Fludarabine and Total-Body Irradiation Conditioning before Ablative Haploidentical Transplantation: Long-Term Safety and Efficacy.


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:
11 2019
Historique:
received: 08 05 2019
revised: 09 06 2019
accepted: 17 06 2019
pubmed: 28 6 2019
medline: 18 8 2020
entrez: 28 6 2019
Statut: ppublish

Résumé

Although myeloablative conditioning (MAC) before haploidentical donor transplant (HIDT) with post-transplant cyclophosphamide is being increasingly used, the optimal preparative regimen remains unclear. In our initial trial, the feasibility of HIDT following a MAC preparative regimen using fludarabine and 12 Gy of total-body irradiation was demonstrated in 30 patients. We now present long-term outcome results, including an additional 52 patients, now with 47 months (16 to 96) median follow-up. Median patient age was 42 (19 to 61) years. The most common diagnoses were acute myelogenous leukemia (51%) and acute lymphoblastic leukemia (33%), and 39% had a high/very high disease risk index (DRI). Engraftment was universal with no cases of primary or secondary graft failure. Grade 3 to 4 acute graft-versus-host disease (GVHD) and moderate to severe chronic GVHD occurred in 17% and 23%, respectively. Nonrelapse mortality (NRM) was 7% at 1 year and 13% at 4 years. Estimated 4-year overall survival (OS), disease-free survival, and cumulative incidence of relapse (CIR) were 67%, 60%, and 27%, respectively. CIR was significantly higher in patients with high/very high- versus low/intermediate-risk DRI (38% versus 20%, P= .032), which led to inferior 4-year OS (50% versus 77%, P = .001). Median time to systemic immunosuppressive therapy (IST) discontinuation was 7.8 months, with 84% of patients off IST at 2 years post-transplant. Current GHVD-free, relapse-free survival (CGRFS) at 2, 3, and 4 years was 60%, 57%, and 60%, respectively. This approach to MAC HIDT results in universal engraftment; low rates of NRM, infection, and clinically significant GVHD; and relatively rapid IST discontinuation, resulting in high rates of CGRFS and survival.

Identifiants

pubmed: 31247313
pii: S1083-8791(19)30381-7
doi: 10.1016/j.bbmt.2019.06.017
pii:
doi:

Substances chimiques

Vidarabine FA2DM6879K
fludarabine P2K93U8740

Types de publication

Clinical Trial Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

2211-2216

Informations de copyright

Copyright © 2019 American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.

Auteurs

Scott R Solomon (SR)

The Blood and Marrow Transplant Program at Northside Hospital, Atlanta, Georgia. Electronic address: ssolomon@bmtga.com.

Melhem Solh (M)

The Blood and Marrow Transplant Program at Northside Hospital, Atlanta, Georgia.

Xu Zhang (X)

School of Public Health, University of Texas, Houston, Texas.

Lawrence E Morris (LE)

The Blood and Marrow Transplant Program at Northside Hospital, Atlanta, Georgia.

H Kent Holland (HK)

The Blood and Marrow Transplant Program at Northside Hospital, Atlanta, Georgia.

Asad Bashey (A)

The Blood and Marrow Transplant Program at Northside Hospital, Atlanta, Georgia.

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Classifications MeSH