| Literature DB >> 22924344 |
Toshihiko Imamura1, Shotaro Iwamoto, Rie Kanai, Akira Shimada, Kiminori Terui, Yuko Osugi, Ryoji Kobayashi, Akio Tawa, Yoshiyuki Kosaka, Koji Kato, Hiroki Hori, Keizo Horibe, Megumi Oda, Souichi Adachi.
Abstract
The acute myeloid leukaemia (AML) 99 trial conducted previously in Japan for the treatment of de novo paediatric AML showed excellent results, with a 5-year overall survival (OS) and event-free survival (EFS) of 75·6% and 61·6%, respectively. To examine reproducibility of these results in another cohort, the outcome of 146 newly diagnosed AML paediatric patients prospectively registered in the Japan Association of Childhood Leukaemia Study (JACLS) from 2003 to 2006 was compared to that of 240 patients in the original AML 99 clinical trial. The 5-year EFS and OS achieved in the new cohort was 66·7 ± 4·0% and 77·7 ± 8·0% respectively, which were comparable to those obtained in the original AML 99 clinical trial, although less frequent core-binding factor (CBF) AML (29·5% vs. 37%) and an almost equal frequency of allogeneic haematopoietic stem cell transplantation (allo-HSCT) during first complete remission (16·5% vs. 19%) were observed. The 5-year EFS in patients with a normal karyotype (NK) (n = 35, 54·9 ± 15·1%) was inferior in the present cohort when compared to the original AML99 trial. This study confirmed the excellent outcome of the original AML99 protocol.Entities:
Mesh:
Year: 2012 PMID: 22924344 DOI: 10.1111/bjh.12030
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998