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血清胃蛋白酶原作为美国胃癌靶向筛查策略的成本效益

Cost-Effectiveness of Serum Pepsinogen as a Gastric Cancer Targeted Screening Strategy in the United States.

作者信息

Oh Aaron, Rustgi Sheila D, Hur Chin, In Haejin

机构信息

Albert Einstein College of Medicine, New York, New York.

Division of Digestive and Liver Diseases, Columbia University Irving Medical Center, New York, New York.

出版信息

Gastro Hep Adv. 2024 Oct 10;4(2):100564. doi: 10.1016/j.gastha.2024.10.004. eCollection 2025.

Abstract

BACKGROUND AND AIMS

Current gastric cancer (GC) screening modalities are invasive and expensive. Noninvasive screening for GC precursors with serum pepsinogen (PG) may improve early detection and prevention. Test characteristics of PG based on US prospective data was recently reported and used to study the cost-effectiveness of PG screening vs no screening in the US.

METHODS

A patient-level state transition microsimulation of gastric adenocarcinoma analyzed noninvasive screening vs no screening in a hypothetical cohort of average risk US individuals. Primary outcomes included life expectancy, quality-adjusted life years, total costs, and incremental cost-effectiveness ratios. Secondary outcomes included total GC incidence and mortality. Base-case PG sensitivity and specificity were 34.1% and 94.7%, respectively, with a wide range of PG performance characteristics also examined.

RESULTS

One-time serum PG screening at age 40 was cost-effective compared to no screening with an incremental cost-effectiveness ratio of $4913.29 per quality-adjusted life year. PG screening resulted in 10.9% relative reduction in lifetime GC incidence and 10.8% relative decrease in cumulative GC mortality. Localized stage at diagnosis increased from 30.5% to 33.6% and metastatic stage decreased from 40.8% to 37.4%. Sensitivity analysis showed PG screening was most sensitive to endoscopy costs, chronic atrophic gastritis quality of life, and PG prevalence. PG screening remained cost-effective across a wide range of test values.

CONCLUSION

PG screening is a cost-effective strategy to improve GC mortality; however, mortality benefit will depend on the test characteristics of the biomarker. Future blood-based screening tests that have better performance characteristics could further improve GC prevention.

摘要

背景与目的

当前的胃癌筛查方式具有侵入性且成本高昂。利用血清胃蛋白酶原(PG)对胃癌前体进行非侵入性筛查可能会改善早期检测与预防。近期报道了基于美国前瞻性数据的PG检测特征,并用于研究在美国进行PG筛查与不筛查的成本效益。

方法

对胃腺癌进行患者水平的状态转换微观模拟,分析在美国普通风险个体的假设队列中进行非侵入性筛查与不筛查的情况。主要结局包括预期寿命、质量调整生命年、总成本以及增量成本效益比。次要结局包括胃癌总发病率和死亡率。基础病例中PG的敏感性和特异性分别为34.1%和94.7%,同时还研究了PG性能特征的广泛范围。

结果

与不筛查相比,40岁时进行一次性血清PG筛查具有成本效益,增量成本效益比为每质量调整生命年4913.29美元。PG筛查使终生胃癌发病率相对降低10.9%,累积胃癌死亡率相对降低10.8%。诊断时的局部阶段从30.5%增加到33.6%,转移阶段从40.8%降至37.4%。敏感性分析表明,PG筛查对内窥镜检查成本、慢性萎缩性胃炎生活质量和PG患病率最为敏感。在广泛的检测值范围内,PG筛查仍具有成本效益。

结论

PG筛查是提高胃癌死亡率的一种具有成本效益的策略;然而,死亡率获益将取决于生物标志物的检测特征。未来具有更好性能特征的基于血液的筛查检测可能会进一步改善胃癌预防。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b915/11762188/9fb6fbf1d647/gr1.jpg

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