| Literature DB >> 23368421 |
Shinichi Kako1, Heiwa Kanamori, Naoki Kobayashi, Akio Shigematsu, Yasuhito Nannya, Mika Nakamae, Kazuyuki Shigeno, Kazumi Suzukawa, Masahiro Takeuchi, Motohiro Tsuzuki, Kensuke Usuki, Kazuo Hatanaka, Kazuei Ogawa, Kinuko Mitani, Yuichiro Nawa, Yoshihiro Hatta, Ishikazu Mizuno, Yoshinobu Kanda.
Abstract
To analyse the outcome of adult patients who developed a first relapse of acute lymphoblastic leukaemia (ALL), we collected the clinical data of 332 patients with Philadelphia-chromosome (Ph) negative ALL, aged 16-65 years, who relapsed after first complete remission (CR1) between 1998 and 2008 in 69 institutions all over Japan, including 58 patients who relapsed after allogeneic haematopoietic stem cell transplantation (Allo-HSCT) in CR1. The overall survival (OS) was 43·4% at 1 year, and 16·3% at 5 years from relapse in patients who received chemotherapy alone in CR1. Among patients who relapsed after chemotherapy alone in CR1, 123 (52·5%) achieved a second remission (CR2) following salvage chemotherapy, of whom 62 subsequently underwent Allo-HSCT during CR2. Allo-HSCT in CR2 was significantly associated with better OS. Moreover, the type of salvage chemotherapy influenced OS from relapse. A doxorubicin, vincristine, and predonisone-based (AdVP-type) regimen was related to better OS in patients with longer CR1 (more than 1 year), but was related to worse OS in patients with shorter CR1. In conclusion, the prognosis of patients with relapsed Ph-negative ALL is poor. Allo-HSCT after a first relapse could improve the prognosis. Selection of the optimal salvage chemotherapy might depend on the duration of CR1.Entities:
Mesh:
Year: 2013 PMID: 23368421 DOI: 10.1111/bjh.12225
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998