Status:

TERMINATED

Erlotinib in Treating Patients With Recurrent Glioblastoma Multiforme or Gliosarcoma

Lead Sponsor:

Michael Prados

Collaborating Sponsors:

National Cancer Institute (NCI)

Genentech, Inc.

Conditions:

Adult Brain Tumors

Eligibility:

All Genders

18+ years

Phase:

PHASE2

Brief Summary

RATIONALE: Erlotinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. PURPOSE: This phase II trial is studying how well erlotinib works in treating patients ...

Detailed Description

OBJECTIVES: Primary * Determine the objective response rate in patients with recurrent epidermal growth factor receptor (EGFR)-positive and PTEN wild-type glioblastoma multiforme or gliosarcoma trea...

Eligibility Criteria

Inclusion

  • INclusion Criteria:
  • Diagnosis of glioblastoma multiforme (GBM) or gliosarcoma (GS)
  • In first, second, or third relapse
  • History of low-grade glioma with transformation to GBM or GS allowed
  • Considered to be in first relapse at first documented diagnosis of GBM or GS
  • Measurable or evaluable disease by contrast MRI
  • Must have failed prior treatment that included external beam radiotherapy with or without chemotherapy
  • Epidermal growth Factor Receptor-positive and PTEN wild-type by immunohistochemistry
  • PATIENT CHARACTERISTICS:
  • Karnofsky performance status 60-100%
  • WBC ≥ 3,000/mm³
  • Absolute neutrophil count ≥ 1,500/mm³
  • Platelet count ≥ 100,000/mm³
  • Hemoglobin ≥ 10 g/dL (transfusion allowed)
  • SGOT \< 2 times upper limit of normal (ULN)
  • Bilirubin \< 2 times ULN
  • Creatinine \< 1.5 mg/dL OR creatinine clearance ≥ 60 mL/min
  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective hormonal or barrier method contraception before, during, and for at least 12 weeks after completion of study treatment
  • No other cancer within the past 3 years except nonmelanoma skin cancer or carcinoma in situ of the cervix
  • No active infection
  • No other disease that would obscure toxicity or dangerously alter study drug metabolism
  • PRIOR CONCURRENT THERAPY:
  • See Disease Characteristics
  • More than 4 weeks since prior and no concurrent radiotherapy
  • At least 4 weeks since prior and no concurrent cytotoxic chemotherapy agents (e.g., temozolomide) (6 weeks for nitrosoureas)
  • At least 2 weeks since prior and no concurrent noncytotoxic chemotherapy agents
  • At least 4 weeks since prior investigational agents
  • No other concurrent investigational agents
  • No prior erlotinib hydrochloride or other epidermal growth factor receptor tyrosine-kinase inhibitors
  • At least 2 weeks since prior enzyme-inducing antiepileptic drugs (EIAEDs), if not used concurrently with study treatment
  • Concurrent continuous use of EIAEDs allowed provided the patient has received the drug for ≥ 2 weeks prior to study treatment
  • No concurrent immunotherapy or anticancer hormonal therapy
  • No other concurrent antineoplastic or antitumor agents
  • Exclusion Criteria:
  • Patients meeting any of the following criteria are ineligible for study entry:
  • Patients with a history of any other cancer (except non-melanoma skin cancer or carcinoma in-situ of the cervix), unless in complete remission and off of all therapy for that disease for a minimum of 3 years are ineligible.
  • Patients must not have active infection
  • Patients must not be pregnant/breast feeding and must agree to practice adequate contraception. Women of childbearing potential must have a negative B-HCG pregnancy test documented within 14 days prior to treatment. Patients must not be pregnant because of the uncertainty that study drug may be potentially embryotoxic. For this reason, women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control) prior to study entry, for the duration of study participation, and continue approximately 12 weeks after the study is completed. If condoms are used as a barrier contraceptive, a spermicidal agent should be added to ensure that pregnancy does not occur. Should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately.
  • Prior treatment with Tarceva, or other EGFR tyrosine-kinase inhibitors will not be allowed.
  • Patients must not have any disease that will obscure toxicity or dangerously alter drug metabolism.

Exclusion

    Key Trial Info

    Start Date :

    January 1 2007

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ACTUAL

    End Date :

    March 1 2009

    Estimated Enrollment :

    6 Patients enrolled

    Trial Details

    Trial ID

    NCT00387894

    Start Date

    January 1 2007

    End Date

    March 1 2009

    Last Update

    June 4 2013

    Active Locations (1)

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    Page 1 of 1 (1 locations)

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    UCSF Helen Diller Family Comprehensive Cancer Center

    San Francisco, California, United States, 94143