Chromosome 8q24.1/c-MYC abnormality: a marker for high-risk myeloma

Leuk Lymphoma. 2015 Mar;56(3):602-7. doi: 10.3109/10428194.2014.924116. Epub 2014 Aug 18.

Abstract

The proto-oncogene c-MYC is rearranged in about 15% of patients with multiple myeloma (MM). We identified 23 patients with MM and c-MYC. Primary objectives were to describe the clinical characteristics, response to therapy, progression-free survival and overall survival (OS). Twelve out of twenty-three patients presented with or progressed to either plasma cell leukemia (PCL) and/or extramedullary disease (EMD). Induction therapy consisted of an immunomodulatory, proteasome inhibitor-based or conventional chemotherapy regimen. Fifteen patients achieved a partial response and three achieved a very good partial response. Sixteen patients received an autologous and one patient an allogeneic hematopoietic stem cell transplant. Median OS from diagnosis was 20.2 months. Patients with PCL or EMD had significantly shorter OS (15.5 vs. 40.4 months, p = 0.0005). This is the first report describing the clinical characteristics of patients with MM and c-MYC. These abnormalities are associated with an aggressive form of MM, high incidence of PCL/EMD and short OS.

Keywords: c-MYC/8q24; high risk; multiple myeloma; plasma cell leukemia.

MeSH terms

  • Adult
  • Aged
  • Biomarkers, Tumor / genetics*
  • Chromosomes, Human, Pair 8 / genetics*
  • Female
  • Gene Rearrangement / physiology
  • Hematopoiesis, Extramedullary / physiology
  • Humans
  • In Situ Hybridization, Fluorescence
  • Leukemia, Plasma Cell / pathology
  • Male
  • Middle Aged
  • Multiple Myeloma / genetics*
  • Multiple Myeloma / mortality
  • Multiple Myeloma / pathology
  • Proto-Oncogene Mas
  • Proto-Oncogene Proteins c-myc / genetics*
  • Retrospective Studies
  • Young Adult

Substances

  • Biomarkers, Tumor
  • MAS1 protein, human
  • Proto-Oncogene Mas
  • Proto-Oncogene Proteins c-myc