Breast Cancer Clinical Trial

Studying Biomarkers in Nipple Fluid, Urine, and Blood Samples From Women With Newly Diagnosed Ductal Carcinoma In Situ or Stage I or Stage II Breast Cancer and in Women at Risk of Developing Breast Cancer

Summary

RATIONALE: Studying samples of nipple fluid, urine, and blood in the laboratory from patients with cancer and from patients at risk of developing cancer may help doctors identify and learn more about biomarkers related to cancer. It may also help doctors learn more about breast cancer and identify patients at risk of developing breast cancer.

PURPOSE: This laboratory study is looking at biomarkers in nipple fluid, urine, and blood samples from women with newly diagnosed ductal carcinoma in situ or stage I or stage II breast cancer and in women at risk of developing breast cancer.

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Full Description

OBJECTIVES:

To determine the levels of catechol estrogens (CE), CE metabolites, CE-DNA adducts, and CE conjugates in nipple aspirate fluid samples obtained from women with newly diagnosed ductal carcinoma in situ or stage I or II breast cancer and from women at high risk of developing breast cancer.

OUTLINE: Patients with newly diagnosed breast cancer or at high risk of developing breast cancer undergo nipple aspiration. The nipple aspirate fluid is obtained from the unaffected breast and is analyzed for 31 estrogen metabolites, conjugates, and depurinating DNA adducts by high-performance liquid chromatography (LC) with electrochemical and mass spectrometric detectors. All patients undergo urine and serum sample collection. The urine samples are analyzed by ultraperformance LC monitored by tandem mass spectrometry for estrogen metabolites, conjugates, and depurinating DNA adducts.

Patients' charts are reviewed to obtain information about age, race, general health, any endocrine disorders, history of cancer, estrogen and progesterone receptor status, and HER2/neu status (for patients with newly diagnosed breast cancer), menopausal status, reproductive history, history of breast disease, medication use, smoking history, and history of alcohol consumption.

View Eligibility Criteria

Eligibility Criteria

DISEASE CHARACTERISTICS:

Meets 1 of the following criteria:

Newly diagnosed (within 30 calendar days of diagnosis) stage I or II breast cancer

Node-negative or node-positive disease
Newly diagnosed ductal carcinoma in situ (stage 0) of the breast

At high risk of developing breast cancer, as indicated by at least 1 of the following criteria:

Gail model 5-year risk score ≥ 1.66%
Gail model lifetime-risk estimate ≥ 20%
Known deleterious BRCA 1 or 2 gene mutation carrier
History of lobular carcinoma in situ or atypical ductal or lobular hyperplasia

At low or average risk of developing breast cancer (control group)

Gail model 5-year risk score < 1.66% or lifetime risk < 20%
No advanced breast cancer
Hormone receptor status not specified

PATIENT CHARACTERISTICS:

Pre- or post-menopausal

PRIOR CONCURRENT THERAPY:

No prior chemotherapy for breast cancer or any other cancer
More than 3 months since prior and no concurrent estrogen or other hormones
More than 3 months since prior oral contraceptives
No concurrent selective estrogen receptor modulators (tamoxifen citrate or raloxifene)
No concurrent aromatase inhibitors

Study is for people with:

Breast Cancer

Estimated Enrollment:

316

Study ID:

NCT00897208

Recruitment Status:

Completed

Sponsor:

Mayo Clinic

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There is 1 Location for this study

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Mayo Clinic Cancer Center
Rochester Minnesota, 55905, United States

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Estimated Enrollment:

316

Study ID:

NCT00897208

Recruitment Status:

Completed

Sponsor:


Mayo Clinic

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