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 Bornhäuser
  • 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
  • Á Urbano-Ispízua
  • D Blaise
  • L Volin
  • P Chevallier
  • D Caballero
  • H Putter
  • A van Biezen
  • A Henseler
  • S Schönland
  • N Kröger
  • J Schetelig

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.

Bibliographical data

Original languageEnglish
ISSN0268-3369
DOIs
Publication statusPublished - 03.2017
PubMed 27941763