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用于结直肠癌筛查的具有成本效益的血液检测的特征。

Characteristics of a cost-effective blood test for colorectal cancer screening.

机构信息

Engineering and Applied Sciences Department, RAND, Arlington, VA, USA.

Department of Public Health, Erasmus Medical Center, Erasmus University, Rotterdam, The Netherlands.

出版信息

J Natl Cancer Inst. 2024 Oct 1;116(10):1612-1620. doi: 10.1093/jnci/djae124.

Abstract

BACKGROUND

Blood-based biomarker tests can potentially change the landscape of colorectal cancer (CRC) screening. We characterize the conditions under which blood test screening would be as effective and cost-effective as annual fecal immunochemical testing or decennial colonoscopy.

METHODS

We used the 3 Cancer Information and Surveillance Modeling Network-Colon models to compare scenarios of no screening, annual fecal immunochemical testing, decennial colonoscopy, and a blood test meeting Centers for Medicare & Medicaid (CMS) coverage criteria (74% CRC sensitivity and 90% specificity). We varied the sensitivity to detect CRC (74%-92%), advanced adenomas (10%-50%), screening interval (1-3 years), and test cost ($25-$500). Primary outcomes included quality-adjusted life-years (QALY) gained from screening and costs for a US average-risk cohort of individuals aged 45 years.

RESULTS

Annual fecal immunochemical testing yielded 125-163 QALY gained per 1000 at a cost of $3811-$5384 per person, whereas colonoscopy yielded 132-177 QALY gained at a cost of $5375-$7031 per person. A blood test with 92% CRC sensitivity and 50% advanced adenoma sensitivity yielded 117-162 QALY gained if used every 3 years and 133-173 QALY gained if used every year but would not be cost-effective if priced above $125 per test. If used every 3 years, a $500 blood test only meeting CMS coverage criteria yielded 83-116 QALY gained at a cost of $8559-$9413 per person.

CONCLUSION

Blood tests that only meet CMS coverage requirements should not be recommended to patients who would otherwise undergo screening by colonoscopy or fecal immunochemical testing because of lower benefit. Blood tests need higher advanced adenoma sensitivity (above 40%) and lower costs (below $125) to be cost-effective.

摘要

背景

基于血液的生物标志物检测有可能改变结直肠癌(CRC)筛查的格局。我们描述了血液检测在何种情况下与每年的粪便免疫化学检测或每十年结肠镜检查一样有效和具有成本效益。

方法

我们使用 3 个癌症信息和监测建模网络-结肠模型来比较不进行筛查、每年进行粪便免疫化学检测、每十年进行结肠镜检查以及符合医疗保险和医疗补助服务中心(CMS)覆盖标准(CRC 检测敏感性 74%,特异性 90%)的血液检测的方案。我们改变了检测 CRC(74%-92%)、高级腺瘤(10%-50%)、筛查间隔(1-3 年)和检测成本($25-$500)的敏感性。主要结果包括筛查获得的质量调整生命年(QALY)和美国平均风险人群(45 岁)的成本。

结果

每年的粪便免疫化学检测每 1000 人获得 125-163 个 QALY,每人费用为 3811-5384 美元,而结肠镜检查每 1000 人获得 132-177 个 QALY,每人费用为 5375-7031 美元。如果每 3 年使用一次,具有 92%CRC 检测敏感性和 50%高级腺瘤检测敏感性的血液检测可获得 117-162 个 QALY,如果每年使用一次,则可获得 133-173 个 QALY,但如果检测价格超过每个 125 美元,则无成本效益。如果每 3 年使用一次,仅符合 CMS 覆盖标准的 500 美元血液检测,每人费用为 8559-9413 美元,可获得 83-116 个 QALY。

结论

如果患者接受结肠镜检查或粪便免疫化学检测,那么仅符合 CMS 覆盖要求的血液检测不应向患者推荐,因为其获益较低。血液检测需要更高的高级腺瘤检测敏感性(高于 40%)和更低的成本(低于 125 美元)才能具有成本效益。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b13/11461157/6dc6bf2c0b5b/djae124f1.jpg

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