Tyrosine kinase domain mutations in chronic myelogenous leukemia patients: A single center experience

被引:6
作者
Bommannan, K. B. [1 ]
Naseem, S. [1 ]
Binota, J. [1 ]
Varma, N. [1 ]
Malhotra, P. [2 ]
Varma, S. [2 ]
机构
[1] Postgrad Inst Med Educ & Res, Dept Hematol, Chandigarh, India
[2] Postgrad Inst Med Educ & Res, Depg Internal Med, Chandigarh, India
关键词
ASO-PCR; imatinib resistance; tyrosine kinase domain mutations; CHRONIC MYELOID-LEUKEMIA; IMATINIB RESISTANCE; INHIBITOR; RECOMMENDATIONS; MANAGEMENT;
D O I
10.4103/jpgm.JPGM_781_20
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Despite the impressive responses achieved with tyrosine kinase inhibitor (TKI) therapy, treatment resistance develops in 16-33% of patients of chronic myelogenous leukemia (CML). Of the BCR-ABL1 dependent mechanisms, mutations in the tyrosine kinase domain (TKD) are the commonest cause of resistance. Material and Methods: Allele specific oligonucleotide - polymerase chain reaction (ASO-PCR) was done for testing the six common TKD mutations, T315I, G250E, E255K, M244V, M351T, and Y253F. Results and Conclusion: TKD mutation study was done on 83 patients. Of these 44 (53%) were positive for one or more mutations. On analyzing specific mutations, E255K was the commonest mutation seen in 24 (29%) cases, followed by T315I in 23(28%) cases. Y253F mutation was not seen in the present study sample. In the present cohort of 83 patients, 29 (35%) cases were positive for single mutation, 12 (14%) had two mutations and 3 (4%) had three mutations.
引用
收藏
页码:93 / 97
页数:5
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