| Literature DB >> 27941763 |
M van Gelder1, L C de Wreede2,3, M Bornhäuser4, D Niederwieser5, M Karas6, N S Anderson7, M Gramatzki8, P Dreger9, M Michallet10, E Petersen11, D Bunjes12, M Potter13, D Beelen14, J J Cornelissen15, I Yakoub-Agha16, N H Russell17, J Finke18, H Schoemans19, A Vitek20, Á Urbano-Ispízua21, D Blaise22, L Volin23, P Chevallier24, D Caballero25, H Putter3, A van Biezen3, A Henseler3, S Schönland9, N Kröger26, J Schetelig2,4.
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.Entities:
Mesh:
Year: 2016 PMID: 27941763 DOI: 10.1038/bmt.2016.282
Source DB: PubMed Journal: Bone Marrow Transplant ISSN: 0268-3369 Impact factor: 5.483