[Drug induced hepatotoxicity in targeted therapy for lung cancer]
Xueqin Chen1, Shaoyu Yang1, Shenglin Ma1
1Department of Medical Oncology, Affiliated Hangzhou Hospital (Hangzhou First People's Hospital), Nanjing Medical University, Hangzhou 310006, China.
Abstract:
Targeted drugs aimed at driver gene, such as Gefitinib, Erlotinib and Crizotinib, have an irreplaceable position in the therapy of advanced non-small cell lung cancer. These drugs bring benefit to patients, however, higher hepatotoxicity is also presented. Now, drug induced hepatotoxicity and its mechanism are reviewed.
Insights
Targeted therapies like Gefitinib for non-small cell lung cancer offer benefits but can cause liver damage. This review examines drug-induced hepatotoxicity and its underlying mechanisms.
Area of Science:
- Oncology
- Pharmacology
- Toxicology
Context:
- Targeted therapies targeting driver genes are crucial for advanced non-small cell lung cancer (NSCLC).
- Drugs such as Gefitinib, Erlotinib, and Crizotinib are standard treatments for NSCLC.
- These targeted drugs are associated with increased risks of hepatotoxicity.
Purpose:
- To review the mechanisms of drug-induced liver injury (DILI) in NSCLC patients.
- To discuss the clinical presentation and management of DILI associated with targeted therapies.
- To highlight the importance of monitoring liver function during treatment.
Summary:
- Gefitinib, Erlotinib, and Crizotinib are effective in treating advanced NSCLC by targeting specific driver genes.
- Hepatotoxicity is a significant adverse effect of these targeted drugs.
- Understanding the mechanisms of DILI is essential for mitigating risks and improving patient outcomes.
Impact:
- Provides a comprehensive overview of DILI in the context of NSCLC targeted therapy.
- Aids clinicians in identifying and managing liver-related adverse events.
- Contributes to safer and more effective cancer treatment strategies.
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