前列腺癌
医学
阉割
癌症
肿瘤科
癌症研究
内科学
前列腺
激素
作者
Petra Deegen,Oliver S. Thomas,Olivier Nolan-Stevaux,Shyun Li,Joachim Wahl,Pamela Bogner,Famke Aeffner,Matthias Friedrich,Michael Z. Liao,Katja Matthes,Doris Rau,Benno Rattel,Tobias Raum,Peter Kufer,Angela Coxon,Julie M. Bailis
标识
DOI:10.1158/1078-0432.ccr-20-3725
摘要
PURPOSE: Metastatic castration-resistant prostate cancer (mCRPC) remains a disease with high unmet medical need, as most patients do not achieve durable response with available treatments. Prostate-specific membrane antigen (PSMA) is a compelling target for mCRPC. It is highly expressed by primary and metastatic prostate cancer cells, with increased expression after progression on androgen deprivation therapy. EXPERIMENTAL DESIGN: and in mCRPC xenograft models. AMG 160 tolerability was assessed in nonhuman primates (NHP). AMG 160 activity as monotherapy and in combination with a PSMA-imaging agent, novel hormonal therapy, and immune checkpoint blockade was evaluated. RESULTS: , AMG 160 administered weekly at 0.2 mg/kg engages T cells administered systemically and promotes regression of established 22Rv-1 mCRPC xenograft tumors. AMG 160 is compatible with the imaging agent gallium 68-labeled PSMA-11, and shows enhanced cytotoxic activity when combined with enzalutamide or an anti-programmed death-1 antibody. AMG 160 exhibits an extended half-life and has an acceptable safety profile in NHPs. CONCLUSIONS: .
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