Ridaforolimus: a promising drug in the treatment of soft-tissue sarcoma and other malignancies

被引:1
作者
Dancey, Janet E. [1 ]
Monzon, Jose [1 ]
机构
[1] Queens Univ, NCIC Clin Trials Grp, Kingston, ON K7L 3N6, Canada
关键词
mTOR; ridaforolimus; sarcoma; PHASE-I TRIAL; RAPAMYCIN INHIBITOR; MAMMALIAN TARGET; DEFOROLIMUS AP23573; MK-8669; GEMCITABINE; THERAPY;
D O I
10.2217/FON.11.57
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Ridaforolimus (deforolimus; AP23573; MK-8669) is a novel sirolimus derivative manufactured by ARIAD Pharmaceuticals and acquired by Merck. It is a small-molecule kinase inhibitor of the mTOR in clinical development for the treatment of cancer. Both intravenous and oral formulations of the agent are being tested in cancer clinical trials. In preclinical and clinical studies, ridaforolimus exhibited significant antitumor activity with acceptable safety and tolerability. With single-agent ridaforolimus, mucositis and myelosuppression were dose-limiting toxicities. In advanced soft-tissue sarcoma, single-agent ridaforolimus was associated with a 29% clinical benefit rate and 2% partial response rate. A Phase III trial has recently been reported to have met its primary end point.
引用
收藏
页码:827 / 839
页数:13
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