Osimertinib-Induced Cardiomyopathy
Shruti R Patel1, Sherry-Ann N Brown2, Jilan E Kubusek3
1Department of Internal Medicine, Mayo Clinic, Rochester, Minnesota.
Abstract:
Osimertinib is the preferred treatment in patients with metastatic non-small cell lung cancer with epidermal growth factor receptor mutations. We report a case series of acute cardiomyopathy with heart failure exacerbation during osimertinib treatment. We suggest that cardiotoxicity from osimertinib is reversible and occurs at a dose of 80 mg/day. (Level of Difficulty: Intermediate.).
Insights
Osimertinib can cause acute heart failure in patients with metastatic non-small cell lung cancer. This cardiotoxicity appears reversible and linked to an 80 mg/day dose, suggesting careful monitoring during treatment.
Area of Science:
- Oncology
- Cardiology
- Pharmacology
Background:
- Osimertinib is a targeted therapy for metastatic non-small cell lung cancer (NSCLC) with specific epidermal growth factor receptor (EGFR) mutations.
- Standard osimertinib dosage is 80 mg/day, and it is generally well-tolerated.
Observation:
- A case series identified acute cardiomyopathy and heart failure exacerbation in patients undergoing osimertinib treatment.
- These cardiac events manifested during therapy with osimertinib at the standard 80 mg/day dose.
Findings:
- The observed cardiotoxicity associated with osimertinib treatment was reversible.
- The cardiac adverse events were dose-dependent, specifically noted at 80 mg/day.
Implications:
- Cardiotoxicity is a potential adverse effect of osimertinib that requires clinical awareness.
- Monitoring cardiac function in patients receiving osimertinib may be warranted, especially at the standard 80 mg/day dose.
- The reversibility of osimertinib-induced cardiotoxicity suggests potential for management and continued oncologic therapy.
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