How I treat high-risk myeloma

Blood. 2015 Sep 24;126(13):1536-43. doi: 10.1182/blood-2015-06-653261. Epub 2015 Aug 13.

Abstract

The treatment of patients with myeloma has dramatically changed over the past decade due in part to the development of new agents and myeloma-specific targets. Despite these advancements, a group for whom the long-term benefit remains less clear are patients with genetically or clinically defined high-risk myeloma. In order to successfully treat these patients, it is important to first identify these patients, treat them with aggressive combination therapy, and employ the use of aggressive long-term maintenance therapy. Future directions include the use of new immune-based treatments (antibodies or cellular-based therapies) as well as target-driven approaches. Until these treatment approaches are better defined, this review will provide a potential treatment approach for standard- and high-risk myeloma that can be followed using agents and strategies that are currently available with the goal of improving progression-free and overall survival for these patients today.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Antineoplastic Agents / therapeutic use*
  • Bortezomib / therapeutic use
  • Female
  • Hematopoietic Stem Cell Transplantation* / methods
  • Humans
  • Immunosuppressive Agents / therapeutic use*
  • Lenalidomide
  • Multiple Myeloma / drug therapy
  • Multiple Myeloma / pathology*
  • Multiple Myeloma / therapy*
  • Oligopeptides / therapeutic use
  • Proteasome Inhibitors / therapeutic use
  • Thalidomide / analogs & derivatives
  • Thalidomide / therapeutic use

Substances

  • Antineoplastic Agents
  • Immunosuppressive Agents
  • Oligopeptides
  • Proteasome Inhibitors
  • Thalidomide
  • Bortezomib
  • carfilzomib
  • pomalidomide
  • Lenalidomide