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Reduced-intensity conditioning is effective for allogeneic hematopoietic stem cell transplantation in infants with MECOM-associated syndrome
Mutations in the MECOM encoding EVI1 are observed in infants who have radioulnar synostosis with amegakaryocytic thrombocytopenia. MECOM-associated syndrome was proposed based on clinical heterogeneity. Allogeneic hematopoietic stem cell transplantation (HSCT) is a curative treatment for progressive...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Nature Singapore
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10063491/ https://www.ncbi.nlm.nih.gov/pubmed/36515795 http://dx.doi.org/10.1007/s12185-022-03505-7 |
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author | Irie, Masahiro Niihori, Tetsuya Nakano, Tomohiro Suzuki, Tasuku Katayama, Saori Moriya, Kunihiko Niizuma, Hidetaka Suzuki, Nobu Saito-Nanjo, Yuka Onuma, Masaei Rikiishi, Takeshi Sato, Atsushi Hangai, Mayumi Hiwatari, Mitsuteru Ikeda, Junji Tanoshima, Reo Shiba, Norio Yuza, Yuki Yamamoto, Nobuyuki Hashii, Yoshiko Kato, Motohiro Takita, Junko Maeda, Miho Aoki, Yoko Imaizumi, Masue Sasahara, Yoji |
author_facet | Irie, Masahiro Niihori, Tetsuya Nakano, Tomohiro Suzuki, Tasuku Katayama, Saori Moriya, Kunihiko Niizuma, Hidetaka Suzuki, Nobu Saito-Nanjo, Yuka Onuma, Masaei Rikiishi, Takeshi Sato, Atsushi Hangai, Mayumi Hiwatari, Mitsuteru Ikeda, Junji Tanoshima, Reo Shiba, Norio Yuza, Yuki Yamamoto, Nobuyuki Hashii, Yoshiko Kato, Motohiro Takita, Junko Maeda, Miho Aoki, Yoko Imaizumi, Masue Sasahara, Yoji |
author_sort | Irie, Masahiro |
collection | PubMed |
description | Mutations in the MECOM encoding EVI1 are observed in infants who have radioulnar synostosis with amegakaryocytic thrombocytopenia. MECOM-associated syndrome was proposed based on clinical heterogeneity. Allogeneic hematopoietic stem cell transplantation (HSCT) is a curative treatment for progressive bone marrow failure. However, data regarding allogeneic HSCT for this rare disease are limited. We retrospectively assessed overall survival, conditioning regimen, regimen-related toxicities and long-term sequelae in six patients treated with allogeneic HSCT. All patients received a reduced-intensity conditioning (RIC) regimen consisting of fludarabine, cyclophosphamide or melphalan, and rabbit anti-thymocyte globulin and/or low-dose total body/thoracic-abdominal/total lymphoid irradiation, followed by allogeneic bone marrow or cord blood transplantation from unrelated donors between 4 and 18 months of age. All patients survived and achieved stable engraftment and complete chimerization with the donor type. Moreover, no patient experienced severe regimen-related toxicities, and only lower grades of acute graft-versus-host disease were observed. Three patients treated with low-dose irradiation had relatively short stature compared to three patients not treated with irradiation. Therefore, allogeneic HSCT with RIC is an effective and feasible treatment for infants with MECOM-associated syndrome. Future studies are needed to evaluate the use of low-dose irradiation to avoid risks of other long-term sequelae. |
format | Online Article Text |
id | pubmed-10063491 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Nature Singapore |
record_format | MEDLINE/PubMed |
spelling | pubmed-100634912023-04-01 Reduced-intensity conditioning is effective for allogeneic hematopoietic stem cell transplantation in infants with MECOM-associated syndrome Irie, Masahiro Niihori, Tetsuya Nakano, Tomohiro Suzuki, Tasuku Katayama, Saori Moriya, Kunihiko Niizuma, Hidetaka Suzuki, Nobu Saito-Nanjo, Yuka Onuma, Masaei Rikiishi, Takeshi Sato, Atsushi Hangai, Mayumi Hiwatari, Mitsuteru Ikeda, Junji Tanoshima, Reo Shiba, Norio Yuza, Yuki Yamamoto, Nobuyuki Hashii, Yoshiko Kato, Motohiro Takita, Junko Maeda, Miho Aoki, Yoko Imaizumi, Masue Sasahara, Yoji Int J Hematol Original Article Mutations in the MECOM encoding EVI1 are observed in infants who have radioulnar synostosis with amegakaryocytic thrombocytopenia. MECOM-associated syndrome was proposed based on clinical heterogeneity. Allogeneic hematopoietic stem cell transplantation (HSCT) is a curative treatment for progressive bone marrow failure. However, data regarding allogeneic HSCT for this rare disease are limited. We retrospectively assessed overall survival, conditioning regimen, regimen-related toxicities and long-term sequelae in six patients treated with allogeneic HSCT. All patients received a reduced-intensity conditioning (RIC) regimen consisting of fludarabine, cyclophosphamide or melphalan, and rabbit anti-thymocyte globulin and/or low-dose total body/thoracic-abdominal/total lymphoid irradiation, followed by allogeneic bone marrow or cord blood transplantation from unrelated donors between 4 and 18 months of age. All patients survived and achieved stable engraftment and complete chimerization with the donor type. Moreover, no patient experienced severe regimen-related toxicities, and only lower grades of acute graft-versus-host disease were observed. Three patients treated with low-dose irradiation had relatively short stature compared to three patients not treated with irradiation. Therefore, allogeneic HSCT with RIC is an effective and feasible treatment for infants with MECOM-associated syndrome. Future studies are needed to evaluate the use of low-dose irradiation to avoid risks of other long-term sequelae. Springer Nature Singapore 2022-12-14 2023 /pmc/articles/PMC10063491/ /pubmed/36515795 http://dx.doi.org/10.1007/s12185-022-03505-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Article Irie, Masahiro Niihori, Tetsuya Nakano, Tomohiro Suzuki, Tasuku Katayama, Saori Moriya, Kunihiko Niizuma, Hidetaka Suzuki, Nobu Saito-Nanjo, Yuka Onuma, Masaei Rikiishi, Takeshi Sato, Atsushi Hangai, Mayumi Hiwatari, Mitsuteru Ikeda, Junji Tanoshima, Reo Shiba, Norio Yuza, Yuki Yamamoto, Nobuyuki Hashii, Yoshiko Kato, Motohiro Takita, Junko Maeda, Miho Aoki, Yoko Imaizumi, Masue Sasahara, Yoji Reduced-intensity conditioning is effective for allogeneic hematopoietic stem cell transplantation in infants with MECOM-associated syndrome |
title | Reduced-intensity conditioning is effective for allogeneic hematopoietic stem cell transplantation in infants with MECOM-associated syndrome |
title_full | Reduced-intensity conditioning is effective for allogeneic hematopoietic stem cell transplantation in infants with MECOM-associated syndrome |
title_fullStr | Reduced-intensity conditioning is effective for allogeneic hematopoietic stem cell transplantation in infants with MECOM-associated syndrome |
title_full_unstemmed | Reduced-intensity conditioning is effective for allogeneic hematopoietic stem cell transplantation in infants with MECOM-associated syndrome |
title_short | Reduced-intensity conditioning is effective for allogeneic hematopoietic stem cell transplantation in infants with MECOM-associated syndrome |
title_sort | reduced-intensity conditioning is effective for allogeneic hematopoietic stem cell transplantation in infants with mecom-associated syndrome |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10063491/ https://www.ncbi.nlm.nih.gov/pubmed/36515795 http://dx.doi.org/10.1007/s12185-022-03505-7 |
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