Allogeneic Hematopoietic Cell Transplantation for Myeloma: When and in Whom Does It Work

Curr Hematol Malig Rep. 2017 Apr;12(2):126-135. doi: 10.1007/s11899-017-0374-1.

Abstract

The growing list of available therapies for patients with multiple myeloma has resulted in tremendously high response rates and prolonged survival. However, the cure remains elusive. A continued effort at developing strategies to utilize all available treatment modalities in the most effective manner is needed. Allogeneic hematopoietic cell transplantation (allo-HCT) is a robust platform, associated with high response rates, and provides a unique foundation on which immune therapies and novel agents can be employed to improve clinical outcomes. Patients with high-risk myeloma and those relapsing after novel agent-based therapies or early after an autologous HCT should be considered for allo-HCT, ideally in a clinical trial setting. Results from several ongoing studies are expected to provide important information that will help determine the place of allo-HCT in the myeloma treatment algorithm.

Keywords: Allo-HCT; Allogeneic hematopoietic cell transplantation; Autologous HCT; Multiple myeloma; Stem cell transplantation.

Publication types

  • Review

MeSH terms

  • Clinical Trials as Topic
  • Combined Modality Therapy
  • Graft vs Host Disease / etiology
  • Graft vs Tumor Effect / immunology
  • Hematopoietic Stem Cell Transplantation* / adverse effects
  • Hematopoietic Stem Cell Transplantation* / methods
  • Humans
  • Killer Cells, Natural / immunology
  • Killer Cells, Natural / metabolism
  • Maintenance Chemotherapy
  • Multiple Myeloma / diagnosis
  • Multiple Myeloma / immunology
  • Multiple Myeloma / metabolism
  • Multiple Myeloma / therapy*
  • Neoplasm, Residual / pathology
  • Receptors, KIR / metabolism
  • Retreatment
  • Tissue Donors
  • Transplantation Conditioning / adverse effects
  • Transplantation Conditioning / methods
  • Transplantation, Autologous
  • Transplantation, Homologous
  • Transplantation, Isogeneic

Substances

  • Receptors, KIR