| Literature DB >> 33692532 |
Hirotoshi Sakaguchi1,2, Takako Miyamura3, Daisuke Tomizawa4, Takashi Taga5, Hiroyuki Ishida6, Yasuhiro Okamoto7, Katsuyoshi Koh8, Tomoko Yokosuka9, Nao Yoshida10, Maho Sato11, Maiko Noguchi12, Keiko Okada13, Tsukasa Hori14, Masanobu Takeuchi15, Yoshiyuki Kosaka16, Masami Inoue11, Yoshiko Hashii3,17, Yoshiko Atsuta18,19.
Abstract
Children with acute myeloid leukemia (AML) commonly develop extramedullary disease (EMD), which comprises central nervous system (CNS) lesions and myeloid sarcoma (MS). In this retrospective analysis, we aimed to determine the effect of EMD on the outcomes of allogeneic hematopoietic cell transplantation (HCT) in 678 pediatric patients with de novo AML (median age, 7 years; range, 0.3-15 years) between 2006 and 2016. We compared the outcomes between patients with (EMD group, n = 158; CNS lesion, n = 47, CNS lesion + MS, n = 9, and MS, n = 102) and without EMD at diagnosis (non-EMD group, n = 520). Survivors were followed for a median of 4.5 years, and the 4-year overall survival (OS) rates were 60.6% and 56.4% in the EMD and non-EMD groups, respectively (P = 0.60). No significant differences in OS were observed with respect to the EMD site, except bone lesions, which were associated with poor OS after HCT in a non-remission status. A multivariate analysis revealed that EMD did not affect the outcomes of HCT. In conclusion, the study findings suggest that EMD should not be considered a poor prognostic factor in HCT for children with AML.Entities:
Mesh:
Year: 2021 PMID: 33692532 DOI: 10.1038/s41409-021-01250-9
Source DB: PubMed Journal: Bone Marrow Transplant ISSN: 0268-3369 Impact factor: 5.174