Department of Hematology/Oncology, University of California-San Francisco, San Francisco, CA 94143-1270, USA.
Hematology Am Soc Hematol Educ Program. 2011;2011:121-7. doi: 10.1182/asheducation-2011.1.121.
The 21st century ushered in the dawn of a new era of targeted therapeutics and a dramatic shift in the management of chronic-phase chronic myeloid leukemia (CP-CML) patients. Groundbreaking scientific and translational studies have led to the rapid development and approval of several effective BCR-ABL tyrosine kinase inhibitors (TKIs). In the United States, there are currently 3 approved BCR-ABL TKIs for newly diagnosed CP-CML patients. It is anticipated that clinical outcomes will continue to improve as more TKIs that address unmet medical needs are approved. However, to achieve this goal, it is critical to carefully monitor and optimally manage patients. To this end, the latest seminal clinical trial results of approved and investigational BCR-ABL TKIs and some of the salient unique features of each of these agents are summarized herein.
21 世纪迎来了靶向治疗的新时代,慢性期慢性髓性白血病(CP-CML)患者的治疗管理也发生了重大转变。开创性的科学和转化研究导致了几种有效的 BCR-ABL 酪氨酸激酶抑制剂(TKI)的快速开发和批准。在美国,目前有 3 种批准用于新诊断 CP-CML 患者的 BCR-ABL TKI。随着更多满足未满足医疗需求的 TKI 的批准,预计临床结果将继续改善。然而,要实现这一目标,关键是要仔细监测和优化患者的治疗。为此,本文总结了已批准和研究性 BCR-ABL TKI 的最新主要临床试验结果,以及这些药物的一些独特特征。