Deininger Michael W N, Holyoake Tessa L
Oregon Health and Science University, USA.
Blood. 2005 Mar 1;105(5):1840-1. doi: 10.1182/blood-2004-12-4764.
In patients with chronic myelogenous leukemia (CML) mutations of the BCR-ABL kinase domain (KD) have been identified as the leading cause of acquired resistance to imatinib, while the mechanisms underlying the persistence of minimal residual disease (MRD) are unknown. In this issue of Blood, Chu and colleagues report several patients with KD mutations at the time of complete cytogenetic response (CCR), implicating mutations as a cause of disease persistence.
在慢性髓性白血病(CML)患者中,BCR-ABL激酶结构域(KD)的突变已被确定为对伊马替尼获得性耐药的主要原因,而微小残留病(MRD)持续存在的潜在机制尚不清楚。在本期《血液》杂志中,朱及其同事报告了几例在完全细胞遗传学缓解(CCR)时出现KD突变的患者,提示突变是疾病持续存在的一个原因。