Cardiotoxicity is a therapy-limiting toxicity with anthracyclines. Keefe proposed an algorithm for monitoring anthracycline chemotherapy in order to minimize the risk of cardiotoxicity. The author is from Memorial Sloan Kettering Cancer Center in New York City.
Parameters:
(1) body surface area in square meters
(2) cumulative dose of anthracycline in doxorubicin equivalents
(3) risk status
A patient is considered high risk for cardiotoxicity if the patient has any of the following:
(1) pre-existing heart disease
(2) radiation therapy to left lung or mediastinum
(3) hypertension
Monitoring is done with:
(1) echocardiography
(2) radionuclide angiography
Monitoring |
High Risk |
Low Risk |
start monitoring |
200 mg per square meter |
300 mg per square meter |
need for closer monitoring (monitor after every 2 cycles) |
300 mg per square meter |
400 mg per square meter |
need for very close monitoring (monitor after every cycle) |
400 mg per square meter |
NA (consider after 500 mg per square meter) |
followup after therapy completed |
every 3 months |
every 3 months |
Endpoint to stop anthracycline therapy based on cardiotoxicity is based upon the left ventricular ejection fraction
(1) caution should be used if < 50%
(2) anthracycline chemotherapy should be discontinued when < 45%
Purpose: To monitor a patient for cardiotoxicity associated with anthracycline chemotherapy using the algorithm of Keefe.
Specialty: Hematology Oncology, Cardiology
Objective: options, adverse effects
ICD-10: T45.1,