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TerminatedNCT00131924Updated Jun 11, 2012

High-Dose Esterified Estrogens in Treating Postmenopausal Women With Metastatic Breast Cancer That Has Failed Previous Hormone Therapy

A Phase 2 interventional study of esterified estrogens in Breast Cancer, sponsored by Northwestern University. Terminated at 1 site in United States. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2012-06-11.

Sponsored by Northwestern University · Phase 2, Interventional, and Treatment

Why this study was terminated
Data Monitoring Committee recommended closure due to poor accrual.
Phase
Phase 2
Study type
Interventional
Enrollment
1
Ages
18 Years and older
Sex
Female
01

Study summary

RATIONALE: High doses of esterified estrogens may stop the growth of breast cancer cells that no longer respond to hormone therapy.

PURPOSE: This phase II trial is studying how well high-dose esterified estrogens work in treating postmenopausal women with metastatic breast cancer that has failed previous hormone therapy.

Read the detailed description

OBJECTIVES:

Primary

  • Determine the clinical response rate in postmenopausal women with estrogen and/or progesterone receptor-positive metastatic breast cancer that has failed prior sequential endocrine therapy treated with high-dose esterified estrogens (Menest\^®).

Secondary

  • Determine time to disease progression in patients treated with this drug.
  • Determine the toxic effects of this drug in these patients.

OUTLINE: Patients receive oral high-dose esterified estrogens (Menest\^®) 3 times daily. Treatment continues in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed for 2 months.

PROJECTED ACCRUAL: A total of 18-35 patients will be accrued for this study within 2 years.

02

Conditions studied

  • Breast Cancer

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Keywords

  • recurrent breast cancer
  • stage IV breast cancer
03

In context

Breast Neoplasms

12,544 studies on the registry are indexed under Breast Neoplasms; 2,892 are open to participants now.

This study's enrollment of 1 is below the median of 72 across 9,303 interventional studies indexed under Breast Neoplasms.

Browse Breast Neoplasms studies →

Lead sponsor

Northwestern University is the lead sponsor of 1,396 studies on the registry; 199 are open to participants now.

Of its 102 completed or terminated interventional studies of FDA-regulated products, 73 (72%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
No

Eligibility criteria

DISEASE CHARACTERISTICS:

  • Histologically confirmed breast cancer

    • Metastatic disease
  • Documented disease progression

    • Must have received and subsequently failed (due to disease progression) ≥ 2 prior sequential endocrine therapies for treatment of metastatic breast cancer

      • Disease progression during adjuvant tamoxifen is considered 1 prior therapy
      • The 2 most recent treatments must have been endocrine agents
  • At least 1 objective measurable disease parameter
  • Brain metastases allowed provided both of the following criteria are met:

    • Brain metastases were previously treated AND are currently stable
    • Brain metastases are not the only site of metastatic disease
  • Hormone receptor status

    • Estrogen and/or progesterone receptor-positive tumor

PATIENT CHARACTERISTICS:

Age

  • 18 and over

Sex

  • Female

Menopausal status

  • Postmenopausal, as defined by any of the following:

    • At least 50 years of age with an intact uterus AND amenorrheic for the past 12 months
    • At least 50 years of age without a uterus AND follicle-stimulating hormone (FSH) level within postmenopausal range
    • Under 50 years of age and FSH level within postmenopausal range
    • Prior bilateral oophorectomy

Performance status

  • ECOG 0-2

Life expectancy

  • At least 6 months

Hematopoietic

  • Adequate hematologic function

Hepatic

  • Adequate hepatic function
  • Bilirubin ≤ 1.5 times upper limit of normal
  • No history of hepatic adenoma

Renal

  • Adequate renal function
  • No history of hypercalcemia or severe hypocalcemia

Cardiovascular

  • No history of thrombophlebitis or thromboembolic disorders associated with prior estrogen use
  • No active thrombophlebitis or thromboembolic disorders
  • No history of uncontrolled hypertension

Other

  • Not pregnant
  • No undiagnosed abnormal vaginal bleeding
  • No other serious medical illness
  • No psychiatric illness that would preclude giving informed consent
  • No other invasive malignancy within the past 5 years except curatively treated basal cell or squamous cell skin cancer or carcinoma in situ of the cervix

PRIOR CONCURRENT THERAPY:

Biologic therapy

  • Not specified

Chemotherapy

  • Prior chemotherapy for metastatic disease allowed
  • Prior adjuvant chemotherapy allowed

Endocrine therapy

  • See Disease Characteristics

Radiotherapy

  • Prior radiotherapy allowed provided the only site of measurable disease was not irradiated

Surgery

  • Not specified
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Masking
None (open label)
Enrollment
1 participant (actual)

Interventions

  • Biologicalesterified estrogens
06

What researchers measure

Primary outcomes

  1. Clinical response rate

Secondary outcomes

  1. Time to disease progression

  2. Toxicity

07

Study locations

1 site
  • Robert H. Lurie Comprehensive Cancer Center at Northwestern University
    Chicago, Illinois 60611-3013, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 11, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00131924
Lead sponsor
Northwestern University
Collaborators
National Cancer Institute (NCI)
Responsible party
Sponsor
First posted
Aug 19, 2005
Start date
Mar 2004
Primary completion
Jan 2006
Completion
Jan 2006
Last update
Jun 11, 2012

Study contacts

William J. Gradishar, MD
principal investigator · Robert H. Lurie Cancer Center
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Jun 2012. You cannot join it, but the record below documents what was studied.

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