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Trastuzumab and Letrozole in Treating Postmenopausal Women With Progressive Advanced Breast Cancer

Trastuzumab Monotherapy Followed By the Combination of Trastuzumab and Letrozole in Post-Menopausal Women With ER-Positive, HER-2 Positive Advanced Breast Cancer Resistant to a Nonsteroidal Aromatase Inhibitor: A Multicenter Two-Step Phase II Trial

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00238290
Enrollment
13
Registered
2005-10-13
Start date
2005-05-31
Completion date
2011-04-30
Last updated
2019-05-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer

Keywords

recurrent breast cancer, stage IIIA breast cancer, stage IIIB breast cancer, stage IIIC breast cancer, stage IV breast cancer

Brief summary

RATIONALE: Monoclonal antibodies, such as trastuzumab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Estrogen can cause the growth of breast cancer cells. Hormone therapy using letrozole may fight breast cancer by lowering the amount of estrogen the body makes. Giving trastuzumab together with letrozole after disease progression may be an effective treatment for breast cancer. PURPOSE: This phase II trial is studying how well giving trastuzumab together with letrozole works in treating postmenopausal women with progressive advanced breast cancer.

Detailed description

OBJECTIVES: Primary * Determine the efficacy of trastuzumab (Herceptin®) monotherapy followed by trastuzumab and letrozole in women with progressive advanced breast cancer that is resistant to prior treatment with a nonsteroidal aromatase inhibitor. Secondary * Determine the safety profile of this regimen in these patients. * Correlate HER-2-extracellular domain (ECD) levels with response to treatment in these patients. * Determine the efficacy of this regimen in these patients. * Correlate response and time to tumor progression with changes in serum HER-2-ECD levels in patients treated with this regimen. OUTLINE: This is a multicenter study. Patients receive trastuzumab (Herceptin®) IV over 30-90 minutes once in weeks 1-3 OR once in week 1. Courses repeat every 3 weeks in the absence of disease progression or unacceptable toxicity. Patients experiencing disease progression after 9 weeks receive trastuzumab as before and oral letrozole once daily in the absence of further disease progression or unacceptable toxicity. After completion of study treatment, patients are followed every 12 weeks until disease progression and then at 6 months. PROJECTED ACCRUAL: A total of 30-40 patients will be accrued for this study.

Interventions

DRUGTrastuzumab + Letrozole

Patients receive trastuzumab (Herceptin®) IV over 30-90 minutes once in weeks 1-3 OR once in week 1. Courses repeat every 3 weeks in the absence of disease progression or unacceptable toxicity. Patients experiencing disease progression after 9 weeks receive trastuzumab as before and oral letrozole once daily in the absence of further disease progression or unacceptable toxicity.

Sponsors

Swiss Cancer Institute
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 120 Years
Healthy volunteers
No

Inclusion criteria

DISEASE CHARACTERISTICS: * Histologically or cytologically confirmed breast cancer * Advanced disease * Measurable disease, defined as ≥ 1 unidimensionally measurable lesion outside previously irradiated areas that is ≥ 20 mm OR ≥ 10 mm if the slice thickness of the CT scan or MRI is ≤ 5 mm * No nonmeasurable lesions as the only site of measurable disease, including any of the following: * Osteoblastic bone metastases * Ascites * Pleural or pericardial effusions * Carcinomatous lymphangitis of the lung * Progressive disease after prior treatment with a nonsteroidal aromatase inhibitor (e.g., letrozole or anastrozole) in an adjuvant or advanced disease setting * HER-2 amplification ≥ 2 by fluorescence in situ hybridization * No clinical symptoms or history of CNS or leptomeningeal metastases (no imaging is required) * No visceral involvement with risk for organ dysfunction * Hormone receptor status: * Estrogen receptor- and/or progesterone receptor-positive tumor PATIENT CHARACTERISTICS: Age * 18 and over Sex * Female Menopausal status * Postmenopausal, defined by 1 of the following: * At least 55 years of age * Less than 55 years of age with spontaneous cessation of menses for ≥ 1 year * Less than 55 years of age with spontaneous cessation of menses within the past year, but amenorrheic with biochemical evidence of postmenopausal status * Underwent prior bilateral oophorectomy * Radiation or chemically induced menopause (treatment with luteinizing hormone-releasing hormone antagonists must continue during study treatment) Performance status * WHO 0-1 Life expectancy * Not specified Hematopoietic * WBC ≥ 3,000/mm\^3 * Platelet count ≥ 100,000/mm\^3 Hepatic * AST and ALT ≤ 2 times upper limit of normal Renal * Creatinine clearance \> 30 mL/min Cardiovascular * No uncontrolled cardiac disease, including any of the following: * Unstable angina * Arrhythmia * Hypertension * No history of congestive heart failure * No myocardial infarction within the past 6 months * LVEF \> 50% by echocardiogram Pulmonary * No severe dyspnea at rest Other * No other malignancy within the past 5 years except adequately treated carcinoma in situ of the cervix or localized nonmelanoma skin cancer * No psychiatric disability that would preclude study participation or giving informed consent * No active autoimmune disease * No uncontrolled diabetes * No other serious underlying medical condition that would preclude study participation PRIOR CONCURRENT THERAPY: Biologic therapy * No prior trastuzumab (Herceptin®) Chemotherapy * Prior neoadjuvant or adjuvant chemotherapy allowed * No prior palliative chemotherapy Endocrine therapy * See Disease Characteristics Radiotherapy * See Disease Characteristics Surgery * Not specified Other * More than 1 month since prior experimental drugs on another clinical trial * No concurrent drugs that contraindicate study treatment * No other concurrent anticancer drugs * No other concurrent investigational drugs

Design outcomes

Primary

MeasureTime frame
Objective response rate as assessed by CT scan or MRI every 3 months3 months

Secondary

MeasureTime frame
Time to tumor progression (TTP) every 3 months3 months
Overall survival every 3 months3 months
Toxicity every 3 months3 months

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026