Acute cardiotoxicity after initiation of the novel tyrosine kinase inhibitor gilteritinib for acute myeloid leukemia
Autor: | Daniel Addison, Sumithira Vasu, Haseeb Nawaz, Lisa Kim, Patrick Ruz, Courtney M. Campbell, Ajay Vallakati, Jeremy Slivnick, Yaquta Kaka, Brian Fowler, Ragavendra R. Baliga |
---|---|
Rok vydání: | 2021 |
Předmět: |
medicine.medical_specialty
Myocarditis medicine.drug_class Cardiomyopathy Case Report Tyrosine-kinase inhibitor Cardiac magnetic resonance imaging Internal medicine Medicine Diseases of the circulatory (Cardiovascular) system Cardiac MRI RC254-282 Cardiotoxicity Ejection fraction Acute myeloid leukemia medicine.diagnostic_test business.industry Myeloid leukemia Neoplasms. Tumors. Oncology. Including cancer and carcinogens Gilteritinib General Medicine medicine.disease Cardio-oncology FLT3-mutation Heart failure RC666-701 Cardiology business |
Zdroj: | Cardio-oncology Cardio-Oncology, Vol 7, Iss 1, Pp 1-6 (2021) |
ISSN: | 2057-3804 |
Popis: | Background Gilteritinib is a novel FMS-like tyrosine kinase 3 inhibitor recently approved by the United States Food and Drug Administration in 2018 for relapsed or refractory acute myeloid leukemia. However, gilteritinib may be associated with underrecognized cardiotoxicities. Case presentation This case describes a patient with a history significant for hyperlipidemia who was diagnosed with relapsed acute myeloid leukemia. After four doses of gilteritinib monotherapy, she abruptly developed acute systolic heart failure with global hypokinesis and septal wall motion abnormalities. Two days after discontinuation, cardiac magnetic resonance imaging showed partial recovery of her left ventricular ejection fraction as well as myocardial edema and non-ischemic fibrosis suggestive of inflammatory cardiomyopathy. She underwent intravenous diuresis and eventually started guideline-directed heart failure therapy. Follow-up cardiac magnetic resonance imaging five months later showed improved ejection fraction with mild non-ischemic fibrosis and resolution of myocardial edema and inflammation. She later received an allogeneic stem cell transplant from a matched unrelated donor. Conclusions Gilteritinib may be associated with early cardiotoxicities, including non-ischemic cardiomyopathy and myocarditis. Cardiac magnetic resonance imaging can be an important modality to help differentiate or diagnose early cardiotoxicities associated with novel targeted therapies. |
Databáze: | OpenAIRE |
Externí odkaz: |