突变
医学
血小板增多症
髓系白血病
酪氨酸激酶
断点群集区域
相伴的
阿布勒
突变频率
费城染色体
癌症研究
内科学
肿瘤科
生物
遗传学
血小板
染色体易位
受体
基因
作者
Nasir Ahmad,Saima Qayum,Abid Jameel,Asif Ali,Sami Siraj,Johar Ali,Yasar Mehmood Yousafzai
出处
期刊:PubMed
日期:2021-11-01
卷期号:34 (6(Supplementary)): 2289-2295
被引量:1
摘要
Chronic Myeloid Leukaemia (CML) is characterized by BCR-ABL1 mutation. A number of research studies have published reports of concomitant JAK2-V617F mutation in BCR-ABL positive Chronic Myeloid Leukaemia. This study aims to investigate the frequency of JAK2-V617F mutation in BCR-ABL positive CML cases. After approval from ethical committee, participants were enrolled in the study. A total of 103 samples from CML patients were analysed for the presence of JAK2-V617F mutation using real-time polymerase chain reaction. Patients were monitored for treatment response using real-time quantitative PCR for BCR-ABL1 mutation. Out of 103 samples analysed, 2 patients tested positive for JAK2-V617F mutation. These two patients when treated with standard Tyrosine Kinase Inhibitors (TKI) therapy achieved molecular response and normalized the haemoglobin and white cell counts. However, one patient has sustained thrombocytosis. JAK2 remained positive throughout the treatment course. We could not follow the second patient till the end of the study. JAK2 mutation in BCR-ABL1 mutated CML appears to be rare. Treatment with TKI does not appear to reduce JAK2 mutation burden despite a decrease in BCR-ABL1 copy numbers.
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