PI3K Inhibitors in Cancer: Clinical Implications and Adverse Effects

Rosalin Mishra1, Hima Patel1, Samar Alanazi1

  • 1Department of Pharmaceutical Sciences, College of Pharmacy, University of Cincinnati, Cincinnati, OH 45267-0514, USA.

Insights

The phosphatidylinositol-3 kinase (PI3K) pathway is vital in many cancers. This review examines PI3K inhibitors in clinical trials, discussing their efficacy, toxicities, and potential for future cancer treatments.

Area of Science:

  • Oncology
  • Molecular Biology
  • Pharmacology

Background:

  • The phosphatidylinositol-3 kinase (PI3K) pathway is frequently dysregulated in various cancers, including breast, gastric, and prostate cancers.
  • PI3K signaling is critical for cancer cell survival, angiogenesis, and metastasis, positioning it as a key therapeutic target.

Purpose of the Study:

  • To review the current landscape of phosphatidylinositol-3 kinase (PI3K) inhibitors in clinical trials for various cancer types.
  • To analyze the efficacy, safety, and challenges associated with PI3K inhibitors as monotherapy or combination treatments.
  • To highlight novel PI3K-targeting drugs with potential for clinical translation.

Main Methods:

  • Comprehensive review of ongoing and completed clinical trials involving pan-PI3K, isoform-specific, and dual PI3K/mTOR inhibitors.
  • Analysis of treatment outcomes, drug-related toxicities, and adverse events reported in clinical studies.
  • Evaluation of resistance mechanisms and challenges in PI3K inhibitor therapy.

Main Results:

  • PI3K inhibitors show promise in various cancer types, with ongoing trials evaluating their efficacy in monotherapy and combination regimens.
  • Drug-related toxicities and adverse events are significant challenges impacting treatment outcomes and leading to treatment failure.
  • Understanding resistance mechanisms is crucial for optimizing PI3K inhibitor therapy.

Conclusions:

  • PI3K inhibitors represent a promising therapeutic strategy for a range of cancers, but careful management of toxicities and overcoming resistance are essential.
  • Further research and development of novel PI3K inhibitors are needed to improve clinical outcomes and expand treatment options.

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