Literature DB >> 32653621

Outcomes after Haploidentical Stem Cell Transplantation with Post-Transplantation Cyclophosphamide in Patients with Primary Immunodeficiency Diseases.

Juliana Folloni Fernandes1, Samantha Nichele2, Leonardo Javier Arcuri3, Lisandro Ribeiro2, Gabriele Zamperlini-Netto3, Gisele Loth4, Ana Luiza Melo Rodrigues5, Cilmara Kuwahara5, Adriana Koliski6, Joanna Trennepohl2, Julia Lopes Garcia7, Liane Esteves Daudt8, Adriana Seber9, Alessandra Araujo Gomes10, Anders Fasth11, Ricardo Pasquini2, Nelson Hamerschlak3, Vanderson Rocha12, Carmem Bonfim13.   

Abstract

Allogeneic hematopoietic stem cell transplantation (HCT) can cure primary immunodeficiency diseases (PID). When a HLA-matched donor is not available, a haploidentical family donor may be considered. The use of T cell-replete haploidentical HCT with post-transplantation cyclophosphamide (haplo-PTCy) in children with PID has been reported in few case series. A donor is usually readily available, and haplo-PTCy can be used in urgent cases. We studied the outcomes of 73 patients with PID who underwent haplo-PTCy, including 55 patients who did so as a first transplantation and 18 who did so as a salvage transplantation after graft failure of previous HCT. The median patient age was 1.6 years. Most of the children were male (n = 54) and had active infection at the time of transplantation (n = 50); 10 children had severe organ damage. The diagnosis was severe combined immunodeficiency (SCID) in 34 patients and non-SCID in 39 (Wiskott-Aldrich syndrome; n = 14; chronic granulomatous disease, n = 10; other PID, n = 15). The median duration of follow-up of survivors was 2 years. The cumulative incidence of neutrophil recovery was 88% in the SCID group and 84% in non-SCID group and was 81% for first transplantations and 83% after a salvage graft. At 100 days, the cumulative incidence of acute GVHD grade II-IV and III-IV was 33% and 14%, respectively. The majority of patients reached 200/μL CD4+ and 1000/μL CD3+ cell counts between 3 and 6 months. The estimated 2-year overall survival was 66%; it was 64% for SCID patients and 65% for non-SCID patients and 63% for first HCT and 77% for salvage transplantations. Twenty-five patients died, most of them due to infection early after transplantation (before 100 days). In conclusion, haplo-PTCy is a feasible procedure, can cure two-thirds of children with PID, and can be used as rescue treatment for previous graft failure. © 2020 American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc.
Copyright © 2020 American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Haploidentical transplantation; Outcomes; Post-transplantation cyclophosphamide; Primary immunodeficiency disease

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Substances:

Year:  2020        PMID: 32653621     DOI: 10.1016/j.bbmt.2020.07.003

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


  4 in total

Review 1.  Conditioning regimens for inborn errors of immunity: current perspectives and future strategies.

Authors:  Akira Nishimura; Satoshi Miyamoto; Kohsuke Imai; Tomohiro Morio
Journal:  Int J Hematol       Date:  2022-06-08       Impact factor: 2.490

Review 2.  Unresolved issues in allogeneic hematopoietic cell transplantation for non-malignant diseases.

Authors:  Katsutsugu Umeda
Journal:  Int J Hematol       Date:  2022-05-14       Impact factor: 2.490

3.  TCRαβ/CD19 depleted HSCT from an HLA-haploidentical relative to treat children with different nonmalignant disorders.

Authors:  Pietro Merli; Daria Pagliara; Federica Galaverna; Giuseppina Li Pira; Marco Andreani; Giovanna Leone; Donato Amodio; Rita Maria Pinto; Alice Bertaina; Valentina Bertaina; Angela Mastronuzzi; Luisa Strocchio; Emilia Boccieri; Daniela Pende; Michela Falco; Matteo Di Nardo; Francesca Del Bufalo; Mattia Algeri; Franco Locatelli
Journal:  Blood Adv       Date:  2022-01-11

Review 4.  Hematopoietic Stem Cell Therapy for Wiskott-Aldrich Syndrome: Improved Outcome and Quality of Life.

Authors:  Kanwaldeep K Mallhi; Aleksandra Petrovic; Hans D Ochs
Journal:  J Blood Med       Date:  2021-06-11
  4 in total

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