Comparison of Simulated Outcomes Between Stool- and Blood-Based Colorectal Cancer Screening Tests

被引:4
作者
Fendrick, A. Mark [1 ,2 ,6 ,7 ]
Vahdat, Vahab [3 ]
Chen, Jing Voon [3 ]
Lieberman, David [4 ]
Limburg, Paul J. [3 ]
Ozbay, A. Burak [3 ]
Kisiel, John B. [5 ]
机构
[1] Univ Michigan, Dept Internal Med, Div Gen Med, Ann Arbor, MI USA
[2] Univ Michigan, Dept Hlth Management & Policy, Div Gen Med, Ann Arbor, MI USA
[3] Exact Sci Corp, Madison, WI USA
[4] Oregon Hlth & Sci Univ, Sch Med, Div Gastroenterol & Hepatol, Portland, OR USA
[5] Mayo Clin, Div Gastroenterol & Hepatol, Rochester, MN USA
[6] Univ Michigan, Dept Internal Med, Div Gen Med, North Campus Res Complex,2800 Plymouth Rd,Bldg 16-, Ann Arbor, MI 48109 USA
[7] Univ Michigan, Dept Hlth Management & Policy, Div Gen Med, North Campus Res Complex,2800 Plymouth Rd,Bldg 16-, Ann Arbor, MI 48109 USA
基金
美国医疗保健研究与质量局;
关键词
colorectal neoplasms; prevention and control; liquid biopsy; biomarker; adenoma; Medicare; COLONOSCOPY; VALIDATION; MODELS;
D O I
10.1089/pop.2023.0037
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
The Centers for Medicare & Medicaid Services (CMS) recommend covering blood-based tests meeting proposed minimum performance thresholds for colorectal cancer (CRC) screening. Outcomes were compared between currently available stool-based screening tests and a hypothetical blood-based test meeting CMS minimum thresholds. Using the Colorectal Cancer and Adenoma Incidence and Mortality Microsimulation Model (CRC-AIM), outcomes were simulated for average-risk individuals screened between ages 45 and 75 years with triennial multitarget stool DNA (mt-sDNA), annual fecal immunochemical test (FIT), and annual fecal occult blood test (FOBT). Per CMS guidance, blood-based CRC screening was modeled triennially, with 74% CRC sensitivity and 90% specificity. Although not specified by CMS, adenoma sensitivity was set between 10% and 20%. Published adenoma and CRC sensitivity and specificity were used for stool-based tests. Adherence was set at (1) 100%, (2) 30%-70%, in 10% increments, and (3) real-world rates for stool-based tests (mt-sDNA = 65.6%; FIT = 42.6%; FOBT = 34.4%). Assuming perfect adherence, a blood-based test produced & GE;19 lower life-years gained (LYG) than stool-based strategies. At the best-case scenario for blood-based tests (100% adherence and 20% adenoma sensitivity), mt-sDNA at real-world adherence achieved more LYG (287.2 vs. 297.1, respectively) with 14% fewer colonoscopies. At 100% blood-based test adherence and real-world mt-sDNA and FIT adherence, the blood-based test would require advanced adenoma sensitivity of 30% to reach the LYG of mt-sDNA (297.1) and & SIM;15% sensitivity to reach the LYG of FIT (258.9). This model suggests that blood-based tests with CMS minimally acceptable CRC sensitivity and low advanced adenoma sensitivity will frequently yield inferior outcomes to stool-based testing across a wide range of adherence assumptions.
引用
收藏
页码:239 / 245
页数:7
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