The Ontario Institute for Cancer Research, MaRS Centre, 101 College Street, Toronto, ON, Canada.
Semin Oncol. 2009 Dec;36 Suppl 3:S46-58. doi: 10.1053/j.seminoncol.2009.10.010.
Activation of mammalian target of rapamycin (mTOR) signaling occurs in a wide variety of human tumors and can lead to increased susceptibility to mTOR inhibitors. Temsirolimus, a novel analog of rapamycin, has shown promising preclinical and early clinical anti-tumor activity in various solid and hematologic tumor types, either alone or in combination with chemotherapy or other targeted agents. Randomized phase III trials have already demonstrated significant clinical benefits of treatment with single-agent temsirolimus in advanced renal cell carcinoma and relapsed and/or refractory mantle cell lymphoma. Other malignancies studied in the phase I and II trial settings include glioblastoma, breast cancer, endometrial cancer, non-Hodgkin lymphomas, and multiple myeloma. This article reviews a comprehensive collection of the clinical trial results reported to date for temsirolimus in various solid and hematologic malignancies, as well as current strategies being tested in ongoing trials. The findings with temsirolimus in multiple tumors provide a valuable framework for future development of temsirolimus and other mTOR inhibitors.
哺乳动物雷帕霉素靶蛋白(mTOR)信号的激活发生在多种人类肿瘤中,并且可能导致对 mTOR 抑制剂的敏感性增加。替西罗莫司是一种新型雷帕霉素类似物,在各种实体瘤和血液系统肿瘤类型中,无论是单独使用还是与化疗或其他靶向药物联合使用,都显示出有希望的临床前和早期抗肿瘤活性。随机 III 期试验已经证明了单药替西罗莫司治疗晚期肾细胞癌和复发性和/或难治性套细胞淋巴瘤的显著临床益处。在 I 期和 II 期试验中研究的其他恶性肿瘤包括胶质母细胞瘤、乳腺癌、子宫内膜癌、非霍奇金淋巴瘤和多发性骨髓瘤。本文综述了迄今为止报告的替西罗莫司在各种实体瘤和血液系统恶性肿瘤中的临床试验结果,以及目前正在进行的试验中正在测试的当前策略。替西罗莫司在多种肿瘤中的研究结果为替西罗莫司和其他 mTOR 抑制剂的未来开发提供了有价值的框架。