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Published on: July 17, 2020
A Review of PI3K Inhibitors in B-Cell Malignancies
Laura Cannon1, Emmeline C Academia2, Ashley E Glode2
1The University of Texas at Austin College of Pharmacy and The University of Texas at Austin Dell Medical School LIVESTRONG Cancer Institutes, Austin, Texas.
Phosphoinositide 3-kinase (PI3K) pathway inhibitors are crucial in treating B-cell malignancies. This review covers approved PI3K inhibitors, their applications, and managing adverse events for advanced practitioners.
Area of Science:
- Oncology
- Pharmacology
Background:
- The phosphoinositide 3-kinase (PI3K) pathway is vital for cell growth and metabolism.
- Targeting the PI3K pathway is a key strategy in cancer drug development.
Purpose of the Study:
- To review current data on U.S. Food & Drug Administration-approved PI3K inhibitors for B-cell malignancies.
- To discuss adverse event management and clinical implications for healthcare providers.
Main Methods:
- Review of current clinical data and FDA-approved PI3K inhibitors.
- Analysis of drug selectivity, indications, dosing, and toxicities.
- Discussion of ongoing research for expanded use and combination therapies.
Main Results:
- Idelalisib, copanlisib, and duvelisib are approved for hematologic malignancies.
- These inhibitors vary in isoform selectivity, indications, and toxicity profiles.
- Ongoing studies explore new applications and combination regimens.
Conclusions:
- Approved PI3K inhibitors offer therapeutic options for B-cell malignancies.
- Understanding individual drug profiles and managing toxicities is essential.
- Further research will likely expand the role of PI3K inhibitors in oncology.
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