Development of a Pharmacogenomic Panel for Early Detection of Chemotherapy- and Immunotherapy-Induced Cardiotoxicity.

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorBeneficência Portuguesa de São Paulo

About this trial

To evaluate the use of a pharmacogenetic and pharmacoepigenetic panel for predicting chemotherapy- and immunotherapy-induced cardiotoxicity in cancer patients.

Eligibility criteria

Qualifiers

Patients with a confirmed diagnosis of breast cancer who are scheduled to initiate treatment with anthracyclines and/or HER2-targeted therapies (anti-HER2 therapies).

Disqualifiers

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;

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

1,000 Participants
are grouped into 4 trial groups

Locations

6
Instituto do Câncer do Ceará60430-230, FortalezaCeará, Brazil
Complexo Hospitar HUOC/PROCAPE50100-130, RecifePernambuco, Brazil
Universidade Federal de Santa Catarina88040-900, FlorianópolisSanta Catarina, Brazil
Hospital Beneficente UNIMAR17525-160, MaríliaSão Paulo, Brazil

Sponsors and collaborators

Beneficência Portuguesa de São Paulo

Lead sponsor