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引用次数: 0
摘要
大环激酶抑制剂对多种激酶具有高结合亲和力和选择性,这些激酶包括哺乳动物雷帕霉素靶复合物 1/2、janus 激酶/Fms 类酪氨酸激酶、细胞周期蛋白依赖性激酶和无性淋巴瘤激酶1。最近,一些大环激酶抑制剂已进入临床试验阶段,用于治疗不同类型的癌症,包括白血病、非小细胞肺癌、骨髓纤维化、乳腺癌、胶质母细胞瘤和淋巴瘤。其中,ridaforomilus 已完成 III 期临床试验,正在等待批准用于治疗乳腺癌和晚期白血病。帕克替尼(Pacritinib)目前也正在进行治疗骨髓纤维化的III期临床试验,而罗拉替尼(loratinib)则正在进行治疗晚期ALK基因阳性非小细胞肺癌的评估。广谱细胞周期蛋白依赖性激酶抑制剂 TGO2 也已进入治疗胶质母细胞瘤和晚期白血病的 II 期临床试验。
A review on macrocyclic kinase inhibitors in clinical trials
Macrocyclic kinase inhibitors have high binding affinity and selectivity towards a variety of kinases including mammalian target of rapamycin complex 1/2, janus kinases/ Fms like tyrosine kinase, cyclin-dependent kinases and anaplastic lymphoma kinase1. Recently, few macrocyclic kinase inhibitors have entered clinical trial for treatment different types of cancers including leukemia, non-small cell lung cancer, myelofibrosis, breast cancer, glioblastoma and lymphoma. Of them, ridaforomilus has completed Phase III clinical trial and is waiting to be approved for treatment of breast cancer and advanced leukemia. Pacritinib is also currently being tested in phase III clinical trial for treatment of myelofibrosis and, loratinib is being evaluated for advanced ALK gene positive nonsmall cell lung carcinoma. The broad-spectrum cyclin-dependent kinases inhibitor, TGO2, has also entered phase II clinical trial for treatment of glioblastoma and advanced leukemia.