Theranostic Potential of the iPSMA-Bombesin Radioligand in Patients with Metastatic Prostate Cancer: A Pilot Study
<b>Background/Objectives:</b> Prostate cancer (PC) represents the second most diagnosed form of cancer in men on a global scale. Despite the theranostic efficacy of prostate-specific membrane antigen (PSMA) radioligands, there is a spectrum of PC disease in which PSMA expression is low or absent. The gastrin-releasing peptide receptor (GRPR), also known as the bombesin type 2 receptor, has been identified as a target in both the early and advanced stages of PC. The objective of this study was to prepare and preclinically evaluate [<sup>99m</sup>Tc]Tc-iPSMA-Bombesin ([<sup>99m</sup>Tc]Tc-iPSMA-BN), estimate dosimetry in healthy subjects, and assess the diagnostic efficacy of the radiotracer in patients with metastatic PC, with the hypothesis of non-inferiority to one of the gold standards, [<sup>18</sup>F]-PSMA-1007. Moreover, the potential of [<sup>99m</sup>Tc]Tc-iPSMA-BN as a theranostic pair with [<sup>177</sup>Lu]Lu-iPSMA-BN was investigated. <b>Methods:</b> [<sup>99m</sup>Tc]Tc-iPSMA-BN was prepared under GMP conditions with radiochemical purities > 95%, showing specific recognition by PSMA and GRP receptors in prostate cancer cells and mice bearing PC tumors. Six healthy volunteers were enrolled, and [<sup>99m</sup>Tc]Tc-iPSMA-BN SPECT/CT imaging (740 MBq) was performed to estimate the dosimetry. The pilot clinical study included seven mCRPC and four mCSPC patients with prior androgen deprivation therapy. All patients had a recent [<sup>18</sup>F]-PSMA-PET/CT scan and were enrolled in this prospective study on their own signed behalf. Volumetric lesion target-to-background ratios (TBRs) were obtained from PET/CT and SPECT/CT images. <b>Results:</b> [<sup>99m</sup>Tc]Tc-iPSMA-BN effective radiation dose was 1.94 ± 0.39 mSv/740 MBq. A total of 178 lesions were detected via CT, 162 via [<sup>18</sup>F]-PSMA-1007 PET, and 155 via [<sup>99m</sup>Tc]Tc-iPSMA-BN SPECT. Three patients with mCRPC had higher TBR values on SPECT than on PET. [<sup>99m</sup>Tc]Tc-iPSMA-BN appears to have better lesion detection in patients with aggressive histologic transformation. Two-way ANOVA analysis revealed a significant difference in TBR values between patients with mCRPC and mCSPC (<i>p</i> < 0.05) but no difference between [<sup>18</sup>F]-PSMA-1007 and [<sup>99m</sup>Tc]Tc-iPSMA-BN (<i>p</i> > 0.05). In one patient, [<sup>177</sup>Lu]Lu-iPSMA-BN showed a high correlation with [<sup>99m</sup>Tc]Tc-iPSMA-BN for lesions that concentrated radioactivity. <b>Conclusions:</b> [<sup>99m</sup>Tc]Tc-iPSMA-BN SPECT/CT is a promising alternative not only for diagnostic purposes but also for broadening the spectrum of PC patients who may benefit from radionuclide theranostics. The results justify the development of a clinical trial involving a significant number of patients with PC.
Authors
- Guillermina Ferro‐Flores (ORCID: https://orcid.org/0000-0003-0296-7605)
- Myrna Luna‐Gutiérrez (ORCID: https://orcid.org/0000-0002-4082-3816)
- Clara Santos‐Cuevas (ORCID: https://orcid.org/0000-0001-5903-1598)
- Blanca Ocampo‐García (ORCID: https://orcid.org/0000-0002-5831-8412)
- Joel E. Vargas-Ahumada (ORCID: https://orcid.org/0009-0003-9057-6109)
- Francisco O. García-Pérez (ORCID: https://orcid.org/0000-0002-1781-0793)
- Laura Meléndez‐Alafort (ORCID: https://orcid.org/0000-0003-0701-3616)
- Gerardo Ramírez-Nava (ORCID: https://orcid.org/0000-0002-3128-1744)
- Erika Azorín‐Vega (ORCID: https://orcid.org/0000-0002-7520-461X)
- Sofía Denisse González-Rueda (ORCID: https://orcid.org/0009-0003-1079-0464)
Institutions
- Instituto Nacional de Investigaciones Nucleares (MX)
- Istituto Oncologico Veneto (IT)
- Instituto Nacional de Cancerología (MX)
- Tecnológico de Monterrey (MX)
Publication Details
- Journal
- Pharmaceutics
- Published
- 2024-10-24
- DOI
- https://doi.org/10.3390/pharmaceutics16111358
- Citations
- 3
- Primary Topic
- Prostate Cancer Treatment and Research
- Type
- article
- Field-Weighted Citation Impact
- 1.26
Funders
- International Atomic Energy Agency