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Guangcai Mao

Publications and source records attributed to Guangcai Mao.

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An Estimand-Focused Approach for AUC Generalization and Cross-Study Benchmarking

The area under the ROC curve (AUC) is the standard measure of a biomarker's discriminatory accuracy; however, AUC is rarely treated as a population-specific estimand. When validation cohorts differ from the intended target population in case mix, Naïve AUC estimates can mislead both generalization and cross-study comparison. We develop an estimand-focused framework that anchors biomarker AUC inference to a prespecified target population, aligning with the ICH E9(R1) estimand perspective adapted to discrimination rather than treatment effect. The framework supports two scientific goals: generalizing a study-specific AUC to a clinically relevant target population, and benchmarking AUCs across studies on a common population footing. Methodologically, we extend calibration weighting to the U-statistic formulation of AUC, allowing valid estimation even when the target population is characterized only by summary-level covariate information. This setting is common in biomarker validation, where individual-level target data are often unavailable and existing transportability methods may not be applicable. When patient-level real-world data are accessible, the proposed augmented variants provide double robustness and improved efficiency. We establish asymptotic properties and study their performances through comprehensive simulations. Furthermore, we demonstrate the proposed framework on the POWER trials, evaluating baseline stair-climb power (SCP) as a prognostic marker for 6-month survival in advanced non-small-cell lung cancer (NSCLC). Unlike prior work on transporting model-based predictive accuracy, our framework targets the biomarker-level estimand directly and addresses cross-study comparability - an issue not resolved by current methods.

stat.ME

Statistical Inference for Heterogeneous Treatment Effect with Right-censored Data from Synthesizing Randomized Clinical Trials and Real-world Data

The heterogeneous treatment effect plays a crucial role in precision medicine.There is evidence that real-world data, even subject to biases, can be employed as supplementary evidence for randomized clinical trials to improve the statistical efficiency of the heterogeneous treatment effect estimation. In this paper, for survival data with right censoring, we consider estimating the heterogeneous treatment effect, defined as the difference of the treatment-specific conditional restricted mean survival times given covariates, by synthesizing evidence from randomized clinical trials and the real-world data with possible biases. We define an omnibus bias function to characterize the effect of biases caused by unmeasured confounders, censoring, and outcome heterogeneity, and further, identify it by combining the trial and real-world data. We propose a penalized sieve method to estimate the heterogeneous treatment effect and the bias function. We further study the theoretical properties of the proposed integrative estimators based on the theory of reproducing kernel Hilbert space and empirical process. The proposed methodology outperforms the approach solely based on the trial data through simulation studies and an integrative analysis of the data from a randomized trial and a real-world registry on early-stage non-small-cell lung cancer.

stat.ME