| Literature DB >> 35687207 |
Giulio Francolini1, Mauro Loi2, Lucia Pia Ciccone3, Beatrice Detti2, Vanessa Di Cataldo2, Pamela Pinzani3, Francesca Salvianti3, Giulia Salvatore3, Mariangela Sottili3, Costanza Santini3, Giulio Frosini3, Luca Visani2, Luca Burchini3, Chiara Mattioli3, Andrea Gaetano Allegra3, Marianna Valzano3, Cecilia Cerbai3, Michele Aquilano3, Viola Salvestrini3, Isacco Desideri3, Monica Mangoni2,3, Icro Meattini2,3, Lorenzo Livi2,3.
Abstract
Circulating tumor cells detection and ARV7 expression are associated with worse clinical outcomes in metastatic Castration-Resistant Prostate Cancer (mCRPC) undergoing Androgen Receptor Targeted Agents. ARFL, PSMA and PSA may help to refine prognostic models. In our institution, a prospective observational trial testing CTC detection in mCPRC undergoing I line ARTA therapy terminated the planned enrollment in 2020. Here, we present a pre-planned interim analysis with 18 months of median follow-up. RT-qPCR was used to determine the CTC expression of PSA, PSMA, AR and ARV7 before starting ARTA. PSA-drop, Progression-Free and Overall Survival (PFS and OS) and their correlation with CTC detection were reported. Forty-four patients were included. CTC were detected in 43.2% of patients, of whom 8.94% expressed PSA, 15.78% showed ARV7, 63.15% and 73.68% displayed ARFL and PSMA, respectively. Biochemical response was significantly improved in CTC + vs CTC- patients, with median PSA-drop of 18.5 vs 2.5 ng/ml (p = 0.03). After a median follow-up of 18 months, 50% of patients progressed. PFS was significantly longer in CTC- patients (NR vs 16 months). Eight (18.2%) patients died, a non-significant trend in terms of OS was detected in favor of CTC- patients (NR vs 29 months, p = 0.05). AR, PSA and PSMA expression in CTC + had no significant impact on PSA-drop, PFS or OS. PRIMERA-trial confirmed the CTC detection predictive importance in mCRPC patients.Entities:
Keywords: AR splice variants; Biomarker; CTCs; Metastatic castration-resistant prostate cancer; PSMA
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Year: 2022 PMID: 35687207 DOI: 10.1007/s12032-022-01756-2
Source DB: PubMed Journal: Med Oncol ISSN: 1357-0560 Impact factor: 3.064