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ABSTRACT: Background
BRCA1/2 mutation carriers are suggested with regular breast cancer surveillance screening strategies using mammography with supplementary MRI as an adjunct tool in Western countries. From a cost-effectiveness perspective, however, the benefits of screening modalities remain controversial among different mutated genes and screening schedules.Methods
We searched the MEDLINE/PubMed, Embase, Cochrane Library, Scopus, and Web of Science databases to collect and compare the results of different cost-effectiveness analyses. A simulated model was used to predict the impact of screening strategies in the target group on cost, life-year gained, quality-adjusted life years, and incremental cost-effectiveness ratio (ICER).Results
Nine cost-effectiveness studies were included. Combined mammography and MRI strategy is cost-effective in BRCA1 mutation carriers for the middle-aged group (age 35 to 54). BRCA2 mutation carriers are less likely to benefit from adjunct MRI screening, which implies that mammography alone would be sufficient from a cost-effectiveness perspective, regardless of dense breast cancer.Conclusions
Precision screening strategies among BRCA1/2 mutation carriers should be conducted according to the acceptable ICER, i.e., a combination of mammography and MRI for BRCA1 mutation carriers and mammography alone for BRCA2 mutation carriers.Systematic review registration
PROSPERO, identifier CRD42020205471.
SUBMITTER: Li J
PROVIDER: S-EPMC8785233 | biostudies-literature | 2021
REPOSITORIES: biostudies-literature
Li Jiaxin J Jia Ziqi Z Zhang Menglu M Liu Gang G Xing Zeyu Z Wang Xin X Huang Xin X Feng Kexin K Wu Jiang J Wang Wenyan W Wang Jie J Liu Jiaqi J Wang Xiang X
Frontiers in oncology 20220110
<h4>Background</h4><i>BRCA1/2</i> mutation carriers are suggested with regular breast cancer surveillance screening strategies using mammography with supplementary MRI as an adjunct tool in Western countries. From a cost-effectiveness perspective, however, the benefits of screening modalities remain controversial among different mutated genes and screening schedules.<h4>Methods</h4>We searched the MEDLINE/PubMed, Embase, Cochrane Library, Scopus, and Web of Science databases to collect and compa ...[more]