Key result
A 70-year-old female treated with osimertinib for metastatic lung adenocarcinoma developed severe QTc prolongation (581 msec) and new-onset cardiomyopathy, which improved upon correction of hypokalemia.
Why the study?
Osimertinib is associated with cardiac-related adverse events, including cardiac dysfunction and prolonged QTc interval, highlighting the need for comprehensive cardiovascular evaluation and monitoring.
Case Report (n=1)
Osimertinib therapy can be associated with severe cardiotoxicity, including QTc prolongation and cardiomyopathy, necessitating vigilant monitoring of electrolytes and cardiac function.
Osimertinib cardiotoxicity may require close QTc and LVEF monitoring with electrolyte correction; this case report leaves open the true incidence and risk factors.
Background: Osimertinib has improved outcomes and is indicated by Food and Drug Administration (FDA) for epidermal growth factor receptor (EGFR)-mutated lung cancer. Osimertinib use is associated with cardiac-related adverse events, including cardiac dysfunction and or prolonged QTc interval. There is an increasing need for a comprehensive evaluation prior to the initiation of Osimertinib with detailed assessment of clinical history particularly looking at the cardiovascular risk factors, a protocol driven close cardio-oncology with periodic electrolyte and ECG monitoring during the therapy, as these high risk patients are associated with higher rates of cardiotoxicity compared with the low risk patient population.Case presentation: We report a patient who presented with cardiomyopathy, manifested by prolonged QTc interval, new valvular and left ventricular systolic dysfunction, six months into her treatment with Osimertinib. With a timely detection and treatment of her electrolyte abnormality and poor oral intake, we were able to correct the markedly prolonged QTc interval and to prevent potential life threatening arrhythmia. Conclusions: Patients receiving third generation tyrosine kinase inhibitor, Osimertinib, should be carefully monitored for development of cancer treatment-related cardiac dysfunction (CTRCD). Significant number of these patients also have other associated cardiac risk factors and comorbidities including poor nutrition. With poor po intake due to comorbidities this sub group of patients are even more susceptible to significant electrolyte abnormalities. Our case highlights the importance of close monitoring of especially these patients with regular electrocardiograms (EKGs), electrolyte panels, along with assessment of left ventricular function when needed to detect and intervene Osimertinib related cardiotoxicity.
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Medepalli et al. (2021) conducted a case report in Metastatic lung adenocarcinoma (n=1). Osimertinib was evaluated on Development of prolonged QTc interval and cardiomyopathy. A 70-year-old female treated with osimertinib for metastatic lung adenocarcinoma developed severe QTc prolongation (581 msec) and new-onset cardiomyopathy, which improved upon correction of hypokalemia.
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