Registry for patients with inflammatory breast cancer and MRD testing
Official title: Multi-center MRD Registry for Inflammatory Breast Cancer
Run by M.D. Anderson Cancer Center · NCT06966050 · Data updated 2026-11-12
This study is looking at patients with inflammatory breast cancer to see how often they test positive for minimal residual disease before surgery and how this affects their treatment and quality of life.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 200 (estimated) |
| Sponsor | M.D. Anderson Cancer Center Academic / other |
| Locations | 1 site (Houston, Texas) |
| Status | Recruiting |
| Started | May 5, 2025 |
| Main results expected | May 31, 2030 |
| Study ends | May 31, 2032 |
| Registry record updated | May 20, 2026 |
| Trial ID | NCT06966050 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are adults aged 18 and older with a clinical diagnosis of stage III or IV inflammatory breast cancer who have undergone MRD testing.
✕Probably not a fit
Patients who are not diagnosed with inflammatory breast cancer or those who have already undergone breast surgery for their diagnosis 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 collect data from participants diagnosed with inflammatory breast cancer (IBC) who may have undergone minimal residual disease (MRD) testing and are planning for surgery. The primary objective is to determine the incidence of MRD positivity before surgery, while secondary objectives include evaluating the feasibility of multi-institutional data collection, assessing the relationship between MRD and pathologic response, and understanding the impact of MRD results on patients' quality of life. Participants will also provide longitudinal MRD data to track recurrence and the effects of adjuvant therapies.
Why it matters
Potential benefit: If successful, this study could enhance understanding of MRD in IBC and improve patient management strategies.
How similar studies have gone: While the approach of collecting MRD data in IBC is relatively novel, similar studies in other cancer types have shown promising results.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Female or males ≥18 years of age with the ability to understand and sign a written * Participants who have a clinical diagnosis of stage III or IV inflammatory breast cancer (IBC). * Participants who are planning to have or already completed a minimum of one blood draw for Signatera testing, for which the result and clinical data can be deposited into the study database. * Participants must be within eight months of diagnosis and have not undergone breast surgery for this diagnosis of breast cancer. * Participants must be English-speaking. Exclusion Criteria: \-
Where it's running
-
MD Anderson Cancer Center
Houston, Texas, United States Recruiting
Study contacts
- Principal investigator: Sadia Saleem, MD — M.D. Anderson Cancer Center
- Study coordinator: Sadia Saleem, MD
- Email: ssaleem@mdanderson.org
- Phone: 281-566-1900
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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.