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Recruiting NCT02610426

Whole Exome Sequencing in Finding Causative Variants in Germline DNA Samples From Patients With Congestive Heart Failure Receiving Therapy for Breast Cancer

Observational Breast Carcinoma

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: Laboratory Biomarker Analysis.
Who it may be relevant to
Registry conditions: Breast Carcinoma. Basic parameters: No limits · All.
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 →
Official title

Exploratory Next Generation Sequencing to Identify Causative Variants for Therapy-Induced Congestive Heart Failure From Breast Cancer Study E5103 Germline DNA Samples

Overview

This research trial studies whole exome sequencing in finding causative variants in germline deoxyribonucleic acid (DNA) samples from patients with congestive heart failure receiving therapy for breast cancer. Studying samples of germline DNA in the laboratory from patients with congestive heart failure receiving therapy for breast cancer may help doctors learn more about changes that occur in DNA and identify biomarkers related to congestive heart failure.

Detailed description

PRIMARY OBJECTIVES:

I. To identify, using next generation sequencing, rare variants of large effect size that impact the risk of congestive heart failure (CHF) in patients from the clinical trial ECOG-5103 (E5103).

OUTLINE:

Previously collected germline DNA samples are analyzed via whole exome sequencing.

Interventions

  • Other Laboratory Biomarker Analysis
    Correlative studies

Primary outcome measures

  • Identification of rare coding variants of large effect that predict the risk of CHF [Time frame: Baseline]

Eligibility criteria

Inclusion criteria

  • European American patients with DNA available
  • European American patients who developed CHF and patients who did not develop CHF following a full course of treatment with an anthracycline and bevacizumab
  • African American cases (based on a drop in left ventricular ejection fraction \[LVEF\] < 50 or a drop from baseline > 20 points) and African American controls

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
Case-control

Study locations

United States · 1 center
  • Eastern Cooperative Oncology Group — Boston

Identifiers

NCT: NCT02610426 · NCI-2013-02291 · NCI-2013-02291 · ECOG-E5103T3 · E5103T3 · E5103T3 · U10CA180820

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗