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Should a matched sibling donor still be considered the primary option for allogeneic hematopoietic cell transplantation in patients over 50 years of age with myelodysplastic syndrome?
Human leukocyte antigen (HLA)-matched sibling donors (MSDs) are the preferred choice for allogeneic hematopoietic cell transplantation (HCT). However, as myelodysplastic syndrome (MDS) is most frequently diagnosed in the elderly, MSDs are also likely to be of advanced age. It is unclear whether an M...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10400426/ https://www.ncbi.nlm.nih.gov/pubmed/37156881 http://dx.doi.org/10.1038/s41409-023-01997-3 |
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author | Konuma, Takaaki Itonaga, Hidehiro Ishiyama, Ken Doki, Noriko Uchida, Naoyuki Sawa, Masashi Katayama, Yuta Tanaka, Masatsugu Ueda, Yasunori Onizuka, Makoto Miyakoshi, Shigesaburo Ozawa, Yukiyasu Fukuda, Takahiro Matsuoka, Ken-ichi Tanaka, Junji Kimura, Takafumi Ichinohe, Tatsuo Atsuta, Yoshiko |
author_facet | Konuma, Takaaki Itonaga, Hidehiro Ishiyama, Ken Doki, Noriko Uchida, Naoyuki Sawa, Masashi Katayama, Yuta Tanaka, Masatsugu Ueda, Yasunori Onizuka, Makoto Miyakoshi, Shigesaburo Ozawa, Yukiyasu Fukuda, Takahiro Matsuoka, Ken-ichi Tanaka, Junji Kimura, Takafumi Ichinohe, Tatsuo Atsuta, Yoshiko |
author_sort | Konuma, Takaaki |
collection | PubMed |
description | Human leukocyte antigen (HLA)-matched sibling donors (MSDs) are the preferred choice for allogeneic hematopoietic cell transplantation (HCT). However, as myelodysplastic syndrome (MDS) is most frequently diagnosed in the elderly, MSDs are also likely to be of advanced age. It is unclear whether an MSD should be considered the primary choice for allogeneic HCT in elderly patients with MDS. We retrospectively compared survival and other outcomes in 1787 patients with MDS over 50 years of age and receiving allogeneic HCT between 2014 and 2020, using either MSD (n = 214), 8/8 allele-matched unrelated donor (MUD) (n = 562), 7/8 allele-MUD (n = 334), or unrelated cord blood (UCB) (n = 677) in Japan. In multivariate analysis, compared to MSD transplants, the risk of relapse was significantly lower following 8/8MUD transplants (hazard ratio [HR], 0.74; P = 0.047), whereas non-relapse mortality was significantly higher following UCB transplants (HR, 1.43; P = 0.041). However, donor type did not determine overall survival, disease-free survival, or graft-versus-host disease (GVHD)-free, relapse-free survival, but chronic GVHD-free, relapse-free survival was better after UCB (HR, 0.80; P = 0.025) and 8/8MUD (HR, 0.81; P = 0.032) compared to MSD transplants. Our study demonstrated that MSDs are not superior to alternative HCT methods, such as 8/8MUD, 7/8MUD, or UCB, in this population. |
format | Online Article Text |
id | pubmed-10400426 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-104004262023-08-05 Should a matched sibling donor still be considered the primary option for allogeneic hematopoietic cell transplantation in patients over 50 years of age with myelodysplastic syndrome? Konuma, Takaaki Itonaga, Hidehiro Ishiyama, Ken Doki, Noriko Uchida, Naoyuki Sawa, Masashi Katayama, Yuta Tanaka, Masatsugu Ueda, Yasunori Onizuka, Makoto Miyakoshi, Shigesaburo Ozawa, Yukiyasu Fukuda, Takahiro Matsuoka, Ken-ichi Tanaka, Junji Kimura, Takafumi Ichinohe, Tatsuo Atsuta, Yoshiko Bone Marrow Transplant Article Human leukocyte antigen (HLA)-matched sibling donors (MSDs) are the preferred choice for allogeneic hematopoietic cell transplantation (HCT). However, as myelodysplastic syndrome (MDS) is most frequently diagnosed in the elderly, MSDs are also likely to be of advanced age. It is unclear whether an MSD should be considered the primary choice for allogeneic HCT in elderly patients with MDS. We retrospectively compared survival and other outcomes in 1787 patients with MDS over 50 years of age and receiving allogeneic HCT between 2014 and 2020, using either MSD (n = 214), 8/8 allele-matched unrelated donor (MUD) (n = 562), 7/8 allele-MUD (n = 334), or unrelated cord blood (UCB) (n = 677) in Japan. In multivariate analysis, compared to MSD transplants, the risk of relapse was significantly lower following 8/8MUD transplants (hazard ratio [HR], 0.74; P = 0.047), whereas non-relapse mortality was significantly higher following UCB transplants (HR, 1.43; P = 0.041). However, donor type did not determine overall survival, disease-free survival, or graft-versus-host disease (GVHD)-free, relapse-free survival, but chronic GVHD-free, relapse-free survival was better after UCB (HR, 0.80; P = 0.025) and 8/8MUD (HR, 0.81; P = 0.032) compared to MSD transplants. Our study demonstrated that MSDs are not superior to alternative HCT methods, such as 8/8MUD, 7/8MUD, or UCB, in this population. Nature Publishing Group UK 2023-05-08 2023 /pmc/articles/PMC10400426/ /pubmed/37156881 http://dx.doi.org/10.1038/s41409-023-01997-3 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Konuma, Takaaki Itonaga, Hidehiro Ishiyama, Ken Doki, Noriko Uchida, Naoyuki Sawa, Masashi Katayama, Yuta Tanaka, Masatsugu Ueda, Yasunori Onizuka, Makoto Miyakoshi, Shigesaburo Ozawa, Yukiyasu Fukuda, Takahiro Matsuoka, Ken-ichi Tanaka, Junji Kimura, Takafumi Ichinohe, Tatsuo Atsuta, Yoshiko Should a matched sibling donor still be considered the primary option for allogeneic hematopoietic cell transplantation in patients over 50 years of age with myelodysplastic syndrome? |
title | Should a matched sibling donor still be considered the primary option for allogeneic hematopoietic cell transplantation in patients over 50 years of age with myelodysplastic syndrome? |
title_full | Should a matched sibling donor still be considered the primary option for allogeneic hematopoietic cell transplantation in patients over 50 years of age with myelodysplastic syndrome? |
title_fullStr | Should a matched sibling donor still be considered the primary option for allogeneic hematopoietic cell transplantation in patients over 50 years of age with myelodysplastic syndrome? |
title_full_unstemmed | Should a matched sibling donor still be considered the primary option for allogeneic hematopoietic cell transplantation in patients over 50 years of age with myelodysplastic syndrome? |
title_short | Should a matched sibling donor still be considered the primary option for allogeneic hematopoietic cell transplantation in patients over 50 years of age with myelodysplastic syndrome? |
title_sort | should a matched sibling donor still be considered the primary option for allogeneic hematopoietic cell transplantation in patients over 50 years of age with myelodysplastic syndrome? |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10400426/ https://www.ncbi.nlm.nih.gov/pubmed/37156881 http://dx.doi.org/10.1038/s41409-023-01997-3 |
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