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Breast Cancer Prevention Clinical Services
Breast Cancer Risk and Prevention Options
Click on Breast Cancer and Risk Factors and
Prevention Options
to download information on these topics.
Clinical Services
Prevention Consultation
To prepare for your visit to the Breast Cancer Prevention Program, we will ask you to fill out several short forms that will help our providers identify your individual risk factors for breast cancer and create a personalized follow-up plan for
surveillance and prevention.
The physician will present the individualized risk assessment.
In addition, our nurse practitioner will explain basic breast anatomy and breast cancer development.
You will have a thorough breast exam and receive instruction on breast self-examination. The nurse practitioner
and/or physician will perform the breast examination, including an extensive breast mapping. Basic recommendations
and information will be provided on nutrition, exercise, and general lifestyle modifications. In addition, a genetic
counselor will be available if you are interested in discussing family history and the possibility of genetic testing.
If you require a mammogram, we will try to schedule one for the day of the appointment. At the completion of the appointment,
you will be provided with a copy of your breast map in addition to your personal risk profile. Follow-up appointments will be made
with the Nurse Practitioner or other staff members. Participants will be kept aware of clinical trials as they become available.
Topics covered during a clinic visit include the following:
- Risk management strategies (chemprevention, surgical prophylaxis, lifestyle changes)
- Cutting edge clinical trials
- Putting breast cancer risk in context of other health risks
- Breast Cancer biology
- Family history of cancer
- Nutrition
Ductal Lavage and Ductoscopy
Ductal Lavage is a new procedure that allows clinicians to access cells and fluid in the breast. Many breast cancers begin to form in the cells lining the milk ducts. Ductal lavage allows us to collect samples of cells from these ducts. These cells are analyzed by a cytopathologist, who determines whether they are normal, atypical or cancerous.
Figures 1 and 2 allow you to visualize how the clinician is able to access the milk duct. First, suction is applied to the nipple and this will draw out breast fluid. Second, the ducts that release breast fluid are marked and the clinician attempts to insert a tiny catheter into the duct to allow for available cells to be collected. The cells that are collected are sent to a laboratory for analysis.
Figures used with permission from Cytyc Health, Inc.
Please visit: www.ductallavage.com for more information on this technique.
Ductoscopy is a similar procedure that allows clinicians to visualize the inside of the breast duct by inserting a tiny camera
through the duct. Cells can also be collected from the duct during this procedure.
For more information on ductoscopy, please visit www.acueity.com.
Genetic Counseling - Cancer Risk Program
Nearly everyone has at least one family member with cancer. When several family members are affected, suspicions are raised about heritability - especially when cancer occurs at a young age. In some families, genetic testing may identify altered genes that predispose to cancer and are passed from parent to child. Genetic testing results, whether positive or negative, can have profound effects on individuals and their families. Family members with cancer may wish to learn their risk of a second cancer. Family members without cancer who inherit mutant genes may have an increased lifetime risk of developing cancer. These individuals must make critical decisions about surveillance, preventive surgery, and other treatment options.
The UCSF Cancer Risk Program (CRP) was established in 1996 as a multi-disciplinary, genetic counseling service for families with hereditary cancer. Counselors verify the family pedigree, provide education sessions, and offer testing for heritable genetic mutations. Based on the family pedigree and on test results, the counselors and consultant physicians provide an individualized risk management program for each client that includes recommendations for preventive measures and follow-up.
For more information on the Cancer Risk Program, please visit: http://www.cc.ucsf.edu/risk/index.html
Clinical Trials
For information about specific clinical trials, please call (415) 353-7070 or email breastcare.prevention@ucsfmedctr.org
We are currently recruiting patients for one clinical trial:
STAR: Study of Tamoxifen and Raloxifene for the Prevention of Breast Cancer
Click to download the Consent Form.
Summary: This study will determine if raloxifene is either more or less effective than tamoxifen in reducing the incidence of invasive breast cancer in postmenopausal women who are at increased risk for the disease. A secondary goal is to determine whether raloxifene reduces the endometrial cancer rates compared to tamoxifen. Approximately 22,000 postmenopausal women 35 years of age or older who are at increased risk for the development of breast cancer will be randomly assigned in this double-blind trial to receive daily either 20 mg of tamoxifen plus a placebo or 60 mg of raloxifene plus a placebo, for a period of 5 years. Women will be eligible for this trial if they are postmenopausal and their projected 5-year probability of developing invasive breast cancer is at least 1.66%, or if they are postmenopausal and they have a history of lobular carcinoma in situ (LCIS). The estimated 5-year probability of invasive breast cancer will be determined using the breast cancer Risk Assessment Profile (RAP) generated by the NSABP Biostatistical Center. To meet these criteria, a woman's risk will be evaluated using present age, number of first-degree relatives with breast cancer, history of previous breast biopsies, history of atypical hyperplasia of the breast, nulliparity, age at first live birth, and age at menarche. Participants will receive follow-up examinations on a regular basis, including an annual mammogram and gynecologic exam.
Inclusion Criteria
- Postmenopausal.
- 35 years of age or more.
- Histological diagnosis of lobular carcinoma in situ (LCIS) treated by local excision, OR a minimum projected 5-year probability of invasive breast cancer of at least 1.66% as determined by the Gail Model.
- Patients with history of benign neutropenia are eligible if the granulocyte counts is greater than/equal to 1500 cu mm.
- Adequate hepatic and renal function.
Exclusion Criteria
- Prior or suspected invasive breast cancer of any type; DCIS or LCIS treated by mastectomy, radiation, or systemic adjuvant therapy.
- Bilateral or unilateral prophylactic mastectomy.
- Participating in any other cancer prevention study or osteoporosis prevention study involving pharmacologic intervention(s) (NSABP Protocol P-1 participants who received placebo are eligible.).
- Prior malignancy of any type that occurred less than 10 years previously;
- Existing non-malignant disease that would preclude the administration of tamoxifen or raloxifene.
- Prior history of deep-vein thrombosis or pulmonary embolus;
- Prior history of documented cerebral vascular accident or documented transient ischemic attack.
- Estrogen- or progesterone-replacement therapy, oral contraceptives, or androgens (Women who discontinue these drugs for at least 3 months prior to randomization will be eligible.).
- Tamoxifen, raloxifene, or other SERM therapy (Women who have received these therapies for less than 3 months duration and discontinue the drugs at least 3 months prior to randomization are eligible.).
- Current use of coumadin or cholestyramine.
- Current use of chemotherapy for benign disease.
Upcoming Trials
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