| Literature DB >> 31186516 |
Hiroaki Shimizu1, Noriko Doki2, Heiwa Kanamori3, Toru Sakura4, Takehiko Mori5, Shinichiro Machida6, Satoshi Takahashi7, Chikako Ohwada8, Shin Fujisawa9, Shingo Yano10, Maki Hagihara11, Yoshinobu Kanda12, Masahiro Onoda13, Moritaka Gotoh14, Shinichi Kako15, Jun Taguchi16, Kensuke Usuki17, Nobutaka Kawai18, Nobuyuki Aotsuka19, Shinichiro Okamoto5.
Abstract
Although cytogenetic abnormalities at diagnosis are recognized as an important prognostic factor in patients with Philadelphia chromosome (Ph)-negative acute lymphoblastic leukemia (ALL), the prognostic impact has not been evaluated in allogeneic stem cell transplant (allo-SCT) recipients. Thus, we assessed 373 Ph-negative ALL patients who underwent allo-SCT. The high-risk (HR) group included those with t(4;11), t(8;14), low hypodiploidy, and complex karyotype, and the standard risk (SR) group included all other karyotypes. Among the 204 patients who underwent a transplant during the first remission (167 in the SR group and 37 in the HR group), the overall survival (OS) rates were similar between these groups (64.1% vs. 80.0% at 5 years, respectively; p = 0.12). Conversely, among the 106 patients who underwent a transplant while not in remission (84 in the SR group and 22 in the HR group), patients in the SR group showed a significantly superior OS rate compared to the HR group (15.4% vs. 4.5% at 5 years, respectively; p = 0.022). These results suggested that treatment outcomes of Ph-negative ALL patients with HR cytogenetic abnormalities may improve following allo-SCT, especially in the first remission. Innovative transplant approaches are warranted in patients who are not in remission.Entities:
Mesh:
Year: 2019 PMID: 31186516 DOI: 10.1038/s41409-019-0585-2
Source DB: PubMed Journal: Bone Marrow Transplant ISSN: 0268-3369 Impact factor: 5.483