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A systematic comparison of microsimulation models of colorectal cancer: the role of assumptions about adenoma progression.

机译:大肠癌微观模拟模型的系统比较:关于腺瘤进展的假设的作用。

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BACKGROUND: As the complexity of microsimulation models increases, concerns about model transparency are heightened. METHODS: The authors conducted model experiments using 3 colorectal cancer (CRC) models. All natural history models were calibrated to match observed data on adenoma prevalence and cancer incidence but varied in their underlying specification of the adenocarcinoma process. The authors projected CRC incidence among individuals with an underlying adenoma or preclinical cancer v. those without any underlying condition and examined the impact of removing adenomas. They calculated the percentage of simulated CRC cases arising from adenomas that developed within 10 or 20 years prior to cancer diagnosis and estimated dwell time-defined as the time from the development of an adenoma to symptom-detected cancer in the absence of screening among individuals with a CRC diagnosis. RESULTS: The 20-year CRC incidence among 55-year-old individuals with an adenoma or preclinical cancer was 7 to 75 times greater than in the condition-free group. The removal of all adenomas among the subgroup with an underlying adenoma or cancer resulted in a reduction of 30% to 89% in cumulative incidence. Among CRCs diagnosed at age 65 years, the proportion arising from adenomas formed within 10 years ranged between 4% and 67%. The mean dwell time varied from 10.6 to 25.8 years. CONCLUSIONS: Models that all match observed data on adenoma prevalence and cancer incidence can produce quite different dwell times and very different answers with respect to the effectiveness of interventions. When conducting applied analyses to inform policy, using multiple models provides a sensitivity analysis on key (unobserved) deep additional research and validation.
机译:背景:随着微观仿真模型的复杂性增加,人们对模型透明度的关注也越来越高。方法:作者使用3种大肠癌(CRC)模型进行了模型实验。所有自然历史模型均经过校准,以匹配有关腺瘤患病率和癌症发生率的观察数据,但在腺癌过程的基础规范方面有所不同。作者预测患有基础腺瘤或临床前癌症患者与无基础疾病的个体之间的CRC发生率,并研究了去除腺瘤的影响。他们计算了在癌症诊断前10或20年内由腺瘤引起的模拟CRC病例的百分比,并估计了保压时间,定义为从无腺瘤发展到无症状筛查的症状检测到的癌症的时间。 CRC诊断。结果:55岁的腺瘤或临床前癌症患者的20年CRC发病率是无病组的7至75倍。除去具有潜在腺瘤或癌症的亚组中的所有腺瘤,可使累积发生率降低30%至89%。在确诊为65岁的CRC中,由腺瘤在10年内形成的比例在4%至67%之间。平均停留时间从10.6年到25.8年不等。结论:所有与腺瘤患病率和癌症发生率的观察数据相匹配的模型在干预效果方面可以产生截然不同的停留时间和不同的答案。在进行应用分析以为政策提供信息时,使用多个模型可对关键的(未观察到的)深度附加研究和验证进行敏感性分析。

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