The University of Texas, MD Anderson Cancer Center, Houston, TX.
Clin Lymphoma Myeloma Leuk. 2013 Oct;13(5):515-29. doi: 10.1016/j.clml.2013.03.018. Epub 2013 Jul 26.
The development of tyrosine kinase inhibitors (TKIs) has led to extended lifespans for many patients with chronic myelogenous leukemia (CML). However, 20% to 30% of patients fail to respond, respond suboptimally, or experience disease relapse after treatment with imatinib. A key factor is drug resistance. The molecular mechanisms implicated in this resistance include those that involve upregulation or mutation of BCR-ABL kinase and those that are BCR-ABL independent. The clinical consequences of these molecular mechanisms of resistance for disease pathogenesis remain open for debate. This review summarizes the molecular mechanisms and clinical consequences of TKI resistance and addresses the current and future treatment approaches for patients with TKI-resistant CML.
酪氨酸激酶抑制剂(TKIs)的发展使许多慢性髓性白血病(CML)患者的寿命得以延长。然而,仍有 20%至 30%的患者对伊马替尼治疗无反应、反应不佳或出现疾病复发。一个关键因素是药物耐药性。涉及 BCR-ABL 激酶上调或突变以及 BCR-ABL 不依赖的耐药机制与这种耐药性有关。这些耐药分子机制对疾病发病机制的临床后果仍存在争议。本文综述了 TKI 耐药的分子机制和临床后果,并探讨了 TKI 耐药 CML 患者目前和未来的治疗方法。