Study of Ductal Lavage in Women at High Risk for Breast Cancer

Breast Cancer Clinical Trial

Official title:

Ductal Lavage to Monitor and Treat High Risk Women

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00429988
• Other study ID #: CDR0000378088
• Secondary ID: UCSF-TEMP01
• Status: Completed
• Phase: N/A
• First received: January 30, 2007
• Last updated: September 25, 2012
• Start date: August 2002
• Est. completion date: June 2004

Study information

• Verified date: September 2012
• Source: University of California, San Francisco
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Federal Government
• Study type: Observational

Clinical Trial Summary

RATIONALE: Collecting samples of fluid using ductal lavage and nipple aspiration from participants at high risk for breast cancer to study in the laboratory may help doctors learn more about changes that may occur in DNA and identify biomarkers related to cancer.

PURPOSE: This clinical trial is using ductal lavage to collect fluid from women at high risk for breast cancer.

Description:

OBJECTIVES:

Primary

• Determine the volume of atypical cells collected from ductal lavage in women at increased risk for breast cancer.

Secondary

• Determine assay techniques to analyze nipple aspirate fluid and ductal lavage fluid samples from these participants.

• Analyze the nipple aspirate fluid from these participants for specific and global protein signatures.

• Determine the replicability of markers in serial assays of these participants.

• Determine the percentage of participants with atypia on ductal lavage in which ductal lesions can be identified using ductoscopy.

OUTLINE: This is a multicenter study.

Participants undergo nipple aspirate fluid and ductal lavage fluid collection. Fluid samples are analyzed using cytological analysis, immunohistochemistry, fluorescent in situ hybridization, or in situ polymerase chain reaction. Protein patterns are identified using mass spectrometry.

Participants found to have atypia undergo repeat lavage at 3-6 months and 1 year. Participants with normal fluid samples undergo repeat lavage at 1 year.

PROJECTED ACCRUAL: A total of 30 participants will accrued for this study within 2-3 months.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 30
• Est. completion date: June 2004
• Est. primary completion date: June 2004
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

DISEASE CHARACTERISTICS:

• High risk for breast cancer defined as 1 of the following:

• History of atypical hyperplasia or atypia found on biopsy, fine-needle aspiration, or ductal lavage

• Family history of cancer meeting at least 1 of the following criteria:

• Single relative with multiple primary cancers

• One or more relative under 40 years of age with breast cancer OR bilateral breast cancer

• Two or more relatives with ovarian cancer

• Two or more relatives with breast cancer and 1 is under 50 years of age

• One or more relative with breast cancer plus = 1 relative with ovarian cancer

• Ashkenazi Jewish descent AND relative with breast cancer under 50 years of age OR ovarian cancer at any age

• BRCA1 and/or BRCA2 mutation

• Prior breast cancer in contralateral breast

• Gail risk > 1.7%

• Spontaneous nipple discharge

• Serum estradiol > 10 pmol/L

• Hormone receptor status:

• Not specified

PATIENT CHARACTERISTICS:

Age

• Over 18

Sex

• Female

Menopausal status

• Not specified

Performance status

• Not specified

Life expectancy

• Not specified

Hematopoietic

• Not specified

Hepatic

• Not specified

Renal

• Not specified

Other

• Able to obtain breast duct fluids

PRIOR CONCURRENT THERAPY:

Biologic therapy

• Not specified

Chemotherapy

• Not specified

Endocrine therapy

• More than 4 months since prior tamoxifen or raloxifene

Radiotherapy

• No prior radiotherapy to the breast

Surgery

• No prior incisional or excisional biopsy within 1.5 cm of nipple

Other

• No prior neoadjuvant therapy

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

• Breast Cancer
• Breast Neoplasms

Intervention

Genetic:
• fluorescence in situ hybridization

• polymerase chain reaction

• proteomic profiling

Other:
• cytology specimen collection procedure

• immunohistochemistry staining method

Procedure:
• breast duct lavage

Locations

Country	Name	City	State
United States	UCSF Comprehensive Cancer Center	San Francisco	California

Sponsors (2)

Lead Sponsor	Collaborator
University of California, San Francisco	National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Average number of atypical cells per ductal lavage sample			No
Secondary	Assay techniques development for nipple aspirate fluid and ductal lavage fluid analysis			No
Secondary	Specific and global protein signature analysis of nipple aspirate			No
Secondary	Replicability of markers in serial assays			No
Secondary	Percentage of participants with atypia on ductal lavage in which ductal lesions can be identified using ductoscopy			No