What Do We Have to Know about PD-L1 Expression in Prostate Cancer? A Systematic Literature Review. Part 2: Clinic–Pathologic Correlations
Many studies have investigated the potential prognostic and predictive role of PD-L1 in prostatic carcinoma (PC). We performed a systematic literature review (PRISMA guidelines) to critically evaluate human tissue-based studies (immunohistochemistry, molecular analysis, etc.), experimental research...
Ausführliche Beschreibung
Autor*in: |
Andrea Palicelli [verfasserIn] Martina Bonacini [verfasserIn] Stefania Croci [verfasserIn] Cristina Magi-Galluzzi [verfasserIn] Sofia Cañete-Portillo [verfasserIn] Alcides Chaux [verfasserIn] Alessandra Bisagni [verfasserIn] Eleonora Zanetti [verfasserIn] Dario De Biase [verfasserIn] Beatrice Melli [verfasserIn] Francesca Sanguedolce [verfasserIn] Magda Zanelli [verfasserIn] Maria Paola Bonasoni [verfasserIn] Loredana De Marco [verfasserIn] Alessandra Soriano [verfasserIn] Stefano Ascani [verfasserIn] Maurizio Zizzo [verfasserIn] Carolina Castro Ruiz [verfasserIn] Antonio De Leo [verfasserIn] Guido Giordano [verfasserIn] Matteo Landriscina [verfasserIn] Giuseppe Carrieri [verfasserIn] Luigi Cormio [verfasserIn] Daniel M. Berney [verfasserIn] Jatin Gandhi [verfasserIn] Giacomo Santandrea [verfasserIn] Maria Carolina Gelli [verfasserIn] Alessandro Tafuni [verfasserIn] Moira Ragazzi [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2021 |
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In: Cells - MDPI AG, 2012, 10(2021), 11, p 3165 |
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Übergeordnetes Werk: |
volume:10 ; year:2021 ; number:11, p 3165 |
Links: |
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DOI / URN: |
10.3390/cells10113165 |
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Katalog-ID: |
DOAJ073495417 |
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10.3390/cells10113165 doi (DE-627)DOAJ073495417 (DE-599)DOAJ49bdba14c7fc4b88b941d1f188ef305f DE-627 ger DE-627 rakwb eng QH573-671 Andrea Palicelli verfasserin aut What Do We Have to Know about PD-L1 Expression in Prostate Cancer? A Systematic Literature Review. Part 2: Clinic–Pathologic Correlations 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Many studies have investigated the potential prognostic and predictive role of PD-L1 in prostatic carcinoma (PC). We performed a systematic literature review (PRISMA guidelines) to critically evaluate human tissue-based studies (immunohistochemistry, molecular analysis, etc.), experimental research (cell lines, mouse models), and clinical trials. Despite some controversial results and study limitations, PD-L1 expression by tumor cells may be related to clinic–pathologic features of adverse outcome, including advanced tumor stage (high pT, presence of lymph node, and distant metastases), positivity of surgical margins, high Grade Group, and castration resistance. Different PD-L1 positivity rates may be observed in matched primary PCs and various metastatic sites of the same patients. Over-fixation, type/duration of decalcification, and PD-L1 antibody clone may influence the immunohistochemical analysis of PD-L1 on bone metastases. PD-L1 seemed expressed more frequently by castration-resistant PCs (49%) as compared to hormone-sensitive PCs (17%). Some series found that PD-L1 positivity was associated with decreased time to castration resistance. Treatment with ipilimumab, cyclophosphamide/GVAX/degarelix, or degarelix alone may increase PD-L1 expression. Correlation of PD-L1 positivity with overall survival and outcomes related to tumor recurrence were rarely investigated; the few analyzed series produced conflicting results and sometimes showed limitations. Further studies are required. The testing and scoring of PD-L1 should be standardized. PD-L1 prostate cancer adenocarcinoma immunohistochemistry target-therapy Cytology Martina Bonacini verfasserin aut Stefania Croci verfasserin aut Cristina Magi-Galluzzi verfasserin aut Sofia Cañete-Portillo verfasserin aut Alcides Chaux verfasserin aut Alessandra Bisagni verfasserin aut Eleonora Zanetti verfasserin aut Dario De Biase verfasserin aut Beatrice Melli verfasserin aut Francesca Sanguedolce verfasserin aut Magda Zanelli verfasserin aut Maria Paola Bonasoni verfasserin aut Loredana De Marco verfasserin aut Alessandra Soriano verfasserin aut Stefano Ascani verfasserin aut Maurizio Zizzo verfasserin aut Carolina Castro Ruiz verfasserin aut Antonio De Leo verfasserin aut Guido Giordano verfasserin aut Matteo Landriscina verfasserin aut Giuseppe Carrieri verfasserin aut Luigi Cormio verfasserin aut Daniel M. Berney verfasserin aut Jatin Gandhi verfasserin aut Giacomo Santandrea verfasserin aut Maria Carolina Gelli verfasserin aut Alessandro Tafuni verfasserin aut Moira Ragazzi verfasserin aut In Cells MDPI AG, 2012 10(2021), 11, p 3165 (DE-627)718622081 (DE-600)2661518-6 20734409 nnns volume:10 year:2021 number:11, p 3165 https://doi.org/10.3390/cells10113165 kostenfrei https://doaj.org/article/49bdba14c7fc4b88b941d1f188ef305f kostenfrei https://www.mdpi.com/2073-4409/10/11/3165 kostenfrei https://doaj.org/toc/2073-4409 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_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 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_2011 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 10 2021 11, p 3165 |
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10.3390/cells10113165 doi (DE-627)DOAJ073495417 (DE-599)DOAJ49bdba14c7fc4b88b941d1f188ef305f DE-627 ger DE-627 rakwb eng QH573-671 Andrea Palicelli verfasserin aut What Do We Have to Know about PD-L1 Expression in Prostate Cancer? A Systematic Literature Review. Part 2: Clinic–Pathologic Correlations 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Many studies have investigated the potential prognostic and predictive role of PD-L1 in prostatic carcinoma (PC). We performed a systematic literature review (PRISMA guidelines) to critically evaluate human tissue-based studies (immunohistochemistry, molecular analysis, etc.), experimental research (cell lines, mouse models), and clinical trials. Despite some controversial results and study limitations, PD-L1 expression by tumor cells may be related to clinic–pathologic features of adverse outcome, including advanced tumor stage (high pT, presence of lymph node, and distant metastases), positivity of surgical margins, high Grade Group, and castration resistance. Different PD-L1 positivity rates may be observed in matched primary PCs and various metastatic sites of the same patients. Over-fixation, type/duration of decalcification, and PD-L1 antibody clone may influence the immunohistochemical analysis of PD-L1 on bone metastases. PD-L1 seemed expressed more frequently by castration-resistant PCs (49%) as compared to hormone-sensitive PCs (17%). Some series found that PD-L1 positivity was associated with decreased time to castration resistance. Treatment with ipilimumab, cyclophosphamide/GVAX/degarelix, or degarelix alone may increase PD-L1 expression. Correlation of PD-L1 positivity with overall survival and outcomes related to tumor recurrence were rarely investigated; the few analyzed series produced conflicting results and sometimes showed limitations. Further studies are required. The testing and scoring of PD-L1 should be standardized. PD-L1 prostate cancer adenocarcinoma immunohistochemistry target-therapy Cytology Martina Bonacini verfasserin aut Stefania Croci verfasserin aut Cristina Magi-Galluzzi verfasserin aut Sofia Cañete-Portillo verfasserin aut Alcides Chaux verfasserin aut Alessandra Bisagni verfasserin aut Eleonora Zanetti verfasserin aut Dario De Biase verfasserin aut Beatrice Melli verfasserin aut Francesca Sanguedolce verfasserin aut Magda Zanelli verfasserin aut Maria Paola Bonasoni verfasserin aut Loredana De Marco verfasserin aut Alessandra Soriano verfasserin aut Stefano Ascani verfasserin aut Maurizio Zizzo verfasserin aut Carolina Castro Ruiz verfasserin aut Antonio De Leo verfasserin aut Guido Giordano verfasserin aut Matteo Landriscina verfasserin aut Giuseppe Carrieri verfasserin aut Luigi Cormio verfasserin aut Daniel M. Berney verfasserin aut Jatin Gandhi verfasserin aut Giacomo Santandrea verfasserin aut Maria Carolina Gelli verfasserin aut Alessandro Tafuni verfasserin aut Moira Ragazzi verfasserin aut In Cells MDPI AG, 2012 10(2021), 11, p 3165 (DE-627)718622081 (DE-600)2661518-6 20734409 nnns volume:10 year:2021 number:11, p 3165 https://doi.org/10.3390/cells10113165 kostenfrei https://doaj.org/article/49bdba14c7fc4b88b941d1f188ef305f kostenfrei https://www.mdpi.com/2073-4409/10/11/3165 kostenfrei https://doaj.org/toc/2073-4409 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_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 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_2011 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 10 2021 11, p 3165 |
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10.3390/cells10113165 doi (DE-627)DOAJ073495417 (DE-599)DOAJ49bdba14c7fc4b88b941d1f188ef305f DE-627 ger DE-627 rakwb eng QH573-671 Andrea Palicelli verfasserin aut What Do We Have to Know about PD-L1 Expression in Prostate Cancer? A Systematic Literature Review. Part 2: Clinic–Pathologic Correlations 2021 Text txt rdacontent Computermedien c rdamedia Online-Ressource cr rdacarrier Many studies have investigated the potential prognostic and predictive role of PD-L1 in prostatic carcinoma (PC). We performed a systematic literature review (PRISMA guidelines) to critically evaluate human tissue-based studies (immunohistochemistry, molecular analysis, etc.), experimental research (cell lines, mouse models), and clinical trials. Despite some controversial results and study limitations, PD-L1 expression by tumor cells may be related to clinic–pathologic features of adverse outcome, including advanced tumor stage (high pT, presence of lymph node, and distant metastases), positivity of surgical margins, high Grade Group, and castration resistance. Different PD-L1 positivity rates may be observed in matched primary PCs and various metastatic sites of the same patients. Over-fixation, type/duration of decalcification, and PD-L1 antibody clone may influence the immunohistochemical analysis of PD-L1 on bone metastases. PD-L1 seemed expressed more frequently by castration-resistant PCs (49%) as compared to hormone-sensitive PCs (17%). Some series found that PD-L1 positivity was associated with decreased time to castration resistance. Treatment with ipilimumab, cyclophosphamide/GVAX/degarelix, or degarelix alone may increase PD-L1 expression. Correlation of PD-L1 positivity with overall survival and outcomes related to tumor recurrence were rarely investigated; the few analyzed series produced conflicting results and sometimes showed limitations. Further studies are required. The testing and scoring of PD-L1 should be standardized. PD-L1 prostate cancer adenocarcinoma immunohistochemistry target-therapy Cytology Martina Bonacini verfasserin aut Stefania Croci verfasserin aut Cristina Magi-Galluzzi verfasserin aut Sofia Cañete-Portillo verfasserin aut Alcides Chaux verfasserin aut Alessandra Bisagni verfasserin aut Eleonora Zanetti verfasserin aut Dario De Biase verfasserin aut Beatrice Melli verfasserin aut Francesca Sanguedolce verfasserin aut Magda Zanelli verfasserin aut Maria Paola Bonasoni verfasserin aut Loredana De Marco verfasserin aut Alessandra Soriano verfasserin aut Stefano Ascani verfasserin aut Maurizio Zizzo verfasserin aut Carolina Castro Ruiz verfasserin aut Antonio De Leo verfasserin aut Guido Giordano verfasserin aut Matteo Landriscina verfasserin aut Giuseppe Carrieri verfasserin aut Luigi Cormio verfasserin aut Daniel M. Berney verfasserin aut Jatin Gandhi verfasserin aut Giacomo Santandrea verfasserin aut Maria Carolina Gelli verfasserin aut Alessandro Tafuni verfasserin aut Moira Ragazzi verfasserin aut In Cells MDPI AG, 2012 10(2021), 11, p 3165 (DE-627)718622081 (DE-600)2661518-6 20734409 nnns volume:10 year:2021 number:11, p 3165 https://doi.org/10.3390/cells10113165 kostenfrei https://doaj.org/article/49bdba14c7fc4b88b941d1f188ef305f kostenfrei https://www.mdpi.com/2073-4409/10/11/3165 kostenfrei https://doaj.org/toc/2073-4409 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_62 GBV_ILN_63 GBV_ILN_65 GBV_ILN_69 GBV_ILN_70 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_2011 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 10 2021 11, p 3165 |
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Andrea Palicelli @@aut@@ Martina Bonacini @@aut@@ Stefania Croci @@aut@@ Cristina Magi-Galluzzi @@aut@@ Sofia Cañete-Portillo @@aut@@ Alcides Chaux @@aut@@ Alessandra Bisagni @@aut@@ Eleonora Zanetti @@aut@@ Dario De Biase @@aut@@ Beatrice Melli @@aut@@ Francesca Sanguedolce @@aut@@ Magda Zanelli @@aut@@ Maria Paola Bonasoni @@aut@@ Loredana De Marco @@aut@@ Alessandra Soriano @@aut@@ Stefano Ascani @@aut@@ Maurizio Zizzo @@aut@@ Carolina Castro Ruiz @@aut@@ Antonio De Leo @@aut@@ Guido Giordano @@aut@@ Matteo Landriscina @@aut@@ Giuseppe Carrieri @@aut@@ Luigi Cormio @@aut@@ Daniel M. Berney @@aut@@ Jatin Gandhi @@aut@@ Giacomo Santandrea @@aut@@ Maria Carolina Gelli @@aut@@ Alessandro Tafuni @@aut@@ Moira Ragazzi @@aut@@ |
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QH573-671 What Do We Have to Know about PD-L1 Expression in Prostate Cancer? A Systematic Literature Review. Part 2: Clinic–Pathologic Correlations PD-L1 prostate cancer adenocarcinoma immunohistochemistry target-therapy |
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What Do We Have to Know about PD-L1 Expression in Prostate Cancer? A Systematic Literature Review. Part 2: Clinic–Pathologic Correlations |
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Many studies have investigated the potential prognostic and predictive role of PD-L1 in prostatic carcinoma (PC). We performed a systematic literature review (PRISMA guidelines) to critically evaluate human tissue-based studies (immunohistochemistry, molecular analysis, etc.), experimental research (cell lines, mouse models), and clinical trials. Despite some controversial results and study limitations, PD-L1 expression by tumor cells may be related to clinic–pathologic features of adverse outcome, including advanced tumor stage (high pT, presence of lymph node, and distant metastases), positivity of surgical margins, high Grade Group, and castration resistance. Different PD-L1 positivity rates may be observed in matched primary PCs and various metastatic sites of the same patients. Over-fixation, type/duration of decalcification, and PD-L1 antibody clone may influence the immunohistochemical analysis of PD-L1 on bone metastases. PD-L1 seemed expressed more frequently by castration-resistant PCs (49%) as compared to hormone-sensitive PCs (17%). Some series found that PD-L1 positivity was associated with decreased time to castration resistance. Treatment with ipilimumab, cyclophosphamide/GVAX/degarelix, or degarelix alone may increase PD-L1 expression. Correlation of PD-L1 positivity with overall survival and outcomes related to tumor recurrence were rarely investigated; the few analyzed series produced conflicting results and sometimes showed limitations. Further studies are required. The testing and scoring of PD-L1 should be standardized. |
abstractGer |
Many studies have investigated the potential prognostic and predictive role of PD-L1 in prostatic carcinoma (PC). We performed a systematic literature review (PRISMA guidelines) to critically evaluate human tissue-based studies (immunohistochemistry, molecular analysis, etc.), experimental research (cell lines, mouse models), and clinical trials. Despite some controversial results and study limitations, PD-L1 expression by tumor cells may be related to clinic–pathologic features of adverse outcome, including advanced tumor stage (high pT, presence of lymph node, and distant metastases), positivity of surgical margins, high Grade Group, and castration resistance. Different PD-L1 positivity rates may be observed in matched primary PCs and various metastatic sites of the same patients. Over-fixation, type/duration of decalcification, and PD-L1 antibody clone may influence the immunohistochemical analysis of PD-L1 on bone metastases. PD-L1 seemed expressed more frequently by castration-resistant PCs (49%) as compared to hormone-sensitive PCs (17%). Some series found that PD-L1 positivity was associated with decreased time to castration resistance. Treatment with ipilimumab, cyclophosphamide/GVAX/degarelix, or degarelix alone may increase PD-L1 expression. Correlation of PD-L1 positivity with overall survival and outcomes related to tumor recurrence were rarely investigated; the few analyzed series produced conflicting results and sometimes showed limitations. Further studies are required. The testing and scoring of PD-L1 should be standardized. |
abstract_unstemmed |
Many studies have investigated the potential prognostic and predictive role of PD-L1 in prostatic carcinoma (PC). We performed a systematic literature review (PRISMA guidelines) to critically evaluate human tissue-based studies (immunohistochemistry, molecular analysis, etc.), experimental research (cell lines, mouse models), and clinical trials. Despite some controversial results and study limitations, PD-L1 expression by tumor cells may be related to clinic–pathologic features of adverse outcome, including advanced tumor stage (high pT, presence of lymph node, and distant metastases), positivity of surgical margins, high Grade Group, and castration resistance. Different PD-L1 positivity rates may be observed in matched primary PCs and various metastatic sites of the same patients. Over-fixation, type/duration of decalcification, and PD-L1 antibody clone may influence the immunohistochemical analysis of PD-L1 on bone metastases. PD-L1 seemed expressed more frequently by castration-resistant PCs (49%) as compared to hormone-sensitive PCs (17%). Some series found that PD-L1 positivity was associated with decreased time to castration resistance. Treatment with ipilimumab, cyclophosphamide/GVAX/degarelix, or degarelix alone may increase PD-L1 expression. Correlation of PD-L1 positivity with overall survival and outcomes related to tumor recurrence were rarely investigated; the few analyzed series produced conflicting results and sometimes showed limitations. Further studies are required. The testing and scoring of PD-L1 should be standardized. |
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