Clinical trial Recruiting at 1 site Observational Ages 18 and up

Pharmacogenomic panel to predict chemotherapy- and immunotherapy-induced heart damage

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

Run by Beneficência Portuguesa de São Paulo · NCT07663357 · Data updated 2026-11-12

A pharmacogenomic and pharmacoepigenetic panel is being tested to see if it can predict which breast cancer patients will develop heart damage from chemotherapy or immunotherapy.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment1000 (estimated)
SponsorBeneficência Portuguesa de São Paulo
Academic / other
Drugs / interventionschemotherapy, immunotherapy
Locations6 sites (Fortaleza, Ceará and 5 other locations)
StatusRecruiting
StartedMay 11, 2026
Main results expectedMarch 1, 2029
Study endsDecember 30, 2029
Registry record updatedJune 23, 2026
Trial IDNCT07663357 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults with confirmed breast cancer who are about to start anthracycline- and/or HER2-targeted therapies and who meet the specific health criteria outlined (e.g., LVEF ≥ 50%, adequate kidney function, controlled blood pressure).

Probably not a fit

Patients with existing significant heart disease, poor kidney function, or uncontrolled hypertension may not benefit from this panel.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This observational study aims to develop a genetic and epigenetic test to forecast cardiotoxicity in cancer patients receiving chemotherapy or immunotherapy. It plans to enroll 1,000 breast cancer patients who are about to start anthracycline or HER2-targeted therapies and follow them for 12 months. Participants will undergo regular cardiac evaluations, including ECG, echocardiography with strain, and biomarkers such as Pro-BNP, BNP, and Troponin I. The goal is to enable early preventive strategies before cancer treatment begins to reduce the risk of left ventricular dysfunction and heart failure related to cancer therapies.

Why it matters

Potential benefit: If successful, patients could avoid or lessen treatment-related heart damage through earlier risk identification and prevention.

How similar studies have gone: Previous research supports pharmacogenomic approaches for predicting adverse treatment effects, but this exact panel for cardiotoxicity is being developed in this study.

Who can join: the full rules

Show full inclusion / exclusion criteria
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.

Where it's running

  • Hospital BP - A Beneficência Portuguesa de São Paulo
    São Paulo, São Paulo, Brazil
    Recruiting
  • Instituto do Câncer do Ceará
    Fortaleza, Ceará, Brazil
    Not yet recruiting
  • Complexo Hospitar HUOC/PROCAPE
    Recife, Pernambuco, Brazil
    Not yet recruiting
  • Universidade Federal de Santa Catarina
    Florianópolis, Santa Catarina, Brazil
    Not yet recruiting
  • Hospital Beneficente UNIMAR
    Marília, São Paulo, Brazil
    Not yet recruiting
  • FAMERP - Faculdade de Medicina de São José do Rio Preto
    São José do Rio Preto, São Paulo, Brazil
    Not yet recruiting

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.