Comprehensive Assessment of Clinical Features and Biomarkers to Identify Patients with Advanced or Metastatic Breast Cancer for Marker Driven Trials in Humans (CATCH)

Status: Recruiting
Location: See all (12) locations...
Intervention Type: Other
Study Type: Observational
SUMMARY

CATCH is an indication-specific diagnostic platform, which drives the implementation of integrative, genomic profiling for metastatic breast cancer into the clinics. The main objective of this approach is to identify biomarkers and drug targets to guide targeted therapeutic interventions. Eligible are all metastatic breast cancer patients (independent of gender), irrespective of molecular subtype. At initial diagnosis of distant metastasis or progress at disease progression, biopsy samples from a prognostic-relevant metastasis are retrieved during standard-of-care procedures for central analyses, together with blood samples. In parallel to all standard-diagnostic measures, genomic and transcriptomic profiling is conducted to infer the underlying biology of the disease and identify patients who might profit from biomarker-guided interventions in clinical trials. 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 to i) identify clinically-actionable biomarkers and drug targets that drive genomics-guided therapies and ii) couple the observational, diagnostic registry platform to an increasing number of independent, biomarker-stratified clinical therapy trials (CATCH-GUIDE).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 14
Maximum Age: 100
Healthy Volunteers: f
View:

• Female and male breast cancer patients ≥ 18 or if the legal guardian has agreed to the respective informed consent form (ICF)

• Patients with advanced or metastatic breast cancer (irrespective of clinical parameters such as TNM, subgroups, therapy lines)

• Patients, who agreed to and were able to sign the informed consent form.

Locations
Other Locations
Germany
University Hospital Augsburg
RECRUITING
Augsburg
Charité
RECRUITING
Berlin
University Hospital Köln
NOT_YET_RECRUITING
Cologne
Medical Faculty and University Hospital Carl Gustav Carus
RECRUITING
Dresden
University Hospital Erlangen
RECRUITING
Erlangen
University Hospital Essen
RECRUITING
Essen
National Center for Tumor Diseases
RECRUITING
Heidelberg
Caritas Hospital St. Josef
RECRUITING
Regensburg
Robert-Bosch-Krankenhaus Stuttgart
RECRUITING
Stuttgart
University Hospital Tübingen
RECRUITING
Tübingen
University Hospital Ulm
RECRUITING
Ulm
University Hospital Würzburg
RECRUITING
Würzburg
Contact Information
Primary
Andreas Schneeweiss, MD
Andreas.Schneeweiss@med.uni-heidelberg.de
0049-6221-5636051
Backup
Peter Lichter, PhD
Peter.Lichter@Dkfz-Heidelberg.de
0049-6221-424609
Time Frame
Start Date: 2017-06-12
Estimated Completion Date: 2030-12-31
Participants
Target number of participants: 5000
Related Therapeutic Areas
Sponsors
Leads: German Cancer Research Center
Collaborators: University Hospital Heidelberg

This content was sourced from clinicaltrials.gov

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