Clinical Trials Directory

Trials / Completed

CompletedNCT00066339

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

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)

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
44 (actual)
Sponsor
European Organisation for Research and Treatment of Cancer - EORTC · Network
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Detailed 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.

Conditions

Interventions

TypeNameDescription
DRUGgefitinib

Timeline

Start date
2003-05-01
Primary completion
2004-01-01
First posted
2003-08-07
Last updated
2012-07-18

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT00066339. Inclusion in this directory is not an endorsement.