Title | Imaging Patients with Metastatic Castration-Resistant Prostate Cancer Using Zr-DFO-MSTP2109A Anti-STEAP1 Antibody. |
Publication Type | Journal Article |
Year of Publication | 2019 |
Authors | Carrasquillo JA, Fine BM, Pandit-Taskar N, Larson SM, Fleming SE, Fox JJ, Cheal SM, O'Donoghue JA, Ruan S, Ragupathi G, Lyashchenko SK, Humm JL, Scher HI, Gönen M, Williams SP, Danila DC, Morris MJ |
Journal | J Nucl Med |
Volume | 60 |
Issue | 11 |
Pagination | 1517-1523 |
Date Published | 2019 11 |
ISSN | 1535-5667 |
Keywords | Aged, Aged, 80 and over, Antigens, Neoplasm, Humans, Immunoconjugates, Male, Middle Aged, Neoplasm Metastasis, Oxidoreductases, Positron Emission Tomography Computed Tomography, Prostatic Neoplasms, Castration-Resistant, Radioisotopes, Radiometry, Tissue Distribution, Zirconium |
Abstract | Six-transmembrane epithelial antigen of prostate-1 (STEAP1) is a relatively newly identified target in prostate cancer. We evaluated the ability of PET/CT with Zr-DFO-MSTP2109A, an antibody that recognizes STEAP1, to detect lesions in patients with metastatic castration-resistant prostate cancer (mCRPC). Nineteen mCRPC patients were prospectively imaged using approximately 185 MBq/10 mg of Zr-DFO-MSTP2109A. Zr-DFO-MSTP2109A PET/CT images obtained 4-7 d after injection were compared with bone and CT scans. Uptake in lesions was measured. Fifteen patients were treated with an antibody-drug conjugate (ADC) based on MSTP2109A; ADC treatment-related data were correlated with tumor uptake by PET imaging. Bone or soft-tissue biopsy samples were evaluated. No significant toxicity occurred. Excellent uptake was observed in bone and soft-tissue disease. Median SUV was 20.6 in bone and 16.8 in soft tissue. Sixteen of 17 lesions biopsied were positive on Zr-DFO-MSTP2109A, and all sites were histologically positive (1 on repeat biopsy). Bayesian analysis resulted in a best estimate of 86% of histologically positive lesions being true-positive on imaging (95% confidence interval, 75%-100%). There was no correlation between SUV tumor uptake and STEAP1 immunohistochemistry, survival after ADC treatment, number of ADC treatment cycles, or change in prostate-specific antigen level. Zr-DFO-MSTP2109A is well tolerated and shows localization in mCRPC sites in bone and soft tissue. Given the high SUV in tumor and localization of a large number of lesions, this reagent warrants further exploration as a companion diagnostic in patients undergoing STEAP1-directed therapy. |
DOI | 10.2967/jnumed.118.222844 |
Alternate Journal | J Nucl Med |
PubMed ID | 31053681 |
PubMed Central ID | PMC6836860 |
Grant List | P30 CA008748 / CA / NCI NIH HHS / United States |
Related Institute:
Molecular Imaging Innovations Institute (MI3)