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Value of 18F-fluorocholine PET/CT in predicting response to radical radiotherapy in patients with localized prostate cancer

PURPOSE: This study aims to establish whether metabolic parameters obtainable from FCH PET/CT can predict long-term response to radical radiotherapy (rRT) in patients with localized prostate cancer (PCa). METHODS: Drawing on a single-center database, we retrospectively reviewed the pre-treatment FCH...

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Autores principales: Sepulcri, Matteo, Fusella, Marco, Cuppari, Lea, Zorz, Alessandra, Paiusco, Marta, Evangelista, Laura
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8361027/
https://www.ncbi.nlm.nih.gov/pubmed/34409175
http://dx.doi.org/10.1016/j.ctro.2021.07.002
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author Sepulcri, Matteo
Fusella, Marco
Cuppari, Lea
Zorz, Alessandra
Paiusco, Marta
Evangelista, Laura
author_facet Sepulcri, Matteo
Fusella, Marco
Cuppari, Lea
Zorz, Alessandra
Paiusco, Marta
Evangelista, Laura
author_sort Sepulcri, Matteo
collection PubMed
description PURPOSE: This study aims to establish whether metabolic parameters obtainable from FCH PET/CT can predict long-term response to radical radiotherapy (rRT) in patients with localized prostate cancer (PCa). METHODS: Drawing on a single-center database, we retrospectively reviewed the pre-treatment FCH PET/CT scans of 50 patients who underwent rRT between 2012 and 2017. Patients were enrolled if they had a follow-up of at least 3 years after rRT. Various metabolic parameters were considered for each PET/CT, including FCH multifocality. rRT was administered to all patients for a total equivalent dose of 76–80 Gy, using a standard or hypofractionated schedule. Patients were classified as disease-free (DF) if their PSA levels after rRT rose by <2 ng/mL vis-à-vis their PSA nadir, or as not disease free (NDF) if their PSA levels rose by more than 2 ng/ml. RESULTS: A multifocal FCH uptake in the prostate gland was identified in 27 patients (54%). At 3-year follow-up, 37 patients (74%) were judged DF, and 13 (26%) were NDF. The SUVmax and SUVmean, and the sum of the two values in all FCH foci in the prostate gland were significantly higher for NDF patients than for DF patients (all p < 0.005). The sum of the TLCKA levels in all FCH foci was likewise significantly higher in patients who were NDF than in those found DF (median 54.5 vs. 29.4; p < 0.05). At univariate analysis, the most of PET-metrics and Gleason Score were predictors of biochemical relapse after 3-year follow-up (all p < 0.05). CONCLUSION: Higher SUVs seems predict a worse outcome for patients with multifocal intraprostatic lesions who are candidates for rRT.
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spelling pubmed-83610272021-08-17 Value of 18F-fluorocholine PET/CT in predicting response to radical radiotherapy in patients with localized prostate cancer Sepulcri, Matteo Fusella, Marco Cuppari, Lea Zorz, Alessandra Paiusco, Marta Evangelista, Laura Clin Transl Radiat Oncol Article PURPOSE: This study aims to establish whether metabolic parameters obtainable from FCH PET/CT can predict long-term response to radical radiotherapy (rRT) in patients with localized prostate cancer (PCa). METHODS: Drawing on a single-center database, we retrospectively reviewed the pre-treatment FCH PET/CT scans of 50 patients who underwent rRT between 2012 and 2017. Patients were enrolled if they had a follow-up of at least 3 years after rRT. Various metabolic parameters were considered for each PET/CT, including FCH multifocality. rRT was administered to all patients for a total equivalent dose of 76–80 Gy, using a standard or hypofractionated schedule. Patients were classified as disease-free (DF) if their PSA levels after rRT rose by <2 ng/mL vis-à-vis their PSA nadir, or as not disease free (NDF) if their PSA levels rose by more than 2 ng/ml. RESULTS: A multifocal FCH uptake in the prostate gland was identified in 27 patients (54%). At 3-year follow-up, 37 patients (74%) were judged DF, and 13 (26%) were NDF. The SUVmax and SUVmean, and the sum of the two values in all FCH foci in the prostate gland were significantly higher for NDF patients than for DF patients (all p < 0.005). The sum of the TLCKA levels in all FCH foci was likewise significantly higher in patients who were NDF than in those found DF (median 54.5 vs. 29.4; p < 0.05). At univariate analysis, the most of PET-metrics and Gleason Score were predictors of biochemical relapse after 3-year follow-up (all p < 0.05). CONCLUSION: Higher SUVs seems predict a worse outcome for patients with multifocal intraprostatic lesions who are candidates for rRT. Elsevier 2021-07-27 /pmc/articles/PMC8361027/ /pubmed/34409175 http://dx.doi.org/10.1016/j.ctro.2021.07.002 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Sepulcri, Matteo
Fusella, Marco
Cuppari, Lea
Zorz, Alessandra
Paiusco, Marta
Evangelista, Laura
Value of 18F-fluorocholine PET/CT in predicting response to radical radiotherapy in patients with localized prostate cancer
title Value of 18F-fluorocholine PET/CT in predicting response to radical radiotherapy in patients with localized prostate cancer
title_full Value of 18F-fluorocholine PET/CT in predicting response to radical radiotherapy in patients with localized prostate cancer
title_fullStr Value of 18F-fluorocholine PET/CT in predicting response to radical radiotherapy in patients with localized prostate cancer
title_full_unstemmed Value of 18F-fluorocholine PET/CT in predicting response to radical radiotherapy in patients with localized prostate cancer
title_short Value of 18F-fluorocholine PET/CT in predicting response to radical radiotherapy in patients with localized prostate cancer
title_sort value of 18f-fluorocholine pet/ct in predicting response to radical radiotherapy in patients with localized prostate cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8361027/
https://www.ncbi.nlm.nih.gov/pubmed/34409175
http://dx.doi.org/10.1016/j.ctro.2021.07.002
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