Trastuzumab With or Without Tamoxifen in Treating Women With Progressive Stage IV Breast Cancer

• Status: Withdrawn
• Trial end date: 1969-12-31
• Target enrollment: 0
• Participant gender: All

Summary

RATIONALE: Monoclonal antibodies such as trastuzumab can locate tumor cells and either kill them or deliver tumor-killing substances to them without harming normal cells. Estrogen can stimulate the growth of breast cancer cells. Hormone therapy using tamoxifen may fight breast cancer by blocking the uptake of estrogen. Combining trastuzumab with tamoxifen may kill more tumor cells.

PURPOSE: Randomized phase III trial to compare the effectiveness of trastuzumab with or without trastuzumab in treating women who have invasive stage IV breast cancer.

• Phase: Phase 3
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Alliance for Clinical Trials in Oncology
• Collaborator: National Cancer Institute (NCI)
• Treatments: Tamoxifen; Trastuzumab

Criteria

DISEASE CHARACTERISTICS:

• Histologically confirmed invasive stage IV breast cancer

• Hormone receptor status:

• HER2/neu positive (3+ by immunohistochemical [IHC] assay or fluorescent in situ hybridization [FISH])

• Estrogen receptor or progesterone receptor positive

• Measurable or evaluable disease

• Must have disease progression within 6 months of initiation of tamoxifen (administered in the adjuvant or metastatic setting) or during aromatase inhibitor therapy

PATIENT CHARACTERISTICS:

Age

• 18 and over

Sex

• Female

Performance status

• ECOG 0-2

Hematopoietic

• Absolute neutrophil count at least 1,000/mm^3

• Platelet count at least 75,000/mm^3

Hepatic

• Bilirubin no greater than 1.5 times upper limit of normal (ULN)

• SGOT and SGPT no greater than 2.5 times ULN

Cardiovascular

• LVEF normal by MUGA

Other

• Not pregnant or nursing

• Fertile patients must use effective nonhormonal contraception during and for at least 2 months after study completion

• No other concurrent active malignancy except nonmelanoma skin cancer

• Patients who have completed prior therapy and are at less than 30% risk of relapse are not considered to have an active malignancy

PRIOR CONCURRENT THERAPY:

Biologic therapy

• No prior trastuzumab (Herceptin) in the adjuvant or metastatic setting

Chemotherapy

• No more than 1 prior chemotherapy regimen in the metastatic setting

• No concurrent chemotherapy

Endocrine therapy

• See Disease Characteristics

• No more than 1 prior hormonal therapy regimen for metastatic disease

• Prior aromatase inhibitor therapy administered in the first-line metastatic or adjuvant setting is allowed provided there is disease progression on tamoxifen

• No other concurrent hormonal therapy except the following:

• Steroids for adrenal failure

• Hormones for nondisease-related conditions (e.g., insulin for diabetes)

• Intermittent use of dexamethasone as an antiemetic

• Vaginal estrogen (or Estring®) for vaginal dryness

Radiotherapy

• No concurrent palliative radiotherapy except whole brain irradiation for CNS disease

Other

• Concurrent bisphosphonates allowed

• No concurrent cardioprotective drugs