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Differentiating pulmonary hypertension associated with protein kinase inhibitors

Protein kinase inhibitors (PKIs) have been implicated in pulmonary vascular toxicities including risk factors for at least three of the five World Health Organization groups of pulmonary hypertension (PH). These toxicities include direct drug‐induced pulmonary arterial hypertension, an increase in c...

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Detalles Bibliográficos
Autores principales: Jacobs, Joshua A., Jahangir, Eiman, Ryan, John J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9248793/
https://www.ncbi.nlm.nih.gov/pubmed/35795494
http://dx.doi.org/10.1002/pul2.12075
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author Jacobs, Joshua A.
Jahangir, Eiman
Ryan, John J.
author_facet Jacobs, Joshua A.
Jahangir, Eiman
Ryan, John J.
author_sort Jacobs, Joshua A.
collection PubMed
description Protein kinase inhibitors (PKIs) have been implicated in pulmonary vascular toxicities including risk factors for at least three of the five World Health Organization groups of pulmonary hypertension (PH). These toxicities include direct drug‐induced pulmonary arterial hypertension, an increase in cardiomyopathies, and an increase in interstitial lung disease. On‐ and off‐target toxicities are common within multitargeted PKIs leading to cardiopulmonary toxicities. This review highlights the incidence, possible mechanisms, and management strategies for each group of possible PKI‐induced PH. Future identification and clarification of protein kinase pathways for both mechanisms of toxicity and pathophysiology for PH could lead to improvements in patient care in oncology and pulmonary vascular diseases.
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spelling pubmed-92487932022-07-05 Differentiating pulmonary hypertension associated with protein kinase inhibitors Jacobs, Joshua A. Jahangir, Eiman Ryan, John J. Pulm Circ Review Articles Protein kinase inhibitors (PKIs) have been implicated in pulmonary vascular toxicities including risk factors for at least three of the five World Health Organization groups of pulmonary hypertension (PH). These toxicities include direct drug‐induced pulmonary arterial hypertension, an increase in cardiomyopathies, and an increase in interstitial lung disease. On‐ and off‐target toxicities are common within multitargeted PKIs leading to cardiopulmonary toxicities. This review highlights the incidence, possible mechanisms, and management strategies for each group of possible PKI‐induced PH. Future identification and clarification of protein kinase pathways for both mechanisms of toxicity and pathophysiology for PH could lead to improvements in patient care in oncology and pulmonary vascular diseases. John Wiley and Sons Inc. 2022-05-11 /pmc/articles/PMC9248793/ /pubmed/35795494 http://dx.doi.org/10.1002/pul2.12075 Text en © 2022 The Authors. Pulmonary Circulation published by John Wiley & Sons Ltd on behalf of Pulmonary Vascular Research Institute. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Review Articles
Jacobs, Joshua A.
Jahangir, Eiman
Ryan, John J.
Differentiating pulmonary hypertension associated with protein kinase inhibitors
title Differentiating pulmonary hypertension associated with protein kinase inhibitors
title_full Differentiating pulmonary hypertension associated with protein kinase inhibitors
title_fullStr Differentiating pulmonary hypertension associated with protein kinase inhibitors
title_full_unstemmed Differentiating pulmonary hypertension associated with protein kinase inhibitors
title_short Differentiating pulmonary hypertension associated with protein kinase inhibitors
title_sort differentiating pulmonary hypertension associated with protein kinase inhibitors
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9248793/
https://www.ncbi.nlm.nih.gov/pubmed/35795494
http://dx.doi.org/10.1002/pul2.12075
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