Jabbour Elias, El Ahdab Samih, Cortes Jorge, Kantarjian Hagop
The University of Texas, MD Anderson Cancer Center, Department of Leukemia, Unit 428, 1515 Holcombe Blvd, Houston, TX 77030, USA.
Expert Opin Investig Drugs. 2008 Jul;17(7):1127-36. doi: 10.1517/13543784.17.7.1127.
The successful introduction of the tyrosine kinase inhibitors has initiated a new era in the management of chronic myeloid leukemia (CML). Imatinib mesilate therapy has significantly improved the prognosis of CML. A minority of patients in chronic-phase CML--and more patients in advanced phases--are resistant to imatinib, or develop resistance during treatment. This is attributed, in 40-50% of cases, to the development of mutations in the Bcr-Abl tyrosine kinase domain that impair imatinib binding. Nilotinib (Tasigna) is a novel potent selective oral kinase inhibitor. Preclinical and clinical investigations demonstrate that nilotinib effectively overcomes imatinib resistance, and has induced high rates of hematologic and cytogenetic responses in CML post imatinib failure.
酪氨酸激酶抑制剂的成功引入开启了慢性髓性白血病(CML)治疗的新纪元。甲磺酸伊马替尼治疗显著改善了CML的预后。少数慢性期CML患者以及更多晚期患者对伊马替尼耐药,或在治疗过程中产生耐药性。在40%-50%的病例中,这归因于Bcr-Abl酪氨酸激酶结构域发生突变,损害了伊马替尼的结合。尼罗替尼(达希纳)是一种新型强效选择性口服激酶抑制剂。临床前和临床研究表明,尼罗替尼能有效克服伊马替尼耐药,并在伊马替尼治疗失败后的CML患者中诱导出高比例的血液学和细胞遗传学反应。