A Study of the Safety and Efficacy of Tarceva in Patients With First Relapse of Grade IV Glioma (Glioblastoma Multiforme)

NCT ID: NCT00337883

Last Updated: 2014-03-04

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 110 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2003-07-31
• Study Completion Date: 2005-10-31

Brief Summary

This is a Phase II, open-label, multicenter trial of single-agent treatment with Tarceva in patients with histologically confirmed GBM in first relapse. This study seeks to estimate the objective response rate and will investigate whether response rate is related to EGFR amplification status.

Conditions

Glioblastoma

Study Design

• Primary Study Purpose: TREATMENT

Interventions

Erlotinib HCl (OSI-774)

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Signed informed consent
• Age >= 18 years
• Histologically confirmed GBM in first relapse
• Disease progression in those patients following prior implantation with Gliadel(R) wafer(s) (polifeprosan 20 with carmustine implant) must be confirmed by biopsy. Prior therapy with Gliadel(R) is allowed only as a component of primary surgery. Patients with Gliadel(R) implants after a secondary resection are not eligible.
• Radiographic evidence of disease progression, as assessed by the investigator, on magnetic resonance imaging (MRI) or CT scan
• Bi-dimensionally measurable disease with a minimum measurement of 1 cm on MRI or CT scan performed within 14 days prior to study entry
• Prior radiotherapy
• Availability of tissue to allow central confirmation of GBM diagnosis (all original slides are preferred)
• Availability of paraffin blocks or slides to allow determination of EGFR amplification status
• Recovery from the toxic effects of a prior therapy, including 4 weeks from prior cytotoxic agents (except 6 weeks from prior nitrosoureas, 3 weeks from prior procarbazine administration, 2 weeks from prior vincristine, or 3 weeks from irinotecan [CPT-11] when given on a weekly schedule), 4 weeks from any prior investigational agent, and 1 week from prior non-cytotoxic agents (e.g., interferon, tamoxifen, thalidomide, 13-cis-retinoic acid, etc.)
• If receiving corticosteroids, patients must be on a stable, non-increasing dose of corticosteroids for >= 2 weeks prior to baseline MRI scan
• ECOG performance status of 0 or 1
• Life expectancy > 12 weeks
• Use of an effective means of contraception in males and in females of childbearing potential

Exclusion Criteria

• Prior treatment with Gleevec (e.g., imatinib mesylate) or agents directed at EGFR (e.g., Iressa)
• Prior treatment with Gliadel(R) following second (salvage or debulking) therapy
• History of any other malignancy within 5 years (except non-melanoma skin cancer or carcinoma in situ of the cervix)
• More than one prior chemotherapy regimen
• ANC < 1500/uL
• Platelets < 100,000/uL
• Total bilirubin > 1.6 mg/dL
• AST/ALT >= 2.5 x upper limit of normal (ULN)
• Creatinine > 1.5 x ULN
• Pregnant or nursing females
• Unstable systemic disease, including active infection, uncontrolled hypertension, unstable angina, congestive heart failure, or myocardial infarction within 6 months prior to study entry, or serious cardiac arrhythmia requiring medication
• Major surgical procedure 2 weeks prior to study entry or anticipation of need for major surgical procedure during the course of the study
• Inability to take oral medication

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Genentech, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Barbara Klencke, M.D.

Role: STUDY_DIRECTOR

Genentech, Inc.

Other Identifiers

OSI2691g

Identifier Type: -

Identifier Source: org_study_id

NCT00090883

Identifier Type: -

Identifier Source: nct_alias