TY - JOUR
T1 - 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
AU - Andersen, Niels Smedegaard
AU - Bornhäuser, Martin
AU - Gramatzki, Martin
AU - Dreger, Peter
AU - Vitek, Antonin
AU - Karas, Michal
AU - Michallet, Mauricette
AU - Moreno, Carol
AU - van Gelder, Michel
AU - Henseler, Anja
AU - de Wreede, Liesbeth C
AU - Schönland, Stefan
AU - Kröger, Nicolaus
AU - Schetelig, Johannes
AU - CLL subcommittee, Chronic Malignancies Working Party
PY - 2019/11
Y1 - 2019/11
N2 - 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.
AB - 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.
KW - Adult
KW - Aged
KW - Antineoplastic Combined Chemotherapy Protocols/therapeutic use
KW - Busulfan/administration & dosage
KW - Combined Modality Therapy
KW - Cyclophosphamide/administration & dosage
KW - Female
KW - Follow-Up Studies
KW - Graft vs Host Disease/epidemiology
KW - Hematopoietic Stem Cell Transplantation/mortality
KW - Humans
KW - Incidence
KW - Leukemia, Lymphocytic, Chronic, B-Cell/mortality
KW - Male
KW - Melphalan/administration & dosage
KW - Middle Aged
KW - Prognosis
KW - Remission Induction
KW - Retrospective Studies
KW - Survival Rate
KW - Transplantation Conditioning/mortality
KW - Transplantation, Homologous
KW - Young Adult
U2 - 10.1007/s00432-019-03014-x
DO - 10.1007/s00432-019-03014-x
M3 - Journal article
C2 - 31468122
VL - 145
SP - 2823
EP - 2834
JO - Zeitschrift fur Krebsforschung und Klinische Onkologie
JF - Zeitschrift fur Krebsforschung und Klinische Onkologie
SN - 0171-5216
IS - 11
ER -