锯齿状路径对大肠癌筛查试验模拟比较效果的影响。

IF 3.4 Q2 ONCOLOGY JNCI Cancer Spectrum Pub Date : 2024-09-02 DOI:10.1093/jncics/pkae077
Reinier G S Meester, Uri Ladabaum
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引用次数: 0

摘要

背景:大肠癌(CRC)由腺瘤或无柄锯齿状病变(SSL)引起,腺瘤可产生粪便隐血,可通过内镜检测到,而无柄锯齿状病变很少出血,可能更难检测到。为 CRC 筛查政策提供信息的模型应反映这两种途径,并考虑到不确定性:方法:建立新颖的 CRC 腺瘤和锯齿状病变途径决策分析模型 (ANSER),比较当前和新出现的筛查策略,并考虑到腺瘤和 SSL 的不同检测灵敏度以及不确定性。筛查策略包括每 10 年进行一次结肠镜检查、每 1-3 年进行一次粪便 DNA/FIT (sDNA-FIT) 或从 45-75 岁开始每年进行一次粪便免疫化学检测 (FIT)。结果包括 CRC 病例和死亡人数、成本效益(成本/获得的质量调整生命年 (QALY))和负担效益(结肠镜检查次数/获得的生命年),以及 95% 不确定区间 (95%UIs):ANSER预测,在不进行筛查的情况下,每1,000名45岁人群终生CRC病例数为62.5(95%UI,58.8-66.3)例,CRC死亡率为24.1(95%UI,22.5-25.7)例;而在进行筛查的情况下,CRC死亡率降低了78%-87%。在获得的 QALYs 方面,这些试验的结果分布有所重叠,但在所需的结肠镜检查和成本方面则有所区别。与 FIT 相比,所有策略的成本均为 500,000 美元/QALY。由于更多的 CRC 来自于 SSL,根据临床获益和成本效益,结肠镜检查仍是首选,但下一代 sDNA-FIT 的成本效益有所提高:结论:当考虑到锯齿状路径时,建模表明结肠镜检查与 FIT 相比具有成本效益。相比之下,尽管 sDNA-FIT 对锯齿状路径的敏感性更高,但建模结果表明,sDNA-FIT 与 FIT 相比并不具有成本效益,即使有相当一部分的 CRC 是由锯齿状路径引起的:荷兰研究理事会(NWO)。
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Impact of the serrated pathway on the simulated comparative effectiveness of colorectal cancer screening tests.

Background: Colorectal cancers (CRCs) arise from adenomas, which can produce fecal occult blood and can be detected endoscopically, or sessile serrated lesions (SSLs), which rarely bleed and may be more challenging to detect. Models informing CRC screening policy should reflect both pathways, accounting for uncertainty.

Methods: Novel decision-analytic model of the adenoma and serrated pathways for CRC (ANSER) to compare current and emerging screening strategies, accounting for differential test sensitivities for adenomas and SSLs, and uncertainty. Strategies included colonoscopy every 10 years, stool-DNA/FIT (sDNA-FIT) every 1-3 years, or fecal immunochemical testing (FIT) every year from age 45 to 75 years. Outcomes included CRC cases and deaths, cost-effectiveness (cost/quality-adjusted life-year [QALY] gained), and burden-benefit (colonoscopies/life-year gained), with 95% uncertainty intervals (UIs).

Results: ANSER predicted 62.5 (95% UI = 58.8-66.3) lifetime CRC cases and 24.1 (95% UI = 22.5-25.7) CRC deaths/1000 45-year-olds without screening, and 78%-87% CRC mortality reductions with screening. The tests' outcome distributions overlapped for QALYs gained but separated for required colonoscopies and costs. All strategies cost less than $100 000/QALY gained vs no screening. Colonoscopy was the most effective and cost-effective, costing $9300/life-year gained (95% UI = $500-$21 900) vs FIT. sDNA-FIT cost more than $500 000/QALY gained vs FIT. As more CRCs arose from SSLs, colonoscopy remained preferred based on clinical benefit and cost-effectiveness, but cost-effectiveness improved for a next-generation sDNA-FIT.

Conclusion: When the serrated pathway is considered, modeling suggests that colonoscopy is cost-effective vs FIT. In contrast, modeling suggests that sDNA-FIT is not cost-effective vs FIT despite its greater sensitivity for SSLs, even if a substantial minority of CRCs arise from SSLs.

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来源期刊
JNCI Cancer Spectrum
JNCI Cancer Spectrum Medicine-Oncology
CiteScore
7.70
自引率
0.00%
发文量
80
审稿时长
18 weeks
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