Generalizing Treatment Effect to a Target Population Without Individual Patient Data in a Real-World Setting

被引:0
|
作者
Quan, Hui [1 ]
Li, Tong [1 ]
Chen, Xun [1 ]
Li, Gang [2 ]
机构
[1] Sanofi, Biostat & Programming, Bridgewater, NJ 08807 USA
[2] Eisai Inc, Nutley, NJ USA
关键词
double inverse probability weighting (DIPW); individual patient data; propensity score; real-world data; real-world evidence; PROPENSITY SCORE; GENERALIZABILITY; TRIALS; BIAS;
D O I
10.1002/pst.2435
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The innovative use of real-world data (RWD) can answer questions that cannot be addressed using data from randomized clinical trials (RCTs). While the sponsors of RCTs have a central database containing all individual patient data (IPD) collected from trials, analysts of RWD face a challenge: regulations on patient privacy make access to IPD from all regions logistically prohibitive. In this research, we propose a double inverse probability weighting (DIPW) approach for the analysis sponsor to estimate the population average treatment effect (PATE) for a target population without the need to access IPD. One probability weighting is for achieving comparable distributions in confounders across treatment groups; another probability weighting is for generalizing the result from a subpopulation of patients who have data on the endpoint to the whole target population. The likelihood expressions for propensity scores and the DIPW estimator of the PATE can be written to only rely on regional summary statistics that do not require IPD. Our approach hinges upon the positivity and conditional independency assumptions, prerequisites to most RWD analysis approaches. Simulations are conducted to compare the performances of the proposed method against a modified meta-analysis and a regular meta-analysis.
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页数:11
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