Nadal E, Olavarria E
Haematology Department, Hammersmith Hospital, Imperial College, London, UK.
Int J Clin Pract. 2004 May;58(5):511-6. doi: 10.1111/j.1368-5031.2004.00173.x.
Imatinib mesylate (Gleevec/Glivec, Novartis, Basel, Switzerland), formerly called STI571, is a specific and potent inhibitor of the BCR-ABL tyrosine kinase, the molecular hallmark of chronic myeloid leukaemia. Several clinical trials have demonstrated the efficacy of imatinib in different phases of this disease. On the other hand, imatinib is also active against other tyrosine kinases, such as ABL, the stem cell factor receptor (c-kit) and the platelet-derived growth factor receptor, whose inhibition might have potential implications for the treatment of several malignancies. In this regard, imatinib has already shown a remarkable activity in patients with hypereosinophilic syndrome and gastrointestinal stromal tumours. Imatinib is an example of how a better understanding of the pathogenetic mechanisms of a neoplastic disease can lead to the development of a molecular-targeted therapy.
甲磺酸伊马替尼(格列卫,诺华公司,瑞士巴塞尔),曾称STI571,是一种特异性强效BCR-ABL酪氨酸激酶抑制剂,而BCR-ABL酪氨酸激酶是慢性髓性白血病的分子标志。多项临床试验已证明伊马替尼在该疾病不同阶段的疗效。另一方面,伊马替尼对其他酪氨酸激酶也有活性,如ABL、干细胞因子受体(c-kit)和血小板衍生生长因子受体,抑制这些激酶可能对多种恶性肿瘤的治疗具有潜在意义。在这方面,伊马替尼已在高嗜酸性粒细胞综合征和胃肠道间质瘤患者中显示出显著活性。伊马替尼是一个例子,说明对肿瘤疾病发病机制的更好理解如何能够促成分子靶向治疗的发展。