Department of Leukemia, The University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA.
Semin Hematol. 2010 Oct;47(4):371-80. doi: 10.1053/j.seminhematol.2010.06.004.
Imatinib is considered standard frontline therapy for the management of patients with chronic myeloid leukemia (CML). However, it is estimated that approximately one third of patients will fail imatinib therapy. The recommended therapeutic approach for those patients is the use of a second-generation tyrosine kinase inhibitor (TKI) such as nilotinib or dasatinib. With these agents, approximately 50% of patients achieve a complete cytogenetic response (0% Philadelphia chromosome-positive [Ph(+)] bone marrow metaphases), the duration of which has not yet been established. For the remainder, the options are limited to allogeneic stem cell transplantation (SCT) or enrollment on a clinical trial with an investigational agent. Third-generation TKIs and non-adenosine triphosphate (non-ATP) mimetic compounds with activity against ABL1 mutations associated with failure to approved TKIs are under development for patients who either have failed sequential therapy with at least two TKIs or carry the highly resistant T315I mutation. Some of these agents have already shown promising clinical activity.
伊马替尼被认为是治疗慢性髓性白血病(CML)患者的标准一线治疗方法。然而,据估计,大约有三分之一的患者会对伊马替尼治疗产生耐药。对于这些患者,推荐使用第二代酪氨酸激酶抑制剂(TKI),如尼洛替尼或达沙替尼。使用这些药物,约有 50%的患者达到完全细胞遗传学缓解(0%费城染色体阳性[Ph(+)]骨髓中期),其持续时间尚未确定。对于其余患者,选择有限,包括异体干细胞移植(SCT)或参加临床试验,使用针对与批准的 TKI 耐药相关的 ABL1 突变的研究药物。对于那些已经至少接受两种 TKI 序贯治疗失败或携带高度耐药 T315I 突变的患者,正在开发针对 ABL1 突变的第三代 TKI 和非三磷酸腺苷(非-ATP)模拟化合物,这些药物具有活性。其中一些药物已经显示出有希望的临床活性。