Overview

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

Status:
Completed
Trial end date:
2011-04-01
Target enrollment:
0
Participant gender:
Female
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.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Swiss Group for Clinical Cancer Research
Treatments:
Letrozole
Trastuzumab
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