Literature DB >> 24296490

HLA-haploidentical donor lymphocyte infusions for patients with relapsed hematologic malignancies after related HLA-haploidentical bone marrow transplantation.

Amer M Zeidan1, Patrick M Forde1, Heather Symons1, Allen Chen1, B Douglas Smith1, Keith Pratz1, Hetty Carraway1, Douglas E Gladstone1, Ephraim J Fuchs1, Leo Luznik1, Richard J Jones1, Javier Bolaños-Meade2.   

Abstract

Treatment of relapse after related HLA-haploidentical T cell-replete bone marrow transplantation (haploBMT) with post-transplantation cyclophosphamide (PTCy) using haploidentical donor lymphocyte infusion (haploDLI) is not documented. All patients who received haploDLI after haploBMT with PTCy between June 2003 and October 2012 were identified and assessed for graft-versus-host disease (GVHD) and outcomes. Forty patients received 52 haploDLI doses. Sixteen patients had acute myeloid leukemia, 11 had lymphomas, and 34 had nonmyeloablative conditioning before haploBMT. The median time from haploBMT to relapse was 183 (range, 0 to 1399) days. The median age at haploDLI was 48 (range, 3 to 70) years. The first haploDLI doses were 1 × 10(5) CD3(+) cells/kg with subsequent escalation. The most commonly used first haploDLI dose was 1 × 10(6) CD3(+) cells/kg. The median follow-up after haploDLI was 7 (mean, 15.4; range, .5 to 96) months for the entire cohort, and 17.5 (mean, 28; range, 2.4 to 96) months for the responders. Acute GVHD developed in 10 patients (25%), 6 patients had grade 3 to 4, and 3 developed chronic GVHD. Twelve (30%) patients achieved a complete response (CR) with a median duration of 11.8 (mean, 22.5; range, .4 to 94) months. At last follow-up, 8 responders were alive in CR; 6 for over a year. HaploDLI for relapse after haploBMT is associated with acceptable toxicities and can result in durable responses.
Copyright © 2014 American Society for Blood and Marrow Transplantation. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Bone marrow transplantation (BMT); Donor lymphocyte infusion (DLI); Haploidentical; Human leukocyte antigen (HLA); Stem cell transplantation

Mesh:

Substances:

Year:  2013        PMID: 24296490      PMCID: PMC4010132          DOI: 10.1016/j.bbmt.2013.11.020

Source DB:  PubMed          Journal:  Biol Blood Marrow Transplant        ISSN: 1083-8791            Impact factor:   5.742


  23 in total

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Review 5.  High-dose cyclophosphamide for graft-versus-host disease prevention.

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7.  DLI after haploidentical BMT with post-transplant CY.

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8.  Major Histocompatibility Mismatch and Donor Choice for Second Allogeneic Bone Marrow Transplantation.

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