Abstract
Background: PSMA is a highly restricted cell-surface protein whose expression is increased with grade, stage, and attenuated AR signaling. J591 is a mAb against the external domain of PSMA and has demonstrated safety in numerous human-studies with anti-tumor activity when radiolabeled and conjugated with drug, with PSA and CTC declines. It was originally engineered to elicit antibody-dependent cellular cytotoxicity (ADCC) and we have made 2 important options leading to the current prospective clinical trials. First, studies of 177Lu-J591 have demonstrated >90% CTC control. While initially thought to represent delivery of 177Lu into CTCs and tumors, we retrospectively observed 4 of 7 patients with CTC count decline with a small amount (20 mg) of J591 without an effector molecule when used for imaging. Second, we analyzed long-term follow up from a 2001 study in men with biochemically recurrent or metastatic CRPC where men received unlabeled J591 plus low dose IL-2. Using validated nomograms, pen with biochemical relapse survived a median on 87 months longer than predicted without metastatic disease and in the pre-docetaxel era, men with mCRPC lived a median of 28.5 months longer than predicted. Based upon the preliminary data pointing towards CTC clearance and long-term survival, we have launched 2 prospective clinical trials.
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CITATION STYLE
Tagawa, S. T., Scherr, D., Batra, J., Jhanwar, Y., Robinson, B., Nanus, D., … Bander, N. (2016). Anti-prostate-specific membrane antigen (PSMA) monoclonal antibody (mAb) J591 immunotherapy for prostate cancer. Annals of Oncology, 27, vi265. https://doi.org/10.1093/annonc/mdw372.55
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