The Impact of PSMA-PET on Oncologic Control in Prostate Cancer Patients Who Experienced PSA Persistence or Recurrence.

PSMA-PET PSMA-guided salvage treatment hormone sensitive prostate cancer recurrent prostate cancer survival

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
30 Dec 2022
Historique:
received: 17 11 2022
revised: 22 12 2022
accepted: 27 12 2022
entrez: 8 1 2023
pubmed: 9 1 2023
medline: 9 1 2023
Statut: epublish

Résumé

Background: Prostate Specific Membrane Antigen-Positron Emission Tomography (PSMA-PET) is currently recommended to restage prostate cancer (PCa) and to guide the delivery of salvage treatments. We aim to evaluate the oncologic outcomes of patients with recurrent PCa who received PSMA-PET. Methods: 324 hormone-sensitive PCa with PSA relapse after radical prostatectomy who underwent PSMA-PET in three high-volume European Centres. Patients have been stratified as pre-salvage who never received salvage treatments (n = 134), and post-salvage, including patients who received previous salvage therapies (n = 190). Patients with oligorecurrent (≤3 lesions), PSMA-positive disease underwent PSMA-directed treatments: salvage radiotherapy (sRT) or Metastases-directed therapy (MDT). Patients with polirecurrent (>3 lesions) PSMA-positive disease were treated with systemic therapy. Patients with negative PSMA-PET were treated with sRT or systemic therapies or observation. The primary outcome of the study was Progression-free survival (PFS). Secondary outcomes were: Metastases-free survival (MFS) and Castration Resistant Pca free survival (CRPC-FS). Results: median follow up was 23 months. In the pre-salvage setting, the PFS, MFS and CRPC-FS estimates at 3 years were 66.2% vs. 38.9%, 95.2% vs. 73.7% and 94.9% vs. 93.1% in patients with negative vs. positive PSMA-PET, respectively (all p ≥ 0.2). In the post-salvage setting, the PFS, MFS and CRPC-FS estimates at 3 years were 59.5% vs. 29.1%, 92.7% vs. 65.1% and 98.8% vs. 88.8% in patients with negative vs. positive PSMA-PET, respectively (all p ≤ 0.01). At multivariable analyses, a positive PSMA-PET was an independent predictor of progression (HR = 2.15) and metastatic disease (HR 2.37; all p ≤ 0.03). Conclusion: PSMA-PET in recurrent PCa detects the site of recurrence guiding salvage treatments and has a prognostic role in patients who received previous salvage treatments.

Identifiants

pubmed: 36612242
pii: cancers15010247
doi: 10.3390/cancers15010247
pmc: PMC9818949
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Lorenzo Bianchi (L)

Division of Urology, IRCCS Azienda Ospedaliero-University of Bologna, 40138 Bologna, Italy.
University of Bologna, 40126 Bologna, Italy.

Francesco Ceci (F)

Division of Nuclear Medicine, IEO European Institute of Oncology IRCCS, 20141 Milan, Italy.
Department of Oncology and Hemato-Oncology, University of Milan, 20122 Milan, Italy.

Francesco Costa (F)

Division of Urology, IRCCS Azienda Ospedaliero-University of Bologna, 40138 Bologna, Italy.

Eleonora Balestrazzi (E)

Division of Urology, IRCCS Azienda Ospedaliero-University of Bologna, 40138 Bologna, Italy.

Matteo Droghetti (M)

Division of Urology, IRCCS Azienda Ospedaliero-University of Bologna, 40138 Bologna, Italy.

Pietro Piazza (P)

Division of Urology, IRCCS Azienda Ospedaliero-University of Bologna, 40138 Bologna, Italy.

Alessandro Pissavini (A)

Division of Urology, IRCCS Azienda Ospedaliero-University of Bologna, 40138 Bologna, Italy.

Riccardo Mei (R)

Nuclear Medicine, IRCCS Azienda Ospedaliero-University of Bologna, 40138 Bologna, Italy.

Andrea Farolfi (A)

Nuclear Medicine, IRCCS Azienda Ospedaliero-University of Bologna, 40138 Bologna, Italy.

Paolo Castellucci (P)

Nuclear Medicine, IRCCS Azienda Ospedaliero-University of Bologna, 40138 Bologna, Italy.

Stefano Puliatti (S)

Department of Urology, University of Modena and Reggio Emilia, 41122 Modena, Italy.
Department of Urology, Onze-Lieve-Vrouwziekenhuis, 9300 Aalst, Belgium.
ORSI Academy, 9300 Melle, Belgium.

Alessandro Larcher (A)

Unit of Urology, Division of Experimental Oncology, Urological Research Institute, IRCCS San Raffaele Scientific Institute, Vita-Salute San Raffaele University, 20132 Milan, Italy.

Giorgio Gandaglia (G)

Unit of Urology, Division of Experimental Oncology, Urological Research Institute, IRCCS San Raffaele Scientific Institute, Vita-Salute San Raffaele University, 20132 Milan, Italy.

Daniele Robesti (D)

Unit of Urology, Division of Experimental Oncology, Urological Research Institute, IRCCS San Raffaele Scientific Institute, Vita-Salute San Raffaele University, 20132 Milan, Italy.

Alexandre Mottrie (A)

Department of Urology, Onze-Lieve-Vrouwziekenhuis, 9300 Aalst, Belgium.
ORSI Academy, 9300 Melle, Belgium.

Alberto Briganti (A)

Unit of Urology, Division of Experimental Oncology, Urological Research Institute, IRCCS San Raffaele Scientific Institute, Vita-Salute San Raffaele University, 20132 Milan, Italy.

Alessio Giuseppe Morganti (AG)

Radiation Oncology, IRCCS Azienda Ospedaliero, University of Bologna, 40138 Bologna, Italy.

Stefano Fanti (S)

Nuclear Medicine, IRCCS Azienda Ospedaliero-University of Bologna, 40138 Bologna, Italy.

Francesco Montorsi (F)

Unit of Urology, Division of Experimental Oncology, Urological Research Institute, IRCCS San Raffaele Scientific Institute, Vita-Salute San Raffaele University, 20132 Milan, Italy.

Riccardo Schiavina (R)

Division of Urology, IRCCS Azienda Ospedaliero-University of Bologna, 40138 Bologna, Italy.
University of Bologna, 40126 Bologna, Italy.

Eugenio Brunocilla (E)

Division of Urology, IRCCS Azienda Ospedaliero-University of Bologna, 40138 Bologna, Italy.
University of Bologna, 40126 Bologna, Italy.

Classifications MeSH