Chemotherapy's hidden heart toll: study probes lasting damage in breast cancer survivors
NCT ID NCT07680855
First seen Jul 02, 2026 · Last updated Jul 02, 2026
Summary
This observational study looks at how anthracycline chemotherapy affects inflammation, oxidative stress, and heart function in adult women who had breast cancer. Researchers measure blood markers and use echocardiograms to assess heart changes about 10 years after treatment. The goal is to understand long-term heart risks in survivors.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- anthracycline chemotherapy
- What this could lead to
- If successful, this study could help identify early markers of heart damage in breast cancer survivors, potentially guiding future monitoring and prevention strategies.
- What could go wrong
- This is a small observational study with only 17 participants and no comparison group, so findings may not apply broadly. It aims to observe long-term effects, not test a new treatment.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
-
17 people
The number who actually took part.
- Started
-
Feb 2011
- Finished
-
Apr 2026
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Adult women with breast cancer treated at Hospital del Salvador, Santiago, Chile. Patients were consecutively recruited between 2010 and 2013 from a prospective cohort of individuals initiating anthracycline-based chemotherapy. A protocol amendment approved by the local ethics committee allowed long-term follow-up of the original cohort at 10 years for cardiovascular, inflammatory, and oxidative stress assessment.
- Ages
-
18 to 75 years
- Sex
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Female participants only
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Female patients with histologically confirmed breast cancer * Age between 18 and 75 years * Indication for anthracycline-based chemotherapy (\>200 mg/m²) * Eastern Cooperative Oncology Group (ECOG) performance status 0-2 * Written informed consent signed prior to study participation * Availability for baseline cardiovascular and biomarker assessment and long-term follow-up Exclusion Criteria: * History of heart failure or left ventricular dysfunction (LVEF \<53%) * Known coronary artery disease or clinically significant ischemic heart disease * History of clinically significant arrhythmias or requirement for antiarrhythmic therapy * Dilated or hypertrophic cardiomyopathy * Moderate to severe valvular heart disease (mitral or aortic stenosis or regurgitation) * Congenital heart disease (including atrial or ventricular septal defects, patent ductus arteriosus, Ebstein anomaly, tetralogy of Fallot, coarctation of the aorta) * Chronic kidney disease (creatinine \>2 mg/dL) * Hepatic failure (bilirubin \>3 mg/dL, albumin \<3.5 g/dL, or prothrombin activity \<60% in absence of anticoagulation)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
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