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Real‐world experience: Introduction of T cell replete haploidentical transplantations in a single center

OBJECTIVES: The aim of this study was to describe real‐world data on outcomes of T cell replete haploidentical hematopoietic stem cell transplantation (HSCT) after the introduction of this modality in a single center and to compare them with different donor types. METHOD: Outcomes of 30 consecutive...

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Autores principales: van Gorkom, Gwendolyn, Billen, Evy, Van Elssen, Catharina, van Gelder, Michel, Bos, Gerard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9175800/
https://www.ncbi.nlm.nih.gov/pubmed/35844710
http://dx.doi.org/10.1002/jha2.203
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author van Gorkom, Gwendolyn
Billen, Evy
Van Elssen, Catharina
van Gelder, Michel
Bos, Gerard
author_facet van Gorkom, Gwendolyn
Billen, Evy
Van Elssen, Catharina
van Gelder, Michel
Bos, Gerard
author_sort van Gorkom, Gwendolyn
collection PubMed
description OBJECTIVES: The aim of this study was to describe real‐world data on outcomes of T cell replete haploidentical hematopoietic stem cell transplantation (HSCT) after the introduction of this modality in a single center and to compare them with different donor types. METHOD: Outcomes of 30 consecutive patients with hematological malignancies that received T cell replete haploidentical HSCT with posttransplantation cyclophosphamide (PTCY) from 2016 to 2018 in our center were analyzed and compared to the outcome of human leukocyte antigen (HLA)‐related and unrelated matched donor HSCT (n = 97) and to a historical cohort of T cell depleted haploidentical HSCT (n = 11). RESULTS: One year graft‐versus‐host‐free, relapse‐free survival in haploidentical HSCT was comparable with other donor types (haplo 40%, matched related donor [MRD] 33%, matched unrelated donor [MUD] 25%, p = 0.55). Non relapse mortality was high in haploidentical HSCT (50%), mostly due to infectious complications. However, relapse rates were only 3%, and OS and progression‐free survival after 1 year were 47% and thereby also similar to HLA‐matched HSCT in our center (MRD 53%, MUD 48%). CONCLUSION: Our data show that T cell replete haploidentical HSCT has similar outcomes to HLA identical HSCT after introduction in our center. More strict adaptation on infection prevention was a crucial aspect of our learning curve. Overall, this type of transplantation is a feasible option when lacking an HLA‐identical donor. This option has advantages over an unrelated donor as it brings less logistical challenges than MUD transplantations.
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spelling pubmed-91758002022-07-14 Real‐world experience: Introduction of T cell replete haploidentical transplantations in a single center van Gorkom, Gwendolyn Billen, Evy Van Elssen, Catharina van Gelder, Michel Bos, Gerard EJHaem Haematologic Malignancy ‐ Cellular Therapy OBJECTIVES: The aim of this study was to describe real‐world data on outcomes of T cell replete haploidentical hematopoietic stem cell transplantation (HSCT) after the introduction of this modality in a single center and to compare them with different donor types. METHOD: Outcomes of 30 consecutive patients with hematological malignancies that received T cell replete haploidentical HSCT with posttransplantation cyclophosphamide (PTCY) from 2016 to 2018 in our center were analyzed and compared to the outcome of human leukocyte antigen (HLA)‐related and unrelated matched donor HSCT (n = 97) and to a historical cohort of T cell depleted haploidentical HSCT (n = 11). RESULTS: One year graft‐versus‐host‐free, relapse‐free survival in haploidentical HSCT was comparable with other donor types (haplo 40%, matched related donor [MRD] 33%, matched unrelated donor [MUD] 25%, p = 0.55). Non relapse mortality was high in haploidentical HSCT (50%), mostly due to infectious complications. However, relapse rates were only 3%, and OS and progression‐free survival after 1 year were 47% and thereby also similar to HLA‐matched HSCT in our center (MRD 53%, MUD 48%). CONCLUSION: Our data show that T cell replete haploidentical HSCT has similar outcomes to HLA identical HSCT after introduction in our center. More strict adaptation on infection prevention was a crucial aspect of our learning curve. Overall, this type of transplantation is a feasible option when lacking an HLA‐identical donor. This option has advantages over an unrelated donor as it brings less logistical challenges than MUD transplantations. John Wiley and Sons Inc. 2021-05-26 /pmc/articles/PMC9175800/ /pubmed/35844710 http://dx.doi.org/10.1002/jha2.203 Text en © 2021 The Authors. eJHaem published by British Society for Haematology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Haematologic Malignancy ‐ Cellular Therapy
van Gorkom, Gwendolyn
Billen, Evy
Van Elssen, Catharina
van Gelder, Michel
Bos, Gerard
Real‐world experience: Introduction of T cell replete haploidentical transplantations in a single center
title Real‐world experience: Introduction of T cell replete haploidentical transplantations in a single center
title_full Real‐world experience: Introduction of T cell replete haploidentical transplantations in a single center
title_fullStr Real‐world experience: Introduction of T cell replete haploidentical transplantations in a single center
title_full_unstemmed Real‐world experience: Introduction of T cell replete haploidentical transplantations in a single center
title_short Real‐world experience: Introduction of T cell replete haploidentical transplantations in a single center
title_sort real‐world experience: introduction of t cell replete haploidentical transplantations in a single center
topic Haematologic Malignancy ‐ Cellular Therapy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9175800/
https://www.ncbi.nlm.nih.gov/pubmed/35844710
http://dx.doi.org/10.1002/jha2.203
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