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[A Case of Significant Ejection Fraction Reduction and Heart Failure Induced by Osimertinib]
Shunsuke Ito1, Aoi Otsuka, Hiroshi Ishii
1Dept. of Respiratory Medicine, Japan Organization of Occupational Health and Safety, Kanto Rosai Hospital.
Background:
In recent years, osimertinib has been increasingly used as a therapeutic drug for epidermal growth factor receptor(EGFR)mutation-positive lung cancer, with heart failure rarely reported as an adverse event. We report here a case of a significantly decreased ejection fraction and heart failure that were induced by osimertinib. We consider the case important and include a discussion of relevant previous reports.
Case:
The patient was a 73-year-old woman who had been on oral gefitinib as first-line treatment for EGFR mutation-positive(exon19 deletion)non-small cell lung cancer for approximately 1 year and 2 months. Thereafter, she tested positive for an EGFR resistance mutation(T790M); and accordingly, oral osimerti- nib was started at 80mg/day as second-line treatment. After continuing this treatment for 6 months with no particular adverse events, she visited our hospital and was found to have dyspnea on exertion and increased pleural effusion. Based on these findings, cancer relapse was suspected, and the patient was hospitalized for detailed examinations. She was diagnosed with heart failure based on the elevated BNP level that was found in a blood test and CT and echocardiography findings, and her ejection fraction deteriorated to 19% from a pretreatment level of 59%. The conditions improved after diuretic and b- blocker treatment. Given the absence of any possible cause of heart failure or reduced ejection fraction in her past history of illness and medication, we concluded that these conditions were induced by osimertinib.
Conclusion:
While heart failure induced by EGFR-TKIs has been rarely reported, osimertinib may cause cardiomyopathy due to human epidermal growth factor receptor type 2(HER2)inhibitory activity.
Insights
Osimertinib, a treatment for EGFR-mutation-positive lung cancer, can rarely cause heart failure. This case highlights potential cardiac adverse events, emphasizing the need for monitoring during treatment.
Area of Science:
- Cardiology
- Oncology
- Pharmacology
Background:
- Osimertinib is a key therapy for epidermal growth factor receptor (EGFR) mutation-positive non-small cell lung cancer.
- Heart failure is an infrequently reported adverse event associated with EGFR-tyrosine kinase inhibitors (TKIs).
Observation:
- A 73-year-old woman developed heart failure with a significantly reduced ejection fraction (19%) after 6 months of osimertinib treatment.
- The patient presented with dyspnea on exertion and increased pleural effusion, initially suspected as cancer relapse.
Findings:
- Cardiac function significantly improved with standard heart failure management, including diuretics and beta-blockers.
- The adverse cardiac event was attributed to osimertinib due to the absence of other contributing factors.
Implications:
- This case underscores the potential for osimertinib to induce cardiomyopathy, possibly through inhibition of human epidermal growth factor receptor type 2 (HER2).
- Clinicians should consider monitoring cardiac function in patients receiving osimertinib, particularly those with pre-existing cardiac risk factors.
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