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Biomarkers in renal cell carcinoma: Towards a more selective immune checkpoint inhibition

Immune checkpoint inhibitors such as programmed death protein 1/programmed death-ligand 1 and cytotoxic T-lymphocyte–associated protein 4 inhibitors are already playing a central role in the treatment of metastatic renal cell carcinoma. However, they seem to be only effective in a subset of patients...

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Detalles Bibliográficos
Autores principales: Sarkis, J., Assaf, J., Alkassis, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Neoplasia Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985395/
https://www.ncbi.nlm.nih.gov/pubmed/33744727
http://dx.doi.org/10.1016/j.tranon.2021.101071
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author Sarkis, J.
Assaf, J.
Alkassis, M.
author_facet Sarkis, J.
Assaf, J.
Alkassis, M.
author_sort Sarkis, J.
collection PubMed
description Immune checkpoint inhibitors such as programmed death protein 1/programmed death-ligand 1 and cytotoxic T-lymphocyte–associated protein 4 inhibitors are already playing a central role in the treatment of metastatic renal cell carcinoma. However, they seem to be only effective in a subset of patients, with a high risk of innate and adaptive tumor resistance. Consequently, biomarkers capable of predicting immune treatment efficacy in advanced renal cancer are needed both in the clinical and the experimental setting. We hereby present a brief summary of evidence on the most studied biomarkers in metastatic renal cell carcinoma with a focus on the possible future place of T cell immunoglobulin and mucin domain-3 (TIM-3).
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spelling pubmed-79853952021-04-01 Biomarkers in renal cell carcinoma: Towards a more selective immune checkpoint inhibition Sarkis, J. Assaf, J. Alkassis, M. Transl Oncol Perspective Immune checkpoint inhibitors such as programmed death protein 1/programmed death-ligand 1 and cytotoxic T-lymphocyte–associated protein 4 inhibitors are already playing a central role in the treatment of metastatic renal cell carcinoma. However, they seem to be only effective in a subset of patients, with a high risk of innate and adaptive tumor resistance. Consequently, biomarkers capable of predicting immune treatment efficacy in advanced renal cancer are needed both in the clinical and the experimental setting. We hereby present a brief summary of evidence on the most studied biomarkers in metastatic renal cell carcinoma with a focus on the possible future place of T cell immunoglobulin and mucin domain-3 (TIM-3). Neoplasia Press 2021-03-18 /pmc/articles/PMC7985395/ /pubmed/33744727 http://dx.doi.org/10.1016/j.tranon.2021.101071 Text en © 2021 The Authors. Published by Elsevier Inc. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Perspective
Sarkis, J.
Assaf, J.
Alkassis, M.
Biomarkers in renal cell carcinoma: Towards a more selective immune checkpoint inhibition
title Biomarkers in renal cell carcinoma: Towards a more selective immune checkpoint inhibition
title_full Biomarkers in renal cell carcinoma: Towards a more selective immune checkpoint inhibition
title_fullStr Biomarkers in renal cell carcinoma: Towards a more selective immune checkpoint inhibition
title_full_unstemmed Biomarkers in renal cell carcinoma: Towards a more selective immune checkpoint inhibition
title_short Biomarkers in renal cell carcinoma: Towards a more selective immune checkpoint inhibition
title_sort biomarkers in renal cell carcinoma: towards a more selective immune checkpoint inhibition
topic Perspective
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7985395/
https://www.ncbi.nlm.nih.gov/pubmed/33744727
http://dx.doi.org/10.1016/j.tranon.2021.101071
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