Stringer Erica M, Fleming Gini F
Fellow.
Professor of Medicine, Department of Medicine, Section of Hematology Oncology, University of Chicago Medical Center, Chicago, IL, US.
Eur Endocrinol. 2013 Mar;9(1):18-21. doi: 10.17925/EE.2013.09.01.18. Epub 2013 Mar 15.
Hormonal therapies such as progestins have only modest activity in the treatment of advanced endometrial cancer. Mechanisms of resistance to progestin therapy are not well understood. However, activation of the PI3K/AKT/mammalian target of rapamycin (mTOR) pathway has been associated with resistance to hormonal therapy and alterations in components of the PI3K/AKT/mTOR pathway, including inactivating mutations in PTEN, activating mutations in PIK3CA and mutations in PIK3R1, are very common in endometrial carcinomas. mTOR inhibitors, including temsirolimus, everolimus and ridaforolimus, are also known to be active against endometrial cancer, and interest has been stimulated in combinations of hormonal treatment with mTOR inhibitors, as both therapies have single-agent activity, and it is hypothesised that mTOR inhibition would enhance sensitivity to hormonal therapy.
诸如孕激素之类的激素疗法在晚期子宫内膜癌的治疗中仅有适度的活性。对孕激素疗法的耐药机制尚未完全了解。然而,PI3K/AKT/雷帕霉素哺乳动物靶蛋白(mTOR)通路的激活与激素疗法耐药相关,并且PI3K/AKT/mTOR通路成分的改变,包括PTEN的失活突变、PIK3CA的激活突变和PIK3R1的突变,在子宫内膜癌中非常常见。mTOR抑制剂,包括替西罗莫司、依维莫司和瑞达福莫司,也已知对子宫内膜癌有活性,并且激素治疗与mTOR抑制剂联合使用引起了人们的兴趣,因为这两种疗法都有单药活性,并且据推测mTOR抑制会增强对激素疗法的敏感性。