Druker B
Department of Medicine, Division of Hematology and Medical Oncology, Oregon Health and Science University, Portland, OR 97201, USA.
Semin Hematol. 2001 Jul;38(3 Suppl 8):9-14. doi: 10.1016/s0037-1963(01)90112-x.
The tyrosine kinase inhibitor, imatinib mesylate (Gleevec, Novartis Pharmaceuticals Corp, East Hanover, NJ) (formerly STI571) showed significant antileukemic activity with minimal toxicity in preclinical studies. Based on these data, a phase I clinical trial was conducted in patients with chronic myeloid leukemia (CML) who failed other treatment options. Once therapeutic doses were attained, 53 of 54 patients (98%) in the chronic phase achieved hematologic remissions. With prolonged therapy of 2 to 5 months duration, a growing percentage of patients achieved cytogenetic responses. Imatinib mesylate also has activity as a single agent in CML blast crisis and in patients with Ph(+) acute lymphocytic leukemia (ALL). Although responses tend not to be durable, 20% of patients with myeloid blast crisis are in continuous remission for periods up to 1 year. Ongoing clinical studies are directed at optimizing the use of imatinib mesylate.
酪氨酸激酶抑制剂甲磺酸伊马替尼(格列卫,诺华制药公司,新泽西州东哈嫩)(原STI571)在临床前研究中显示出显著的抗白血病活性且毒性极小。基于这些数据,对其他治疗方案无效的慢性髓性白血病(CML)患者进行了I期临床试验。一旦达到治疗剂量,54例慢性期患者中有53例(98%)实现血液学缓解。经过2至5个月的延长治疗,实现细胞遗传学缓解的患者比例不断增加。甲磺酸伊马替尼作为单一药物在CML急变期和Ph(+)急性淋巴细胞白血病(ALL)患者中也有活性。尽管缓解往往不持久,但20%的髓性急变期患者持续缓解长达1年。正在进行的临床研究旨在优化甲磺酸伊马替尼的使用。