TY - JOUR
T1 - Unrelated female-to-male bone marrow transplantation would be preferred over cord blood transplantation in male patients
AU - Tamaki, Masaharu
AU - Akahoshi, Yu
AU - Okada, Yosuke
AU - Uchida, Naoyuki
AU - Tanaka, Masatsugu
AU - Doki, Noriko
AU - Sawa, Masashi
AU - Maruyama, Yumiko
AU - Ueda, Yasunori
AU - Miyakoshi, Shigesaburo
AU - Katayama, Yuta
AU - Kawakita, Toshiro
AU - Kimura, Takafumi
AU - Onizuka, Makoto
AU - Fukuda, Takahiro
AU - Atsuta, Yoshiko
AU - Yanagisawa, Ryu
AU - Yakushijin, Kimikazu
AU - Kanda, Junya
AU - Nakasone, Hideki
N1 - Publisher Copyright:
© 2023 International Society for Cell & Gene Therapy
PY - 2023/11
Y1 - 2023/11
N2 - Background aims: Allogeneic hematopoietic stem cell transplantation from female donors to male recipients (female-to-male allo-HCT) is a well-established risk factor for a greater incidence of non-relapse mortality (NRM) and chronic graft-versus-host disease (GVHD). In contrast, unrelated cord blood transplantation (UCBT) is associated with a lower incidence of chronic GVHD. In this study, survival outcomes were compared between the UCBT and unrelated female-to-male bone marrow transplantation (UFMBMT) groups. Methods: We evaluated male allo-HCT recipients who underwent UCBT or UFMBMT between 2012 and 2020 in Japan. There were 2517 cases in the UCBT group, 456 cases in the HLA-matched UFMBMT group and 457 cases in the HLA-mismatched UFMBMT group. Results: HLA-mismatched UFMBMT was significantly associated with a decreased risk of relapse (hazard ratio [HR] 0.74; 95% confidence interval [CI] 0.57–0.98], P = 0.033) and HLA-matched UFMBMT had the tendency of a decreased risk of relapse (HR 0.78; 95% CI 0.61–1.01, P = 0.059). HLA-matched UFMBMT was also associated with favorable OS (HR 0.82; 95% CI 0.69–0.97, P = 0.021). The relationship between the donor sources and relapse was similarly observed in the lymphoid malignancy cohort. Conclusions: The difference of graft-versus leukemia effect by H-Y immunity according to donor sources might contribute to the difference in clinical impact. It might be desirable for patients who could sufficiently wait for donor coordination to select BMT rather than UCBT, even if only unrelated female donors are available for male recipients.
AB - Background aims: Allogeneic hematopoietic stem cell transplantation from female donors to male recipients (female-to-male allo-HCT) is a well-established risk factor for a greater incidence of non-relapse mortality (NRM) and chronic graft-versus-host disease (GVHD). In contrast, unrelated cord blood transplantation (UCBT) is associated with a lower incidence of chronic GVHD. In this study, survival outcomes were compared between the UCBT and unrelated female-to-male bone marrow transplantation (UFMBMT) groups. Methods: We evaluated male allo-HCT recipients who underwent UCBT or UFMBMT between 2012 and 2020 in Japan. There were 2517 cases in the UCBT group, 456 cases in the HLA-matched UFMBMT group and 457 cases in the HLA-mismatched UFMBMT group. Results: HLA-mismatched UFMBMT was significantly associated with a decreased risk of relapse (hazard ratio [HR] 0.74; 95% confidence interval [CI] 0.57–0.98], P = 0.033) and HLA-matched UFMBMT had the tendency of a decreased risk of relapse (HR 0.78; 95% CI 0.61–1.01, P = 0.059). HLA-matched UFMBMT was also associated with favorable OS (HR 0.82; 95% CI 0.69–0.97, P = 0.021). The relationship between the donor sources and relapse was similarly observed in the lymphoid malignancy cohort. Conclusions: The difference of graft-versus leukemia effect by H-Y immunity according to donor sources might contribute to the difference in clinical impact. It might be desirable for patients who could sufficiently wait for donor coordination to select BMT rather than UCBT, even if only unrelated female donors are available for male recipients.
KW - H-Y antigens
KW - allogeneic hematopoietic stem cell transplantation
KW - bone marrow
KW - cord blood
KW - sex-mismatch transplantation
UR - http://www.scopus.com/inward/record.url?scp=85169910633&partnerID=8YFLogxK
U2 - 10.1016/j.jcyt.2023.06.002
DO - 10.1016/j.jcyt.2023.06.002
M3 - Article
C2 - 37341665
AN - SCOPUS:85169910633
SN - 1465-3249
VL - 25
SP - 1220
EP - 1228
JO - Cytotherapy
JF - Cytotherapy
IS - 11
ER -