論文

査読有り 国際誌
2019年12月

Prognostic impact of cytogenetic abnormalities in adult patients with Philadelphia chromosome-negative ALL who underwent an allogeneic transplant.

Bone marrow transplantation
  • Hiroaki Shimizu
  • Noriko Doki
  • Heiwa Kanamori
  • Toru Sakura
  • Takehiko Mori
  • Shinichiro Machida
  • Satoshi Takahashi
  • Chikako Ohwada
  • Shin Fujisawa
  • Shingo Yano
  • Maki Hagihara
  • Yoshinobu Kanda
  • Masahiro Onoda
  • Moritaka Gotoh
  • Shinichi Kako
  • Jun Taguchi
  • Kensuke Usuki
  • Nobutaka Kawai
  • Nobuyuki Aotsuka
  • Shinichiro Okamoto
  • 全て表示

54
12
開始ページ
2020
終了ページ
2026
記述言語
英語
掲載種別
研究論文(学術雑誌)
DOI
10.1038/s41409-019-0585-2

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.

リンク情報
DOI
https://doi.org/10.1038/s41409-019-0585-2
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/31186516
ID情報
  • DOI : 10.1038/s41409-019-0585-2
  • PubMed ID : 31186516

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