MISC

査読有り
2012年8月

Clinical significance of minimal residual disease detected by multidimensional flow cytometry: Serial monitoring after allogeneic stem cell transplantation for acute leukemia

LEUKEMIA RESEARCH
  • Takuya Miyazaki
  • Hiroyuki Fujita
  • Katsumichi Fujimaki
  • Takeshi Hosoyama
  • Reina Watanabe
  • Takayoshi Tachibana
  • Atsuko Fujita
  • Kenji Matsumoto
  • Masatsugu Tanaka
  • Hideyuki Koharazawa
  • Jun Taguchi
  • Naoto Tomita
  • Rika Sakai
  • Shin Fujisawa
  • Heiwa Kanamori
  • Yoshiaki Ishigatsubo
  • 全て表示

36
8
開始ページ
998
終了ページ
1003
記述言語
英語
掲載種別
DOI
10.1016/j.leukres.2012.04.005
出版者・発行元
PERGAMON-ELSEVIER SCIENCE LTD

We analyzed minimal residual disease (MRD) by multidimensional flow cytometry (MFC) after allogeneic stem cell transplantation in 41 patients with acute myeloid leukemia (AML) (n = 31) or acute lymphoblastic leukemia (ALL) (n = 10). Aberrant antigen expression was compared with the results of quantitative PCR for WT1 mRNA (n = 41) and leukemia-specific fusion transcripts (n = 12; AML in seven, ALL in five). There was a significant correlation between detection of MRD by MFC and WT1 mRNA, as well as between MFC and fusion transcripts. Serial monitoring of MRD by the three techniques correlated in parallel to the clinical course in most of the patients, but three patients were only positive for WT1 during hematological remission. The overall survival time of patients with complete remission was significantly associated with the appearance of aberrant expression after transplantation. In conclusion, MFC is valuable for clinical management decisions after transplantation. (C) 2012 Elsevier Ltd. All rights reserved.

リンク情報
DOI
https://doi.org/10.1016/j.leukres.2012.04.005
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/22551655
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000305823000020&DestApp=WOS_CPL
ID情報
  • DOI : 10.1016/j.leukres.2012.04.005
  • ISSN : 0145-2126
  • PubMed ID : 22551655
  • Web of Science ID : WOS:000305823000020

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