Alternate Title
Basic Trial Information
Objectives
Entry Criteria
Expected Enrollment
Outcomes
Outline
Trial Contact Information
Registry Information

Alternate Title

Exemestane in Reducing Breast Density in Postmenopausal Women at Risk for Breast Cancer

Basic Trial Information

Phase Type Status Age Sponsor Protocol IDs No phase specified Prevention Closed Postmenopausal Other CAN-NCIC-MAP2 PFIZER-971-ONC-0028-088, NCT00066586, MAP2

Objectives

1. Determine the efficacy of exemestane in decreasing breast density at least 1 grade in postmenopausal women with increased radiological breast density at increased risk for breast cancer.
2. Determine whether the decrease in breast density is sustained 1 year after the cessation of this drug in these participants.
3. Correlate the grade of breast density with bone density at baseline and at 1 year in participants treated with this drug.
4. Determine the overall safety of this drug, in terms of bone and lipid metabolism and toxicity, in these participants.
5. Determine the menopause-specific quality of life of participants treated with this drug.

Entry Criteria

Disease Characteristics:

• Radiologically confirmed density occupying at least 25% of the breast tissue on baseline mammogram*
  • Grade 2, 3, 4, 5, or 6 (Boyd classification)
    • Participants with different grades between the 2 breasts should be classified according to a higher grade

   [Note: *Performed within 6 months before study entry]




• Bone mineral density T-score of either posterior-anterior spine or hip (femoral neck) must be no greater than 2.0 standard deviations below the mean value of peak bone mass in young normal women as determined by DEXA scan within the past 6 months



• No concurrent breast cancer



• No prior invasive breast cancer or ductal carcinoma in situ



• No breast implants



• Hormone receptor status:
  • Not specified

Prior/Concurrent Therapy:

Biologic therapy

• No prior immunotherapy
• No concurrent immunotherapy

Chemotherapy

• No prior chemotherapy
• No concurrent chemotherapy

Endocrine therapy

• More than 3 months since prior exogenous estrogen and/or progesterone/progestin therapy
• More than 6 months since prior selective estrogen-receptor modulators (e.g., tamoxifen, toremifene, or raloxifene)
• No concurrent selective estrogen-receptor modulators (e.g., tamoxifen, toremifene, or raloxifene)
• No concurrent steroids
• Vaginal estrogens allowed (e.g., Estring® or Vagifem®)
  • No concurrent compounded creams

Radiotherapy

• Not specified

Surgery

• Not specified

Other

• More than 4 weeks since prior investigational agents
• No other concurrent medications that would preclude study endpoints
• No concurrent over-the-counter products or supplements considered to have an estrogenic effect, including any of the following:
  • Ginseng
  • Ginkgo biloba
  • Black cohosh
  • Dong quai
  • Fortified soy supplements (e.g., phytoestrogen preparations)

Patient Characteristics:

Age

• Postmenopausal

Sex

• Female

Menopausal status

• Postmenopausal, defined as 1 of the following:
  • Over 50 years of age with no spontaneous menses for at least 1 year
  • 50 years of age and under with no menses (e.g., spontaneous or secondary to hysterectomy) within the past year AND a follicle-stimulating hormone level within institution postmenopausal range
  • Bilateral oophorectomy

Performance status

• Not specified

Life expectancy

• Not specified

Hematopoietic

• Not specified

Hepatic

• Not specified

Renal

• Not specified

Cardiovascular

• No cardiovascular disease
• No history of myocardial infarction
• No history of stroke
• No uncontrolled high blood pressure

Other

• No uncontrolled metabolic or endocrine disease
• No malabsorption syndrome
• No known hypersensitivity to exemestane or its excipients
• No other malignancy within the past 5 years except curatively treated squamous cell or basal cell skin cancer or carcinoma in situ of the cervix

Expected Enrollment

A total of 120 participants (60 per treatment arm) will be accrued for this study.

Outcomes

Change in breast density as measured by Boyd Scale at 1 year

Outline

This is a randomized, double-blind, placebo-controlled, multicenter study. Participants are stratified according to baseline mammographic density grade (2 vs 3 vs 4 vs 5 vs 6). Participants are randomized to 1 of 2 treatment arms.

• Arm I: Participants receive oral exemestane once daily for 1 year.



• Arm II: Participants receive oral placebo once daily for 1 year.

In both arms, treatment continues in the absence of disease or unacceptable toxicity.

Quality of life is assessed at baseline and then at 3, 6, 9, 12, 18, and 24 months.

Participants are followed at 18 and 24 months.

Trial Contact Information

Trial Lead Organizations

NCIC-Clinical Trials Group

Paul Goss, MD, PhD, Protocol chair		Ph: 617-724-3118; 877-726-5130

Registry Information
Official Title		A Randomized Study Of The Effect Of Exemestane (Aromasin) Versus Placebo On Breast Density In Postmenopausal Women At Increased Risk For Development Of Breast Cancer
Trial Start Date		2001-08-01
Registered in ClinicalTrials.gov		NCT00066586
Date Submitted to PDQ		2003-06-18
Information Last Verified		2006-07-24

Back to Top