TY - JOUR
T1 - Clinical Trials with External Control
T2 - Beyond Propensity Score Matching
AU - Wang, Hongwei
AU - Fang, Yixin
AU - He, Weili
AU - Chen, Ruizhe
AU - Chen, Su
N1 - Funding Information:
This study was funded by AbbVie.
Publisher Copyright:
© 2022, The Author(s) under exclusive licence to International Chinese Statistical Association.
PY - 2022/7
Y1 - 2022/7
N2 - Real-world data (RWD) is playing an increasingly important role in drug development from early discovery throughout the life-cycle management. This includes leveraging RWD in randomized clinical trial (RCT) design and study conduct. In many scenarios, a concurrent control arm may not be viable for ethical or practical considerations, and inclusion of an external control arm can greatly facilitate the decision-making and interpretation of findings. We summarize the strengths and limitations of typical external data sources including historical RCT, aggregated data at study level from literature, patient registry, health insurance claims, electronic health records in terms of fit-for-purpose data selection. To address the inherent confounding due to lack of randomization, propensity score matching method has the advantages of separating the design from analysis and providing the ability to explicitly examine the degree of overlap in confounders. Within the framework of causal inference, however, many alternatives have been proposed with desirable theoretical properties. In this article, we review key steps from study design conceptualization to data source selection, and focus on several methods for evaluation of performance in the context of creating external control for clinical trials. We conducted a focused simulation studies to assess bias reduction and statistical properties when underlying assumptions are violated or models are mis-specified. The results support that analysis using matched group improve bias reduction when sample size is not a limiting factor, and targeted maximum likelihood estimation coupled with super learner is robust when estimating both average treatment effects and average treatment effects among treated.
AB - Real-world data (RWD) is playing an increasingly important role in drug development from early discovery throughout the life-cycle management. This includes leveraging RWD in randomized clinical trial (RCT) design and study conduct. In many scenarios, a concurrent control arm may not be viable for ethical or practical considerations, and inclusion of an external control arm can greatly facilitate the decision-making and interpretation of findings. We summarize the strengths and limitations of typical external data sources including historical RCT, aggregated data at study level from literature, patient registry, health insurance claims, electronic health records in terms of fit-for-purpose data selection. To address the inherent confounding due to lack of randomization, propensity score matching method has the advantages of separating the design from analysis and providing the ability to explicitly examine the degree of overlap in confounders. Within the framework of causal inference, however, many alternatives have been proposed with desirable theoretical properties. In this article, we review key steps from study design conceptualization to data source selection, and focus on several methods for evaluation of performance in the context of creating external control for clinical trials. We conducted a focused simulation studies to assess bias reduction and statistical properties when underlying assumptions are violated or models are mis-specified. The results support that analysis using matched group improve bias reduction when sample size is not a limiting factor, and targeted maximum likelihood estimation coupled with super learner is robust when estimating both average treatment effects and average treatment effects among treated.
KW - Causal inference
KW - Clinical trials
KW - Doubly robust
KW - External control
KW - Propensity score
KW - Targeted MLE
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U2 - 10.1007/s12561-022-09341-x
DO - 10.1007/s12561-022-09341-x
M3 - Article
AN - SCOPUS:85127526766
SN - 1867-1764
VL - 14
SP - 304
EP - 317
JO - Statistics in Biosciences
JF - Statistics in Biosciences
IS - 2
ER -