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
Language English Country Germany Media print-electronic
Document type Comparative Study, Journal Article
PubMed
31468122
PubMed Central
PMC11810217
DOI
10.1007/s00432-019-03014-x
PII: 10.1007/s00432-019-03014-x
Knihovny.cz E-resources
- Keywords
- Allogeneic hematopoietic stem cell transplantation, Nonmyeloablative/reduced intensity conditioning, Relapsed/refractory chronic lymphocytic leukemia,
- MeSH
- Busulfan administration & dosage MeSH
- Leukemia, Lymphocytic, Chronic, B-Cell mortality pathology therapy MeSH
- Cyclophosphamide administration & dosage MeSH
- Adult MeSH
- Transplantation, Homologous MeSH
- Incidence MeSH
- Remission Induction MeSH
- Combined Modality Therapy MeSH
- Middle Aged MeSH
- Humans MeSH
- Melphalan administration & dosage MeSH
- Survival Rate MeSH
- Young Adult MeSH
- Follow-Up Studies MeSH
- Graft vs Host Disease epidemiology mortality MeSH
- Transplantation Conditioning mortality MeSH
- Prognosis MeSH
- Antineoplastic Combined Chemotherapy Protocols therapeutic use MeSH
- Retrospective Studies MeSH
- Aged MeSH
- Hematopoietic Stem Cell Transplantation mortality MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Young Adult MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Comparative Study MeSH
- Names of Substances
- Busulfan MeSH
- Cyclophosphamide MeSH
- Melphalan MeSH
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.
BMT Unit Department of Hematology Rigshospitalet Copenhagen Denmark
Bone Marrow Transplantation Centre University Hospital Eppendorf Hamburg Germany
Centre Hospitalier Lyon Sud Hématologie Lyon France
Department of Biomedical Data Sciences Leiden University Medical Center Leiden The Netherlands
Department of Haematology Institute of Hematology and Blood Transfusion Prague Czech Republic
Department of Hematology Oncology Charles University Hospital Pilsen Czech Republic
Department of Internal Medicine Hematology University Hospital Maastricht Maastricht The Netherlands
Hematologia Hospital de la Santa Creu i Sant Pau Barcelona Spain
Medizinische Klinik u Poliklinik 5 University of Heidelberg Heidelberg Germany
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