Correlation of [<sup>68</sup>Ga]Ga-PSMA PET/CT response and PSA decline in first-line enzalutamide for metastatic castration-resistant prostate cancer patients.
prospective_cohort · Level II
Where this comes from
- Record sourced from PubMed, PMID 39207484.
- Also identified by DOI 10.1007/s00259-024-06887-4 and PMC identifier 11599341.
- Licence recorded as CC BY-NC-ND.
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Abstract
to assess the utility of response monitoring to enzalutamide by using [<sup>68</sup>Ga]Ga-PSMA PET in mCRPC patients treated with enzalutamide as first-line therapy. patients underwent [<sup>68</sup>Ga]Ga-PSMA PET less than 8 weeks before and 3 months after starting enzalutamide. On the basis of EAU/EANM criteria, patients were categorized as PSMA responders (PET-R) or PSMA non-responders (PET-NR), whilst, based on PSA, they were classified as biochemical responders (PSA-R) or non-responders (PSA-NR). Survival analysis was performed using the Cox regression hazard model and the Kaplan-Meier method. 69 patients were considered fully evaluable. We observed 47.8% of concordance between [68Ga]Ga-PSMA PET and PSA monitoring at 3 months after starting enzalutamide. For discordant cases, the PSA reduction has a weak impact on PFS and a significant impact on OS in PET-NR patients, whilst this change has no impact either for PFS and OS in PET-R ones. [<sup>68</sup>Ga]Ga-PSMA PET could be a useful imaging tool for monitoring response to enzalutamide in mCRPC patients, being more informative than PSA in this setting, and possibly better guiding clinicians in therapeutic decisions.
Medical subject headings
- Benzamides
- Nitriles
- Phenylthiohydantoin
- Gallium Radioisotopes
- Prostatic Neoplasms, Castration-Resistant
- Positron Emission Tomography Computed Tomography
- Gallium Isotopes
- Prostate-Specific Antigen
- Edetic Acid
- Neoplasm Metastasis