Gefitinib in Treating Patients With Metastatic Breast Cancer That Has Progressed After Antiestrogen and Nonsteroidal Aromatase Inhibitor Therapy

Breast Cancer Clinical Trial

Official title:

An IDBBC Single Arm Phase II Trial Evaluating The Activity Of Iressa (ZD1839) In Metastatic Breast Cancer Patients Pretreated With An Antiestrogen And A Non-Steroidal Aromatase Inhibitor (Anastrozole Or Letrozole)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00066339
• Other study ID #: EORTC-10012
• Secondary ID: EORTC-10012IDBBC
• Status: Completed
• Phase: Phase 2
• First received: August 6, 2003
• Last updated: July 17, 2012
• Start date: May 2003

Study information

• Verified date: July 2012
• Source: European Organisation for Research and Treatment of Cancer - EORTC
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Federal Government
• Study type: Interventional

Clinical Trial Summary

RATIONALE: Gefitinib may stop the growth of tumor cells by blocking the enzymes necessary for tumor cell growth.

PURPOSE: Phase II trial to study the effectiveness of gefitinib in treating patients who have metastatic breast cancer that has not responded to antiestrogen and nonsteroidal aromatase inhibitor therapy.

Description:

OBJECTIVES:

• Determine the clinical benefit rate, defined as complete response, partial response, or stable disease after at least 24 weeks, in patients receiving gefitinib for metastatic breast cancer who progressed after prior antiestrogen and nonsteroidal aromatase inhibitor therapy.

• Determine the best overall response rate of patients treated with this drug.

• Determine the progression-free survival of patients treated with this drug.

• Determine the duration of response in patients treated with this drug.

• Determine the safety of this drug in these patients.

OUTLINE: This is a nonrandomized, open-label, multicenter study.

Patients receive oral gefitinib once daily. Treatment continues in the absence of disease progression or unacceptable toxicity.

Patients who go off study in the absence of disease progression are followed every 8 weeks until disease progression.

PROJECTED ACCRUAL: A total of 44 patients will be accrued for this study.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 44
• Est. primary completion date: January 2004
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

DISEASE CHARACTERISTICS:

• Histologically confirmed breast cancer

• Radiological and/or clinical evidence of metastatic disease

• Progressive disease after prior therapy with an antiestrogen (e.g., tamoxifen or faslodex) and a nonsteroidal aromatase inhibitor (e.g., anastrozole or letrozole) in the adjuvant and/or metastatic setting* NOTE: *Endocrine therapy must be the last treatment before study entry

• Unidimensionally measurable disease

• No rapidly progressive visceral metastases

• No uncontrolled CNS metastases

• Hormone receptor status:

• Estrogen receptor and/or progesterone receptor positive

PATIENT CHARACTERISTICS:

Age

• 18 and over

Sex

• Not specified

Menopausal status

• Postmenopausal, defined as any of the following:

• Natural menopause with at least 1 year since last menses

• Radiation-induced oophorectomy with last menses more than 1 year ago

• Chemotherapy-induced menopause with 1 year since last menses and serum follicle-stimulating hormone, luteinizing hormone, and plasma estradiol levels 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 severe or uncontrolled hepatic disease

Renal

• No severe or uncontrolled renal disease

Cardiovascular

• No severe or uncontrolled cardiac disease

Pulmonary

• No severe or uncontrolled respiratory disease

• No evidence of clinically active interstitial lung disease

• Asymptomatic chronic stable radiographic changes allowed

Other

• No other malignancy within the past 5 years except adequately treated carcinoma in situ of the cervix, contralateral breast cancer, or nonmelanoma skin cancer

• No psychological, familial, sociological, or geographical condition that would preclude study compliance and follow-up

• No other severe or uncontrolled systemic disease

• No known hypersensitivity to any excipients of gefitinib

• No unresolved chronic toxicity greater than grade 2

PRIOR CONCURRENT THERAPY:

Biologic therapy

• No concurrent biologic agents

Chemotherapy

• No more than 1 prior chemotherapy regimen for metastatic breast cancer

• No concurrent chemotherapy

Endocrine therapy

• See Disease Characteristics

• No concurrent hormonal therapy

Radiotherapy

• Prior radiotherapy allowed

• No concurrent radiotherapy to any metastatic site

Surgery

• No surgery within 4 days after study drug administration

Other

• No prior epidermal growth factor receptor inhibitor therapy

• More than 30 days since prior investigational drugs

• No concurrent use of any of the following:

• Phenytoin

• Carbamazepine

• Rifampin

• Phenobarbital

• Hypericum perforatum (St. John's Wort)

• No concurrent systemic retinoids

• No other concurrent investigational drugs or treatments

• No other concurrent anticancer treatments

• Concurrent bisphosphonates for the treatment and prevention of bony metastases are allowed provided therapy was initiated before study enrollment* NOTE: *Bisphosphonates may be initiated during study participation for the treatment of hypercalcemia only

Study Design

Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Breast Cancer
• Breast Neoplasms

Intervention

Drug:
• gefitinib

Locations

Country	Name	City	State
Belgium	Institut Jules Bordet	Brussels

Sponsors (1)

Lead Sponsor	Collaborator
European Organisation for Research and Treatment of Cancer - EORTC

Country where clinical trial is conducted

Belgium,