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Real-world data analyses unveiled the immune-related adverse effects of immune checkpoint inhibitors across cancer types

Immune checkpoint inhibitors have demonstrated significant survival benefits in treating many types of cancers. However, their immune-related adverse events (irAEs) have not been systematically evaluated across cancer types in large-scale real-world populations. To address this gap, we conducted rea...

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Autores principales: Wang, Feicheng, Yang, Shihao, Palmer, Nathan, Fox, Kathe, Kohane, Isaac S., Liao, Katherine P., Yu, Kun-Hsing, Kou, S. C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8433190/
https://www.ncbi.nlm.nih.gov/pubmed/34508179
http://dx.doi.org/10.1038/s41698-021-00223-x
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author Wang, Feicheng
Yang, Shihao
Palmer, Nathan
Fox, Kathe
Kohane, Isaac S.
Liao, Katherine P.
Yu, Kun-Hsing
Kou, S. C.
author_facet Wang, Feicheng
Yang, Shihao
Palmer, Nathan
Fox, Kathe
Kohane, Isaac S.
Liao, Katherine P.
Yu, Kun-Hsing
Kou, S. C.
author_sort Wang, Feicheng
collection PubMed
description Immune checkpoint inhibitors have demonstrated significant survival benefits in treating many types of cancers. However, their immune-related adverse events (irAEs) have not been systematically evaluated across cancer types in large-scale real-world populations. To address this gap, we conducted real-world data analyses using nationwide insurance claims data with 85.97 million enrollees across 8 years. We identified a significantly increased risk of developing irAEs among patients receiving immunotherapy agents in all seven cancer types commonly treated with immune checkpoint inhibitors. By six months after treatment initialization, those receiving immunotherapy were 1.50–4.00 times (95% CI, lower bound from 1.15 to 2.16, upper bound from 1.69 to 20.36) more likely to develop irAEs in the first 6 months of treatment, compared to matched chemotherapy or targeted therapy groups, with a total of 92,858 patients. The risk of developing irAEs among patients using nivolumab is higher compared to those using pembrolizumab. These results confirmed the need for clinicians to assess irAEs among cancer patients undergoing immunotherapy as part of management. Our methods are extensible to characterizing the effectiveness and adverse effects of novel treatments in large populations in an efficient and economical fashion.
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spelling pubmed-84331902021-09-24 Real-world data analyses unveiled the immune-related adverse effects of immune checkpoint inhibitors across cancer types Wang, Feicheng Yang, Shihao Palmer, Nathan Fox, Kathe Kohane, Isaac S. Liao, Katherine P. Yu, Kun-Hsing Kou, S. C. NPJ Precis Oncol Article Immune checkpoint inhibitors have demonstrated significant survival benefits in treating many types of cancers. However, their immune-related adverse events (irAEs) have not been systematically evaluated across cancer types in large-scale real-world populations. To address this gap, we conducted real-world data analyses using nationwide insurance claims data with 85.97 million enrollees across 8 years. We identified a significantly increased risk of developing irAEs among patients receiving immunotherapy agents in all seven cancer types commonly treated with immune checkpoint inhibitors. By six months after treatment initialization, those receiving immunotherapy were 1.50–4.00 times (95% CI, lower bound from 1.15 to 2.16, upper bound from 1.69 to 20.36) more likely to develop irAEs in the first 6 months of treatment, compared to matched chemotherapy or targeted therapy groups, with a total of 92,858 patients. The risk of developing irAEs among patients using nivolumab is higher compared to those using pembrolizumab. These results confirmed the need for clinicians to assess irAEs among cancer patients undergoing immunotherapy as part of management. Our methods are extensible to characterizing the effectiveness and adverse effects of novel treatments in large populations in an efficient and economical fashion. Nature Publishing Group UK 2021-09-10 /pmc/articles/PMC8433190/ /pubmed/34508179 http://dx.doi.org/10.1038/s41698-021-00223-x Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Wang, Feicheng
Yang, Shihao
Palmer, Nathan
Fox, Kathe
Kohane, Isaac S.
Liao, Katherine P.
Yu, Kun-Hsing
Kou, S. C.
Real-world data analyses unveiled the immune-related adverse effects of immune checkpoint inhibitors across cancer types
title Real-world data analyses unveiled the immune-related adverse effects of immune checkpoint inhibitors across cancer types
title_full Real-world data analyses unveiled the immune-related adverse effects of immune checkpoint inhibitors across cancer types
title_fullStr Real-world data analyses unveiled the immune-related adverse effects of immune checkpoint inhibitors across cancer types
title_full_unstemmed Real-world data analyses unveiled the immune-related adverse effects of immune checkpoint inhibitors across cancer types
title_short Real-world data analyses unveiled the immune-related adverse effects of immune checkpoint inhibitors across cancer types
title_sort real-world data analyses unveiled the immune-related adverse effects of immune checkpoint inhibitors across cancer types
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8433190/
https://www.ncbi.nlm.nih.gov/pubmed/34508179
http://dx.doi.org/10.1038/s41698-021-00223-x
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