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Molecular predictors of response to pembrolizumab in thymic carcinoma

Thymic carcinoma is rare and has a poorer prognosis than thymomas. The treatment options are limited after failure of platinum-based chemotherapy. We previously performed a single-center phase II study of pembrolizumab in patients with advanced thymic carcinoma, showing a 22.5% response rate. Here,...

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Autores principales: He, Yongfeng, Ramesh, Archana, Gusev, Yuriy, Bhuvaneshwar, Krithika, Giaccone, Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8484507/
https://www.ncbi.nlm.nih.gov/pubmed/34622229
http://dx.doi.org/10.1016/j.xcrm.2021.100392
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author He, Yongfeng
Ramesh, Archana
Gusev, Yuriy
Bhuvaneshwar, Krithika
Giaccone, Giuseppe
author_facet He, Yongfeng
Ramesh, Archana
Gusev, Yuriy
Bhuvaneshwar, Krithika
Giaccone, Giuseppe
author_sort He, Yongfeng
collection PubMed
description Thymic carcinoma is rare and has a poorer prognosis than thymomas. The treatment options are limited after failure of platinum-based chemotherapy. We previously performed a single-center phase II study of pembrolizumab in patients with advanced thymic carcinoma, showing a 22.5% response rate. Here, we characterize the genomic and transcriptomic profile of thymic carcinoma samples from 10 patients (5 non-responders versus 5 responders) in this cohort, with the main aim of identifying potential predictors of response to immunotherapy. We find that expression of PDL1 and alterations in genes or pathways that correlated with PD-L1 expression (CYLD and BAP1) could be potential predictors for response or resistance to immunotherapy in patients with advanced thymic carcinoma. Our study provides insights into potential predictive markers/pathways to select patients with thymic carcinoma for anti-PD-1 immunotherapy.
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spelling pubmed-84845072021-10-06 Molecular predictors of response to pembrolizumab in thymic carcinoma He, Yongfeng Ramesh, Archana Gusev, Yuriy Bhuvaneshwar, Krithika Giaccone, Giuseppe Cell Rep Med Article Thymic carcinoma is rare and has a poorer prognosis than thymomas. The treatment options are limited after failure of platinum-based chemotherapy. We previously performed a single-center phase II study of pembrolizumab in patients with advanced thymic carcinoma, showing a 22.5% response rate. Here, we characterize the genomic and transcriptomic profile of thymic carcinoma samples from 10 patients (5 non-responders versus 5 responders) in this cohort, with the main aim of identifying potential predictors of response to immunotherapy. We find that expression of PDL1 and alterations in genes or pathways that correlated with PD-L1 expression (CYLD and BAP1) could be potential predictors for response or resistance to immunotherapy in patients with advanced thymic carcinoma. Our study provides insights into potential predictive markers/pathways to select patients with thymic carcinoma for anti-PD-1 immunotherapy. Elsevier 2021-09-03 /pmc/articles/PMC8484507/ /pubmed/34622229 http://dx.doi.org/10.1016/j.xcrm.2021.100392 Text en © 2021 The Author(s) https://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 Article
He, Yongfeng
Ramesh, Archana
Gusev, Yuriy
Bhuvaneshwar, Krithika
Giaccone, Giuseppe
Molecular predictors of response to pembrolizumab in thymic carcinoma
title Molecular predictors of response to pembrolizumab in thymic carcinoma
title_full Molecular predictors of response to pembrolizumab in thymic carcinoma
title_fullStr Molecular predictors of response to pembrolizumab in thymic carcinoma
title_full_unstemmed Molecular predictors of response to pembrolizumab in thymic carcinoma
title_short Molecular predictors of response to pembrolizumab in thymic carcinoma
title_sort molecular predictors of response to pembrolizumab in thymic carcinoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8484507/
https://www.ncbi.nlm.nih.gov/pubmed/34622229
http://dx.doi.org/10.1016/j.xcrm.2021.100392
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