Buparlisib

From WikiMD's Food, Medicine & Wellness Encyclopedia

Buparlisib (BKM120) is a highly specific oral inhibitor of the phosphatidylinositol-3-kinase (PI3K) family, a group of enzymes involved in cellular functions such as cell growth, proliferation, differentiation, motility, survival, and intracellular trafficking, which are integral to the development and progression of cancers. Buparlisib has shown potential in targeting the PI3K pathway in cancer cells, making it a subject of interest in oncology research for its therapeutic potential in various cancers.

Mechanism of Action[edit | edit source]

Buparlisib inhibits the activity of the PI3K enzymes by binding to the ATP-binding cleft of these enzymes. This inhibition prevents the activation of the PI3K/AKT/mTOR pathway, a signaling pathway that is often overactive in many types of cancer cells, leading to uncontrolled cell growth and survival. By targeting this pathway, buparlisib aims to reduce tumor growth and proliferation.

Clinical Trials[edit | edit source]

Clinical trials have been conducted to evaluate the efficacy and safety of buparlisib in various cancers, including breast cancer, non-small cell lung cancer (NSCLC), and glioblastoma. These studies have explored buparlisib as both a monotherapy and in combination with other cancer therapies. While some trials have shown promise, the results have been mixed, with challenges such as toxicity and the development of resistance limiting its effectiveness in some cases.

Adverse Effects[edit | edit source]

The most common adverse effects associated with buparlisib include hyperglycemia, nausea, rash, fatigue, and mood changes. These side effects are generally manageable but have led to dose reductions or discontinuation in some patients. The risk of serious adverse events underscores the importance of careful patient monitoring during treatment with buparlisib.

Current Status[edit | edit source]

As of the last update, buparlisib is not yet approved by regulatory agencies such as the U.S. Food and Drug Administration (FDA) for the treatment of any cancer. Research and development efforts continue, with ongoing clinical trials aiming to better understand its therapeutic potential and to identify patient populations that may benefit most from this treatment.

Future Directions[edit | edit source]

Future research on buparlisib includes further clinical trials to optimize its use, including combination therapy strategies, dose optimization, and the identification of biomarkers to predict response to therapy. The development of strategies to manage or prevent resistance to buparlisib is also a critical area of focus.

See Also[edit | edit source]




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Contributors: Prab R. Tumpati, MD