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Detection Rate and Clinical Impact of PET/CT with (18)F-FACBC in Patients with Biochemical Recurrence of Prostate Cancer: A Retrospective Bicentric Study

Our aim was to assess the detection rate (DR) of positron emission computed tomography (PET/CT) with anti-1-amino-3-[(18)F]-flurocyclobutane-1-carboxylic acid ((18)F-FACBC) in patients with biochemical recurrence (BCR) from prostate cancer (PC). As a secondary endpoint, we evaluated (18)F-FACBC PET/...

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Autores principales: Filippi, Luca, Bagni, Oreste, Crisafulli, Carmelo, Cerio, Ivan, Brunotti, Gabriele, Chiaravalloti, Agostino, Schillaci, Orazio, Dore, Franca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8773479/
https://www.ncbi.nlm.nih.gov/pubmed/35052856
http://dx.doi.org/10.3390/biomedicines10010177
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author Filippi, Luca
Bagni, Oreste
Crisafulli, Carmelo
Cerio, Ivan
Brunotti, Gabriele
Chiaravalloti, Agostino
Schillaci, Orazio
Dore, Franca
author_facet Filippi, Luca
Bagni, Oreste
Crisafulli, Carmelo
Cerio, Ivan
Brunotti, Gabriele
Chiaravalloti, Agostino
Schillaci, Orazio
Dore, Franca
author_sort Filippi, Luca
collection PubMed
description Our aim was to assess the detection rate (DR) of positron emission computed tomography (PET/CT) with anti-1-amino-3-[(18)F]-flurocyclobutane-1-carboxylic acid ((18)F-FACBC) in patients with biochemical recurrence (BCR) from prostate cancer (PC). As a secondary endpoint, we evaluated (18)F-FACBC PET/CT’s impact on patients management. Clinical records of 81 patients submitted to (18)F-FACBC PET/CT due to PC BCR in two Italian Nuclear Medicine Units were retrospectively assessed. DR was gauged in the whole cohort and stratifying patients by discrete intervals of PSA levels. PET/CT’s impact on clinical management was scored as (1) major if it entailed an intermodality change (e.g., from systemic to loco-regional therapy); (2) minor if it led to an intramodality change (e.g., modified radiotherapy field). PET/CT’s DR resulted in 76.9% in the whole cohort, with a positive predictive value of 96.7%. Stratified by PSA quartile intervals, PET/CT’s DR was 66.7%, 71.4%, 78.9% and 90% for PSA 0.2–0.57 ng/mL, 0.58–0.99 ng/mL, 1–1.5 ng/mL and >1.5 ng/mL without significant difference among groups (p = 0.81). The most common sites of relapse were prostate bed and pelvic lymph nodes (59.3%). PET/CT impacted on clinical management in 33/81 cases (40.7%), leading to a major change in 30 subjects (90.9%). (18)F-FACBC PET/CT localized recurrence in patients with BCR, with meaningful DR also at low PSA levels and significantly impacted on clinical management.
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spelling pubmed-87734792022-01-21 Detection Rate and Clinical Impact of PET/CT with (18)F-FACBC in Patients with Biochemical Recurrence of Prostate Cancer: A Retrospective Bicentric Study Filippi, Luca Bagni, Oreste Crisafulli, Carmelo Cerio, Ivan Brunotti, Gabriele Chiaravalloti, Agostino Schillaci, Orazio Dore, Franca Biomedicines Article Our aim was to assess the detection rate (DR) of positron emission computed tomography (PET/CT) with anti-1-amino-3-[(18)F]-flurocyclobutane-1-carboxylic acid ((18)F-FACBC) in patients with biochemical recurrence (BCR) from prostate cancer (PC). As a secondary endpoint, we evaluated (18)F-FACBC PET/CT’s impact on patients management. Clinical records of 81 patients submitted to (18)F-FACBC PET/CT due to PC BCR in two Italian Nuclear Medicine Units were retrospectively assessed. DR was gauged in the whole cohort and stratifying patients by discrete intervals of PSA levels. PET/CT’s impact on clinical management was scored as (1) major if it entailed an intermodality change (e.g., from systemic to loco-regional therapy); (2) minor if it led to an intramodality change (e.g., modified radiotherapy field). PET/CT’s DR resulted in 76.9% in the whole cohort, with a positive predictive value of 96.7%. Stratified by PSA quartile intervals, PET/CT’s DR was 66.7%, 71.4%, 78.9% and 90% for PSA 0.2–0.57 ng/mL, 0.58–0.99 ng/mL, 1–1.5 ng/mL and >1.5 ng/mL without significant difference among groups (p = 0.81). The most common sites of relapse were prostate bed and pelvic lymph nodes (59.3%). PET/CT impacted on clinical management in 33/81 cases (40.7%), leading to a major change in 30 subjects (90.9%). (18)F-FACBC PET/CT localized recurrence in patients with BCR, with meaningful DR also at low PSA levels and significantly impacted on clinical management. MDPI 2022-01-15 /pmc/articles/PMC8773479/ /pubmed/35052856 http://dx.doi.org/10.3390/biomedicines10010177 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Filippi, Luca
Bagni, Oreste
Crisafulli, Carmelo
Cerio, Ivan
Brunotti, Gabriele
Chiaravalloti, Agostino
Schillaci, Orazio
Dore, Franca
Detection Rate and Clinical Impact of PET/CT with (18)F-FACBC in Patients with Biochemical Recurrence of Prostate Cancer: A Retrospective Bicentric Study
title Detection Rate and Clinical Impact of PET/CT with (18)F-FACBC in Patients with Biochemical Recurrence of Prostate Cancer: A Retrospective Bicentric Study
title_full Detection Rate and Clinical Impact of PET/CT with (18)F-FACBC in Patients with Biochemical Recurrence of Prostate Cancer: A Retrospective Bicentric Study
title_fullStr Detection Rate and Clinical Impact of PET/CT with (18)F-FACBC in Patients with Biochemical Recurrence of Prostate Cancer: A Retrospective Bicentric Study
title_full_unstemmed Detection Rate and Clinical Impact of PET/CT with (18)F-FACBC in Patients with Biochemical Recurrence of Prostate Cancer: A Retrospective Bicentric Study
title_short Detection Rate and Clinical Impact of PET/CT with (18)F-FACBC in Patients with Biochemical Recurrence of Prostate Cancer: A Retrospective Bicentric Study
title_sort detection rate and clinical impact of pet/ct with (18)f-facbc in patients with biochemical recurrence of prostate cancer: a retrospective bicentric study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8773479/
https://www.ncbi.nlm.nih.gov/pubmed/35052856
http://dx.doi.org/10.3390/biomedicines10010177
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