CDKN2A
多重连接依赖探针扩增
造血干细胞移植
微小残留病
肿瘤科
移植
白血病
癌症研究
医学
内科学
拷贝数变化
生物
免疫学
基因
遗传学
癌症
基因组
外显子
作者
Makoto Onizuka,Eri Kikkawa,Shinichiro Machida,Masako Toyosaki,Rikio Suzuki,Daisuke Ogiya,Yasuyuki Aoyama,Jun Amaki,Kaito Harada,Ryujiro Hara,Sawako Shiraiwa,Yoshiaki Ogawa,Hiroshi Kawada,Kiyoshi Ando
出处
期刊:Blood cell therapy
[Asia-Pacific Blood and Marrow Transplantation Group]
日期:2023-01-01
卷期号:6 (3)
标识
DOI:10.31547/bct-2023-004
摘要
The most important prognostic factor for Philadelphia chromosome-positive acute lymphoblastic leukemia (Ph+ALL) is minimal residual disease (MRD).Previous studies have reported copy number variants of genes such as IKZF1, CDKN2A/2B, and PAX5.These gene mutations can be analyzed using multiplex ligation-dependent probe amplification (MLPA), which is less costly and easier to perform than large-scale gene mutation analyses.In this study, we performed copy number variant analysis of leukemia cells at the first onset of Ph+ALL in a case series of allogeneic hematopoietic stem cell transplantation (allo-HSCT) using the MLPA method.We analyzed how it influenced allo-HSCT prognosis together with MRD information.CDKN2A/2B copy number variations significantly increased the rate of post-transplant recurrence (P=0.025) and significantly reduced disease-free survival (P=0.015).Additionally, patients with IKZF1 deletions had a significantly higher post-transplant recurrence rate (P=0.042).Although they were positive for pre-transplant MRD, no relapse was observed in patients with wild-type copy number variations in IKZF1 or CDKN2A/2B.CDKN2A/2B copy number variation is a crucial factor that can be confirmed at initial onset as a post-transplant prognostic factor of Ph+ALL.
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