Coexistence of BCR-ABL1 reassortment and JAK2 V617F mutation in chronic myeloid leukaemia.

Jianjun Yang Cheeloo, Kehong Bi, Zhaoguang Zhang
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Abstract

Myeloproliferative neoplasms (MPNs) can be classified into two major categories, namely chronic myeloid leukaemia (CML) and Philadelphia-negative MPNs (PN-MPNs). BCR- ABL1 reassortment is an irreplaceable indicator for the diagnosis of typical CML, while the V617F mutation on the Janus kinase 2 (JAK2) gene is common in PN-MPNs patients. Generally, these two genetic abnormalities are considered unable to coexist. We report a patient with CML who had both genetic changes, suggesting that when tyrosine kinase inhibitors (TKIs) monotherapy cannot obtain satisfactory treatment outcomes in CML patients, another possibility besides disease progression is a mutation on the JAK2 V617F gene.

BCR-ABL1重组和JAK2 V617F突变在慢性髓性白血病中的共存
骨髓增生性肿瘤(mpn)可分为两大类,即慢性髓性白血病(CML)和费城阴性mpn (pn - mpn)。BCR- ABL1重排是诊断典型CML不可替代的指标,而JAK2基因V617F突变在PN-MPNs患者中很常见。一般来说,这两种基因异常被认为是不能共存的。我们报道了一名同时存在两种基因改变的CML患者,这表明当酪氨酸激酶抑制剂(TKIs)单药治疗在CML患者中不能获得满意的治疗结果时,除了疾病进展外,另一种可能性是JAK2 V617F基因突变。
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