| Literature DB >> 30065100 |
Song Cho1, Francesca Zammarchi2, David G Williams3, Carin E G Havenith4, Noel R Monks5, Peter Tyrer3, Francois D'Hooge3, Ryan Fleming5, Kapil Vashisht5, Nazzareno Dimasi5, Francois Bertelli3, Simon Corbett3,6, Lauren Adams3, Halla W Reinert6, Sandamali Dissanayake4, Charles E Britten4, Wanda King5, Karma Dacosta5, Ravinder Tammali5, Kevin Schifferli5, Patrick Strout5, Martin Korade5, Mary Jane Masson Hinrichs5, Simon Chivers4, Eva Corey7, He Liu8, Sae Kim8, Neil H Bander8, Philip W Howard3, John A Hartley3,6, Steve Coats5, David A Tice5, Ronald Herbst5, Patrick H van Berkel4.
Abstract
Prostate-specific membrane antigen (PSMA) is a membrane-bound glutamate carboxypeptidase that is highly expressed in nearly all prostate cancers with the highest expression in metastatic castration-resistant prostate cancer (mCRPC). The prevalence of increased surface expression and constitutive internalization of PSMA make it an attractive target for an antibody-drug conjugate (ADC) approach to treating patients with mCRPC. MEDI3726 (previously known as ADCT-401) is an ADC consisting of an engineered version of the anti-PSMA antibody J591 site specifically conjugated to the pyrrolobenzodiazepine (PBD) dimer tesirine. MEDI3726 specifically binds the extracellular domain of PSMA and, once internalized, releases the PBD dimer to crosslink DNA and trigger cell death. In vitro, MEDI3726 demonstrated potent and specific cytotoxicity in a panel of PSMA-positive prostate cancer cell lines, consistent with internalization and DNA interstrand crosslinking. In vivo, MEDI3726 showed robust antitumor activity against the LNCaP and the castration-resistant CWR22Rv1 prostate cancer cell line xenografts. MEDI3726 also demonstrated durable antitumor activity in the PSMA-positive human prostate cancer patient-derived xenograft (PDX) LuCaP models. This activity correlated with increased phosphorylated Histone H2AX in tumor xenografts treated with MEDI3726. MEDI3726 is being evaluated in a phase I clinical trial as a treatment for patients with metastatic castrate-resistant prostate cancer (NCT02991911). Mol Cancer Ther; 17(10); 2176-86. ©2018 AACR. ©2018 American Association for Cancer Research.Entities:
Mesh:
Substances:
Year: 2018 PMID: 30065100 DOI: 10.1158/1535-7163.MCT-17-0982
Source DB: PubMed Journal: Mol Cancer Ther ISSN: 1535-7163 Impact factor: 6.261