Clinical trial · Interventional
Gefitinib Plus Temozolomide in Treating Patients With Malignant Primary Glioma
A Phase I Study Of ZD 1839 And Temozolomide For The Treatment Of Gliomas
NCT00027625CI-TRIAL-00033486completedPhase 1ClinicalTrials.gov clinicaltrialsProvenance
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
RATIONALE: Biological therapies such as gefitinib may interfere with the growth of cancer cells and slow the growth of the tumor. Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining gefitinib with chemotherapy may kill more tumor cells. PURPOSE: Phase I trial to study the effectiveness of combining gefitinib with temozolomide in treating patients who have malignant primary glioma.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Brain and Central Nervous System Tumors | — | UNRESOLVED | — |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| gefitinib | Drug | Gefitinib | ALIAS |
| temozolomide | Drug | Temozolomide | ALIAS |
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 120 Years
Show eligibility criteria text
DISEASE CHARACTERISTICS: * Histologically confirmed malignant primary glioma * Glioblastoma multiforme * Anaplastic astrocytoma * Anaplastic oligodendroglioma * Anaplastic mixed oligoastrocytoma * Malignant astrocytoma not otherwise specified * Stable or progressive disease * Progressive disease after interstitial brachytherapy or stereotactic radiosurgery must be confirmed by positron emission tomography or thallium scan, magnetic resonance spectroscopy, or surgical biopsy * Prior treatment for no more than 3 prior relapses allowed PATIENT CHARACTERISTICS: Age: * 18 and over Performance status: * Karnofsky 60-100% Life expectancy: * More than 8 weeks Hematopoietic: * WBC greater than 3,000/mm\^3 * Absolute neutrophil count greater than 1,500/mm\^3 * Platelet count greater than 120,000/mm\^3 * Hemoglobin greater than 10 g/dL (transfusion allowed) Hepatic: * Bilirubin less than 1.5 times upper limit of normal (ULN) * SGOT less than 1.5 times ULN Renal: * Creatinine less than 1.5 mg/dL OR * Creatinine clearance greater than 60 mL/min Other: * Not pregnant * Negative pregnancy test * Fertile patients must use effective contraception * No active infection * No other concurrent significant medical illness that would preclude study participation * No significant gastrointestinal risk factors (e.g., active ulcerative colitis) within the past 6 months * No other malignancy within the past 3 years except non-melanoma skin cancer or carcinoma in situ of the cervix PRIOR CONCURRENT THERAPY: Biologic therapy: * At least 1 week since prior interferon * No concurrent filgrastim (G-CSF) during the first course of study therapy Chemotherapy: * At least 2 weeks since prior vincristine * At least 3 weeks since prior procarbazine * At least 6 weeks since prior nitrosoureas * Prior or concurrent temozolomide allowed if there is no evidence of progression while receiving therapy Endocrine therapy: * At least 1 week since prior tamoxifen * Must be on a stable dose of corticosteroids for at least 5 days Radiotherapy: * See Disease Characteristics * At least 3 weeks since prior radiotherapy Surgery: * See Disease Characteristics * At least 1 week since prior surgical resection Other: * Recovered from all prior therapy * No prior gefitinib * At least 1 week since prior non-cytotoxic agents except radiosensitizers * At least 4 weeks since prior cytotoxic therapy * At least 4 weeks since prior investigational agents * At least 3 years since prior therapy for other malignancy * Concurrent therapeutic agents allowed at stable dosage * Concurrent enzyme-inducing anti-epileptic drugs allowed if continued during study participation
References
Publications (1)
- RESULTPrados MD, Yung WK, Wen PY, Junck L, Cloughesy T, Fink K, Chang S, Robins HI, Dancey J, Kuhn J. Phase-1 trial of gefitinib and temozolomide in patients with malignant glioma: a North American brain tumor consortium study. Cancer Chemother Pharmacol. 2008 May;61(6):1059-67. doi: 10.1007/s00280-007-0556-y. Epub 2007 Aug 11. PMID 17694310