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地福司明(AP23573)是一种处于临床开发阶段的新型雷帕霉素靶蛋白(mTOR)抑制剂。

Deforolimus (AP23573) a novel mTOR inhibitor in clinical development.

作者信息

Mita Monica, Sankhala Kamalesh, Abdel-Karim Issam, Mita Alain, Giles Francis

机构信息

Institute for Drug Development, Cancer Therapy and Research Center, UT Health Science Center, San Antonio, USA.

出版信息

Expert Opin Investig Drugs. 2008 Dec;17(12):1947-54. doi: 10.1517/13543780802556485.

Abstract

mTOR was determined to be a promising anticancer target and several drug inhibitors of mTOR are currently in clinical development. Rapamycin (RAP) was the first mTOR inhibitor discovered. However, RAP has poor aqueous solubility and chemical stability and therefore its utilization at doses susceptible to produce an effect as an anticancer agent is limited. This represented the main rationale for developing new RAP analogs. The RAP analogs currently in clinical development as anticancer agents include temsirolimus (CCI-779), everolimus (RAD-001), and deforolimus (AP23573). These agents have demonstrated antiproliferative activity against a diverse range of malignancies in preclinical studies, and clinical evaluations have been very encouraging thus far. Deforolimus (AP23573), a non-RAP prodrug, has been tested in Phase I and II clinical trials and shows promising results in several tumor types including sarcoma. A Phase III study in patients with sarcoma is currently ongoing. The preclinical and clinical studies with deforolimus will be presented.

摘要

mTOR被确定为一个有前景的抗癌靶点,目前有几种mTOR药物抑制剂正处于临床开发阶段。雷帕霉素(RAP)是最早发现的mTOR抑制剂。然而,RAP的水溶性和化学稳定性较差,因此其作为抗癌药物在有效剂量下的应用受到限制。这是开发新型RAP类似物的主要理论依据。目前作为抗癌药物正在进行临床开发的RAP类似物包括替西罗莫司(CCI-779)、依维莫司(RAD-001)和地福罗莫司(AP23573)。在临床前研究中,这些药物已证明对多种恶性肿瘤具有抗增殖活性,并且迄今为止临床评估结果非常令人鼓舞。地福罗莫司(AP23573)是一种非RAP前药,已在I期和II期临床试验中进行了测试,并在包括肉瘤在内的几种肿瘤类型中显示出有前景的结果。目前正在对肉瘤患者进行III期研究。将介绍地福罗莫司的临床前和临床研究情况。

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