三种预测欧洲结直肠癌筛查益处的区域微观模拟模型的开发和验证。

IF 1.7
MDM policy & practice Pub Date : 2021-01-29 eCollection Date: 2021-01-01 DOI:10.1177/2381468320984974
Andrea Gini, Maaike Buskermolen, Carlo Senore, Ahti Anttila, Dominika Novak Mlakar, Piret Veerus, Marcell Csanádi, Erik E L Jansen, Nadine Zielonke, Sirpa Heinävaara, György Széles, Nereo Segnan, Harry J de Koning, Iris Lansdorp-Vogelaar
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引用次数: 5

摘要

背景。经过验证的微模拟模型已被证明是提供结肠直肠癌(CRC)筛查决策支持的有用工具。为了帮助欧洲国家降低结直肠癌死亡率,我们开发并验证了三个评估欧洲结直肠癌筛查的区域模型。方法。意大利、斯洛文尼亚和芬兰的微模拟筛选分析- colon (MISCAN-Colon)模型版本使用来自不同国家机构的数据进行量化。这些模型是根据其所在地区(如果有的话)筛查有效性的最佳证据进行验证的:意大利的结肠直肠筛查(SCORE)试验和佛罗伦萨粪便免疫化学试验(FIT)筛查研究;挪威结直肠癌预防(NORCCAP)试验和愈创木粪潜血试验(ggft)芬兰人口为基础的芬兰研究。当没有公开的证据可用时(斯洛文尼亚),使用癌症登记数据验证该模型。结果。我们的三个模型再现了筛查前期年龄特异性CRC发病率和分期分布。此外,意大利和芬兰的模型(合理地)很好地复制了CRC死亡率的降低,与现有的最佳证据相反。预测的结直肠癌死亡率下降幅度略大于观察到的结果(佛罗伦萨FIT研究除外),但始终在相应的95%置信区间内。结论。我们的研究结果证实了MISCAN-Colon在支持CRC筛查决策方面的可靠性。此外,我们的研究为另一个工具(EU-TOPIA CRC评估工具:http://miscan.eu-topia.org)提供了模型结构,旨在帮助政策制定者和研究人员监测或改善欧洲的CRC筛查。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Development and Validation of Three Regional Microsimulation Models for Predicting Colorectal Cancer Screening Benefits in Europe.

Development and Validation of Three Regional Microsimulation Models for Predicting Colorectal Cancer Screening Benefits in Europe.

Development and Validation of Three Regional Microsimulation Models for Predicting Colorectal Cancer Screening Benefits in Europe.

Development and Validation of Three Regional Microsimulation Models for Predicting Colorectal Cancer Screening Benefits in Europe.

Background. Validated microsimulation models have been shown to be useful tools in providing support for colorectal cancer (CRC) screening decisions. Aiming to assist European countries in reducing CRC mortality, we developed and validated three regional models for evaluating CRC screening in Europe. Methods. Microsimulation Screening Analysis-Colon (MISCAN-Colon) model versions for Italy, Slovenia, and Finland were quantified using data from different national institutions. These models were validated against the best available evidence for the effectiveness of screening from their region (when available): the Screening for COlon REctum (SCORE) trial and the Florentine fecal immunochemical test (FIT) screening study for Italy; the Norwegian Colorectal Cancer Prevention (NORCCAP) trial and the guaiac fecal occult blood test (gFOBT) Finnish population-based study for Finland. When published evidence was not available (Slovenia), the model was validated using cancer registry data. Results. Our three models reproduced age-specific CRC incidence rates and stage distributions in the prescreening period. Moreover, the Italian and Finnish models replicated CRC mortality reductions (reasonably) well against the best available evidence. CRC mortality reductions were predicted slightly larger than those observed (except for the Florentine FIT study), but consistently within the corresponding 95% confidence intervals. Conclusions. Our findings corroborate the MISCAN-Colon reliability in supporting decision making on CRC screening. Furthermore, our study provides the model structure for an additional tool (EU-TOPIA CRC evaluation tool: http://miscan.eu-topia.org) that aims to help policymakers and researchers monitoring or improving CRC screening in Europe.

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