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Deletion of Y chromosome before allogeneic hematopoietic stem cell transplantation in male recipients with female donors

The graft-versus-leukemia (GVL) effect is one of the curative mechanisms of allogeneic hematopoietic stem cell transplantation (allo-HCT). H-Y antigens, which are encoded by Y chromosome, are important targets of the GVL effect. Thus, deletion of the Y chromosome (del[Y]) might cause the GVL effect...

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Detalles Bibliográficos
Autores principales: Tamaki, Masaharu, Kameda, Kazuaki, Kimura, Shun-ichi, Harada, Naonori, Uchida, Naoyuki, Doki, Noriko, Tanaka, Masatsugu, Ikegame, Kazuhiro, Sawa, Masashi, Katayama, Yuta, Miyakoshi, Shigesaburo, Ara, Takahide, Kanda, Junya, Onizuka, Makoto, Fukuda, Takahiro, Atsuta, Yoshiko, Kanda, Yoshinobu, Yakushijin, Kimikazu, Nakasone, Hideki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Hematology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8941451/
https://www.ncbi.nlm.nih.gov/pubmed/35108728
http://dx.doi.org/10.1182/bloodadvances.2021006456
Descripción
Sumario:The graft-versus-leukemia (GVL) effect is one of the curative mechanisms of allogeneic hematopoietic stem cell transplantation (allo-HCT). H-Y antigens, which are encoded by Y chromosome, are important targets of the GVL effect. Thus, deletion of the Y chromosome (del[Y]) might cause the GVL effect to deteriorate in a transplantation involving a female donor and male recipient, although the clinical significance of the del(Y) group remains to be elucidated. In this study, we evaluated adult male patients who underwent allo-HCT between 2010 and 2019 in Japan. There were 155 cases in the del(Y) group and 4149 cases without del(Y) who underwent female-to-male allo-HCT. Del(Y) was significantly associated with inferior overall survival (hazard ratio [HR], 1.24; 95% confidence interval [CI], 1.00-1.53; P = .049) and an increased risk of relapse (HR, 1.40; 95% CI, 1.08-1.80; P = .0098) in multivariate analyses. There was no significant difference in nonrelapse mortality between recipients with and without del(Y) (HR, 1.08; 95% CI, 0.769-1.51; P = .67). In contrast, del(Y) was not significantly associated with any clinical outcomes in the cohort of male-to-male allo-HCT. A higher incidence of relapse might have been caused by attenuation of the GVL effect resulting from a lack of H-Y antigens. Because a GVL effect resulting from sex mismatch may not be expected in men with del(Y) who undergo allo-HCT with a female donor, additional post–allo-HCT strategies might be required to prevent disease relapse.