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本页整理公开书目信息,不生成学术质量评分。AI 解读根据题名及所注明的摘要或原文片段生成,未完成全文核验,可能有误;具体假设、证明与结论请核对原文。摘要保留来源文本,未经模型改写。

DOI 首次登记不等于接收或发表日期。部分更正、评论等条目没有独立摘要;缺少可靠材料时保留待补状态。

引用量采用 OpenAlex 单条关联记录,不合计多个记录;关联记录可能包含正式发表版本,不等于此版本单独引用。缺失不视为零,引用指标不代表论文质量。

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分类依据与纠错

AI 根据所提供的论文材料归类:摘要研究医学多类别结局的关联回归与外部信息整合,类别结局并非已明确的离散选择行为,也未提出因果识别。

反馈分类问题

A Generalized Integration Approach to Association Analysis with Multi-category Outcome: An Application to a Tumor Sequencing Study of Colorectal Cancer and Smoking

多类别结局关联分析的广义信息整合:结直肠癌与吸烟应用

正在核对关联版本…

代码、数据与补充材料

正在核对对应版本的资源…

关注这篇论文的作者
Jiayin Zheng
Xinyuan Dong
Li Hsu

多类别结局关联分析的广义信息整合:结直肠癌与吸烟应用

研究问题
当肿瘤测序样本有限,而文献中已有总体癌症风险及既知标记的关联信息时,如何提高新肿瘤特征关联分析的效率?
方法与思路
作者在多项逻辑回归中,以约束连接外部汇总信息和目标参数,再最大化个体肿瘤数据与外部信息的联合似然。
材料陈述的贡献
摘要称整合方法提高估计效率,并在 CPS-II 数据中发现吸烟关联随 APC、RNF43 突变状态不同,而常规分析未识别这些关联。
阅读关注点
应核对外部信息与个体样本的兼容条件、汇总估计不确定性的处理、约束构造,以及样本选择对关联分析的影响。
阅读边界
仅据 OpenAlex 索引摘要,稿件版本未注明;外部信息兼容条件未说明,所报吸烟关联不能直接解释为因果效应。

原文摘要

Cancer is a heterogeneous disease, and rapid progress in sequencing and -omics technologies has enabled researchers to characterize tumors comprehensively. This has stimulated an intensive interest in studying how risk factors are associated with various tumor heterogeneous features. The Cancer Prevention Study-II (CPS-II) cohort is one of the largest prospective studies, particularly valuable for elucidating associations between cancer and risk factors. In this paper, we investigate the association of smoking with novel colorectal tumor markers obtained from targeted sequencing. However, due to cost and logistic difficulties, only a limited number of tumors can be assayed, which limits our capability for studying these associations. Meanwhile, there are extensive studies for assessing the association of smoking with overall cancer risk and established colorectal tumor markers. Importantly, such summary information is readily available from the literature. By linking this summary information to parameters of interest with proper constraints, we develop a generalized integration approach for polytomous logistic regression model with outcome characterized by tumor features. The proposed approach gains the efficiency through maximizing the joint likelihood of individual-level tumor data and external summary information under the constraints that narrow the parameter searching space. We apply the proposed method to the CPS-II data and identify the association of smoking with colorectal cancer risk differing by the mutational status of APC and RNF43 genes, neither of which is identified by the conventional analysis of CPS-II individual data only. These results help better understand the role of smoking in the etiology of colorectal cancer.

笔记与分组
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