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Reduced intensity conditioning regimens including alkylating chemotherapy do not alter survival outcomes after allogeneic hematopoietic cell transplantation in chronic lymphocytic leukemia compared to low-intensity non-myeloablative conditioning.

Authors :
Andersen, Niels Smedegaard
Bornhäuser, Martin
Gramatzki, Martin
Dreger, Peter
Vitek, Antonin
Karas, Michal
Michallet, Mauricette
Moreno, Carol
van Gelder, Michel
Henseler, Anja
de Wreede, Liesbeth C.
Schönland, Stefan
Kröger, Nicolaus
Schetelig, Johannes
Source :
Journal of Cancer Research & Clinical Oncology; Nov2019, Vol. 145 Issue 11, p2823-2834, 12p
Publication Year :
2019

Abstract

Purpose: The optimal dose intensity for conditioning prior to allogeneic hematopoietic stem cell transplantation (alloHSCT) for chronic lymphocytic leukemia (CLL) is unknown. Methods: We retrospectively compared outcomes of patients who received a first alloHCST after non-myeloablative (NMA) and reduced intensity conditioning (RIC). Data of 432 patients with a median age of 55 years were included, of which 86 patients underwent NMA and 346 RIC. Results: The median follow-up after alloHSCT was 4.3 years. Compared to the RIC group, more NMA patients had purine-analog-sensitive disease, were in complete remission and received matched related donor transplantation. After RIC, the probabilities for 5-year OS, EFS, CIR, and NRM were 46%, 38%, 28%, and 35% and after NMA the respective probabilities were 52%, 43%, 25%, and 32%. In multivariate analysis, remission status prior to conditioning but not RIC versus NMA conditioning had a significant impact on CIR, EFS, and OS. Conclusion: Presumed higher anti-leukemic activity of RIC versus NMA conditioning did not translate into better outcomes after alloHSCT, but better remission status prior to conditioning did. Effective pathway inhibitor-based salvage therapies combined with NMA conditioning might thus represent the most attractive contemporary approach for alloHSCT for patients with CLL. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01715216
Volume :
145
Issue :
11
Database :
Complementary Index
Journal :
Journal of Cancer Research & Clinical Oncology
Publication Type :
Academic Journal
Accession number :
139215726
Full Text :
https://doi.org/10.1007/s00432-019-03014-x