Targeted Search for Individualized Clinical Decision Rules to Optimize Clinical Outcomes.

Pub Date : 2022-12-01 DOI:10.1007/s12561-022-09343-9
Yanqing Wang, Yingqi Zhao, Yingye Zheng
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Abstract

Novel biomarkers, in combination with currently available clinical information, have been sought to enhance clinical decision making in many branches of medicine, including screening, surveillance and prognosis. An individualized clinical decision rule (ICDR) is a decision rule that matches subgroups of patients with tailored medical regimen based on patient characteristics. We proposed new approaches to identify ICDRs by directly optimizing a risk-adjusted clinical benefit function that acknowledges the tradeoff between detecting disease and over-treating patients with benign conditions. In particular, we developed a novel plug-in algorithm to optimize the risk-adjusted clinical benefit function, which leads to the construction of both nonparametric and linear parametric ICDRs. In addition, we proposed a novel approach based on the direct optimization of a smoothed ramp loss function to further enhance the robustness of a linear ICDR. We studied the asymptotic theories of the proposed estimators. Simulation results demonstrated good finite sample performance for the proposed estimators and improved clinical utilities when compared to standard approaches. The methods were applied to a prostate cancer biomarker study.

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针对性搜索个性化临床决策规则以优化临床结果。
新的生物标志物,结合现有的临床信息,已经寻求在许多医学分支,包括筛查,监测和预后加强临床决策。个体化临床决策规则(ICDR)是一种基于患者特征,为患者亚组匹配量身定制的医疗方案的决策规则。我们提出了通过直接优化风险调整的临床效益函数来识别icdr的新方法,该函数承认在检测疾病和过度治疗良性疾病患者之间的权衡。特别是,我们开发了一种新的插件算法来优化风险调整后的临床效益函数,从而构建了非参数和线性参数icdr。此外,我们提出了一种基于平滑斜坡损失函数的直接优化的新方法,以进一步增强线性ICDR的鲁棒性。我们研究了所提估计量的渐近理论。仿真结果表明,与标准方法相比,所提出的估计器具有良好的有限样本性能,并提高了临床实用性。这些方法被应用于前列腺癌生物标志物研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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