Genomics-guided precision medicine for metastatic breast cancer
Official title: Comprehensive Assessment of Clinical Features and Biomarkers to Identify Patients With Advanced or Metastatic Breast Cancer for Marker Driven Trials in Humans (CATCH)
Run by German Cancer Research Center · NCT05652569 · Data updated 2026-11-12
This study is testing whether using genetic information from tumors and blood samples can help doctors create personalized treatment plans for people with metastatic breast cancer.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 14 Years to 100 Years |
| Sex | All |
| Enrollment | 5000 (estimated) |
| Sponsor | German Cancer Research Center Academic / other |
| Locations | 12 sites (Augsburg and 11 other locations) |
| Status | Recruiting |
| Started | June 12, 2017 |
| Main results expected | December 31, 2030 |
| Study ends | December 31, 2030 |
| Registry record updated | January 28, 2026 |
| Trial ID | NCT05652569 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are adults with advanced or metastatic breast cancer, regardless of gender or molecular subtype.
✕Probably not a fit
Patients with early-stage breast cancer or those unable to provide a tissue biopsy may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
CATCH is an observational study that aims to implement genomics-guided precision medicine for patients with metastatic breast cancer. It involves collecting tumor and blood samples from patients at the time of diagnosis or disease progression to conduct genomic and transcriptomic profiling. This profiling helps identify biomarkers and potential drug targets, guiding personalized therapeutic interventions. The study seeks to integrate these precision oncology workflows into clinical practice to improve treatment outcomes.
Why it matters
Potential benefit: If successful, this approach could lead to more effective, personalized treatment options for patients with metastatic breast cancer.
How similar studies have gone: Other studies have shown promise in using genomics-guided approaches for cancer treatment, indicating that this method has potential for success.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * 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. Exclusion Criteria: * Early breast cancer * Inability to take a tissue bioptic sample due to reasons such as physical location of the lesion or health of the patient * Any physical or mental handicap or severe comorbidities that would hamper the adequate cooperation with the patient.
Where it's running
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University Hospital Augsburg
Augsburg, Germany Recruiting -
Charité
Berlin, Germany Recruiting -
University Hospital Köln
Cologne, Germany Recruiting -
Medical Faculty and University Hospital Carl Gustav Carus
Dresden, Germany Recruiting -
University Hospital Erlangen
Erlangen, Germany Recruiting -
University Hospital Essen
Essen, Germany Recruiting
Show 6 more locations
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National Center for Tumor Diseases
Heidelberg, Germany Recruiting -
Caritas Hospital St. Josef
Regensburg, Germany Recruiting -
Robert-Bosch-Krankenhaus Stuttgart
Stuttgart, Germany Recruiting -
University Hospital Tübingen
Tübingen, Germany Recruiting -
University Hospital Ulm
Ulm, Germany Recruiting -
University Hospital Würzburg
Würzburg, Germany Recruiting
Study contacts
- Principal investigator: Andreas Schneeweiss, MD — National Center for Tumor Diseases, Heidelberg
- Study coordinator: Andreas Schneeweiss, MD
- Email: Andreas.Schneeweiss@med.uni-heidelberg.de
- Phone: 0049-6221-5636051
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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PRT13722 in advanced HR+/HER2- breast cancer
This early study tests PRT13722, by itself and with standard therapies, to see if it is safe and has any signs of activity in adults with HR+/HER2- breast cancer who have progressed on prior treatments.
-
Personalized treatment after endocrine therapy failure in metastatic breast cancer
The study tests whether using a patient’s fresh tumor sample to try different drugs outside the body can help pick the next therapy for hormone receptor-positive, HER2-negative metastatic breast cancer that progressed on endocrine therapy.
-
SSGJ-612 plus a HER2-targeted ADC in HR-positive, HER2-low metastatic breast cancer
This phase II study tests whether adding SSGJ-612 to a HER2-targeted antibody-drug conjugate helps people with HR-positive, HER2-low or ultralow metastatic breast cancer.
-
SMP-656 in HER2-positive advanced breast cancer after ADC therapy
This trial tests whether SMP-656 given by IV every 3 weeks can help people with HER2-positive locally advanced or metastatic breast cancer who progressed after a HER2-targeted antibody-drug conjugate.
-
Entinostat with Pyrotinib and Endocrine Therapy in HER2-positive, HR-positive Advanced Breast Cancer after Trastuzumab Failure
This study tests whether adding entinostat to pyrotinib and hormone therapy is safe and helps patients with advanced HR+/HER2+ breast cancer who progressed after trastuzumab.
-
T-DXd–based therapy followed by targeted HER2 blockade and endocrine therapy in first-line HER2+ / HR+ metastatic breast cancer
This trial tests a sequence of therapies starting with T-DXd plus pertuzumab, then a maintenance phase with dual HER2 blockade, endocrine therapy, and CDK4/6 inhibitor, with a retreatment option of T-DXd if disease progresses.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.