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Early relapse after autologous hematopoietic cell transplantation remains a poor prognostic factor in multiple myeloma but outcomes have improved over time

  • S. K. Kumar
  • , A. DIspenzieri
  • , R. Fraser
  • , F. Mingwei
  • , G. Akpek
  • , R. Cornell
  • , M. Kharfan-Dabaja
  • , C. Freytes
  • , S. Hashmi
  • , G. Hildebrandt
  • , L. Holmberg
  • , R. Kyle
  • , H. Lazarus
  • , C. Lee
  • , J. Mikhael
  • , T. Nishihori
  • , J. Tay
  • , S. Usmani
  • , D. Vesole
  • , R. Vij
  • B. Wirk, A. Krishnan, C. Gasparetto, T. Mark, Y. Nieto, P. Hari, A. D'Souza
  • Mayo Clinic Rochester, MN
  • Medical College of Wisconsin
  • Rush University
  • Vanderbilt University
  • Moffitt Cancer Center
  • University of Texas Health Science Center at San Antonio
  • University of Kentucky
  • Fred Hutchinson Cancer Research Center
  • Case Western Reserve University
  • Royal Adelaide Hospital
  • Mayo Clinic Arizona
  • University of Ottawa
  • Carolinas HealthCare System
  • John Theurer Cancer Center at Hackensack UMC
  • Washington University St. Louis
  • Seattle Cancer Care Alliance
  • City of Hope National Med Center
  • Duke University
  • University of Colorado Anschutz Medical Campus
  • University of Texas Health Science Center at Houston

Research output: Contribution to journalArticlepeer-review

76 Scopus citations

Abstract

Duration of initial disease response remains a strong prognostic factor in multiple myeloma (MM) particularly for upfront autologous hematopoietic cell transplant (AHCT) recipients. We hypothesized that new drug classes and combinations employed prior to AHCT as well as after post-AHCT relapse may have changed the natural history of MM in this population. We analyzed the Center for International Blood and Marrow Transplant Research database to track overall survival (OS) of MM patients receiving single AHCT within 12 months after diagnosis (N=3256) and relapsing early post-AHCT (<24 months), and to identify factors predicting for early vs late relapses (24-48 months post-AHCT). Over three periods (2001-2004, 2005-2008, 2009-2013), patient characteristics were balanced except for lower proportion of Stage III, higher likelihood of one induction therapy with novel triplets and higher rates of planned post-AHCT maintenance over time. The proportion of patients relapsing early was stable over time at 35-38%. Factors reducing risk of early relapse included lower stage, chemosensitivity, transplant after 2008 and post-AHCT maintenance. Shorter post-relapse OS was associated with early relapse, IgA MM, Karnofsky <90, stage III, >1 line of induction and lack of maintenance. Post-AHCT early relapse remains a poor prognostic factor, even though outcomes have improved over time.

Original languageEnglish
Pages (from-to)986-995
Number of pages10
JournalLeukemia
Volume32
Issue number4
DOIs
StatePublished - Apr 1 2018

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