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Anti-thymocyte globulin with CsA and MMF as GVHD prophylaxis in nonmyeloablative HLA-mismatched allogeneic HCT
Nonmyeloablative regimens are used for allogeneic hematopoietic cell transplantation (HCT) of older or medically unfit patients, but successful outcome is still hindered by graft-versus-host disease (GVHD), especially in the setting of HLA-mismatched HCT. New GVHD prophylaxis strategies are emerging...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8214052/ https://www.ncbi.nlm.nih.gov/pubmed/34148060 http://dx.doi.org/10.1038/s41409-021-01369-9 |
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author | van der Velden, Walter J. F. M. Choi, Goda de Witte, Moniek A. van der Meer, Arnold de Haan, Anton F. J. Blijlevens, Nicole M. A. Huls, Gerwin Kuball, Jürgen van Dorp, Suzanne |
author_facet | van der Velden, Walter J. F. M. Choi, Goda de Witte, Moniek A. van der Meer, Arnold de Haan, Anton F. J. Blijlevens, Nicole M. A. Huls, Gerwin Kuball, Jürgen van Dorp, Suzanne |
author_sort | van der Velden, Walter J. F. M. |
collection | PubMed |
description | Nonmyeloablative regimens are used for allogeneic hematopoietic cell transplantation (HCT) of older or medically unfit patients, but successful outcome is still hindered by graft-versus-host disease (GVHD), especially in the setting of HLA-mismatched HCT. New GVHD prophylaxis strategies are emerging, including the triple drug strategy, that improve the GVHD-free and relapse-free survival (GRFS). Because the impact of ATG in HLA-mismatched Flu-TBI-based nonmyeloablative HCT has not been investigated, we did a retrospective analysis in three Dutch centers. 67 patients were evaluable, with a median age of 56 years. Overall survival, relapse-free survival and GRFS at 4 years were 52%, 43%, and 38%, respectively. NRM findings and cumulative incidence of relapse at 4 years were 26% and 31%, respectively. At 1-year grade II-IV had occurred in 40% of the patients, and the incidence of moderate-severe chronic GVHD incidence was 16%. Acknowledging the limitations of retrospective analyses, we conclude that the use of ATG for HLA-mismatched truly nonmyeloablative Flu-TBI HCT is feasible and results in acceptable long term outcomes, especially with regards to GRFS. We consider ATG in combination with cyclosporin and mycophenolate mofetil as an alternative for the triple drug strategy that uses sirolimus for GVHD prophylaxis in this particular setting. |
format | Online Article Text |
id | pubmed-8214052 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82140522021-06-21 Anti-thymocyte globulin with CsA and MMF as GVHD prophylaxis in nonmyeloablative HLA-mismatched allogeneic HCT van der Velden, Walter J. F. M. Choi, Goda de Witte, Moniek A. van der Meer, Arnold de Haan, Anton F. J. Blijlevens, Nicole M. A. Huls, Gerwin Kuball, Jürgen van Dorp, Suzanne Bone Marrow Transplant Article Nonmyeloablative regimens are used for allogeneic hematopoietic cell transplantation (HCT) of older or medically unfit patients, but successful outcome is still hindered by graft-versus-host disease (GVHD), especially in the setting of HLA-mismatched HCT. New GVHD prophylaxis strategies are emerging, including the triple drug strategy, that improve the GVHD-free and relapse-free survival (GRFS). Because the impact of ATG in HLA-mismatched Flu-TBI-based nonmyeloablative HCT has not been investigated, we did a retrospective analysis in three Dutch centers. 67 patients were evaluable, with a median age of 56 years. Overall survival, relapse-free survival and GRFS at 4 years were 52%, 43%, and 38%, respectively. NRM findings and cumulative incidence of relapse at 4 years were 26% and 31%, respectively. At 1-year grade II-IV had occurred in 40% of the patients, and the incidence of moderate-severe chronic GVHD incidence was 16%. Acknowledging the limitations of retrospective analyses, we conclude that the use of ATG for HLA-mismatched truly nonmyeloablative Flu-TBI HCT is feasible and results in acceptable long term outcomes, especially with regards to GRFS. We consider ATG in combination with cyclosporin and mycophenolate mofetil as an alternative for the triple drug strategy that uses sirolimus for GVHD prophylaxis in this particular setting. Nature Publishing Group UK 2021-06-19 2021 /pmc/articles/PMC8214052/ /pubmed/34148060 http://dx.doi.org/10.1038/s41409-021-01369-9 Text en © The Author(s), under exclusive licence to Springer Nature Limited 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Article van der Velden, Walter J. F. M. Choi, Goda de Witte, Moniek A. van der Meer, Arnold de Haan, Anton F. J. Blijlevens, Nicole M. A. Huls, Gerwin Kuball, Jürgen van Dorp, Suzanne Anti-thymocyte globulin with CsA and MMF as GVHD prophylaxis in nonmyeloablative HLA-mismatched allogeneic HCT |
title | Anti-thymocyte globulin with CsA and MMF as GVHD prophylaxis in nonmyeloablative HLA-mismatched allogeneic HCT |
title_full | Anti-thymocyte globulin with CsA and MMF as GVHD prophylaxis in nonmyeloablative HLA-mismatched allogeneic HCT |
title_fullStr | Anti-thymocyte globulin with CsA and MMF as GVHD prophylaxis in nonmyeloablative HLA-mismatched allogeneic HCT |
title_full_unstemmed | Anti-thymocyte globulin with CsA and MMF as GVHD prophylaxis in nonmyeloablative HLA-mismatched allogeneic HCT |
title_short | Anti-thymocyte globulin with CsA and MMF as GVHD prophylaxis in nonmyeloablative HLA-mismatched allogeneic HCT |
title_sort | anti-thymocyte globulin with csa and mmf as gvhd prophylaxis in nonmyeloablative hla-mismatched allogeneic hct |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8214052/ https://www.ncbi.nlm.nih.gov/pubmed/34148060 http://dx.doi.org/10.1038/s41409-021-01369-9 |
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