Thiotepa, Busulfan, and Fludarabine Conditioning Regimen in T Cell-Replete HLA-Haploidentical Hematopoietic Stem Cell 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
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

1407-1415

Informations de copyright

Copyright © 2019. Published by Elsevier Inc.

Auteurs

Rémy Duléry (R)

Department of Hematology and Cellular Therapy, Saint Antoine Hospital, AP-HP, Paris, France; INSERM, UMR 938, Paris, France; Sorbonne Universités, Université Pierre et Marie Curie Paris 6, Paris, France.

Juliana Bastos (J)

Department of Hematology and Cellular Therapy, Saint Antoine Hospital, AP-HP, Paris, France; Department of Hematology, Sao Joao Hospital, Porto, Portugal.

Annalisa Paviglianiti (A)

Department of Hematology and Cellular Therapy, Saint Antoine Hospital, AP-HP, Paris, France.

Florent Malard (F)

Department of Hematology and Cellular Therapy, Saint Antoine Hospital, AP-HP, Paris, France; INSERM, UMR 938, Paris, France; Sorbonne Universités, Université Pierre et Marie Curie Paris 6, Paris, France.

Eolia Brissot (E)

Department of Hematology and Cellular Therapy, Saint Antoine Hospital, AP-HP, Paris, France; INSERM, UMR 938, Paris, France; Sorbonne Universités, Université Pierre et Marie Curie Paris 6, Paris, France.

Giorgia Battipaglia (G)

Department of Hematology and Cellular Therapy, Saint Antoine Hospital, AP-HP, Paris, France; Sorbonne Universités, Université Pierre et Marie Curie Paris 6, Paris, France.

Clémence Médiavilla (C)

Department of Hematology and Cellular Therapy, Saint Antoine Hospital, AP-HP, Paris, France; Sorbonne Universités, Université Pierre et Marie Curie Paris 6, Paris, France.

Federica Giannotti (F)

Department of Hematology and Cellular Therapy, Saint Antoine Hospital, AP-HP, Paris, France.

Anne Banet (A)

Department of Hematology and Cellular Therapy, Saint Antoine Hospital, AP-HP, Paris, France.

Zoé Van de Wyngaert (ZV)

Department of Hematology and Cellular Therapy, Saint Antoine Hospital, AP-HP, Paris, France.

Tounes Ledraa (T)

Department of Hematology and Cellular Therapy, Saint Antoine Hospital, AP-HP, Paris, France.

Ramdane Belhocine (R)

Department of Hematology and Cellular Therapy, Saint Antoine Hospital, AP-HP, Paris, France.

Simona Sestili (S)

Department of Hematology and Cellular Therapy, Saint Antoine Hospital, AP-HP, Paris, France.

Rosa Adaeva (R)

Department of Hematology and Cellular Therapy, Saint Antoine Hospital, AP-HP, Paris, France.

Simona Lapusan (S)

Department of Hematology and Cellular Therapy, Saint Antoine Hospital, AP-HP, Paris, France.

Françoise Isnard (F)

Department of Hematology and Cellular Therapy, Saint Antoine Hospital, AP-HP, Paris, France.

Ollivier Legrand (O)

Department of Hematology and Cellular Therapy, Saint Antoine Hospital, AP-HP, Paris, France; INSERM, UMR 938, Paris, France; Sorbonne Universités, Université Pierre et Marie Curie Paris 6, Paris, France.

Anne Vekhoff (A)

Department of Hematology and Cellular Therapy, Saint Antoine Hospital, AP-HP, Paris, France.

Marie-Thérèse Rubio (MT)

Department of Hematology and Cellular Therapy, Saint Antoine Hospital, AP-HP, Paris, France.

Annalisa Ruggeri (A)

Department of Hematology and Cellular Therapy, Saint Antoine Hospital, AP-HP, Paris, France.

Mohamad Mohty (M)

Department of Hematology and Cellular Therapy, Saint Antoine Hospital, AP-HP, Paris, France; INSERM, UMR 938, Paris, France; Sorbonne Universités, Université Pierre et Marie Curie Paris 6, Paris, France. Electronic address: mohamad.mohty@inserm.fr.

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