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Perspectives on the Risk-Stratified Treatment of Multiple Myeloma

  • Faith E. Davies*
  • , Charlotte Pawlyn
  • , Saad Z. Usmani
  • , Jesus F. San-Miguel
  • , Hermann Einsele
  • , Eileen M. Boyle
  • , Jill Corre
  • , Daniel Auclair
  • , Hearn Jay Cho
  • , Sagar Lonial
  • , Pieter Sonneveld
  • , A. Keith Stewart
  • , P. Leif Bergsagel
  • , Martin F. Kaiser
  • , Katja Weisel
  • , Jonathan J. Keats
  • , Joseph R. Mikhael
  • , Kathryn E. Morgan
  • , Irene M. Ghobrial
  • , Robert Z. Orlowski
  • C. Ola Landgren, Francesca Gay, Joseph Caers, Wee Joo Chng, Ajai Chari, Brian A. Walker, Shaji K. Kumar, Luciano J. Costa, Kenneth C. Anderson, Gareth J. Morgan
*Corresponding author for this work
  • NYU Langone Health
  • Institute of Cancer Research (ICR), London
  • Royal Marsden Hospital, London
  • Memorial Sloan-Kettering Cancer Center
  • University of Navarra
  • University Hospital Würzburg
  • Institut national de la santé et de la recherche médicale
  • Multiple Myeloma Research Foundation
  • Icahn School of Medicine at Mount Sinai
  • Emory University
  • University Health Network
  • Mayo Clinic, Scottsdale, AZ
  • University Medical Center Hamburg-Eppendorf
  • Myeloma Patients Europe
  • University of Texas MD Anderson Cancer Center
  • University of Miami
  • University of Turin
  • CHU and University of Liège
  • Mayo Clinic Rochester, MN
  • University of Alabama at Birmingham
  • Perlmutter Cancer Center (Long Island)
  • Dana-Farber Cancer Institute
  • Indiana University
  • City of Hope Cancer Center (Phoenix)
  • Translational Genomics Research Institute
  • Princess Margaret Hospital Cancer Centre
  • Unité de Génomique du Myélome

Research output: Contribution to journal › Article › Academic › peer-review

41 Citations (Scopus)
93 Downloads (Pure)

Abstract

The multiple myeloma treatment landscape has changed dramatically. This change, paralleled by an increase in scientific knowledge, has resulted in significant improvement in survival. However, heterogeneity remains in clinical outcomes, with a proportion of patients not benefiting from current approaches and continuing to have a poor prognosis. A significant proportion of the variability in outcome can be predicted on the basis of clinical and biochemical parameters and tumor-acquired genetic variants, allowing for risk stratification and a more personalized approach to therapy. This article discusses the principles that can enable the rational and effective development of therapeutic approaches for high-risk multiple myeloma.

Original languageEnglish
Pages (from-to)273-284
Number of pages12
JournalBlood cancer discovery
Volume3
Issue number7
DOIs
Publication statusPublished - 1 Jul 2022

Bibliographical note

Publisher Copyright: ©2022 The Authors; Published by the American Association for Cancer Research.

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