Augmenting external control arms using Bayesian borrowing: a case study in first-line non-small cell lung cancer

医学 随机对照试验 危险系数 内科学 西妥昔单抗 肺癌 人口 肿瘤科 贝伐单抗 化疗 癌症 置信区间 结直肠癌 环境卫生
作者
Alessandria Struebing,Chelsea McKibbon,Haoyao Ruan,Emma K. Mackay,Natalie Dennis,Russanthy Velummailum,Philip He,Yôko Tanaka,Yan Xiong,Aaron Springford,Mats Rosenlund
出处
期刊:Journal of Comparative Effectiveness Research [Future Medicine]
卷期号:13 (5)
标识
DOI:10.57264/cer-2023-0175
摘要

Aim: This study aimed to improve comparative effectiveness estimates and discuss challenges encountered through the application of Bayesian borrowing (BB) methods to augment an external control arm (ECA) constructed from real-world data (RWD) using historical clinical trial data in first-line non-small-cell lung cancer (NSCLC). Materials & methods: An ECA for a randomized controlled trial (RCT) in first-line NSCLC was constructed using ConcertAI Patient360™ to assess chemotherapy with or without cetuximab, in the bevacizumab-inappropriate subpopulation. Cardinality matching was used to match patient characteristics between the treatment arm (cetuximab + chemotherapy) and ECA. Overall survival (OS) was assessed as the primary outcome using Cox proportional hazards (PH). BB was conducted using a static power prior under a Weibull PH parameterization with borrowing weights from 0.0 to 1.0 and augmentation of the ECA from a historical control trial. Results: The constructed ECA yielded a higher overall survival (OS) hazard ratio (HR) (HR = 1.53; 95% CI: 1.21–1.93) than observed in the matched population of the RCT (HR = 0.91; 95% CI: 0.73–1.13). The OS HR decreased through the incorporation of BB (HR = 1.30; 95% CI: 1.08–1.54, borrowing weight = 1.0). BB was applied to augment the RCT control arm via a historical control which improved the precision of the observed HR estimate (1.03; 95% CI: 0.86–1.22, borrowing weight = 1.0), in comparison to the matched population of the RCT alone. Conclusion: In this study, the RWD ECA was unable to successfully replicate the OS estimates from the matched population of the selected RCT. The inability to replicate could be due to unmeasured confounding and variations in time-periods, follow-up and subsequent therapy. Despite these findings, we demonstrate how BB can improve precision of comparative effectiveness estimates, potentially aid as a bias assessment tool and mitigate challenges of traditional methods when appropriate external data sources are available.

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