Characterization and monitoring by droplet digital PCR of a novel BCR-ABL1 fusion transcript in a patient with chronic myeloid leukemia

J. Petiti, M. Dragani, A. Castelli, M. Loiacono, C. Fantino, C. Badino, A. Serra, E. Giugliano, G. Andreani, Rosso, E. Gottardi, G. Rege‐Cambrin, G. Saglio, D. Cilloni, C. Fava
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引用次数: 1

Abstract

Chronic myeloid leukemia (CML) is characterized by the t(9;22) (q34;q11) translocation which leads to the generation of the BCR-ABL1 protein with constitutive tyrosine kinase activity. BCR-ABL1 is the molecular marker for the evaluation of minimal residual disease (MRD) and its levels throughout the follow up define the depth of molecular remission and guide clinical decisions like change of tyrosine-kinase inhibitor (TKI) or, more recently, discontinuation of therapy [1].
慢性髓性白血病患者新型BCR-ABL1融合转录物的液滴数字PCR表征和监测
慢性髓性白血病(Chronic myeloid leukemia, CML)的特征是t(9;22) (q34;q11)易位,导致BCR-ABL1蛋白产生具有组成型酪氨酸激酶活性。BCR-ABL1是评估最小残留病(MRD)的分子标志物,其在整个随访中的水平定义了分子缓解的深度,并指导临床决策,如改变酪氨酸激酶抑制剂(TKI)或最近停止治疗[1]。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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