Thiotepa, Busulfan, and Fludarabine Conditioning Regimen in T Cell-Replete HLA-Haploidentical Hematopoietic Stem Cell Transplantation.
Adolescent
Adult
Aged
Busulfan
/ administration & dosage
Cyclosporine
/ administration & dosage
Disease-Free Survival
Female
Graft vs Host Disease
/ metabolism
HLA Antigens
Hematologic Neoplasms
/ metabolism
Hematopoietic Stem Cell Transplantation
Humans
Male
Middle Aged
Mycophenolic Acid
/ administration & dosage
Retrospective Studies
Survival Rate
T-Lymphocytes
/ metabolism
Thiotepa
/ administration & dosage
Transplantation Conditioning
Vidarabine
/ administration & dosage
Antithymocyte globulin
Conditioning
Graft-versus-host disease
Haploidentical transplantation
Journal
Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation
ISSN: 1523-6536
Titre abrégé: Biol Blood Marrow Transplant
Pays: United States
ID NLM: 9600628
Informations de publication
Date de publication:
07 2019
07 2019
Historique:
received:
25
01
2019
accepted:
28
02
2019
pubmed:
16
3
2019
medline:
2
7
2020
entrez:
16
3
2019
Statut:
ppublish
Résumé
We report the outcomes of 51 patients who underwent unmanipulated haploidentical hematopoietic stem cell transplantation (haplo-HSCT) with post-transplantation cyclophosphamide (PT-Cy) and antithymocyte globulin (ATG), from peripheral blood stem cells (PBSCs) or bone marrow, after receipt of a TBF (thiotepa, busulfan, and fludarabine) conditioning regimen. Their median age was 55 years (range, 16 to 72 years). Hematologic diagnoses included acute leukemias (n = 31), lymphoid neoplasm (n = 12), myeloproliferative neoplasm (n = 5), and myelodysplastic syndromes (n = 3). Thirty-seven patients (73%) were in complete remission. Graft-versus-host disease (GVHD) prophylaxis consisted of cyclosporine and mycophenolate for all patients, associated with ATG in 39 patients (76.5%). The median time to neutrophil engraftment was 17 days (range, 12 to 34 days). The cumulative incidences of grade II-IV and grade III-IV acute GVHD were 27.5% and 14%, respectively. In patients receiving a PBSC graft and ATG prophylaxis, grade II-IV aGVHD occurred in 16% of patients. The use of ATG and a lower thiotepa dose (5 mg/kg versus 10 mg/kg) were associated with a reduced cumulative incidence of grade II-IV acute GVHD (P = .03 and .005, respectively). The 2-year cumulative incidence of chronic GVHD was 29% and was significantly reduced to 13% with the lower thiotepa dose (P = .002). After a median follow-up of 25 months (range, 12 to 62 months), the cumulative incidences of nonrelapse mortality, relapse, overall survival (OS), disease-free survival (DFS), and GVHD-free, relapse-free survival (GFRFS) were 20%, 22.5%, 67%, 58%, and 51%, respectively. Pretransplantation disease status (complete remission versus others) was the main factor associated with OS, DFS, and GFRFS. In conclusion, the TBF conditioning regimen is an appealing platform in the haplo-HSCT setting with PT-Cy in terms of engraftment rate, toxicity, and disease control. We found no benefit of a thiotepa dose of 10 mg/kg compared with a dose of 5 mg/kg. ATG reduced the risk of acute GVHD without comprising outcomes.
Identifiants
pubmed: 30871978
pii: S1083-8791(19)30151-X
doi: 10.1016/j.bbmt.2019.02.025
pii:
doi:
Substances chimiques
HLA Antigens
0
Cyclosporine
83HN0GTJ6D
Thiotepa
905Z5W3GKH
Vidarabine
FA2DM6879K
Busulfan
G1LN9045DK
Mycophenolic Acid
HU9DX48N0T
fludarabine
P2K93U8740
Types de publication
Clinical Trial
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1407-1415Informations de copyright
Copyright © 2019. Published by Elsevier Inc.