TY - JOUR
T1 - Comparison of transplant outcomes between haploidentical transplantation and single cord blood transplantation in non-remission acute myeloid leukaemia
T2 - A nationwide retrospective study
AU - Matsuda, Kensuke
AU - Konuma, Takaaki
AU - Fuse, Kyoko
AU - Masuko, Masayoshi
AU - Kawamura, Koji
AU - Hirayama, Masahiro
AU - Uchida, Naoyuki
AU - Ikegame, Kazuhiro
AU - Wake, Atsushi
AU - Eto, Tetsuya
AU - Doki, Noriko
AU - Miyakoshi, Shigesaburo
AU - Tanaka, Masatsugu
AU - Takahashi, Satoshi
AU - Onizuka, Makoto
AU - Kato, Koji
AU - Kimura, Takafumi
AU - Ichinohe, Tatsuo
AU - Takayama, Nobuyuki
AU - Kobayashi, Hikaru
AU - Nakamae, Hirohisa
AU - Atsuta, Yoshiko
AU - Kanda, Junya
AU - Yanada, Masamitsu
N1 - Funding Information:
This work was supported in part by a grant from the Practical Research Project for Allergic Diseases and Immunology (Research Technology of Medical Transplantation) from the Japan Agency for Medical Research and Development (AMED), grant number: 19ek0510023h0003.
Publisher Copyright:
© 2022 British Society for Haematology and John Wiley & Sons Ltd.
PY - 2022
Y1 - 2022
N2 - Allogeneic haematopoietic stem cell transplantation (HSCT) is a potentially curative treatment for some patients with acute myeloid leukaemia (AML) who are refractory to chemotherapy. Cord blood transplantation (CBT) is a reasonable option in such cases because of its rapid availability. Recently, a growing number of human leucocyte antigen (HLA)-haploidentical related donor HSCTs (haplo-HSCTs) have been performed, although its effectiveness remains undetermined. Using the Japanese nationwide transplantation registry data, we identified 2438 patients aged ≥16 years who received CBT or haplo-HSCT as their first transplant for non-remission AML between January 2008 and December 2018. After 2:1 propensity score matching, 918 patients in the CBT group and 459 patients in the haplo-HSCT group were selected. In this matched cohort, no significant difference in overall survival (OS) was observed between the CBT and haplo-HSCT groups (hazard ratio [HR] of haplo-HSCT to CBT 1.02, 95% confidence interval [CI] 0.89–1.16). Similarly, no significant difference in the cumulative incidence of relapse (HR 1.09, 95% CI 0.93–1.28) or non-relapse mortality (HR 0.94, 95% CI 0.76–1.18). Subgroup analysis showed that CBT was significantly associated with preferable OS in patients receiving myeloablative conditioning. Our data showed comparable outcomes between haplo-HSCT and CBT recipients with non-remission AML.
AB - Allogeneic haematopoietic stem cell transplantation (HSCT) is a potentially curative treatment for some patients with acute myeloid leukaemia (AML) who are refractory to chemotherapy. Cord blood transplantation (CBT) is a reasonable option in such cases because of its rapid availability. Recently, a growing number of human leucocyte antigen (HLA)-haploidentical related donor HSCTs (haplo-HSCTs) have been performed, although its effectiveness remains undetermined. Using the Japanese nationwide transplantation registry data, we identified 2438 patients aged ≥16 years who received CBT or haplo-HSCT as their first transplant for non-remission AML between January 2008 and December 2018. After 2:1 propensity score matching, 918 patients in the CBT group and 459 patients in the haplo-HSCT group were selected. In this matched cohort, no significant difference in overall survival (OS) was observed between the CBT and haplo-HSCT groups (hazard ratio [HR] of haplo-HSCT to CBT 1.02, 95% confidence interval [CI] 0.89–1.16). Similarly, no significant difference in the cumulative incidence of relapse (HR 1.09, 95% CI 0.93–1.28) or non-relapse mortality (HR 0.94, 95% CI 0.76–1.18). Subgroup analysis showed that CBT was significantly associated with preferable OS in patients receiving myeloablative conditioning. Our data showed comparable outcomes between haplo-HSCT and CBT recipients with non-remission AML.
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U2 - 10.1111/bjh.18530
DO - 10.1111/bjh.18530
M3 - Article
AN - SCOPUS:85140390643
JO - British Journal of Haematology
JF - British Journal of Haematology
SN - 0007-1048
ER -