Expired Study
This study is not currently recruiting Study Participants on ClinicalConnection.com. If you would like to find active studies please search for clinical trials.

Stanford, California 94305


Purpose:

To evaluate the antitumor activity, toxicity, and effectiveness of the combination of goserelin (Zoladex) and anastrozole (Arimidex) in the treatment of premenopausal women with hormone receptor positive metastatic carcinoma of the breast.


Study summary:

Pre-menopausal women with estrogen and/or progesterone receptor positive, metastatic or recurrent breast cancer were enrolled and treated with goserelin (Zoladex) monthly and began anastrozole (Arimidex) daily for 21 days following the first injection of goserelin. Participants continued on treatment until disease progression or unacceptable toxicity.


Criteria:

INCLUSION CRITERIA - Histologically-confirmed, bi-dimensionally measurable, recurrent or metastatic carcinoma of the breast that is progressive - Premenopausal, defined as any of: 1. Last menstrual period within 3 months, or 2. Post-hysterectomy without bilateral oophorectomy and with follicle-stimulating hormone (FSH) in the premenopausal range, or, 3. If tamoxifen administered within the past 3 months, plasma estradiol must be in the premenopausal range - Either positive estrogen and/or progesterone receptor determination by Immunohistochemistry (IHC) or competitive binding assay on metastatic disease, or if not performed on their metastatic disease a positive result on their primary breast cancer specimen. - Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2 - Granulocytes > 1500/mm^3 - Platelets > 100,000/mm^3 - Serum glutamic oxaloacetic transaminase (SGOT) < 2.5 x upper limit of normal - Total bilirubin < 1.5 mg/dL - May have received irradiation to bony sites of disease for pain control or for prevention of fracture. The irradiated site(s) will NOT be evaluable for disease response. - Must be using effective contraception or not be of childbearing potential - Signed written informed consent INCLUSION CRITERIA - Active, unresolved infection - Active malignancy other than breast cancer, in situ carcinoma of the cervix, or non-melanomatous skin cancers in the past 5 years - Prior treatment with an aromatase inhibitor or inactivator - Prior treatment with an luteinizing hormone-releasing hormone (LH/RH) agonist/antagonist - Adjuvant chemotherapy within 6 months of study entry. - Received chemotherapy or hormonal therapy in the 3 weeks prior to enrollment - Central nervous system metastasis - Lymphangitic pulmonary metastasis - Pregnant or lactating


NCT ID:

NCT00186121


Primary Contact:

Principal Investigator
Melinda Telli, MD
Stanford University


Backup Contact:

N/A


Location Contact:

Stanford, California 94305
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 09, 2019

Modifications to this listing: Only selected fields are shown, please use the link below to view all information about this clinical trial.


Click to view Full Listing

This study is not currently recruiting Study Participants on ClinicalConnection.com. The form below is not enabled.