TY - JOUR
T1 - Patients with acute myeloid leukemia undergoing allogeneic hematopoietic cell transplantation
T2 - trends in survival during the past two decades
AU - Yanada, Masamitsu
AU - Masuko, Masayoshi
AU - Mori, Jinichi
AU - Aoki, Jun
AU - Mizuno, Shohei
AU - Fukuda, Takahiro
AU - Kakihana, Kazuhiko
AU - Ozawa, Yukiyasu
AU - Ota, Shuichi
AU - Kanamori, Heiwa
AU - Mori, Takehiko
AU - Nakamae, Hirohisa
AU - Eto, Tetsuya
AU - Shiratori, Souichi
AU - Maeda, Tetsuo
AU - Iwato, Koji
AU - Ichinohe, Tatsuo
AU - Kanda, Yoshinobu
AU - Tanaka, Junji
AU - Atsuta, Yoshiko
AU - Yano, Shingo
N1 - Funding Information:
Acknowledgements This work was supported in part by the Practical Research Project for Allergic Diseases and Immunology (Research Technology of Medical Transplantation) from Japan Agency for Medical Research and Development (AMED) under the grant number 18ek0510023h0002.
Publisher Copyright:
© 2018, Springer Nature Limited.
PY - 2019/4/1
Y1 - 2019/4/1
N2 - It remains unclear how specific innovations in allogeneic hematopoietic cell transplantation (HCT) attained over the past decades have contributed to improvement in transplantation outcomes. To address this question, we conducted a registry-based study of adults with acute myeloid leukemia in first or second complete remission who underwent allogeneic HCT between 1994 and 2013 from a sibling (N = 1600) or unrelated (N = 2113) donor matched at the antigen level for HLA-A, -B, and -DR. Preliminary analysis led us to focus on comparisons between the 1994–2006 and 2007–2013 periods. Significant improvement in survival was observed in the later cohort compared to the earlier cohort for unrelated HCT (P = 0.004), but not for related HCT (P = 0.767). The improvement in unrelated HCT was solely due to diminished non-relapse mortality (P = 0.001), while incidence of relapse did not change over time (P = 0.934). The percentage of patients receiving transplants from 8/8-matched unrelated donors was significantly higher in the later cohort (P < 0.001), and their survival was significantly better than that of those undergoing mismatched unrelated HCT (P = 0.022). These findings suggest that advances in HLA-typing technology have been vital for improvement in transplantation outcomes.
AB - It remains unclear how specific innovations in allogeneic hematopoietic cell transplantation (HCT) attained over the past decades have contributed to improvement in transplantation outcomes. To address this question, we conducted a registry-based study of adults with acute myeloid leukemia in first or second complete remission who underwent allogeneic HCT between 1994 and 2013 from a sibling (N = 1600) or unrelated (N = 2113) donor matched at the antigen level for HLA-A, -B, and -DR. Preliminary analysis led us to focus on comparisons between the 1994–2006 and 2007–2013 periods. Significant improvement in survival was observed in the later cohort compared to the earlier cohort for unrelated HCT (P = 0.004), but not for related HCT (P = 0.767). The improvement in unrelated HCT was solely due to diminished non-relapse mortality (P = 0.001), while incidence of relapse did not change over time (P = 0.934). The percentage of patients receiving transplants from 8/8-matched unrelated donors was significantly higher in the later cohort (P < 0.001), and their survival was significantly better than that of those undergoing mismatched unrelated HCT (P = 0.022). These findings suggest that advances in HLA-typing technology have been vital for improvement in transplantation outcomes.
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U2 - 10.1038/s41409-018-0301-7
DO - 10.1038/s41409-018-0301-7
M3 - Article
C2 - 30108330
AN - SCOPUS:85052531346
SN - 0268-3369
VL - 54
SP - 578
EP - 586
JO - Bone Marrow Transplantation
JF - Bone Marrow Transplantation
IS - 4
ER -