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NCT Number: NCT00080756

Deslorelin Combined With Low-Dose Add-Back Estradiol and Testosterone in Preventing Breast Cancer in Premenopausal Women Who Are at High Risk for This Disease

RATIONALE: Chemoprevention therapy is the use of certain drugs to try to prevent the development or recurrence of cancer. Deslorelin combined with low-dose add-back estradiol and testosterone (given to replace hormones suppressed by deslorelin) may be effective in preventing breast cancer in at-risk women.

PURPOSE: This phase II trial is studying how well giving deslorelin together with estradiol and testosterone works in preventing breast cancer in premenopausal women who are at high risk for this disease.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

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Key information

Age range

21 year–48 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2

Primary location

City of Hope Medical Center

Duarte, California, 91010-3000, United States

About this study

OBJECTIVES:

I. Assess the effects on the breast of treatment with the gonadotropin-releasing hormone agonist (GnRHA)-based regimen in breast cancer (BRCA) gene mutation carriers, including correlation of changes in mammographic and magnetic resonance imaging (MRI) densities with tissue morphometrics and biomarkers.

II. Evaluate perspectives about risk reduction options and impact on quality-of-life (QOL) measures of participation in the chemopreventive protocol and in risk reduction surgery.

OUTLINE:

GROUP 1: Patients receive deslorelin, estradiol, and testosterone intranasally once daily (QD) for 6 months. Patients then undergo planned risk reduction mastectomy.

GROUP 2: Patients receive deslorelin, estradiol, and testosterone intranasally QD for 10 months. Patients then undergo continued surveillance through 10 months.

After completion of study treatment, patients are followed up every 6 months for 2 years.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients must generally be in good health with lab values and physical examination within normal limits
  • Known high risk of breast cancer due to BRCA mutation or empiric risk > 30% lifetime by the Claus model
  • No evidence or history of pervious cancer, except non-melanoma skin cancer
  • Premenopausal women planning risk reduction mastectomy in 6 months or more (Group 1) or continued surveillance (Group 2)
  • Prior tubal ligation or willing to use a non-hormonal barrier method of contraception
  • Signed the Informed Consent Form document for this study in accordance with all Federal, State and Institutional regulations
  • Must be current non-smoker

Exclusion criteria

  • GnRHA treatment within 12 months of study entry
  • Nasal polyposis, atrophic rhinitis, severe allergic or vasomotor rhinitis, or sinusitis requiring current treatment or treatment for more than 3 months in the previous year
  • Concurrent medications including: corticosteroids (prednisone, prednisolone, cortisone acetate, Decadron, Deltasone, hydrocortisone, Hydrocortone, Medrol), estrogens, progestins or androgens, including oral, implanted, or injected contraceptive; (At least 6 months must have elapsed since the last use of an implanted or injected contraceptive such as Norplant)
  • Pregnant or breast-feeding or have been so in the last six months
  • Immeasurable breast density on mammogram

Treatment and study plan

therapeutic estradiol

Biological

0.35mg/100ul per day as a nasal spray

Deslorelin

Drug

1mg/100ul per day as a nasal spray

Therapeutic Testosterone

Drug

0.275mg/100ul per day as a nasal spray

therapeutic conventional surgery

Procedure

Undergo risk reduction mastectomy

Active Surveillance

Other

Undergo continued surveillance

quality-of-life assessment

Procedure

Ancillary studies

laboratory biomarker analysis

Other

Correlative studies

Primary outcomes

  1. Treatment effects and correlation of changes in morphometrics and biomarkers as assessed by mammogram and magnetic resonance image (MRI) densities on days 1 and 300

    Time frame: Day 300

  2. Perspectives about risk reduction options and their impact on quality of life (QOL) as assessed by Medical Outcomes 36-item short-form version, Health Perceptions scale, and Body Image scale on days 1, 169, and 300, and then every 6 months for 2 years

    Time frame: 2 years

Sponsors and collaborators

Lead sponsor

City of Hope Medical Center

Other

Collaborators

  • National Cancer Institute (NCI)

Registry information

Official study title

Biomarkers, Breast Density And Risk Reduction Perspectives In BRCA Carriers

Important dates

Study start
2004
Primary completion
2024
Study completion
2024
First posted
Apr 8, 2004
Registry last updated
Aug 28, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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