医学
肿瘤科
危险系数
临床试验
总体生存率
置信区间
内科学
统计能力
插补(统计学)
安慰剂
渡线
比例危险模型
时间点
随机对照试验
生存分析
研究设计
样本量测定
缺少数据
医学物理学
统计
统计分析
治疗效果
危害
临床终点
统计模型
临床研究设计
区间(图论)
治疗组和对照组
计算机科学
控制(管理)
点估计
精密医学
交叉研究
无进展生存期
梅德林
标识
DOI:10.1080/10543406.2025.2571224
摘要
In oncology trials, patients in both the control and experimental arms can receive different subsequent anti-cancer therapies (SATs) after discontinuing their randomized study drugs, a phenomenon commonly referred to as treatment switching. SATs may have the potential to extend overall survival (OS) in patients treated with the control and experimental drugs. Without recovering the information from the SATs, the statistical power of the clinical trials could be drastically reduced, thus making it difficult or impossible to meet the efficacy objective. This article presents a novel statistical method for imputing the post-switching survival time multiple times to derive the point estimate of the true hazard ratio (HR) of OS between the experimental and control drugs and the associated 95% confidence interval (CI). The proposed method provides an effective solution for recovering lost information in the OS caused by SATs. It also offers an efficient way to evaluate the true causal treatment effect, potentially increasing the statistical power. Additionally, this method can be used for patients with a crossover from a placebo to an experimental treatment in placebo-controlled trials. Simulation studies demonstrated that the proposed method performed well and reliably, and applications to oncology trials using the simulated data are provided.
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