IRESSA™ (Gefitinib) in Breast Cancer Patients

Phase 2

Completed

• Conditions: Breast Cancer

• Registration Number: NCT00632723
• Lead Sponsor: AstraZeneca

Brief Summary

This is a phase II trial to assess whether IRESSA™ (gefitinib) has anti-tumour efficacy in patients with breast cancer. The trial proposes to enter 27 patients who have acquired resistance to tamoxifen and 27 patients with ER negative tumours. However for each of these two types of patients recruitment will stop after 14 patients have been entered in order to confirm that IRESSA™ (gefitinib)has anti-tumour efficacy. If no patient out of 14 in a group has shown clinical benefit (ie an objective response (CR or PR) or stable disease (SD) for at least 24 weeks) then a clinical benefit rate of \>20% can be ruled out with \>95% certainty. If one or more of the objective response or stable disease (\> 24 weeks) has been seen in the first 14 patients recruited in a group then recruitment to that group will recommence to a total of 27 patients. If 14 patients are entered into an arm but not all 14 patients are available for final analysis and the toxicity/safety and tolerability profile of the therapy is acceptable and documented and a clinical benefit is seen in the patients, enrolment of additional patients beyond the initial 14 may be made based on overall clinical assessment.

Detailed Description

Not available

Study Timeline

• Study Start: 2001-04
• Study Completion: 2005-10
• Study First Submitted: 2008-01-17
• Study First Submitted QC: 2008-03-04
• Study First Posted: 2008-03-11
• Status Verified: 2009-04
• Last Update Submitted: 2009-04-21
• Last Update Posted: 2009-04-22

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 54

Inclusion Criteria

• histological or cytological confirmation of breast cancer that is either

  • a primary tumour in a patient unfit for or who has declined surgery
  • advanced (locally or metastatic) disease

• acquired resistance to tamoxifen or ER negative tumour

• at least one measurable or assessable lesion

• WHO performance status 0 - 2

• life expectancy of 12 weeks or more

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Exclusion Criteria

• more than one previous chemotherapy regimens for advanced disease
• prior anthracycline chemotherapy (> 250 mg/m2 adriamycin)
• radiotherapy completed within 14 days prior to Day 1 of treatment
• incomplete healing from prior oncologic or other major surgery
• signs of neurological symptoms consistent with spinal cord compression
• any evidence of clinically active interstitial lung disease (patients with chronic stable

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
Objective tumour response (complete + partial response) based on Union International Contre le Cancer (UICC) Criteria	Assessed after 24 weeks
Clinical benefit (CR + PR + SD > 24 wks)	After 24 weeks of treatment
Frequency and severity of adverse events (AEs)	Assessed at each visit

Secondary Outcome Measures

Name	Time	Method
Progression-free survival	Time to death
Duration of response	Time to progression