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Long-term survival of patients with CLL after allogeneic transplantation: a report from the European Society for Blood and Marrow Transplantation

  • M. van Gelder
  • , L. C. de Wreede
  • , M. Bornhaeuser
  • , D. Niederwieser
  • , M. Karas
  • , N. S. Anderson
  • , M. Gramatzki
  • , P. Dreger
  • , M. Michallet
  • , E. Petersen
  • , D. Bunjes
  • , M. Potter
  • , D. Beelen
  • , J. J. Cornelissen
  • , I. Yakoub-Agha
  • , N. H. Russell
  • , J. Finke
  • , H. Schoemans
  • , A. Vitek
  • , A. Urbano-Ispizua
  • D. Blaise, L. Volin, P. Chevallier, D. Caballero, H. Putter, A. van Biezen, A. Henseler, S. Schoenland, N. Kroeger, J. Schetelig*, Chronic Malignancy Working Party
*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Even with the availability of targeted drugs, allogeneic hematopoietic cell transplantation (allo-HCT) is the only therapy with curative potential for patients with CLL. Cure can be assessed by comparing long-term survival of patients to the matched general population. Using data from 2589 patients who received allo-HCT between 2000 and 2010, we used landmark analyses and methods from relative survival analysis to calculate excess mortality compared with an age-, sex-and calendar year-matched general population. Estimated event-free survival, overall survival and non-relapse mortality (NRM) 10 years after allo-HCT were 28% (95% confidence interval (CI), 25-31), 35% (95% CI, 32-38) and 40% (95% CI, 37-42), respectively. Patients who passed the 5-year landmark event-free survival (N = 394) had a 79% probability (95% CI, 73-85) of surviving the subsequent 5 years without an event. Relapse and NRM contributed equally to treatment failure. Five-year mortality for 45-and 65-year-old reference patients who were event-free at the 5-year landmark was 8% and 47% compared with 3% and 14% in the matched general population, respectively. The prospect of long-term disease-free survival remains an argument to consider allo-HCT for young patients with high-risk CLL, and programs to understand and prevent late causes of failure for long-term survivors are warranted, especially for older patients.

Original languageEnglish
Pages (from-to)372-380
Number of pages9
JournalBone Marrow Transplantation
Volume52
Issue number3
DOIs
Publication statusPublished - Mar 2017

Keywords

  • CHRONIC LYMPHOCYTIC-LEUKEMIA
  • HEMATOPOIETIC-CELL TRANSPLANTATION
  • LATE MORTALITY
  • FOLLOW-UP
  • RISK CLL
  • OUTCOMES
  • IBRUTINIB
  • RELAPSE
  • ERA

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