Clinical trial · Observational
Genetics and Heart Health After Cancer Therapy
NCT03510689CI-TRIAL-00081658Gene-HEARTcompletedClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The overall objective of this study is to use patient-centered in vitro and in vivo models to answer the fundamental question of whether or not pathogenic mutations in BRCA1/2 result in an increased risk of CV disease
Conditions
Conditions (4)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Breast Cancer | Malignant Breast Neoplasm | CURATED_EXACT | 0.92 |
| Drug-Induced Cardiomyopathy | — | UNRESOLVED | — |
| Heart Diseases | — | UNRESOLVED | — |
| Hereditary Breast/Ovarian Cancer (brca1, Brca2) | — | UNRESOLVED | — |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Blood Collection | Other | — | UNRESOLVED |
| Cardiopulmonary Exercise Testing | Other | — | UNRESOLVED |
| echocardiography | Diagnostic Test | — | UNRESOLVED |
Design
Arms and outcomes
Arms (3)
- label
- Group 1
- description
- Subjects with genetic testing confirming deleterious mutations in BRCA1 or BRCA2 whose prior treatment for breast cancer includes anthracycline exposure. All groups have same schedule of study procedures, including echocardiography, cardiopulmonary exercise testing, and blood collection.
- interventionNames
- Diagnostic Test: echocardiography
- Other: Cardiopulmonary Exercise Testing
- Other: Blood Collection
- label
- Group 2
- description
- Subjects with genetic testing confirming deleterious mutations in BRCA1 or BRCA2 whose prior treatment for breast cancer does not include anthracycline exposure. All groups have same schedule of study procedures, including echocardiography, cardiopulmonary exercise testing, and blood collection.
- interventionNames
- Diagnostic Test: echocardiography
- Other: Cardiopulmonary Exercise Testing
- Other: Blood Collection
- label
- Group 3
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
Inclusion Criteria * ≥18 years of age * Initial diagnosis of Breast Cancer in 2005 or later * Documented BRCA testing (results from a local laboratory are acceptable) showing * confirmation of a germline mutation in BRCA1 or BRCA2 that is predicted or suspected to be deleterious OR * confirmation that no mutation was detected in BRCA1 or BRCA2 * Non-carriers will have been treated with an anthracycline-based chemotherapy regimen; carriers may or may not have been treated with an anthracycline-based chemotherapy regimen. * Approximately at least 12 months from initiation of adjuvant treatment or neo-adjuvant chemotherapy * Able to provide informed consent Exclusion Criteria * Stage IV Breast Cancer * Genetic testing confirming a variant of unknown significance (VUS) or benign polymorphism in BRCA1 or BRCA2 * V02 Testing contraindicated for any reason, including: * Myocardial infarction (within past 3 months) * High-risk unstable angina; * High-risk or uncontrolled cardiac arrhythmias; * Symptomatic severe aortic stenosis; * Uncontrolled symptomatic heart failure; * Acute pulmonary embolus or pulmonary infarction; * Acute myocarditis or pericarditis; * Acute aortic dissection; * Coronary revascularization procedure within the past three months; * Uncontrolled hypertension, defined as systolic blood pressure ≥ 180mmHg or diastolic blood pressure ≥ 100mmHg; * Clinically significant valvular heart disease (severe stenosis or regurgitation); * Known aortic aneurysm; or * Any other condition which, in the opinion of the investigator, may impede testing of the study hypothesis or make it unsafe to engage in the V02 test * Women who are pregnant * Any other clinically significant medical disease or condition that, in the investigator's opinion, may interfere with protocol adherence or a subject's ability to give informed consent
References
Publications (0)
Data not yet available
No reference posted for this study.