Main clinical trials of ADCs in endometrial and cervical cancer
Target | ADC | Trial | Phase | Setting | Treatment | Primary endpoint | Results |
---|---|---|---|---|---|---|---|
HER2 | T-DM1 | NCT02675829 [83] | II | HER2 pos tumors including endometrial cancer | T-DM1 | ORR | ORR: 22% |
NCT02465060 [84] | II | HER2 pos including endometrial and ovarian cancer | T-DM1 | ORR | ORR: 9% | ||
FRα | Mirvetuximab soravtansine | NCT01609556 [60] | I | FRα pos tumors including metastatic endometrial cancer | Mirvetuximab soravtansine | MTD/RP2D | ORR: 0% |
Trop2 | Sacituzumab govitecan | IMMU-132-01(NCT01631552) [85] | I/II | Advanced epithelial cancer including endometrial, cervical and ovarian cancer | Sacituzumab govitecan | Safety (phase I)ORR (phase II) | ORR: 22.2% |
TF | Tisotumab vedotin | InnovaTV 204(NCT03438396) [86] | II | Previously treated recurrent or metastatic cervical cancer | Tisotumab vedotin | ORR | ORR: 24%PFS: 4.2 months |
InnovaTV 205(NCT03786081) [87] | I/II | Recurrent or metastatic cervical cancer, first line | Tisotumab vedotin + carboplatin | DLT (phase I)ORR (phase II) | ORR: 55%PFS: 9.5 months | ||
Recurrent or metastatic cervical cancer, second or third line | Tisotumab vedotin + pembrolizumab | DLT (phase I)ORR (phase II) | ORR: 38%PFS: 5.6 months |
MN and IC contributed to the conception and design of the manuscript. MN and IC wrote the first draft of the manuscript. MN, MDG, CS, and IC contributed to literature analysis. All authors contributed to manuscript revision, read and approved the submitted version.
Ilaria Colombo: travel grants from Tesaro; technical support from: AstraZeneca (AZ), GlaxoSmithKline (GSK), Novartis, Merck Sharpe and Dohme (MSD); institutional grants for clinical trials (PI) from MSD, Bayer, Oasmia. None of the other authors have a conflict of interest.
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© The Author(s) 2022.