A Role for Germline Variants in Multiple Myeloma?

dc.contributor.authorWalker, Brian A.
dc.contributor.departmentMedicine, School of Medicine
dc.date.accessioned2025-06-13T07:22:02Z
dc.date.available2025-06-13T07:22:02Z
dc.date.issued2024
dc.description.abstractIn Blood Cancer Discovery, Thibaud and colleagues report the incidence of pathogenic germline variants (PGV) in patients with multiple myeloma and that these PGVs are associated with DNA repair pathway genes, including BRCA1 and BRCA2. They find an association of patients with PGVs and previous family or personal history of cancer, and that these patients are diagnosed slightly earlier than those without PGVs. Patients with PGVs had a longer progression-free survival than those without PGVs when they received high-dose melphalan and autologous stem cell transplant, providing a therapeutic rationale for diagnostic germline testing in myeloma. See related article by Thibaud et al., p. 428.
dc.eprint.versionFinal published version
dc.identifier.citationWalker BA. A Role for Germline Variants in Multiple Myeloma?. Blood Cancer Discov. 2024;5(6):375-376. doi:10.1158/2643-3230.BCD-24-0226
dc.identifier.urihttps://hdl.handle.net/1805/48670
dc.language.isoen_US
dc.publisherAmerican Association for Cancer Research
dc.relation.isversionof10.1158/2643-3230.BCD-24-0226
dc.relation.journalBlood Cancer Discovery
dc.rightsPublisher Policy
dc.sourcePMC
dc.subjectGenetic predisposition to disease
dc.subjectMultiple myeloma
dc.subjectGerm-line mutation
dc.titleA Role for Germline Variants in Multiple Myeloma?
dc.typeArticle
ul.alternative.fulltexthttps://pmc.ncbi.nlm.nih.gov/articles/PMC11528183/
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