Effect of Neoadjuvant or Adjuvant Systemic Therapy on Breast Cancers, Bone Marrow Cancer Cells, and Circulating Cancer Cells

Purpose

The main purpose of this study is to compare genetic markers present on tumor cells before and after chemotherapy.

Condition

  • Breast Neoplasms

Eligibility

Eligible Ages
Over 18 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

Criteria

Inclusion Criteria:

- Recently diagnosed with clinical stage II, III, or IV breast cancer

- Planning to undergo neoadjuvant or adjuvant systemic therapy; patients who have
already completed neoadjuvant systemic therapy are also eligible

- Must be >= 18 years of age

- If female, must not be pregnant

- Must not have Hepatitis B, C, or HIV

- Must be willing and able to sign informed consent document

Study Design

Phase
Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Arm Groups

ArmDescriptionAssigned Intervention
Tissue, blood, and bone marrow (optional) collection - Undergo neoadjuvant systemic therapy - initial surgery for sentinel lymph node biopsy/portacath placement - definitive cancer surgery (if applicable) - when portacath is removed (1 year, if available) - if metastatic disease develops or is present in accessible sites, a sample may be collected at the time of specimen collection for diagnosis - Undergo Adjuvant Systemic Therapy - initial surgery for a sentinel lymph node biopsy/portacath placement - when portacath is removed (1 year, if available) - If metastatic disease develops or is present in accessible sites, a sample may be collected at the time of specimen collection for diagnosis. - Undergone neoadjuvant systemic therapy - during definitive cancer surgery/portacath removal (if available) - if metastatic disease develops or is present in accessible sites, a sample may be collected at the time of specimen collection for diagnosis
  • Procedure: Peripheral blood draw
  • Procedure: Breast tissue collection
  • Procedure: Bone marrow biopsy

Recruiting Locations

Washington University in St. Louis and nearby locations

Washington University School of Medicine
St Louis 4407066, Missouri 4398678 63119
Contact:
Rebecca Aft, MD, PhD
314-747-0063
aftr@wustl.edu

More Details

NCT ID
NCT00353483
Status
Recruiting
Sponsor
Washington University School of Medicine

Study Contact

Rebecca Aft, MD, PhD
314-747-0063
aftr@wustl.edu

Detailed Description

In this study, the investigators propose that persistent disseminated tumor cells (DTC) present after systemic therapy represent a unique subpopulation of all DTC, are predictors of a poor response to systemic therapy and correlate with poor clinical outcome. The investigators hypothesize that systemic therapy-resistant DTC can be identified by their expression of a unique constellation of tumor marker proteins which may be similar to those expressed by breast cancer stem cells. In this research, the investigators' specific aims are : 1) to characterize tumor markers expressed by DTC which are present after systemic therapy, 2) to compare the expression of these markers to that on DTC detected prior to systemic therapy, 3) to correlate expression of the defined tumor markers on DTC with clinical outcome of breast cancer patients to identify those markers that are predictive of disease recurrence, 4) to utilize biomarkers identified in Specific Aims 1 and 2 to isolate purified DTC for further molecular analysis.