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博舒替尼

Bosutinib.

作者信息

Keller Gunhild, Schafhausen Philippe, Brümmendorf Tim H

机构信息

Department of Hematology and Oncology, University Hospital Aachen, Germany.

出版信息

Recent Results Cancer Res. 2010;184:119-27. doi: 10.1007/978-3-642-01222-8_9.

Abstract

Bosutinib (SKI-606) is a 7-alkoxy-3-quinolinecarbonitrile, which functions as a dual inhibitor of Src and Abl kinases. In biochemical and proliferation assays, the compound was shown to be active against src family kinases and Bcr-Abl at IC50s of 100 and 90 nM, respectively. The bcr-abl fusion gene product, a consecutively activated tyrosine kinase, which is crucial for the development of chronic myeloid leukaemia (CML), is highly sensitive to bosutinib. Interestingly, distinctly lower concentrations of the dual src/abl inhibitor are required to ablate Bcr-Abl phosphorylation when compared to first-generation tyrosine kinase inhibitor imatinib (IM). Bosutinib is a potent inhibitor of CML cell proliferation in vitro and in vivo experiments and has demonstrated promising harbouring results in CML patients resistance or intolerance to IM in ongoing phase I/II clinical trials. Remarkably, bosutinib has been found to be capable of overcoming the majority of IM-resistant bcr-abl mutations. A randomised open label phase III clinical study to compare the efficacy of bosutinib and IM in first-line therapy of Ph+ chronic phase (CP) CML has recently been initiated. In a phase I/II clinical study with subjects suffering from advanced stages of solid tumours, long-term responses have also been reported. In conclusion, Bosutinib is a promising novel small molecule inhibitor for targeted therapy of CML and solid tumours.

摘要

博舒替尼(SKI-606)是一种7-烷氧基-3-喹啉腈,它作为Src和Abl激酶的双重抑制剂发挥作用。在生化和增殖试验中,该化合物对src家族激酶和Bcr-Abl具有活性,其IC50分别为100 nM和90 nM。bcr-abl融合基因产物是一种持续激活的酪氨酸激酶,对慢性髓性白血病(CML)的发展至关重要,对博舒替尼高度敏感。有趣的是,与第一代酪氨酸激酶抑制剂伊马替尼(IM)相比,消除Bcr-Abl磷酸化所需的双重src/abl抑制剂浓度明显更低。在体外和体内实验中,博舒替尼是CML细胞增殖的有效抑制剂,并且在正在进行的I/II期临床试验中,已在对IM耐药或不耐受的CML患者中显示出有前景的疗效。值得注意的是,已发现博舒替尼能够克服大多数IM耐药的bcr-abl突变。最近启动了一项随机开放标签III期临床研究,以比较博舒替尼和IM在Ph+慢性期(CP)CML一线治疗中的疗效。在一项针对患有实体瘤晚期患者的I/II期临床研究中,也报告了长期缓解情况。总之,博舒替尼是一种有前景的新型小分子抑制剂,用于CML和实体瘤的靶向治疗。

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