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CDK 4/6 inhibitors for the treatment of meningioma
Meningiomas are the most common non-metastatic brain tumors, and although the majority are relatively slow-growing and histologically benign, a subset of meningiomas are aggressive and remain challenging to treat. Despite a standard of care that includes surgical resection and radiotherapy, and rece...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9354681/ https://www.ncbi.nlm.nih.gov/pubmed/35936751 http://dx.doi.org/10.3389/fonc.2022.931371 |
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author | Young, Jacob S. Kidwell, Reilly L. Zheng, Allison Haddad, Alex F. Aghi, Manish K. Raleigh, David R. Schulte, Jessica D. Butowski, Nicholas A. |
author_facet | Young, Jacob S. Kidwell, Reilly L. Zheng, Allison Haddad, Alex F. Aghi, Manish K. Raleigh, David R. Schulte, Jessica D. Butowski, Nicholas A. |
author_sort | Young, Jacob S. |
collection | PubMed |
description | Meningiomas are the most common non-metastatic brain tumors, and although the majority are relatively slow-growing and histologically benign, a subset of meningiomas are aggressive and remain challenging to treat. Despite a standard of care that includes surgical resection and radiotherapy, and recent advances in meningioma molecular grouping, there are no systemic medical options for patients with meningiomas that are resistant to standard interventions. Misactivation of the cell cycle at the level of CDK4/6 is common in high-grade or molecularly aggressive meningiomas, and CDK4/6 has emerged as a potential target for systemic meningioma treatments. In this review, we describe the preclinical evidence for CDK4/6 inhibitors as a treatment for high-grade meningiomas and summarize evolving clinical experience with these agents. Further, we highlight upcoming clinical trials for patients meningiomas, and discuss future directions aimed at optimizing the efficacy of these therapies and selecting patients most likely to benefit from their use. |
format | Online Article Text |
id | pubmed-9354681 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93546812022-08-06 CDK 4/6 inhibitors for the treatment of meningioma Young, Jacob S. Kidwell, Reilly L. Zheng, Allison Haddad, Alex F. Aghi, Manish K. Raleigh, David R. Schulte, Jessica D. Butowski, Nicholas A. Front Oncol Oncology Meningiomas are the most common non-metastatic brain tumors, and although the majority are relatively slow-growing and histologically benign, a subset of meningiomas are aggressive and remain challenging to treat. Despite a standard of care that includes surgical resection and radiotherapy, and recent advances in meningioma molecular grouping, there are no systemic medical options for patients with meningiomas that are resistant to standard interventions. Misactivation of the cell cycle at the level of CDK4/6 is common in high-grade or molecularly aggressive meningiomas, and CDK4/6 has emerged as a potential target for systemic meningioma treatments. In this review, we describe the preclinical evidence for CDK4/6 inhibitors as a treatment for high-grade meningiomas and summarize evolving clinical experience with these agents. Further, we highlight upcoming clinical trials for patients meningiomas, and discuss future directions aimed at optimizing the efficacy of these therapies and selecting patients most likely to benefit from their use. Frontiers Media S.A. 2022-07-22 /pmc/articles/PMC9354681/ /pubmed/35936751 http://dx.doi.org/10.3389/fonc.2022.931371 Text en Copyright © 2022 Young, Kidwell, Zheng, Haddad, Aghi, Raleigh, Schulte and Butowski https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author (s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Young, Jacob S. Kidwell, Reilly L. Zheng, Allison Haddad, Alex F. Aghi, Manish K. Raleigh, David R. Schulte, Jessica D. Butowski, Nicholas A. CDK 4/6 inhibitors for the treatment of meningioma |
title | CDK 4/6 inhibitors for the treatment of meningioma |
title_full | CDK 4/6 inhibitors for the treatment of meningioma |
title_fullStr | CDK 4/6 inhibitors for the treatment of meningioma |
title_full_unstemmed | CDK 4/6 inhibitors for the treatment of meningioma |
title_short | CDK 4/6 inhibitors for the treatment of meningioma |
title_sort | cdk 4/6 inhibitors for the treatment of meningioma |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9354681/ https://www.ncbi.nlm.nih.gov/pubmed/35936751 http://dx.doi.org/10.3389/fonc.2022.931371 |
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