arXiv subjects

Yixiang Qu

Publications and source records attributed to Yixiang Qu.

3 recordsLinked to original sources

arXiv2025

Cure Rate Joint Model for Time-to-Event Data and Longitudinal Tumor Burden with Potential Change Points

In non-small cell lung cancer (NSCLC) clinical trials, tumor burden (TB) is a key longitudinal biomarker for assessing treatment effects. Typically, standard-of-care (SOC) therapies and some novel interventions initially decrease TB; however, many patients subsequently experience an increase-indicating disease progression-while others show a continuous decline. In patients with an eventual TB increase, the change point marks the onset of progression and must occur before the time of the event. To capture these distinct dynamics, we propose a novel joint model that integrates time-to-event and longitudinal TB data, classifying patients into a change-point group or a stable group. For the change-point group, our approach flexibly estimates an individualized change point by leveraging time-to-event information. We use a Monte Carlo Expectation-Maximization (MCEM) algorithm for efficient parameter estimation. Simulation studies demonstrate that our model outperforms traditional approaches by accurately capturing diverse disease progression patterns and handling censoring complexities, leading to robust marginal TB outcome estimates. When applied to a Phase 3 NSCLC trial comparing cemiplimab monotherapy to SOC, the treatment group shows prolonged TB reduction and consistently lower TB over time, highlighting the clinical utility of our approach. The implementation code is publicly available on https://github.com/quyixiang/JoCuR.

stat.ME↗

arXiv2024

PrecLLM: A Privacy-Preserving Framework for Efficient Clinical Annotation Extraction from Unstructured EHRs using Small-Scale LLMs

Large Language Models (LLMs) have demonstrated remarkable proficiency in automated text annotation within natural language processing. However, their deployment in clinical settings is severely constrained by strict privacy regulations and the prohibitive computational cost of processing voluminous unstructured Electronic Health Records (EHRs). In this study, we developed a resource-efficient preprocessing technique that can be adopted in existing LLM procedures. This approach is particularly useful for smaller LLMs, which are often more accuracy-challenged, and forms a compact LLM framework optimized for local deployment in computational environments with stringent privacy requirements and restricted access to high-performance GPUs (PrecLLM). The preprocessing step includes both regular expressions (regex) and Retrieval-Augmented Generation (RAG) to extract and highlight key information from unstructured clinical notes. Pre-filtering long and unstructured texts enhanced the performance of smaller LLMs on EHR-related tasks. Evaluation was performed on two distinct cohorts: a locally curated private EHR dataset from the EPIC system for a Head and Neck Cancer (HNC) cohort, and the publicly available EHR dataset (MIMIC-IV). Using MIMIC-IV, we further compared PrecLLM against fine-tuned LLMs. Results demonstrated that PrecLLM substantially enhanced the performance of the original smaller LLMs in terms of sensitivity, specificity, and F1 scores, making it well-suited for privacy-sensitive and resource-constrained applications. This study offers optimized LLM performance for local, secure, and efficient healthcare applications, and provides practical guidance for clinical LLM deployment while addressing challenges related to privacy, computational feasibility, and clinical applicability.

cs.AI↗

arXiv2024

Jointly modeling time-to-event and longitudinal data with individual-specific change points: a case study in modeling tumor burden

In oncology clinical trials, tumor burden (TB) stands as a crucial longitudinal biomarker, reflecting the toll a tumor takes on a patient's prognosis. With certain treatments, the disease's natural progression shows the tumor burden initially receding before rising once more. Biologically, the point of change may be different between individuals and must have occurred between the baseline measurement and progression time of the patient, implying a random effects model obeying a bound constraint. However, in practice, patients may drop out of the study due to progression or death, presenting a non-ignorable missing data problem. In this paper, we introduce a novel joint model that combines time-to-event data and longitudinal data, where the latter is parameterized by a random change point augmented by random pre-slope and post-slope dynamics. Importantly, the model is equipped to incorporate covariates across for the longitudinal and survival models, adding significant flexibility. Adopting a Bayesian approach, we propose an efficient Hamiltonian Monte Carlo algorithm for parameter inference. We demonstrate the superiority of our approach compared to a longitudinal-only model via simulations and apply our method to a data set in oncology.

stat.ME↗