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Rapid and fatal acute heart failure induced by pazopanib
Cédric van Marcke1, Benjamin Ledoux1, Bénédicte Petit1
1Department of Medical Oncology, Hopital de Jolimont, Haine-Saint-Paul, Belgium.
Abstract:
Tyrosine kinase inhibitors, represented by sunitinib, sorafenib, axitinib and pazopanib, are emerging molecules harbouring antitumoural efficacy in multiple neoplasia. We report the case of a 51-year-old woman with right thoracic sarcoma who developed fatal heart failure on pazopanib. The patient had no cardiovascular risk factor, except previous exposure to anthracycline, and her cardiac function was normally controlled before initiating the pazopanib. Despite a rapid tumour response, fatigue rapidly appeared, requiring treatment interruption 2 weeks after pazopanib introduction. After clinical improvement, the pazopanib was reintroduced at reduced dose; however, a few days later, our patient was admitted for worsening dyspnoea and fatigue. Pulmonary embolism was excluded as was pleuropericardial effusion. Brain natriuretic peptide was the only laboratory abnormality, and echocardiography revealed acute and severe heart failure. The patient died despite pazopanib arrest and inotropic support.
Insights
Tyrosine kinase inhibitors like pazopanib show anti-tumor effects but can cause severe heart failure. This case highlights the critical need for cardiac monitoring in patients receiving these treatments.
Area of Science:
- Oncology
- Cardiology
- Pharmacology
Background:
- Tyrosine kinase inhibitors (TKIs) are effective cancer treatments.
- Pazopanib is a TKI used for various cancers.
- Cardiotoxicity is a potential side effect of TKIs.
Observation:
- A 51-year-old woman with thoracic sarcoma developed fatal heart failure while on pazopanib.
- The patient had prior anthracycline exposure but no other cardiovascular risk factors.
- Cardiac function was normal before pazopanib initiation.
Findings:
- Despite initial tumor response, the patient experienced fatigue and required pazopanib interruption.
- Upon reintroduction at a reduced dose, she developed acute, severe heart failure.
- Elevated Brain Natriuretic Peptide and echocardiographic findings confirmed heart failure.
Implications:
- This case underscores the potential for pazopanib-induced cardiotoxicity, even in patients without traditional risk factors.
- Close cardiac monitoring is crucial for patients undergoing TKI therapy.
- Further research into TKI cardiotoxicity mechanisms and prevention strategies is warranted.
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