丙型肝炎感染者肝癌最优m开关监测策略

Qiushi Chen, T. Ayer, J. Chhatwal
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引用次数: 1

摘要

肝细胞癌(HCC)是最常见的肝癌类型,也是美国癌症相关死亡人数增长最快的原因。大多数HCC病例归因于慢性丙型肝炎病毒感染,该病毒影响了近300万美国人和全球1.7亿人。尽管监测丙型肝炎患者的肝细胞癌可以提高生存率,但最佳的监测政策仍然未知。在本研究中,我们开发了一个基于混合整数规划(MIP)的框架,系统地分析了一套丰富的政策,并确定了具有最大社会净效益的最佳HCC监测政策。我们基于mip的框架捕获了两个问题特征,使基于动态规划的公式在计算上难以处理。特别是,我们提出的框架允许(1)明确制定可实施的m开关政策,以及(2)根据可观察到的疾病状态对监测间隔进行分层,从而为每个亚人群量身定制监测政策。我们从理论上分析了HCC监测问题,描述了监测政策何时应适应不同疾病进展率的人群,并量化了降低HCC发病率和提高治疗结果之间的权衡。我们使用临床试验数据、先前验证的模拟模型和已发表的临床研究仔细地参数化了我们的模型。我们的数值分析得出了三个具有重要政策意义的主要结果。首先,我们发现,除了肝硬化患者外,将监测扩大到早期丙型肝炎感染患者可以提高HCC监测的成本效益。第二,与“一刀切”的常规政策相比,我们发现基于丙型肝炎感染阶段分层监测策略,在感染早期较少进行癌症监测具有成本效益。最后,我们发现M-switch策略捕获的策略结构中的一点灵活性足以获得几乎与复杂的全动态策略一样多的收益。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Optimal M-Switch Surveillance Policies for Liver Cancer in Hepatitis C-Infected Population
Hepatocellular carcinoma (HCC) is the most common type of liver cancer and the fastest-growing cause of cancer-related deaths in the United States. Most HCC cases are attributed to chronic hepatitis C virus infection, which affects nearly 3 million Americans and 170 million globally. Although surveillance for HCC in hepatitis C patients can improve survival, the optimal surveillance policies remain unknown. In this study, we develop a mixed-integer programming (MIP)-based framework to systematically analyze a rich set of policies and determine the optimal HCC surveillance policies with the maximum societal net benefit. Our MIP-based framework captures two problem features that make dynamic programming-based formulation computationally intractable. In particular, our proposed framework allows to (1) explicitly formulate M-switch policies that are practical for implementation, and (2) tailor surveillance policies for each subpopulation by stratifying surveillance intervals based on the observable disease states. We theoretically analyze the HCC surveillance problem, characterize when the surveillance policies should be adapted to populations with different disease progression rates, and quantify the trade-off between decreasing HCC incidence and increasing treatment outcomes. We carefully parameterize our model using clinical trial data, a previously validated simulation model, and published clinical studies. Our numerical analyses lead to three main results with important policy implications. First, we find that, in addition to cirrhotic patients, expanding surveillance to patients in earlier stage of hepatitis C infection improves the cost-effectiveness of HCC surveillance. Second, compared with the one-size-fits-all type routine policies, we find that it is cost-effective to stratify surveillance strategies based on the stage of hepatitis C infection with less frequent cancer surveillance in earlier stages of infection. Lastly, we find that a little flexibility in the policy structure as captured by M-switch policies is sufficient to capture almost as much benefit as complex fully dynamic policies.
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