PSMA PET/CT in Castration-Resistant Prostate Cancer: Myth or Reality?
Background: prostate-specific membrane antigen (PSMA) ligand PET has been recently incorporated into international guidelines for several different indications in prostate cancer (PCa) patients. However, there are still some open questions regarding the role of PSMA ligand PET in castration-resistan...
Ausführliche Beschreibung
Autor*in: |
Luca Urso [verfasserIn] Luca Filippi [verfasserIn] Angelo Castello [verfasserIn] Maria Cristina Marzola [verfasserIn] Mirco Bartolomei [verfasserIn] Corrado Cittanti [verfasserIn] Luigia Florimonte [verfasserIn] Massimo Castellani [verfasserIn] Paolo Zucali [verfasserIn] Alessio Bruni [verfasserIn] Roberto Sabbatini [verfasserIn] Massimo Dominici [verfasserIn] Stefano Panareo [verfasserIn] Laura Evangelista [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2023 |
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Schlagwörter: |
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Übergeordnetes Werk: |
In: Journal of Clinical Medicine - MDPI AG, 2013, 12(2023), 22, p 7130 |
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Übergeordnetes Werk: |
volume:12 ; year:2023 ; number:22, p 7130 |
Links: |
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DOI / URN: |
10.3390/jcm12227130 |
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Katalog-ID: |
DOAJ101229356 |
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10.3390/jcm12227130 doi (DE-627)DOAJ101229356 (DE-599)DOAJ6f270d25d81d4eaaa799d22e7675cf72 DE-627 ger DE-627 rakwb eng Luca Urso verfasserin aut PSMA PET/CT in Castration-Resistant Prostate Cancer: Myth or Reality? 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Background: prostate-specific membrane antigen (PSMA) ligand PET has been recently incorporated into international guidelines for several different indications in prostate cancer (PCa) patients. However, there are still some open questions regarding the role of PSMA ligand PET in castration-resistant prostate cancer (CRPC). The aim of this work is to assess the clinical value of PSMA ligand PET/CT in patients with CRPC. Results: PSMA ligand PET has demonstrated higher detection rates in comparison to conventional imaging and allows for a significant reduction in the number of M0 CRPC patients. However, its real impact on patients’ prognosis is still an open question. Moreover, in CRPC patients, PSMA ligand PET presents some sensitivity and specificity limitations. Due to its heterogeneity, CRPC may present a mosaic of neoplastic clones, some of which could be PSMA−/FDG+, or vice versa. Likewise, unspecific bone uptake (UBU) and second primary neoplasms (SNPs) overexpressing PSMA in the neoangiogenic vessels represent potential specificity issues. Integrated multi-tracer imaging (PSMA ligand and [<sup<18</sup<F]FDG PET) together with a multidisciplinary discussion could allow for reaching the most accurate evaluation of each patient from a precision medicine point of view. prostate cancer PCa castration-resistant prostate cancer PSMA PET FDG PET pitfalls Medicine R Luca Filippi verfasserin aut Angelo Castello verfasserin aut Maria Cristina Marzola verfasserin aut Mirco Bartolomei verfasserin aut Corrado Cittanti verfasserin aut Luigia Florimonte verfasserin aut Massimo Castellani verfasserin aut Paolo Zucali verfasserin aut Alessio Bruni verfasserin aut Roberto Sabbatini verfasserin aut Massimo Dominici verfasserin aut Stefano Panareo verfasserin aut Laura Evangelista verfasserin aut In Journal of Clinical Medicine MDPI AG, 2013 12(2023), 22, p 7130 (DE-627)718632478 (DE-600)2662592-1 20770383 nnns volume:12 year:2023 number:22, p 7130 https://doi.org/10.3390/jcm12227130 kostenfrei https://doaj.org/article/6f270d25d81d4eaaa799d22e7675cf72 kostenfrei https://www.mdpi.com/2077-0383/12/22/7130 kostenfrei https://doaj.org/toc/2077-0383 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 12 2023 22, p 7130 |
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10.3390/jcm12227130 doi (DE-627)DOAJ101229356 (DE-599)DOAJ6f270d25d81d4eaaa799d22e7675cf72 DE-627 ger DE-627 rakwb eng Luca Urso verfasserin aut PSMA PET/CT in Castration-Resistant Prostate Cancer: Myth or Reality? 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Background: prostate-specific membrane antigen (PSMA) ligand PET has been recently incorporated into international guidelines for several different indications in prostate cancer (PCa) patients. However, there are still some open questions regarding the role of PSMA ligand PET in castration-resistant prostate cancer (CRPC). The aim of this work is to assess the clinical value of PSMA ligand PET/CT in patients with CRPC. Results: PSMA ligand PET has demonstrated higher detection rates in comparison to conventional imaging and allows for a significant reduction in the number of M0 CRPC patients. However, its real impact on patients’ prognosis is still an open question. Moreover, in CRPC patients, PSMA ligand PET presents some sensitivity and specificity limitations. Due to its heterogeneity, CRPC may present a mosaic of neoplastic clones, some of which could be PSMA−/FDG+, or vice versa. Likewise, unspecific bone uptake (UBU) and second primary neoplasms (SNPs) overexpressing PSMA in the neoangiogenic vessels represent potential specificity issues. Integrated multi-tracer imaging (PSMA ligand and [<sup<18</sup<F]FDG PET) together with a multidisciplinary discussion could allow for reaching the most accurate evaluation of each patient from a precision medicine point of view. prostate cancer PCa castration-resistant prostate cancer PSMA PET FDG PET pitfalls Medicine R Luca Filippi verfasserin aut Angelo Castello verfasserin aut Maria Cristina Marzola verfasserin aut Mirco Bartolomei verfasserin aut Corrado Cittanti verfasserin aut Luigia Florimonte verfasserin aut Massimo Castellani verfasserin aut Paolo Zucali verfasserin aut Alessio Bruni verfasserin aut Roberto Sabbatini verfasserin aut Massimo Dominici verfasserin aut Stefano Panareo verfasserin aut Laura Evangelista verfasserin aut In Journal of Clinical Medicine MDPI AG, 2013 12(2023), 22, p 7130 (DE-627)718632478 (DE-600)2662592-1 20770383 nnns volume:12 year:2023 number:22, p 7130 https://doi.org/10.3390/jcm12227130 kostenfrei https://doaj.org/article/6f270d25d81d4eaaa799d22e7675cf72 kostenfrei https://www.mdpi.com/2077-0383/12/22/7130 kostenfrei https://doaj.org/toc/2077-0383 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 12 2023 22, p 7130 |
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10.3390/jcm12227130 doi (DE-627)DOAJ101229356 (DE-599)DOAJ6f270d25d81d4eaaa799d22e7675cf72 DE-627 ger DE-627 rakwb eng Luca Urso verfasserin aut PSMA PET/CT in Castration-Resistant Prostate Cancer: Myth or Reality? 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Background: prostate-specific membrane antigen (PSMA) ligand PET has been recently incorporated into international guidelines for several different indications in prostate cancer (PCa) patients. However, there are still some open questions regarding the role of PSMA ligand PET in castration-resistant prostate cancer (CRPC). The aim of this work is to assess the clinical value of PSMA ligand PET/CT in patients with CRPC. Results: PSMA ligand PET has demonstrated higher detection rates in comparison to conventional imaging and allows for a significant reduction in the number of M0 CRPC patients. However, its real impact on patients’ prognosis is still an open question. Moreover, in CRPC patients, PSMA ligand PET presents some sensitivity and specificity limitations. Due to its heterogeneity, CRPC may present a mosaic of neoplastic clones, some of which could be PSMA−/FDG+, or vice versa. Likewise, unspecific bone uptake (UBU) and second primary neoplasms (SNPs) overexpressing PSMA in the neoangiogenic vessels represent potential specificity issues. Integrated multi-tracer imaging (PSMA ligand and [<sup<18</sup<F]FDG PET) together with a multidisciplinary discussion could allow for reaching the most accurate evaluation of each patient from a precision medicine point of view. prostate cancer PCa castration-resistant prostate cancer PSMA PET FDG PET pitfalls Medicine R Luca Filippi verfasserin aut Angelo Castello verfasserin aut Maria Cristina Marzola verfasserin aut Mirco Bartolomei verfasserin aut Corrado Cittanti verfasserin aut Luigia Florimonte verfasserin aut Massimo Castellani verfasserin aut Paolo Zucali verfasserin aut Alessio Bruni verfasserin aut Roberto Sabbatini verfasserin aut Massimo Dominici verfasserin aut Stefano Panareo verfasserin aut Laura Evangelista verfasserin aut In Journal of Clinical Medicine MDPI AG, 2013 12(2023), 22, p 7130 (DE-627)718632478 (DE-600)2662592-1 20770383 nnns volume:12 year:2023 number:22, p 7130 https://doi.org/10.3390/jcm12227130 kostenfrei https://doaj.org/article/6f270d25d81d4eaaa799d22e7675cf72 kostenfrei https://www.mdpi.com/2077-0383/12/22/7130 kostenfrei https://doaj.org/toc/2077-0383 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 12 2023 22, p 7130 |
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10.3390/jcm12227130 doi (DE-627)DOAJ101229356 (DE-599)DOAJ6f270d25d81d4eaaa799d22e7675cf72 DE-627 ger DE-627 rakwb eng Luca Urso verfasserin aut PSMA PET/CT in Castration-Resistant Prostate Cancer: Myth or Reality? 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Background: prostate-specific membrane antigen (PSMA) ligand PET has been recently incorporated into international guidelines for several different indications in prostate cancer (PCa) patients. However, there are still some open questions regarding the role of PSMA ligand PET in castration-resistant prostate cancer (CRPC). The aim of this work is to assess the clinical value of PSMA ligand PET/CT in patients with CRPC. Results: PSMA ligand PET has demonstrated higher detection rates in comparison to conventional imaging and allows for a significant reduction in the number of M0 CRPC patients. However, its real impact on patients’ prognosis is still an open question. Moreover, in CRPC patients, PSMA ligand PET presents some sensitivity and specificity limitations. Due to its heterogeneity, CRPC may present a mosaic of neoplastic clones, some of which could be PSMA−/FDG+, or vice versa. Likewise, unspecific bone uptake (UBU) and second primary neoplasms (SNPs) overexpressing PSMA in the neoangiogenic vessels represent potential specificity issues. Integrated multi-tracer imaging (PSMA ligand and [<sup<18</sup<F]FDG PET) together with a multidisciplinary discussion could allow for reaching the most accurate evaluation of each patient from a precision medicine point of view. prostate cancer PCa castration-resistant prostate cancer PSMA PET FDG PET pitfalls Medicine R Luca Filippi verfasserin aut Angelo Castello verfasserin aut Maria Cristina Marzola verfasserin aut Mirco Bartolomei verfasserin aut Corrado Cittanti verfasserin aut Luigia Florimonte verfasserin aut Massimo Castellani verfasserin aut Paolo Zucali verfasserin aut Alessio Bruni verfasserin aut Roberto Sabbatini verfasserin aut Massimo Dominici verfasserin aut Stefano Panareo verfasserin aut Laura Evangelista verfasserin aut In Journal of Clinical Medicine MDPI AG, 2013 12(2023), 22, p 7130 (DE-627)718632478 (DE-600)2662592-1 20770383 nnns volume:12 year:2023 number:22, p 7130 https://doi.org/10.3390/jcm12227130 kostenfrei https://doaj.org/article/6f270d25d81d4eaaa799d22e7675cf72 kostenfrei https://www.mdpi.com/2077-0383/12/22/7130 kostenfrei https://doaj.org/toc/2077-0383 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 12 2023 22, p 7130 |
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10.3390/jcm12227130 doi (DE-627)DOAJ101229356 (DE-599)DOAJ6f270d25d81d4eaaa799d22e7675cf72 DE-627 ger DE-627 rakwb eng Luca Urso verfasserin aut PSMA PET/CT in Castration-Resistant Prostate Cancer: Myth or Reality? 2023 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Background: prostate-specific membrane antigen (PSMA) ligand PET has been recently incorporated into international guidelines for several different indications in prostate cancer (PCa) patients. However, there are still some open questions regarding the role of PSMA ligand PET in castration-resistant prostate cancer (CRPC). The aim of this work is to assess the clinical value of PSMA ligand PET/CT in patients with CRPC. Results: PSMA ligand PET has demonstrated higher detection rates in comparison to conventional imaging and allows for a significant reduction in the number of M0 CRPC patients. However, its real impact on patients’ prognosis is still an open question. Moreover, in CRPC patients, PSMA ligand PET presents some sensitivity and specificity limitations. Due to its heterogeneity, CRPC may present a mosaic of neoplastic clones, some of which could be PSMA−/FDG+, or vice versa. Likewise, unspecific bone uptake (UBU) and second primary neoplasms (SNPs) overexpressing PSMA in the neoangiogenic vessels represent potential specificity issues. Integrated multi-tracer imaging (PSMA ligand and [<sup<18</sup<F]FDG PET) together with a multidisciplinary discussion could allow for reaching the most accurate evaluation of each patient from a precision medicine point of view. prostate cancer PCa castration-resistant prostate cancer PSMA PET FDG PET pitfalls Medicine R Luca Filippi verfasserin aut Angelo Castello verfasserin aut Maria Cristina Marzola verfasserin aut Mirco Bartolomei verfasserin aut Corrado Cittanti verfasserin aut Luigia Florimonte verfasserin aut Massimo Castellani verfasserin aut Paolo Zucali verfasserin aut Alessio Bruni verfasserin aut Roberto Sabbatini verfasserin aut Massimo Dominici verfasserin aut Stefano Panareo verfasserin aut Laura Evangelista verfasserin aut In Journal of Clinical Medicine MDPI AG, 2013 12(2023), 22, p 7130 (DE-627)718632478 (DE-600)2662592-1 20770383 nnns volume:12 year:2023 number:22, p 7130 https://doi.org/10.3390/jcm12227130 kostenfrei https://doaj.org/article/6f270d25d81d4eaaa799d22e7675cf72 kostenfrei https://www.mdpi.com/2077-0383/12/22/7130 kostenfrei https://doaj.org/toc/2077-0383 Journal toc kostenfrei GBV_USEFLAG_A SYSFLAG_A GBV_DOAJ GBV_ILN_20 GBV_ILN_22 GBV_ILN_23 GBV_ILN_24 GBV_ILN_39 GBV_ILN_40 GBV_ILN_60 GBV_ILN_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_73 GBV_ILN_74 GBV_ILN_95 GBV_ILN_105 GBV_ILN_110 GBV_ILN_151 GBV_ILN_161 GBV_ILN_170 GBV_ILN_206 GBV_ILN_213 GBV_ILN_230 GBV_ILN_285 GBV_ILN_293 GBV_ILN_602 GBV_ILN_2005 GBV_ILN_2009 GBV_ILN_2014 GBV_ILN_2055 GBV_ILN_2111 GBV_ILN_4012 GBV_ILN_4037 GBV_ILN_4112 GBV_ILN_4125 GBV_ILN_4126 GBV_ILN_4249 GBV_ILN_4305 GBV_ILN_4306 GBV_ILN_4307 GBV_ILN_4313 GBV_ILN_4322 GBV_ILN_4323 GBV_ILN_4324 GBV_ILN_4325 GBV_ILN_4338 GBV_ILN_4367 GBV_ILN_4700 AR 12 2023 22, p 7130 |
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2023-01-01T00:00:00Z |
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Luca Urso |
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Luca Urso misc prostate cancer misc PCa misc castration-resistant prostate cancer misc PSMA PET misc FDG PET misc pitfalls misc Medicine misc R PSMA PET/CT in Castration-Resistant Prostate Cancer: Myth or Reality? |
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PSMA PET/CT in Castration-Resistant Prostate Cancer: Myth or Reality? prostate cancer PCa castration-resistant prostate cancer PSMA PET FDG PET pitfalls |
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psma pet/ct in castration-resistant prostate cancer: myth or reality? |
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PSMA PET/CT in Castration-Resistant Prostate Cancer: Myth or Reality? |
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Background: prostate-specific membrane antigen (PSMA) ligand PET has been recently incorporated into international guidelines for several different indications in prostate cancer (PCa) patients. However, there are still some open questions regarding the role of PSMA ligand PET in castration-resistant prostate cancer (CRPC). The aim of this work is to assess the clinical value of PSMA ligand PET/CT in patients with CRPC. Results: PSMA ligand PET has demonstrated higher detection rates in comparison to conventional imaging and allows for a significant reduction in the number of M0 CRPC patients. However, its real impact on patients’ prognosis is still an open question. Moreover, in CRPC patients, PSMA ligand PET presents some sensitivity and specificity limitations. Due to its heterogeneity, CRPC may present a mosaic of neoplastic clones, some of which could be PSMA−/FDG+, or vice versa. Likewise, unspecific bone uptake (UBU) and second primary neoplasms (SNPs) overexpressing PSMA in the neoangiogenic vessels represent potential specificity issues. Integrated multi-tracer imaging (PSMA ligand and [<sup<18</sup<F]FDG PET) together with a multidisciplinary discussion could allow for reaching the most accurate evaluation of each patient from a precision medicine point of view. |
abstractGer |
Background: prostate-specific membrane antigen (PSMA) ligand PET has been recently incorporated into international guidelines for several different indications in prostate cancer (PCa) patients. However, there are still some open questions regarding the role of PSMA ligand PET in castration-resistant prostate cancer (CRPC). The aim of this work is to assess the clinical value of PSMA ligand PET/CT in patients with CRPC. Results: PSMA ligand PET has demonstrated higher detection rates in comparison to conventional imaging and allows for a significant reduction in the number of M0 CRPC patients. However, its real impact on patients’ prognosis is still an open question. Moreover, in CRPC patients, PSMA ligand PET presents some sensitivity and specificity limitations. Due to its heterogeneity, CRPC may present a mosaic of neoplastic clones, some of which could be PSMA−/FDG+, or vice versa. Likewise, unspecific bone uptake (UBU) and second primary neoplasms (SNPs) overexpressing PSMA in the neoangiogenic vessels represent potential specificity issues. Integrated multi-tracer imaging (PSMA ligand and [<sup<18</sup<F]FDG PET) together with a multidisciplinary discussion could allow for reaching the most accurate evaluation of each patient from a precision medicine point of view. |
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Background: prostate-specific membrane antigen (PSMA) ligand PET has been recently incorporated into international guidelines for several different indications in prostate cancer (PCa) patients. However, there are still some open questions regarding the role of PSMA ligand PET in castration-resistant prostate cancer (CRPC). The aim of this work is to assess the clinical value of PSMA ligand PET/CT in patients with CRPC. Results: PSMA ligand PET has demonstrated higher detection rates in comparison to conventional imaging and allows for a significant reduction in the number of M0 CRPC patients. However, its real impact on patients’ prognosis is still an open question. Moreover, in CRPC patients, PSMA ligand PET presents some sensitivity and specificity limitations. Due to its heterogeneity, CRPC may present a mosaic of neoplastic clones, some of which could be PSMA−/FDG+, or vice versa. Likewise, unspecific bone uptake (UBU) and second primary neoplasms (SNPs) overexpressing PSMA in the neoangiogenic vessels represent potential specificity issues. Integrated multi-tracer imaging (PSMA ligand and [<sup<18</sup<F]FDG PET) together with a multidisciplinary discussion could allow for reaching the most accurate evaluation of each patient from a precision medicine point of view. |
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