Review Article
Molecular Alterations of PI3K/Akt/mTOR Pathway: A Therapeutic Target in Endometrial Cancer
Table 1
PI3k/Akt/mTOR inhibitors in preclinical and clinical studies.
| Drug | Target kinase | Clinical trial phase | | PR | SD | PFS | References |
| Preclinical studies | | | | | | | | CH5132799 | PI3K | | | | | | [86] | NVP-BEZ235 + RAD001 | PI3K/mTOR | | | | | | [72] | LY294002 + OBP-801/YM753 | PI3K/HDAC | | | | | | [87] | Published studies and abstracts | | | | | | | | Temsirolimus | mTOR | Phase II | 19 | 7–26% | 44–69% | 4.3 months | [65, 88] | Ridaforolimus | mTOR | Phase II | 45, 34 | 7% | 26–53% | 16 weeks | [67, 68] | Everolimus | mTOR | Phase II | 35 | 57% | 43% | ≥8 weeks | [64] | MKC-1 | | Phase II | 9 | 55.5% | 44.4% | 1.8 weeks | [85] | Temsirolimus + megestrol + tamoxifen | mTOR | Phase II | 22 | | | | [82] | Everolimus + letrozole | mTOR | Phase II | 28 | | | ≥8 weeks | [83] | Ridaforolimus versus medroxyprogesterone versus chemotherapy | mTOR | Phase II | 53 | | 35% versus 17% | 3.6 versus 1.9 months | [84] |
|
|
: number of patients; PFS: progression free survival; PR: partial response; SD: stable disease.
|