非比例性的证据。HR 和 RMST 基于测量的治疗效果在统计学意义上是一致的,除了一个例外。HR 的中位数为 0.84(四分位距范围,0.67 至 0.97),RMST 的差值中位数为 1.12 个月(范围,0.22 至 2.75 个月)。HR 与 RMST 比值的平均比值为 1.11(95%置信区间,1.07 至 1.15),各试验间存在较大的变异性(I(2)=86%)。结果在结局类型(总生存与其他结局)和是否存在比例危险假设方面是一致的。
平均而言,HR 提供的治疗效果估计明显大于 RMST 比值。当绝对效果较小时,HR 可能显得较大。具有生存时间结局的随机试验应常规报告 RMST 基于测量的结果。