Collecting samples and data from patients with recurrent or metastatic breast cancer
Official title: Collection of Specimens and Clinical Data for Patients With Recurrent or Metastatic Breast Cancer or Male Breast Cancer
Run by Mayo Clinic · NCT06217874 · Data updated 2026-11-12
This study is collecting blood and tissue samples from patients with recurrent or metastatic breast cancer to learn more about the disease and improve treatment options.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 2000 (estimated) |
| Sponsor | Mayo Clinic Academic / other |
| Locations | 1 site (Rochester, Minnesota) |
| Status | Recruiting |
| Started | June 5, 2014 |
| Main results expected | June 30, 2034 |
| Study ends | June 30, 2034 |
| Registry record updated | February 25, 2026 |
| Trial ID | NCT06217874 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include adult males and females with confirmed invasive breast cancer who are willing to participate.
✕Probably not a fit
Patients with conditions that impair their ability to provide informed consent or those with serious allergic reactions to local anesthetics 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
This observational study aims to gather blood samples and fresh tissue from biopsies of metastatic lesions in patients with recurrent or metastatic breast cancer, including male breast cancer. The collected specimens and clinical data will help enhance the understanding of the disease's development, progression, and treatment options. Participants will undergo blood sample collection, tumor biopsy, and have their medical records reviewed as part of the study. The study is being conducted at the Mayo Clinic in Rochester, Minnesota.
Why it matters
Potential benefit: If successful, this study could lead to improved understanding and treatment options for patients with recurrent or metastatic breast cancer.
How similar studies have gone: Other studies focusing on specimen collection for cancer research have shown success in advancing understanding and treatment, making this approach promising.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Female participants must have histologically or cytologically confirmed invasive breast cancer. * Male participants must have biopsy proven breast cancer. * Age must be \>= 18 years, and all must be able to understand and willing to sign an informed consent document. Exclusion Criteria: * Dementia, altered mental status, or any psychiatric condition that would prohibit the understanding or rendering of informed consent; a history of serious or life-threatening allergic reaction to local anesthetics (i.e. lidocaine, xylocaine). * Any other condition, which in the opinion of the patient's treating oncologist, or the physician performing the biopsy procedure, would make participation in this protocol unreasonably hazardous for the patient.
Where it's running
-
Mayo Clinic in Rochester
Rochester, Minnesota, United States Recruiting
Study contacts
- Principal investigator: Fergus J. Couch, Ph.D. — Mayo Clinic in Rochester
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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.