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Programme death ligand 1 expressions as a surrogate for determining immunotherapy in cervical carcinoma patients

BACKGROUND: The programme death ligand1 and its receptor (PD-1/PD-L1) interaction is a target for blockage by immunotherapy that uses the body’s own immune system. Some studies show that PD-L1 expressing tumours are also more aggressive with poor prognosis. This study evaluated the immunohistochemic...

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Autores principales: Omenai, Sebastian A., Ajani, Mustapha A., Okolo, Clement A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8827435/
https://www.ncbi.nlm.nih.gov/pubmed/35139126
http://dx.doi.org/10.1371/journal.pone.0263615
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author Omenai, Sebastian A.
Ajani, Mustapha A.
Okolo, Clement A.
author_facet Omenai, Sebastian A.
Ajani, Mustapha A.
Okolo, Clement A.
author_sort Omenai, Sebastian A.
collection PubMed
description BACKGROUND: The programme death ligand1 and its receptor (PD-1/PD-L1) interaction is a target for blockage by immunotherapy that uses the body’s own immune system. Some studies show that PD-L1 expressing tumours are also more aggressive with poor prognosis. This study evaluated the immunohistochemical expression of PD-L1 in uterine cervical carcinomas. Women with cervical cancer would benefit from its use as a marker in therapy and prognosis. METHODS: Hospital-based cross-sectional retrospective study was conducted. The study materials included 183 archived formalin fixed and paraffin embedded (FFPE) tissue blocks with histological diagnosis of cervical carcinoma diagnosed in our facility within a five-year period (January 2012 and December 2016) that met the study criteria. Data were extracted from records in the Department and immunohistochemistry was done using polyclonal antibodies to PD-L1 (GTX104763, Genetex). Obtained data were analysed using SPSS version 23. P < 0.05 was considered significant. RESULTS: A hundred and eighty-three cases of cervical cancer were studied. PD-L1 was positive in 57.4% of all cases. The diffuse pattern of staining was the major pattern accounting for 88.5% of positive cases. Poorly differentiated cervical carcinomas are less likely to express PD-L1. Within the histologic types, the squamous cell carcinomas expressed PD-L1 in 58.7%, and 50% of adenocarcinomas were positive. PD-L1 was not expressed in all cases of adenoid cystic carcinomas and basaloid squamous cell carcinomas. CONCLUSION: A significant population of cervical carcinoma expresses PD-L1 by immunohistochemistry. PD-L1 prevalence is lower amongst the poorly differentiated cancers compared to other grades.
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spelling pubmed-88274352022-02-10 Programme death ligand 1 expressions as a surrogate for determining immunotherapy in cervical carcinoma patients Omenai, Sebastian A. Ajani, Mustapha A. Okolo, Clement A. PLoS One Research Article BACKGROUND: The programme death ligand1 and its receptor (PD-1/PD-L1) interaction is a target for blockage by immunotherapy that uses the body’s own immune system. Some studies show that PD-L1 expressing tumours are also more aggressive with poor prognosis. This study evaluated the immunohistochemical expression of PD-L1 in uterine cervical carcinomas. Women with cervical cancer would benefit from its use as a marker in therapy and prognosis. METHODS: Hospital-based cross-sectional retrospective study was conducted. The study materials included 183 archived formalin fixed and paraffin embedded (FFPE) tissue blocks with histological diagnosis of cervical carcinoma diagnosed in our facility within a five-year period (January 2012 and December 2016) that met the study criteria. Data were extracted from records in the Department and immunohistochemistry was done using polyclonal antibodies to PD-L1 (GTX104763, Genetex). Obtained data were analysed using SPSS version 23. P < 0.05 was considered significant. RESULTS: A hundred and eighty-three cases of cervical cancer were studied. PD-L1 was positive in 57.4% of all cases. The diffuse pattern of staining was the major pattern accounting for 88.5% of positive cases. Poorly differentiated cervical carcinomas are less likely to express PD-L1. Within the histologic types, the squamous cell carcinomas expressed PD-L1 in 58.7%, and 50% of adenocarcinomas were positive. PD-L1 was not expressed in all cases of adenoid cystic carcinomas and basaloid squamous cell carcinomas. CONCLUSION: A significant population of cervical carcinoma expresses PD-L1 by immunohistochemistry. PD-L1 prevalence is lower amongst the poorly differentiated cancers compared to other grades. Public Library of Science 2022-02-09 /pmc/articles/PMC8827435/ /pubmed/35139126 http://dx.doi.org/10.1371/journal.pone.0263615 Text en © 2022 Omenai et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed 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, provided the original author and source are credited.
spellingShingle Research Article
Omenai, Sebastian A.
Ajani, Mustapha A.
Okolo, Clement A.
Programme death ligand 1 expressions as a surrogate for determining immunotherapy in cervical carcinoma patients
title Programme death ligand 1 expressions as a surrogate for determining immunotherapy in cervical carcinoma patients
title_full Programme death ligand 1 expressions as a surrogate for determining immunotherapy in cervical carcinoma patients
title_fullStr Programme death ligand 1 expressions as a surrogate for determining immunotherapy in cervical carcinoma patients
title_full_unstemmed Programme death ligand 1 expressions as a surrogate for determining immunotherapy in cervical carcinoma patients
title_short Programme death ligand 1 expressions as a surrogate for determining immunotherapy in cervical carcinoma patients
title_sort programme death ligand 1 expressions as a surrogate for determining immunotherapy in cervical carcinoma patients
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8827435/
https://www.ncbi.nlm.nih.gov/pubmed/35139126
http://dx.doi.org/10.1371/journal.pone.0263615
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