RecruitingNCT05906407

COGNITION: Genomics-Guided Precision Oncology in Early High-Risk Breast Cancer

COGNITION: Comprehensive Assessment of Clinical Features, Genomics and Further Molecular Markers to Identify Patients with Early Breast Cancer for Enrolment on Marker Driven Trials (Molecular Diagnostic Platform)


Sponsor

German Cancer Research Center

Enrollment

2,000 participants

Start Date

Apr 19, 2019

Study Type

OBSERVATIONAL

Conditions

Summary

The COGNITION diagnostic platform elucidates the biomarker profile of neoadjuvant chemotherapy-resistant residual bulk tumors in high risk early breast cancer patients. The major goal is to provide a framework for genomic profiling, which serves as infrastructure for systematic biomarker-screening and -stratification for concise therapy-arm allocation in the interventional clinical phase II trial COGNITION-GUIDE (NCT05332561). In patients, who display a poor response to standard-of-care neoadjuvant chemotherapy, tissue samples before and after neoadjuvant therapy are subjected together with blood samples to comprehensive genomic profiling to identify patients potentially benefiting from biomarker-guided interventions in COGNITION-GUIDE. Samples not required for standard-of-care clinical procedures or genomic profiling are systematically collected in a dedicated bio-repository to fuel translational scientific companion programs. The continuously growing comprehensive database serves as an integrative resource for systematic, prospective multidimensional data collection (clinical records, biomaterial, genomic data). In summary, the overarching goal is to generate a precision oncology platform i) to identify clinically-actionable biomarkers and drug targets that drive genomics-guided therapies and ii) to couple the observational, diagnostic registry platform to the independent, biomarker-stratified clinical therapy trial COGNITION-GUIDE.


Eligibility

Min Age: 18 YearsMax Age: 80 Years

Plain Language Summary

Simplified for easier understanding

This registry study (COGNITION) is collecting genetic and clinical information from breast cancer patients receiving standard care to help researchers understand how tumor genetics can guide more personalized treatment decisions in early-stage, high-risk breast cancer. **You may be eligible if...** - You are 18 or older (men or women) with early-stage breast cancer of any subtype - You are about to start, in the middle of, or have recently completed standard chemotherapy before or after surgery - You are willing to provide a tumor tissue sample - You may also be eligible if you have a localized cancer recurrence that can still be treated with curative intent **You may NOT be eligible if...** - You have refused or withdrawn consent - Tumor tissue cannot be obtained for genetic analysis - You have severe physical or mental conditions that would prevent participation Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

OTHERGenomic Profiling / Sequencing

Procedure: genomic profiling (Whole-Genome- / Exome-Sequencing + RNA-Sequencing) in high-risk early breast cancer patients pre- and post neoadjuvant therapy


Locations(12)

University Hospital Augsburg

Augsburg, Germany

Charité - Berlin

Berlin, Germany

University Hospital Köln

Cologne, Germany

Medical Faculty and University Hospital Carl Gustav Carus

Dresden, Germany

University Hospital Erlangen

Erlangen, Germany

University Hospital Essen

Essen, Germany

National Center for Tumor Diseases (NCT) Heidelberg

Heidelberg, Germany

Caritas Hospital St. Josef

Regensburg, Germany

Robert Bosch Hospital Stuttgart

Stuttgart, Germany

University Hospital Tübingen

Tübingen, Germany

University Hospital Ulm

Ulm, Germany

University Hospital Würzburg

Würzburg, Germany

View Full Details on ClinicalTrials.gov

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NCT05906407


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