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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...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Nature Singapore 2022
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
Descripción
Sumario: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.