Blast phase of chronic myeloid leukemia with concurrent BCR::ABL1 and SET::NUP214: A report of two cases

被引:3
|
作者
Chen, Yan [1 ]
Wang, Qian [1 ]
Cen, Jiannong [1 ]
Xu, Chao [1 ]
Tao, Ting-ting [1 ]
Xie, Jundan [1 ]
Shen, Wenhong [1 ]
Gong, Yanlei [1 ]
Pan, Jinlan [1 ]
Yao, Li [1 ,2 ]
机构
[1] Soochow Univ, Affiliated Hosp 1, NHC Key Lab Thrombosis & Hemostasis, Jiangsu Inst Hematol,Natl Clin Res Ctr Hematol Di, Suzhou, Peoples R China
[2] Soochow Univ, Collaborat Innovat Ctr Hematol, Suzhou, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
BCR; ABL1; blast phase; chronic myeloid leukemia; SET; NUP214; CHRONIC MYELOGENOUS LEUKEMIA; FUSION GENES; SET-NUP214; IMPACT; ERA; RESISTANCE; FEATURES; CML;
D O I
10.1002/mc.23480
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Chronic myeloid leukemia (CML) is a myeloproliferative neoplasm defined by the presence of t(9;22)(q34;q11.2)/BCR::ABL1. Additional chromosomal abnormalities play an important role in the progression to CML. However, the additional fusion gene was rarely reported such as CBFB::MYH11. In this report, we described two cases of the co-occurrence of BCR::ABL1 and SET::NUP214 in CML-BP for the first time, which is associated with poor outcomes during tyrosine kinase inhibitor (TKI) treatment. Meanwhile, we retrospectively analyzed SET::NUP214 fusion transcript of the two cases at initial diagnosis of the CML chronic phase by quantitative RT-PCR, and detected at a ratio of 1.63% and 1.50%, respectively. SET::NUP214 may promote disease progression during the transformation of CML. This study highlights the importance of extended molecular testing at the initial diagnosis of CML-CP at TKI resistance and/or disease transformation.
引用
收藏
页码:117 / 121
页数:5
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