Abstract

Develop a 64Cu labeled radiopharmaceutical targeting prostate specific membrane antigen (PSMA) and investigate its application for prostate cancer imaging. 64Cu-PSMA-BCH was prepared and investigated for stability, PSMA specificity, and micro-PET imaging. With the approval of Ethics Committee of Beijing Cancer Hospital (No. 2017KT97), PET/CT imaging in 4 patients with suspected prostate cancer was performed and the radiation dosimetry was estimated. Then, PSMA PET-ultrasound image-guided biopsies were performed on 3 patients and the fine needle aspirates were further performed for autoradiography and immunohistochemistry analysis. 64Cu-PSMA-BCH was prepared with high radiochemical yield and stability. In vivo study showed higher uptake in PSMA ( +) 22Rv1 cells than PSMA ( -) PC-3 cells (5.59 ± 0.36 and 1.97 ± 0.22 IA%/106 cells at 1h). It accumulated in 22Rv1 tumor with increasing radioactivity uptake and T/N ratios from 1 to 24h post-injection. In patients with suspected prostate cancer, SUVmax and T/N ratios increased within 24h post-injection. Compared with image at 1h post-injection, more tumor lesions were detected at 6h and 24h post-injection. The human organ radiation dosimetry showed gallbladder wall was most critical, liver and kidneys were followed, and the whole-body effective dose was 0.0292mSv/MBq. Two fine needle aspirates obtained by PET-ultrasound-guided targeted biopsy showed high radioactive signal by autoradiography, with 100% PSMA expression in cytoplasm and 30% expression in nucleus. 64Cu-PSMA-BCH was PSMA specific and showed high stability in vivo with lower uptake in liver than 64Cu-PSMA-617. Biodistribution in mice and PCa patients showed similar profile compared with other PSMA ligands and it was safe with moderate effective dosimetry. The increased tumor uptake and T/N ratios by delayed imaging may facilitate the detection of small lesions and guiding targeted biopsies.

Highlights

  • Prostate cancer (PCa) is common among men

  • 64Cu-prostate specific membrane antigen (PSMA)-BCH was prepared with high radiochemical yield and stability

  • Biodistribution in mice and PCa patients showed similar profile compared with other PSMA ligands and it was safe with moderate effective dosimetry

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Summary

Introduction

Prostate cancer (PCa) is common among men. PSMA PET/CT has shown high sensitivity and specificity in identifying sites of PCa, and some studies have demonstrated that PSMA-based PET/CT and PET/MR can give accurate location of tumor lesions in primary PCa superior to MRI [1, 2], which offers the possibility that PSMA PET images prior to biopsy giving a simpler criteria for targeted biopsy. Limited by the short half-life of 68Ga, the images were obtained at 1 h post injection (p.i.) with high radioactivity in bladder, which lead the low contrast between the PCa and background. Radiopharmaceuticals labeled with radionuclides having longer half-life can be used in delayed imaging, potentially leading to higher tumor-to-background contrast. Because of the internalization of PSMA radiotracers, the contrast in tumor lesions increases at longer time points after injection, with the radioactivity in non-target organs significantly decreasing at later time points. Among such radionuclides, copper-64 (64Cu) was deemed to be a good choice due to its moderate half-life (12.7 h) and high resolution [4]

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