To evaluate the use of a pharmacogenetic and pharmacoepigenetic panel for predicting chemotherapy- and immunotherapy-induced cardiotoxicity in cancer patients.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* Patients with a confirmed diagnosis of breast cancer who are scheduled to initiate treatment with anthracyclines and/or HER2-targeted therapies (anti-HER2 therapies).
Exclusion Criteria:
* Patients with a left ventricular ejection fraction (LVEF) \< 50%;
* Patients who have undergone chemotherapy and/or radiotherapy within the previous year;
* Patients with chronic kidney disease and a glomerular filtration rate (GFR) \< 30 mL/min/1.73 m²;
* Patients with uncontrolled hypertension;
* Patients with complex congenital heart disease.
Primary outcome measure(s)
Cardiotoxicity — 1 year Throughout treatment and follow-up, cardiotoxicity will be defined according to the criteria established by the 2022 European Society of Cardiology (ESC) Cardio-Oncology Guidelines.
Trial sites (6)
Facility
City
Region
Status
Instituto do Câncer do Ceará
Fortaleza
Ceará
Not Yet Recruiting
Complexo Hospitar HUOC/PROCAPE
Recife
Pernambuco
Not Yet Recruiting
Universidade Federal de Santa Catarina
Florianópolis
Santa Catarina
Not Yet Recruiting
Hospital Beneficente UNIMAR
Marília
São Paulo
Not Yet Recruiting
FAMERP - Faculdade de Medicina de São José do Rio Preto
São José do Rio Preto
São Paulo
Not Yet Recruiting
Hospital BP - A Beneficência Portuguesa de São Paulo
São Paulo
São Paulo
Recruiting
More Beneficência Portuguesa de São Paulo trials in Brazil
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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