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AI 根据所提供的论文材料归类:摘要核心是个体纵向重复测量及其随机效应建模,与面板数据方向直接相关,但未明确因果识别设计。

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代码、数据与补充材料

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关注这篇论文的作者
Laura A. Hatfield
Mark E. Boye
Bradley P. Carlin

大量零值纵向患者报告结局与生存时间的多层贝叶斯模型

研究问题
如何联合分析含大量零值的纵向患者报告结局与生存时间,并区分症状是否出现、出现后的严重程度及其与治疗的关系?
方法与思路
作者构建层级贝叶斯联合模型,以零增广贝塔似然分别描述症状出现与严重程度,并用潜在随机变量连接纵向结局和生存。
材料陈述的贡献
摘要称,该模型可在患者报告结局的原始尺度上建模,并在间皮瘤试验中揭示治疗相关结局与治疗响应结局的不同变化模式。
阅读关注点
应核对零值机制、纵向与生存子模型的连接方式、先验设定,以及周期性变化和组间差异如何支持作者对不同结局的解释。
阅读边界
仅据 OpenAlex 索引摘要,稿件版本未注明,不能推断刊本变化;摘要未说明完整模型条件、敏感性分析及治疗差异的因果解释边界。

原文摘要

Regulatory approval of new therapies often depends on demonstrating prolonged survival. Particularly when these survival benefits are modest, consideration of therapeutic benefits to patient-reported outcomes (PROs) may add value to the traditional biomedical clinical trial endpoints. We extend a popular class of joint models for longitudinal and survival data to accommodate the excessive zeros common in PROs, building hierarchical Bayesian models that combine information from longitudinal PRO measurements and survival outcomes. The model development is motivated by a clinical trial for malignant pleural mesothelioma, a rapidly fatal form of pulmonary cancer usually associated with asbestos exposure. By separately modeling the presence and severity of PROs, using our zero-augmented beta (ZAB) likelihood, we are able to model PROs on their original scale and learn about individual-level parameters from both presence and severity of symptoms. Correlations among an individual's PROs and survival are modeled using latent random variables, adjusting the fitted trajectories to better accommodate the observed data for each individual. This work contributes to understanding the impact of treatment on two aspects of mesothelioma: patients’ subjective experience of the disease process and their progression-free survival times. We uncover important differences between outcome types that are associated with therapy (periodic, worse in both treatment groups after therapy initiation) and those that are responsive to treatment (aperiodic, gradually widening gap between treatment groups). Finally, our work raises questions for future investigation into multivariate modeling, choice of link functions, and the relative contributions of multiple data sources in joint modeling contexts.

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