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PD-L1 Expression in Medullary Thyroid Carcinoma and Its Association with Clinicopathological Findings

Objective:  Medullary thyroid carcinoma (MTC) is a rare tumor originating from parafollicular C cells. It has more aggressive biologic behavior than differentiated thyroid carcinomas, and it is insensitive to treatment with radioactive iodine. Vandetanib and cabozantinib are the newly approved tyros...

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Autores principales: Kemal, Yasemin, Caliskan, Sultan, Gun, Seda, Kefeli, Mehmet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Federation of Turkish Pathology Societies 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9999690/
https://www.ncbi.nlm.nih.gov/pubmed/34580845
http://dx.doi.org/10.5146/tjpath.2021.01558
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author Kemal, Yasemin
Caliskan, Sultan
Gun, Seda
Kefeli, Mehmet
author_facet Kemal, Yasemin
Caliskan, Sultan
Gun, Seda
Kefeli, Mehmet
author_sort Kemal, Yasemin
collection PubMed
description Objective:  Medullary thyroid carcinoma (MTC) is a rare tumor originating from parafollicular C cells. It has more aggressive biologic behavior than differentiated thyroid carcinomas, and it is insensitive to treatment with radioactive iodine. Vandetanib and cabozantinib are the newly approved tyrosine kinase inhibitors in advanced stages, but novel effective systemic therapeutics could be crucial and needed for the clinical management of these patients. We aimed to evaluate the Programmed death-ligand 1 (PD-L1) expression, which is a novel immunotherapy target, in our MTC cohort, and determine whether it has an association with clinical and pathological features. Material and Method:  This retrospective study involved 41 cases of MTC with a median follow-up of 54 months. PD-L1 monoclonal antibody (SP263 clone) was investigated immunohistochemically. Complete and/or partial membranous staining pattern in more than 1% of tumor cells was considered positive. The correlations of PD-L1 expression with clinicopathologic and prognostic features were analyzed. Results:  PD-L1 positivity was detected in 5 (12.2%) of 41 tumors. The extent of PD-L1 staining was low (<5%) for all tumors. There was no clinicopathologic and prognostic relevance regarding PD-L1 expression in our MTC patients. Conclusion:  Although PD-L1 expression could be a potential biomarker to predict the prognosis of various cancers and response to checkpoint inhibitors, we did not find any significant correlation between PD-L1 expression and clinicopathologic features in our cases. Studies with larger patient numbers are still required to perform a more comprehensive analysis.
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spelling pubmed-99996902023-04-21 PD-L1 Expression in Medullary Thyroid Carcinoma and Its Association with Clinicopathological Findings Kemal, Yasemin Caliskan, Sultan Gun, Seda Kefeli, Mehmet Turk Patoloji Derg Original Article Objective:  Medullary thyroid carcinoma (MTC) is a rare tumor originating from parafollicular C cells. It has more aggressive biologic behavior than differentiated thyroid carcinomas, and it is insensitive to treatment with radioactive iodine. Vandetanib and cabozantinib are the newly approved tyrosine kinase inhibitors in advanced stages, but novel effective systemic therapeutics could be crucial and needed for the clinical management of these patients. We aimed to evaluate the Programmed death-ligand 1 (PD-L1) expression, which is a novel immunotherapy target, in our MTC cohort, and determine whether it has an association with clinical and pathological features. Material and Method:  This retrospective study involved 41 cases of MTC with a median follow-up of 54 months. PD-L1 monoclonal antibody (SP263 clone) was investigated immunohistochemically. Complete and/or partial membranous staining pattern in more than 1% of tumor cells was considered positive. The correlations of PD-L1 expression with clinicopathologic and prognostic features were analyzed. Results:  PD-L1 positivity was detected in 5 (12.2%) of 41 tumors. The extent of PD-L1 staining was low (<5%) for all tumors. There was no clinicopathologic and prognostic relevance regarding PD-L1 expression in our MTC patients. Conclusion:  Although PD-L1 expression could be a potential biomarker to predict the prognosis of various cancers and response to checkpoint inhibitors, we did not find any significant correlation between PD-L1 expression and clinicopathologic features in our cases. Studies with larger patient numbers are still required to perform a more comprehensive analysis. Federation of Turkish Pathology Societies 2022-05-19 /pmc/articles/PMC9999690/ /pubmed/34580845 http://dx.doi.org/10.5146/tjpath.2021.01558 Text en Copyright © 2022 The Author(s). https://creativecommons.org/licenses/by/4.0/This is an open-access article published by Federation of Turkish Pathology Societies under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) which permits unrestricted use, distribution, and reproduction in any medium or format, provided the original work is properly cited. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Original Article
Kemal, Yasemin
Caliskan, Sultan
Gun, Seda
Kefeli, Mehmet
PD-L1 Expression in Medullary Thyroid Carcinoma and Its Association with Clinicopathological Findings
title PD-L1 Expression in Medullary Thyroid Carcinoma and Its Association with Clinicopathological Findings
title_full PD-L1 Expression in Medullary Thyroid Carcinoma and Its Association with Clinicopathological Findings
title_fullStr PD-L1 Expression in Medullary Thyroid Carcinoma and Its Association with Clinicopathological Findings
title_full_unstemmed PD-L1 Expression in Medullary Thyroid Carcinoma and Its Association with Clinicopathological Findings
title_short PD-L1 Expression in Medullary Thyroid Carcinoma and Its Association with Clinicopathological Findings
title_sort pd-l1 expression in medullary thyroid carcinoma and its association with clinicopathological findings
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9999690/
https://www.ncbi.nlm.nih.gov/pubmed/34580845
http://dx.doi.org/10.5146/tjpath.2021.01558
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