On the two-step hybrid design for augmenting randomized trials using real-world data
Jiapeng Xu, Ruben P.A. van Eijk, Alicia Ellis, Tianyu Pan, Lorene M., Nelson, Kit C.B. Roes, Marc van Dijk, Maria Sarno, Leonard H. van den Berg,, Lu Tian, and Ying Lu

TL;DR
This paper introduces four new statistical methods to improve control of type I error in two-step hybrid clinical trial designs that incorporate real-world data, especially when exchangeability assumptions are uncertain.
Contribution
The paper proposes four novel approaches for better controlling type I error in hybrid trial designs, addressing limitations of existing methods under exchangeability violations.
Findings
All proposed methods effectively control type I error, unlike previous approaches.
Simulation results show reduced type I error inflation (6-8%) with new methods.
Bayesian power prior exhibits higher type I error inflation (16%).
Abstract
Hybrid clinical trials, that borrow real-world data (RWD), are gaining interest, especially for rare diseases. They assume RWD and randomized control arm be exchangeable, but violations can bias results, inflate type I error, or reduce power. A two-step hybrid design first tests exchangeability, reducing inappropriate borrowing but potentially inflating type I error (Yuan et al., 2019). We propose four methods to better control type I error. Approach 1 estimates the variance of test statistics, rejecting the null hypothesis based on large sample normal approximation. Approach 2 uses a numerical approach for exact critical value determination. Approach 3 splits type I error rates by equivalence test outcome. Approach 4 adjusts the critical value only when equivalence is established. Simulation studies using a hypothetical ALS scenario, evaluate type I error and power under various…
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Taxonomy
TopicsAdvanced Causal Inference Techniques · Statistical Methods in Clinical Trials
