A Role for Germline Variants in Multiple Myeloma?

Blood Cancer Discov. 2024 Nov 1;5(6):375-376. doi: 10.1158/2643-3230.BCD-24-0226.

Abstract

In 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.

MeSH terms

  • BRCA1 Protein / genetics
  • BRCA2 Protein / genetics
  • Genetic Predisposition to Disease
  • Germ-Line Mutation*
  • Humans
  • Multiple Myeloma* / diagnosis
  • Multiple Myeloma* / genetics
  • Multiple Myeloma* / therapy

Substances

  • BRCA1 Protein
  • BRCA2 Protein