Breast Cancer Clinical Trial

Studying Blood and Tumor Tissue Samples in Women With Invasive Breast Cancer, Ductal or Lobular Carcinoma in Situ, or Benign Breast Disease

Summary

RATIONALE: Collecting and storing samples of blood and tumor tissue from patients with cancer to test in the laboratory may help the study of cancer in the future.

PURPOSE: This clinical trial is studying blood and tumor tissue samples in women with invasive breast cancer, ductal carcinoma in situ, lobular carcinoma in situ, or benign breast disease.

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Full Description

OBJECTIVES:

Primary

To establish a specimen bank from peripheral blood specimens collected from women with a full spectrum of breast disease (invasive breast cancer [IBC], ductal or lobular carcinoma in situ [CIS], or benign breast disease [BBD]) with standardized clinical follow up and serial specimen collection for those with IBC.
To determine the ability of quantitative real-time reverse-transcriptase PCR (qRT-PCR) to discriminate between patients with IBC, CIS, and BBD by comparing baseline assay values from pre-biopsy specimens to the histologic diagnosis.
To determine the ability of qRT-PCR to predict treatment response by comparing serial assay values from patients with evaluable IBC to their objective response.
To determine the ability of qRT-PCR to predict relapse by comparing the serial assay values from all patients with IBC to their disease status.
To determine the ability of qRT-PCR to perform as an independent prognostic factor by comparing baseline assay values from all patients with IBC to their disease status, stratified by known breast cancer prognostic factors.

Secondary

To perform exploratory studies identifying potential targets for novel nucleic acid and proteomic-based early detection assays.

OUTLINE: Patients undergo baseline peripheral blood specimen collection pre-biopsy and then periodically for up to 10 years. Specimens are analyzed for circulating tumor cells via quantitative real-time reverse-transcriptase PCR, immunofluorescence, and bidirectional pyrophosphorolysis-activated polymerization allele-specific amplification; and for protein profiles via mass spectometry, liquid chromatography, enzyme digestion, and tandem mass spectometry. Patients' tumor tissue (invasive breast cancer [IBC] only) is analyzed for p53 via IHC. Medical records are reviewed periodically.

Patients with IBC complete a quality of life assessment at baseline and every 6 months for up to 10 years.

View Eligibility Criteria

Eligibility Criteria

DISEASE CHARACTERISTICS:

Biopsy-confirmed diagnosis of one of the following:

Stage I-IV infiltrating ductal or infiltrating lobular carcinoma

Patients with early-stage disease must not have started systemic treatment; if no systemic treatment is planned, patients must be either preoperative or ≤ 120 days since definitive breast surgery
Patients with locally advanced disease must be scheduled for neoadjuvant chemotherapy prior to initiation of systemic treatment
Ductal carcinoma in situ
Lobular carcinoma in situ

Benign breast disease

Proliferative or non-proliferative
With or without atypia

PATIENT CHARACTERISTICS:

Karnofsky performance status 50-100%
Not pregnant
No prior invasive cancer diagnosis within the past 5 years except for squamous cell or basal cell carcinoma of the skin

PRIOR CONCURRENT THERAPY:

See Disease Characteristics
No prior systemic therapy (chemotherapy or hormonal therapy) for patients with stage I-III disease

Study is for people with:

Breast Cancer

Estimated Enrollment:

563

Study ID:

NCT00898508

Recruitment Status:

Completed

Sponsor:

City of Hope Medical Center

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There are 3 Locations for this study

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Tower Cancer Research Foundation
Beverly Hills California, 90211, United States
City of Hope Comprehensive Cancer Center
Duarte California, 91010, United States
City of Hope Medical Group
Pasadena California, 91105, United States

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Estimated Enrollment:

563

Study ID:

NCT00898508

Recruitment Status:

Completed

Sponsor:


City of Hope Medical Center

How clear is this clinincal trial information?

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