» Articles » PMID: 36551598

Real World Cost-Effectiveness Analysis of Population Screening for BRCA Variants Among Ashkenazi Jews Compared with Family History-Based Strategies

Overview
Journal Cancers (Basel)
Publisher MDPI
Specialty Oncology
Date 2022 Dec 23
PMID 36551598
Authors
Affiliations
Soon will be listed here.
Abstract

Identifying carriers of pathogenic BRCA1/BRCA2 variants reduces cancer morbidity and mortality through surveillance and prevention. We analyzed the cost-effectiveness of BRCA1/BRCA2 population screening (PS) in Ashkenazi Jews (AJ), for whom carrier rate is 2.5%, compared with two existing strategies: cascade testing (CT) in carrier’s relatives (≥25% carrier probability) and international family history (IFH)-based guidelines (>10% probability). We used a decision analytic-model to estimate quality-adjusted life-years (QALY) gained, and incremental cost-effectiveness ratio for PS vs. alternative strategies. Analysis was conducted from payer-perspective, based on actual costs. Per 1000 women, the model predicted 21.6 QALYs gained, a lifetime decrease of three breast cancer (BC) and four ovarian cancer (OC) cases for PS vs. CT, and 6.3 QALYs gained, a lifetime decrease of 1 BC and 1 OC cases comparing PS vs. IFH. PS was less costly compared with CT (−3097 USD/QALY), and more costly than IFH (+42,261 USD/QALY), yet still cost-effective, from a public health policy perspective. Our results are robust to sensitivity analysis; PS was the most effective strategy in all analyses. PS is highly cost-effective, and the most effective screening strategy for breast and ovarian cancer prevention. BRCA testing should be available to all AJ women, irrespective of family history.

Citing Articles

The Use of National Cancer Registry Data for Breast Cancer Family History Assessment in Premenopausal Women.

Chodick G, Silverman B, Keinan-Boker L J Clin Med. 2024; 13(15).

PMID: 39124739 PMC: 11313154. DOI: 10.3390/jcm13154473.

References
1.
Manchanda R, Blyuss O, Gaba F, Gordeev V, Jacobs C, Burnell M . Current detection rates and time-to-detection of all identifiable carriers in the Greater London population. J Med Genet. 2018; 55(8):538-545. DOI: 10.1136/jmedgenet-2017-105195. View

2.
Metcalfe K, Poll A, Royer R, Llacuachaqui M, Tulman A, Sun P . Screening for founder mutations in BRCA1 and BRCA2 in unselected Jewish women. J Clin Oncol. 2009; 28(3):387-91. DOI: 10.1200/JCO.2009.25.0712. View

3.
Smith M, Gerber D, Olsen A, Khouri O, Wang Y, Liu M . Uptake and timing of risk-reducing salpingo-oophorectomy among patients with BRCA1 and BRCA2 mutations. Am J Obstet Gynecol. 2021; 225(5):508.e1-508.e10. DOI: 10.1016/j.ajog.2021.06.070. View

4.
Hadar T, Mor P, Amit G, Lieberman S, Gekhtman D, Rabinovitch R . Presymptomatic Awareness of Germline Pathogenic BRCA Variants and Associated Outcomes in Women With Breast Cancer. JAMA Oncol. 2020; 6(9):1460-1463. PMC: 7349080. DOI: 10.1001/jamaoncol.2020.2059. View

5.
Heemskerk-Gerritsen B, Jager A, Koppert L, Obdeijn A, Collee M, Meijers-Heijboer H . Survival after bilateral risk-reducing mastectomy in healthy BRCA1 and BRCA2 mutation carriers. Breast Cancer Res Treat. 2019; 177(3):723-733. PMC: 6745043. DOI: 10.1007/s10549-019-05345-2. View