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A Review of PI3K Inhibitors in B-Cell Malignancies
The phosphoinositide 3-kinase (PI3K) pathway plays a primary role in cellular proliferation and metabolism. Inhibition of the PI3K pathway is an emerging area of drug development and cancer research. Idelalisib, copanlisib, and duvelisib are currently the only U.S. Food & Drug Administration–app...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Harborside Press LLC
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7517780/ https://www.ncbi.nlm.nih.gov/pubmed/33391855 http://dx.doi.org/10.6004/jadpro.2019.10.7.7 |
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author | Cannon, Laura Academia, Emmeline C. Glode, Ashley E. |
author_facet | Cannon, Laura Academia, Emmeline C. Glode, Ashley E. |
author_sort | Cannon, Laura |
collection | PubMed |
description | The phosphoinositide 3-kinase (PI3K) pathway plays a primary role in cellular proliferation and metabolism. Inhibition of the PI3K pathway is an emerging area of drug development and cancer research. Idelalisib, copanlisib, and duvelisib are currently the only U.S. Food & Drug Administration–approved PI3K inhibitors available for use in hematologic malignancies. These PI3K inhibitors differ in their recommended indications, selectivity of PI3K isoforms, dosing, and potential toxicities. Several ongoing studies are aiming to expand the use of such drugs and identify unique combination regimens. This article discusses the current data supporting their place in therapy for B-cell malignancies, management of adverse events, and the clinical implications for advanced practitioners for the commercially available PI3K inhibitors. |
format | Online Article Text |
id | pubmed-7517780 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Harborside Press LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-75177802020-12-31 A Review of PI3K Inhibitors in B-Cell Malignancies Cannon, Laura Academia, Emmeline C. Glode, Ashley E. J Adv Pract Oncol Prescriber's Corner The phosphoinositide 3-kinase (PI3K) pathway plays a primary role in cellular proliferation and metabolism. Inhibition of the PI3K pathway is an emerging area of drug development and cancer research. Idelalisib, copanlisib, and duvelisib are currently the only U.S. Food & Drug Administration–approved PI3K inhibitors available for use in hematologic malignancies. These PI3K inhibitors differ in their recommended indications, selectivity of PI3K isoforms, dosing, and potential toxicities. Several ongoing studies are aiming to expand the use of such drugs and identify unique combination regimens. This article discusses the current data supporting their place in therapy for B-cell malignancies, management of adverse events, and the clinical implications for advanced practitioners for the commercially available PI3K inhibitors. Harborside Press LLC 2019 2019-09-01 /pmc/articles/PMC7517780/ /pubmed/33391855 http://dx.doi.org/10.6004/jadpro.2019.10.7.7 Text en © 2019 Harborside™ http://creativecommons.org/licenses/by-nc-nd/3.0/ This article is distributed under the terms of the Creative Commons Attribution Non-Commercial Non-Derivative License, which permits unrestricted non-commercial and non-derivative use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Prescriber's Corner Cannon, Laura Academia, Emmeline C. Glode, Ashley E. A Review of PI3K Inhibitors in B-Cell Malignancies |
title | A Review of PI3K Inhibitors in B-Cell Malignancies |
title_full | A Review of PI3K Inhibitors in B-Cell Malignancies |
title_fullStr | A Review of PI3K Inhibitors in B-Cell Malignancies |
title_full_unstemmed | A Review of PI3K Inhibitors in B-Cell Malignancies |
title_short | A Review of PI3K Inhibitors in B-Cell Malignancies |
title_sort | review of pi3k inhibitors in b-cell malignancies |
topic | Prescriber's Corner |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7517780/ https://www.ncbi.nlm.nih.gov/pubmed/33391855 http://dx.doi.org/10.6004/jadpro.2019.10.7.7 |
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