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

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-99
SponsorTempus AI

About this trial

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 criteria

Qualifiers

Willing and able to participate in the research and provide biospecimens

Willing and able to provide informed consent

Must be diagnosed with breast cancer

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

Disqualifiers

Not willing or able to adhere with the study procedures

Active secondary malignancy

Diagnosis of a malignancy within 3 years of breast cancer diagnosis Note: Ductal carcinoma in situ (DCIS, ipsilateral or contralateral) within 3 years is not excluded.

Trial design

Treatments tested in this trial

  • There are no interventions in this observational study.

Treatment groups

900 Participants
are divided into 3 treatment groups

Sponsors and collaborators