Anastrozole With or Without Gefitinib in Treating Postmenopausal Women With Metastatic or Locally Recurrent Breast Cancer

E

European Organisation for Research and Treatment of Cancer (EORTC)

Status and phase

Completed
Phase 2

Conditions

Breast Cancer

Treatments

Drug: gefitinib
Drug: anastrozole

Study type

Interventional

Funder types

NETWORK

Identifiers

NCT00066378
EORTC-10021
IDBBC-10021

Details and patient eligibility

About

RATIONALE: Estrogen can stimulate the growth of breast cancer cells. Hormone therapy using anastrozole may fight breast cancer by reducing the production of estrogen. Gefitinib may stop the growth of tumor cells by blocking the enzymes necessary for their growth. Combining anastrozole with gefitinib may kill more tumor cells. PURPOSE: Randomized phase II trial to compare the effectiveness of anastrozole with or without gefitinib in treating postmenopausal women who have metastatic or locally recurrent breast cancer.

Full description

OBJECTIVES: Compare the 1 year antitumor activity of anastrozole with vs without gefitinib, in terms of progression-free survival, in postmenopausal women with metastatic or locally recurrent advanced breast cancer. Compare the objective tumor response and duration of tumor response in patients treated with these regimens. Compare the progression-free survival of patients treated with these regimens. Compare the safety of these regimens in these patients. OUTLINE: This is a randomized, double-blind, placebo-controlled, multicenter study. Patients are stratified according to participating center, dominant site of metastatic disease (bone alone vs other), prior chemotherapy (no vs yes), stage (metastatic vs locally recurrent), and measurability (measurable vs evaluable). Patients are randomized to 1 of 2 treatment arms. Arm I: Patients receive oral anastrozole and oral gefitinib once daily. Arm II: Patients receive oral anastrozole and an oral placebo once daily. In both arms, treatment continues in the absence of disease progression or unacceptable toxicity. Patients are followed every 8 weeks until disease progression. PROJECTED ACCRUAL: A total of 108 patients (54 per treatment arm) will be accrued for this study.

Enrollment

71 patients

Sex

Female

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

DISEASE CHARACTERISTICS: * Histologically confirmed breast cancer * Radiologically or clinically evident metastatic or locally recurrent disease * Locally advanced disease in elderly patients * Bone metastases only allowed * Failed prior tamoxifen therapy * No rapidly progressive visceral metastases * No uncontrolled CNS metastases * Hormone receptor status: * Estrogen receptor and/or progesterone receptor positive PATIENT CHARACTERISTICS: Age * Postmenopausal Sex * Female Menopausal status * Postmenopausal, defined by any of the following: * Natural menopause with last menses more than 1 year ago * Radiotherapy-induced oophorectomy with last menses more than 1 year ago * Chemotherapy-induced menopause with last menses more than 1 year ago AND serum follicle-stimulating hormone and luteinizing hormone and plasma estradiol levels clearly in the postmenopausal range * Surgical castration Performance status * ECOG 0-2 Life expectancy * Not specified Hematopoietic * Not specified Hepatic * Bilirubin no greater than 1.5 times upper limit of normal (ULN) * Transaminases no greater than 2.5 times ULN * No unstable or uncompensated hepatic disease Renal * No unstable or uncompensated renal disease Cardiovascular * No unstable or uncompensated cardiac disease Pulmonary * No unstable or uncompensated pulmonary disease * No clinically active interstitial lung disease * Asymptomatic chronic stable radiographic changes are allowed Other * No severe or uncontrolled systemic disease * No other malignancy within the past 5 years except adequately treated carcinoma in situ of the cervix, nonmelanoma skin cancer, or contralateral breast cancer * No psychological, familial, sociological or geographical condition that would preclude study compliance and follow-up * No grade 2 or greater unresolved chronic toxicity from prior anticancer therapy * No unresolved ocular inflammation or infection * No known hypersensitivity to anastrozole or gefitinib or any of their excipients PRIOR CONCURRENT THERAPY: Biologic therapy * No prior trastuzumab (Herceptin) * No concurrent biologic therapy Chemotherapy * No more than 1 line of prior chemotherapy in the adjuvant or metastatic setting * No concurrent chemotherapy Endocrine therapy * At least 2 years since prior aromatase inhibitors (e.g., anastrozole, letrozole, or exemestane) in the adjuvant setting * Prior tamoxifen or fulvestrant in the adjuvant and/or metastatic setting allowed * No prior aromatase inhibitors for metastatic disease * No other concurrent hormonal therapy Radiotherapy * No concurrent radiotherapy to any metastatic site Surgery * No surgery during and within 4 days after the last dose of gefitinib Other * At least 30 days since prior investigational drugs * No prior anti-epidermal growth factor therapy * No prior anti-vascular endothelial growth factor therapy (i.e., tyrosine kinase inhibitor receptor) * No concurrent administration of any of the following drugs: * Phenytoin * Carbamazepine * Rifampin * Phenobarbital * Hypericum perforatum (St John's Wort) * No other concurrent investigational drugs or treatment * No other concurrent cancer treatment * No concurrent systemic retinoids * Concurrent bisphosphonate therapy for the treatment and prevention of bony metastases is allowed provided therapy was initiated prior to study entry * Bisphosphonates may be initiated during study only for the treatment of hypercalcemia

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

71 participants in 2 patient groups

Arimidex + Iressa® 250 mg
Experimental group
Description:
Arimidex + Iressa® 250 mg Treatment should be administered until documented disease progression, unacceptable toxicity as judged by the responsible physician or patient refusal
Treatment:
Drug: anastrozole
Drug: gefitinib
Arimidex + Placebo
Active Comparator group
Description:
Treatment should be administered until documented disease progression, unacceptable toxicity as judged by the responsible physician or patient refusal
Treatment:
Drug: anastrozole

Trial contacts and locations

9

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Data sourced from clinicaltrials.gov

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