Adjusting Survival Time Estimates to Account for Treatment Switching in Randomized Controlled Trials—an Economic Evaluation Context

审查(临床试验) 背景(考古学) 计算机科学 反概率 边际结构模型 心理干预 混淆 计量经济学 医学 因果推理 贝叶斯概率 经济 人工智能 后验概率 生物 精神科 病理 古生物学
作者
Nicholas Latimer,Keith R. Abrams,Paul C. Lambert,Michael J. Crowther,Allan Wailoo,James P. Morden,Ron Akehurst,Michael J. Campbell
出处
期刊:Medical Decision Making [SAGE Publishing]
卷期号:34 (3): 387-402 被引量:91
标识
DOI:10.1177/0272989x13520192
摘要

Background. Treatment switching commonly occurs in clinical trials of novel interventions in the advanced or metastatic cancer setting. However, methods to adjust for switching have been used inconsistently and potentially inappropriately in health technology assessments (HTAs). Objective. We present recommendations on the use of methods to adjust survival estimates in the presence of treatment switching in the context of economic evaluations. Methods. We provide background on the treatment switching issue and summarize methods used to adjust for it in HTAs. We discuss the assumptions and limitations associated with adjustment methods and draw on results of a simulation study to make recommendations on their use. Results. We demonstrate that methods used to adjust for treatment switching have important limitations and often produce bias in realistic scenarios. We present an analysis framework that aims to increase the probability that suitable adjustment methods can be identified on a case-by-case basis. We recommend that the characteristics of clinical trials, and the treatment switching mechanism observed within them, should be considered alongside the key assumptions of the adjustment methods. Key assumptions include the “no unmeasured confounders” assumption associated with the inverse probability of censoring weights (IPCW) method and the “common treatment effect” assumption associated with the rank preserving structural failure time model (RPSFTM). Conclusions. The limitations associated with switching adjustment methods such as the RPSFTM and IPCW mean that they are appropriate in different scenarios. In some scenarios, both methods may be prone to bias; “2-stage” methods should be considered, and intention-to-treat analyses may sometimes produce the least bias. The data requirements of adjustment methods also have important implications for clinical trialists.
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