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The prognostic value of (18)F-PSMA-1007 PET/CT in predicting pathological upgrading of newly diagnosed prostate cancer from systematic biopsy to radical prostatectomy

OBJECTIVE: This study aimed to evaluate predictors for upgrading of newly diagnosed prostate cancer from systematic biopsy (SB) to radical prostatectomy (RP) using fluorine-18 prostate-specific membrane antigen 1007 ((18)F-PSMA-1007) positron emission tomography/computed tomography (PET/CT) and asso...

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Autores principales: Zheng, Anqi, Wang, Zhuonan, Luo, Liang, Chang, Ruxi, Gao, Jungang, Wang, Bo, Duan, Xiaoyi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10206242/
https://www.ncbi.nlm.nih.gov/pubmed/37234988
http://dx.doi.org/10.3389/fonc.2023.1169189
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author Zheng, Anqi
Wang, Zhuonan
Luo, Liang
Chang, Ruxi
Gao, Jungang
Wang, Bo
Duan, Xiaoyi
author_facet Zheng, Anqi
Wang, Zhuonan
Luo, Liang
Chang, Ruxi
Gao, Jungang
Wang, Bo
Duan, Xiaoyi
author_sort Zheng, Anqi
collection PubMed
description OBJECTIVE: This study aimed to evaluate predictors for upgrading of newly diagnosed prostate cancer from systematic biopsy (SB) to radical prostatectomy (RP) using fluorine-18 prostate-specific membrane antigen 1007 ((18)F-PSMA-1007) positron emission tomography/computed tomography (PET/CT) and association with clinical parameters. MATERIALS AND METHODS: We retrospectively collected data from biopsy-confirmed prostate cancer (PCa) patients who underwent (18)F-PSMA-1007 PET/CT prior to RP from July 2019 and October 2022. Imaging characteristics derived from (18)F-PSMA-1007 PET/CT and clinical parameters were compared in patients of pathological upgrading and concordance subgroups. Univariable and multivariable logistic regressions were performed to analyze factors predicting histopathological upgrading from SB to RP specimens. Discrimination ability of independent predictors was further evaluated by receiver operating characteristic (ROC) analysis with corresponding area under the curve (AUC). RESULTS: Pathological upgrading occurred in 26.97% (41/152) PCa patients, and 23.03% (35/152) of all patients experienced pathological downgrading. Concordance rate reached 50% (76/152). International Society of Urological Pathology grade group (ISUP GG) 1(77.78%) and ISUP GG 2 (65.22%) biopsies were related with the highest rate of upgrading. Multivariable logistic regression analyses showed that prostate volume (OR= 0.933; 95% CI, 0.887–0.982; p = 0.008), ISUP GG 1 vs. 4 (OR= 13.856; 95% CI: 2.467–77.831; p = 0.003), and total uptake of PSMA-avid lesions (PSMA-TL) (OR = 1.003; 95% CI, 1.000–1.006; p = 0.029) were found to be independent risk factors of pathological upgrading after RP. The AUCs and corresponding sensitivity and specificity of the independent predictors of synthesis for upgrading were 0.839, 78.00%, and 83.30% respectively, which showed good discrimination capacity. CONCLUSION: (18)F-PSMA-1007 PET/CT may help to predict pathological upgrading between biopsy and RP specimens, particularly for ISUP GG 1 and ISUP GG 2 patients with higher PSMA-TL and smaller prostate volume.
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spelling pubmed-102062422023-05-25 The prognostic value of (18)F-PSMA-1007 PET/CT in predicting pathological upgrading of newly diagnosed prostate cancer from systematic biopsy to radical prostatectomy Zheng, Anqi Wang, Zhuonan Luo, Liang Chang, Ruxi Gao, Jungang Wang, Bo Duan, Xiaoyi Front Oncol Oncology OBJECTIVE: This study aimed to evaluate predictors for upgrading of newly diagnosed prostate cancer from systematic biopsy (SB) to radical prostatectomy (RP) using fluorine-18 prostate-specific membrane antigen 1007 ((18)F-PSMA-1007) positron emission tomography/computed tomography (PET/CT) and association with clinical parameters. MATERIALS AND METHODS: We retrospectively collected data from biopsy-confirmed prostate cancer (PCa) patients who underwent (18)F-PSMA-1007 PET/CT prior to RP from July 2019 and October 2022. Imaging characteristics derived from (18)F-PSMA-1007 PET/CT and clinical parameters were compared in patients of pathological upgrading and concordance subgroups. Univariable and multivariable logistic regressions were performed to analyze factors predicting histopathological upgrading from SB to RP specimens. Discrimination ability of independent predictors was further evaluated by receiver operating characteristic (ROC) analysis with corresponding area under the curve (AUC). RESULTS: Pathological upgrading occurred in 26.97% (41/152) PCa patients, and 23.03% (35/152) of all patients experienced pathological downgrading. Concordance rate reached 50% (76/152). International Society of Urological Pathology grade group (ISUP GG) 1(77.78%) and ISUP GG 2 (65.22%) biopsies were related with the highest rate of upgrading. Multivariable logistic regression analyses showed that prostate volume (OR= 0.933; 95% CI, 0.887–0.982; p = 0.008), ISUP GG 1 vs. 4 (OR= 13.856; 95% CI: 2.467–77.831; p = 0.003), and total uptake of PSMA-avid lesions (PSMA-TL) (OR = 1.003; 95% CI, 1.000–1.006; p = 0.029) were found to be independent risk factors of pathological upgrading after RP. The AUCs and corresponding sensitivity and specificity of the independent predictors of synthesis for upgrading were 0.839, 78.00%, and 83.30% respectively, which showed good discrimination capacity. CONCLUSION: (18)F-PSMA-1007 PET/CT may help to predict pathological upgrading between biopsy and RP specimens, particularly for ISUP GG 1 and ISUP GG 2 patients with higher PSMA-TL and smaller prostate volume. Frontiers Media S.A. 2023-05-10 /pmc/articles/PMC10206242/ /pubmed/37234988 http://dx.doi.org/10.3389/fonc.2023.1169189 Text en Copyright © 2023 Zheng, Wang, Luo, Chang, Gao, Wang and Duan https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Zheng, Anqi
Wang, Zhuonan
Luo, Liang
Chang, Ruxi
Gao, Jungang
Wang, Bo
Duan, Xiaoyi
The prognostic value of (18)F-PSMA-1007 PET/CT in predicting pathological upgrading of newly diagnosed prostate cancer from systematic biopsy to radical prostatectomy
title The prognostic value of (18)F-PSMA-1007 PET/CT in predicting pathological upgrading of newly diagnosed prostate cancer from systematic biopsy to radical prostatectomy
title_full The prognostic value of (18)F-PSMA-1007 PET/CT in predicting pathological upgrading of newly diagnosed prostate cancer from systematic biopsy to radical prostatectomy
title_fullStr The prognostic value of (18)F-PSMA-1007 PET/CT in predicting pathological upgrading of newly diagnosed prostate cancer from systematic biopsy to radical prostatectomy
title_full_unstemmed The prognostic value of (18)F-PSMA-1007 PET/CT in predicting pathological upgrading of newly diagnosed prostate cancer from systematic biopsy to radical prostatectomy
title_short The prognostic value of (18)F-PSMA-1007 PET/CT in predicting pathological upgrading of newly diagnosed prostate cancer from systematic biopsy to radical prostatectomy
title_sort prognostic value of (18)f-psma-1007 pet/ct in predicting pathological upgrading of newly diagnosed prostate cancer from systematic biopsy to radical prostatectomy
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10206242/
https://www.ncbi.nlm.nih.gov/pubmed/37234988
http://dx.doi.org/10.3389/fonc.2023.1169189
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