| Literature DB >> 29959436 |
Daisuke Tomizawa1, Masanori Yoshida2, Tadakazu Kondo3, Takako Miyamura4, Takashi Taga5, Souichi Adachi6, Katsuyoshi Koh7, Maiko Noguchi8, Harumi Kakuda9, Kenichiro Watanabe10, Yuko Cho11, Takahiro Fukuda12, Motohiro Kato13,2, Norio Shiba14, Hiroaki Goto15, Keiko Okada16, Masami Inoue17, Yoshiko Hashii4, Yoshiko Atsuta18,19, Hiroyuki Ishida20.
Abstract
Allocating patients with acute myeloid leukemia and high-risk cytogenetic abnormalities (HR-AML) for allogeneic hematopoietic stem cell transplantation (allo-HSCT) is part of the standard treatment protocol; however, whether allo-HSCT truly improves the outcomes in these patients is debatable. Data on 169 children and adolescents with HR-AML who received their first allo-HSCT in first or second remission between 2000 and 2015 were extracted from a nationwide, Japanese HSCT registry. The 3-year disease-free survival (DFS) and overall survival (OS) rates were 55.2% (95% CI, 46.8-62.9%) and 69.6% (61.4-76.3%), respectively, for all the HR-AML patients. In univariate analysis, the cytogenetic subgroup had a significant impact on both the DFS (P = 0.011) and OS (P < 0.001) rates. In particular, 14 patients with t(16;21) showed an extremely poor outcome. Additionally, older age at allo-HSCT (10-19 years old, P = 0.025), myeloablative conditioning with total-body irradiation (P = 0.019), and grade II-IV acute graft-versus-host disease (GVHD, P = 0.049) were associated with inferior OS. The donor type and occurrence of chronic GVHD did not affect the outcome. Multivariate analysis revealed t(16;21) to be associated with increased overall mortality (hazard ratio = 4.416, P < 0.001). Because the outcome of patients with certain HR-AML subgroups, such as t(16;21)-positive cases, is extremely poor even with allo-HSCT in remission, a novel therapy is urgently required.Entities:
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Year: 2018 PMID: 29959436 DOI: 10.1038/s41409-018-0273-7
Source DB: PubMed Journal: Bone Marrow Transplant ISSN: 0268-3369 Impact factor: 5.483