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Evaluating Minimal Residual Disease (MRD) Through Longitudinal Circulating Tumor DNA (ctDNA) Profiling in Breast Malignancies

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

For patients with breast cancer, it's important to find any remaining cancer cells after they've had their main treatment. Even a few cells, called minimal residual disease (MRD), can lead to the cancer coming back later. A way to find these cells is by looking for tiny bits of cancer DNA that are shed into the blood. This is called circulating tumor DNA (ctDNA). A simple blood test, often called a liquid biopsy, can detect this ctDNA. This research aims to see if finding this cancer DNA in the blood can help predict if a patient's cancer will return. It also may help find out if the treatment is working. Ultimately, the results of this research may help doctors better manage breast cancer and develop new and improved tests and treatments.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 99
Healthy Volunteers: f
View:

⁃ All Cohorts:

• Willing and able to participate in the research and provide biospecimens

• Willing and able to provide informed consent

• Must be diagnosed with breast cancer

⁃ Cohort 1: Neoadjuvant Treatment Cohort 1A: Newly Diagnosed, High Risk HR+,HER2-

• A known or suspected HR+, HER2- breast cancer treated with curative intent (Stage II to III disease)

• Patients are considered at high risk of recurrence, defined as 4 or more positive axillary lymph nodes (ALNs), or between 1-3 positive ALNs and either grade 3 disease or tumor size of 5 cm or larger.

⁃ Cohort 1B: HER2+ 1. A known or suspected HER2+ breast cancer treated with curative intent (Stage II to III disease). Inclusive of HR+ or HR- patients.

⁃ Cohort 1C: Triple Negative Breast Cancer

⁃ 1\. A known or suspected triple negative breast cancer treated with curative intent (Stage I to III disease).

⁃ Cohort 2: Adjuvant Therapy / Surveillance Cohort 2A: Newly Diagnosed HR+,HER2-

• A known or suspected HR+, HER2- breast cancer treated with curative intent (Stage II to III disease)

• Patients are considered at high risk of recurrence, defined as 4 or more positive axillary lymph nodes (ALNs), or between 1-3 positive ALNs and either grade 3 disease or tumor size of 5 cm or larger.

• Have undergone curative intent surgery with no clinical evidence of disease.

⁃ Cohort 2B: HER2+

• A known or suspected HER2+ breast cancer treated with curative intent (Stage II to III disease)

• Have undergone curative intent surgery with no clinical evidence of disease.

⁃ Cohort 2C: Triple Negative Breast Cancer

• A known or suspected triple negative breast cancer treated with curative intent (Stage I to III disease)

• Have undergone curative intent surgery with no clinical evidence of disease.

⁃ Cohort 3: 5-Years Post-Diagnosis Surveillance (NED)

• A known HR+, HER2- breast cancer treated with curative intent (Stage II to III disease).

• No Evidence of Disease (NED) ≥ 5 years from initial diagnosis.

• Patients are considered at high risk of recurrence, defined as 4 or more positive axillary lymph nodes (ALNs), or between 1-3 positive ALNs and either grade 3 disease or tumor size of 5 cm or larger.

Locations
United States
Alabama
Birmingham Hematology Associates
RECRUITING
Birmingham
California
PIH Health Whittier Hospital
RECRUITING
Whittier
Illinois
Southern Illinois Hospital Services
RECRUITING
Carbondale
Cancer Care Specialist of Illinois
RECRUITING
O'fallon
Indiana
Goshen Center for Cancer Care
RECRUITING
Goshen
Michigan
Trinity Health
RECRUITING
Ann Arbor
Missouri
Oncology Hematology Associates
RECRUITING
Springfield
New Jersey
Summit Medical Group
RECRUITING
Florham Park
Nevada
Cancer Care Specialist of Reno
RECRUITING
Reno
Tennessee
Nashville General
RECRUITING
Nashville
Washington
Cancer Care Northwest
RECRUITING
Spokane Valley
Wisconsin
Gunderson Health
RECRUITING
La Crosse
Contact Information
Primary
GEMINI Breast Clinical Study Manager
gemini-breast@tempus.com
(833) 514-4187
Time Frame
Start Date: 2025-10-27
Estimated Completion Date: 2033-12
Participants
Target number of participants: 900
Treatments
Cohort 1: Neoadjuvant Therapy
There are no interventions in this observational study. Cohort 1 includes participants who will receive neoadjuvant treatment prior to surgery.
Cohort 2: Adjuvant Therapy / Surveillance
There are no interventions in this observational study. Cohort 2 includes participants who will receive adjuvant therapy after surgery.
Cohort 3: 5 Years Post-Diagnosis Surveillance
There are no interventions in this observational study. Cohort 3 includes participants who have no evidence of disease for at least 5 years post diagnosis.
Related Therapeutic Areas
Sponsors
Leads: Tempus AI

This content was sourced from clinicaltrials.gov