Image

Comparison of the Breast Tumor Microenvironment

Comparison of the Breast Tumor Microenvironment

Non Recruiting
50 years and older
Female
Phase N/A

Powered by AI

Overview

The goal of the project is to identify a molecular signature of tumor stroma from "normal" adjacent breast tissue obtained prospectively at the time of breast conserving surgery before and after receiving intraoperative radiation therapy (IORT) in subjects that have luminal A and triple negative breast cancer. IORT is considered as being standard of care.

Description

There is evidence that the normal tissue around a tumor plays a role in determining how the tumor behaves, including how it will respond to treatments and how likely it is to recur. In breast cancer, radiation is used to decrease the chance of recurrence in the area where the tumor is removed. This risk of recurrence varies between different types of breast cancer. The investigators seek to study the proteins produced in normal tissue surrounding breast tumors. The tissue will be taken from women who are receiving radiation to the breast at the time of their surgery (known as intraoperative radiation), one specimen taken before radiation and one after. A new process will be used to stabilize the tissue rapidly and allow the proteins to be identified before they break down. This will allow us to identify differences in the proteins produced by cells before and after radiation and between two types of breast cancers, luminal A (less likely to recur) and triple negative (more likely to recur). Identifying these differences in proteins may allow them to be used in the future as markers to predict the likelihood of tumors recurring.

Eligibility

Inclusion Criteria:

  • Female, age greater than or equal to 40
  • Core biopsy proven invasive breast carcinoma or ductal carcinoma in situ (DCIS), all subtypes excluding invasive lobular carcinoma due to increased risk for multifocal disease
  • Human epidermal growth factor receptor 2 (HER2) negative regardless of hormone receptor status
  • Clinically less than or equal to 3cm unifocal lesion
  • Clinically node negative
  • Must have diagnostic mammogram performed within last 6 months
  • Eastern Cooperative Oncology Group Performance Status (ECOG PS) less than or equal to 1
  • Appropriate renal, liver, and hematologic lab values
  • Ability to give informed consent

Exclusion Criteria:

  • Multifocal disease
  • Clinically N1 disease at diagnosis
  • Invasive lobular carcinoma
  • Metastatic disease
  • Patients for whom RT would be contraindicated (e.g., connective tissue disorder or prior ipsilateral breast radiation)
  • Patients with known BRCA1/2 mutations
  • Pregnant or nursing

Study details
    Triple Negative Breast Cancer
    Hormone Receptor Positive Malignant Neoplasm of Breast

NCT03165487

Columbia University

21 October 2025

FAQs

Learn more about clinical trials

What is a clinical trial?

A clinical trial is a study designed to test specific interventions or treatments' effectiveness and safety, paving the way for new, innovative healthcare solutions.

Why should I take part in a clinical trial?

Participating in a clinical trial provides early access to potentially effective treatments and directly contributes to the healthcare advancements that benefit us all.

How long does a clinical trial take place?

The duration of clinical trials varies. Some trials last weeks, some years, depending on the phase and intention of the trial.

Do I get compensated for taking part in clinical trials?

Compensation varies per trial. Some offer payment or reimbursement for time and travel, while others may not.

How safe are clinical trials?

Clinical trials follow strict ethical guidelines and protocols to safeguard participants' health. They are closely monitored and safety reviewed regularly.
Add a private note
  • abc Select a piece of text.
  • Add notes visible only to you.
  • Send it to people through a passcode protected link.