Generation of Heart Muscle Cells From Blood or Skin Cells of Breast Cancer Patients
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: skin punch biopsy.
- Who it may be relevant to
- Registry conditions: Breast Cancer. Basic parameters: from 18 years · Female.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Official title
Generation of Induced Pluripotent Stem Cell Derived Cardiomyocytes From Patients Exposed to Trastuzumab Therapy for Breast Cancer
Overview
The purpose of this study is to investigate whether cells from a biopsy taken from the patient skin can be transformed into cardiomyocytes the changes in cardiomyocyte (heart muscle cells) when grown in a special culture medium outside of the body. The structure and function of these cells will then be studied to determine why some patients with breast cancer who are treated with chemotherapy including anthracycline (e.g. Doxorubicin) and anti-HER2 therapy (e.g. Herceptin) develop decreased heart function.
Interventions
- Procedure skin punch biopsy
Primary outcome measures
- derive iPSs from skin fibroblasts [Time frame: 1 day]
Eligibility criteria
Inclusion criteria
- Female
- Age greater than 18 years
- Willing to participate in protocol procedures with signed informed consent
- Assessment of LVEE via echocardiogram, cardiac MRI, or MUGA
Subjects in the cardiotoxicity group (TOX) must meet the following criteria:
- History of HER2 positive breast cancer (stage I-IV)
- Prior/current treatment with anthracycline based chemotherapy followed by anti-HER2 directed therapy or anti-HER2 directed therapy alone
- Assessment of LVEF at baseline prior to initiation of anthracycline or anti-HER2 therapy and during anti-HER2 therapy via echocardiogram, cardiac MRI, or MUGA
- Prior confirmed diagnosis of cardiotoxicity associated with anti-HER2 based therapy, defined as a decrease in LVEF > 10% from baseline to < 53% with symptoms of heart failure (NYHA class II-IV).
Subjects in the no cardiotoxicity group (NO-TOX) must meet the following criteria:
- History of HER2 positive breast cancer (stage I-IV)
- Completion of planned anthracycline and anti-HER2 therapy, or anti-HER2 therapy alone
- No symptoms of heart failure (NYHA class II-IV) during and at the end of anthracycline and anti-HER2 therapy
- Assessment of LVEF at baseline prior to innitiation of anthracycline or anti-HER2 therapy and during anti-HER2 therapy via echocardiogram, cardiac MRI, or MUGA
- Normal LVEF >53% at each assessment during and at the end of trastuzumab therapy.
- Maximum absolute decrease in LVEF <5% from baseline during and at the end of trastuzumab therapy.
- LVEF assessment performed at baseline and at least two time points during trastuzumab therapy.
Exclusion criteria
- Unwilling or unable to give skin biopsies
- Contraindications to punch biopsy including but not limited to bleeding diathesis, as determined by the investigator.
- Known pre-existing CV disease prior to initiation of breast cancer therapy as determined by the investigator, including
- Obstructive coronary artery disease (stenosis >70%)
- Arrhythmia - paroxysmal or persistent atrial arrhythmias, sustained ventricular tachycardia (>30 seconds), ventricular fibrillation, or cardiac arrest
- Cardiomyopathy (EF <53%)
- Heart failure (NYHA class II-IV)
- Valvular heart disease with equal to or greater than moderate stenosis or regurgitation
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
United States · 1 center
- Memorial Sloan-Kettering Cancer Center — New York
Identifiers
NCT: NCT02772367 · 16-025