1 School of Health and Related Research, University of Sheffield, Sheffield, UK.
2 MRC Clinical Trials Unit, University College London, London, UK.
Stat Methods Med Res. 2019 Aug;28(8):2475-2493. doi: 10.1177/0962280218780856. Epub 2018 Jun 25.
Treatment switching often has a crucial impact on estimates of effectiveness and cost-effectiveness of new oncology treatments. Rank preserving structural failure time models (RPSFTM) and two-stage estimation (TSE) methods estimate 'counterfactual' (i.e. had there been no switching) survival times and incorporate re-censoring to guard against informative censoring in the counterfactual dataset. However, re-censoring causes a loss of longer term survival information which is problematic when estimates of long-term survival effects are required, as is often the case for health technology assessment decision making. We present a simulation study designed to investigate applications of the RPSFTM and TSE with and without re-censoring, to determine whether re-censoring should always be recommended within adjustment analyses. We investigate a context where switching is from the control group onto the experimental treatment in scenarios with varying switch proportions, treatment effect sizes, treatment effect changes over time, survival function shapes, disease severity and switcher prognosis. Methods were assessed according to their estimation of control group restricted mean survival that would be observed in the absence of switching, up to the end of trial follow-up. We found that analyses which re-censored usually produced negative bias (i.e. underestimating control group restricted mean survival and overestimating the treatment effect), whereas analyses that did not re-censor consistently produced positive bias which was often smaller in magnitude than the bias associated with re-censored analyses, particularly when the treatment effect was high and the switching proportion was low. The RPSFTM with re-censoring generally resulted in increased bias compared to the other methods. We believe that analyses should be conducted with and without re-censoring, as this may provide decision-makers with useful information on where the true treatment effect is likely to lie. Incorporating re-censoring should not always represent the default approach when the objective is to estimate long-term survival times and treatment effects.
治疗方案转换通常会对新肿瘤治疗的有效性和成本效益估计产生重大影响。排名保持结构失效时间模型(RPSFTM)和两阶段估计(TSE)方法估计“反事实”(即,如果没有转换)生存时间,并纳入再删失,以防止反事实数据集中的信息性删失。然而,再删失会导致长期生存信息的丢失,这在需要估计长期生存效果的情况下是有问题的,因为这通常是健康技术评估决策的情况。我们进行了一项模拟研究,旨在调查 RPSFTM 和 TSE 在有和没有再删失的情况下的应用,以确定在调整分析中是否应始终推荐再删失。我们在转换从对照组到实验组的情况下,在不同的转换比例、治疗效果大小、治疗效果随时间的变化、生存函数形状、疾病严重程度和转换者预后的情况下,调查了一个应用场景。方法是根据它们对控制组在没有转换的情况下观察到的限制平均生存时间的估计进行评估,直到试验随访结束。我们发现,通常会对再删失的分析产生负偏差(即低估控制组限制平均生存时间并高估治疗效果),而不进行再删失的分析则会产生正偏差,这种偏差通常比再删失分析的偏差小,特别是当治疗效果高且转换比例低时。RPSFTM 与再删失通常会导致更大的偏差。我们认为,应该进行有和没有再删失的分析,因为这可以为决策者提供有关真实治疗效果可能在哪里的有用信息。当目标是估计长期生存时间和治疗效果时,纳入再删失不应该总是代表默认方法。