西印度慢性髓系白血病BCR-ABL激酶结构域突变的研究

P. Gadhia, Jessica Jeejan, Vishma Shah, M. Patel, S. Vaniawala
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摘要

背景:BCR-ABL激酶结构域(KD)突变占慢性髓性白血病(CML) -慢行期(CP)伊马替尼耐药的60-80%。接受伊马替尼治疗的CML患者,需要根据欧洲白血病网(ELN)标准进行突变分析,以找出伊马替尼的耐药性。本研究的目的是评估导致印度西部对伊马替尼治疗产生耐药性的不同类型突变。方法:回顾性分析经伊马替尼耐药检测的患者,采用Sanger法对BCR-ABL转录本进行直接测序进行IRMA检测。结果:215例患者进行了伊马替尼耐药分析(IRMA),其中45例(20.93%)检测到突变。T315I位点突变频率最高,其次是M244V位点和G250E位点。结论:IRMA阳性突变率为20.93%,对其耐药情况进行了探讨。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Study on BCR-ABL Kinase Domain Mutations in Chronic Myeloid Leukemia from Western India
Background: BCR-ABL kinase domain(KD) mutations accounts for 60-80% of Imatinib resistance in chronic myeloid leukemia (CML) – chronic phase (CP). Patients with CML who are receiving imatinib treatment, a mutation analysis is required to find out the resistance of imatinib as per European Leukemia Net (ELN) criteria. The present study was carried out to assess for different types of mutations responsible for resistance of imatinib treatment from Western India. Methods: In a retrospective study, the patients who were tested for imatinib resistance were analysed for IRMA testing using direct sequencing of BCR-ABL transcript by Sanger method. Results: A total of 215 patients were tested for Imatinib resistance analysis (IRMA), of which 45 (20.93%) had detectable mutations. The highest frequency of mutation recorded at T315I amino acids site, followed by M244V and G250E sites. Conclusion: The patients who were tested for IRMA showed 20.93 % positive mutations with reference to its resistance are discussed.  
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