遗传性胰腺癌监测成本效益回顾。

IF 1.8 4区 医学 Q3 GENETICS & HEREDITY
Familial Cancer Pub Date : 2024-08-01 Epub Date: 2024-05-25 DOI:10.1007/s10689-024-00392-1
Louise Wang, Rachel Levinson, Catherine Mezzacappa, Bryson W Katona
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引用次数: 0

摘要

有遗传性胰腺癌风险的人包括对胰腺癌(PC)有种系遗传易感性和/或有胰腺癌家族史的高危人群(HRIs)。以前的研究表明,对高危人群进行 PC 监测可以降低 PC 诊断的晚期并延长生存期,因此建议对某些高危人群进行胰腺监测。然而,最佳的监测策略仍不确定,包括监测应采用哪些方式、监测的频率以及哪些 HRI 亚群应接受监测。此外,在理想情况下,PC 监测还应具有成本效益。成本效益分析是一种非常有价值的工具,它可以考虑各种 PC 监测策略的成本、潜在健康益处和风险。在本综述中,我们总结了针对遗传性胰腺癌 HRIs 的各种 PC 监测策略的成本效益,并提供了该领域未来工作的潜在途径。此外,我们还纳入了对散发性胰腺癌高危人群--新发糖尿病(NoD)患者的成本效益研究,作为对比。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Review of the cost-effectiveness of surveillance for hereditary pancreatic cancer.

Review of the cost-effectiveness of surveillance for hereditary pancreatic cancer.

Individuals with hereditary pancreatic cancer risk include high risk individuals (HRIs) with germline genetic susceptibility to pancreatic cancer (PC) and/or a strong family history of PC. Previously, studies have shown that PC surveillance in HRIs can downstage PC diagnosis and extend survival leading to pancreatic surveillance being recommended for certain HRIs. However, the optimal surveillance strategy remains uncertain, including which modalities should be used for surveillance, how frequently should surveillance be performed, and which sub-groups of HRIs should undergo surveillance. Additionally, in the ideal world PC surveillance should also be cost-effective. Cost-effectiveness analysis is a valuable tool that can consider the costs, potential health benefits, and risks among various PC surveillance strategies. In this review, we summarize the cost-effectiveness of various PC surveillance strategies for HRIs for hereditary pancreatic cancer and provide potential avenues for future work in this field. Additionally, we include cost-effectiveness studies among individuals with new-onset diabetes (NoD), a high-risk group for sporadic PC, as a comparison.

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来源期刊
Familial Cancer
Familial Cancer 医学-遗传学
CiteScore
4.10
自引率
4.50%
发文量
36
审稿时长
6-12 weeks
期刊介绍: In recent years clinical cancer genetics has become increasingly important. Several events, in particular the developments in DNA-based technology, have contributed to this evolution. Clinical cancer genetics has now matured to a medical discipline which is truly multidisciplinary in which clinical and molecular geneticists work together with clinical and medical oncologists as well as with psycho-social workers. Due to the multidisciplinary nature of clinical cancer genetics most papers are currently being published in a wide variety of journals on epidemiology, oncology and genetics. Familial Cancer provides a forum bringing these topics together focusing on the interests and needs of the clinician. The journal mainly concentrates on clinical cancer genetics. Most major areas in the field shall be included, such as epidemiology of familial cancer, molecular analysis and diagnosis, clinical expression, treatment and prevention, counselling and the health economics of familial cancer.
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