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Daniel Wojdyla

Publications and source records attributed to Daniel Wojdyla.

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Towards Fair Predictions: Group Conditional Concordance Index to Quantify Fairness in Time-to-Event Prognostication

Fairness metrics are essential for rigorously defining, quantifying, and mitigating biases in predictive models. While most existing metrics focus on binary classification tasks, fairness in time-to-event analyses has received limited attention. To address this gap, we propose a novel group fairness metric, the group-conditional Concordance Index (xCI), which extends Harrell's Concordance Index (CI) by conditioning on group membership. The xCI measures both within-group and cross-group ranking accuracy in the presence of right-censored data. We formally define the xCI, prove that CI is a weighted average of xCIs across all possible group pairs, and develop a consistent estimator using inverse probability of censoring weights (IPCW). We further investigate the relationship between xCI and predicted risk scores through analytical derivations and simulation studies. To demonstrate its practical utility, we present two case studies: (i) assessing the fairness of survival models trained on harmonized data from the Framingham Offspring, MESA, and ARIC studies, and (ii) evaluating fairness in existing cardiovascular disease (CVD) risk prediction models using Truveta, a large-scale electronic health record (EHR) database. Our results show that xCI effectively detects biases across demographic groups that are overlooked by existing metrics. Overall, xCI provides a valuable tool for fairness assessment in survival analysis, particularly in constrained resource allocation settings, and complements existing fairness evaluation approaches.

stat.ME

Improving Event Time Prediction by Learning to Partition the Event Time Space

Recently developed survival analysis methods improve upon existing approaches by predicting the probability of event occurrence in each of a number pre-specified (discrete) time intervals. By avoiding placing strong parametric assumptions on the event density, this approach tends to improve prediction performance, particularly when data are plentiful. However, in clinical settings with limited available data, it is often preferable to judiciously partition the event time space into a limited number of intervals well suited to the prediction task at hand. In this work, we develop a method to learn from data a set of cut points defining such a partition. We show that in two simulated datasets, we are able to recover intervals that match the underlying generative model. We then demonstrate improved prediction performance on three real-world observational datasets, including a large, newly harmonized stroke risk prediction dataset. Finally, we argue that our approach facilitates clinical decision-making by suggesting time intervals that are most appropriate for each task, in the sense that they facilitate more accurate risk prediction.

stat.ML