Clinical trial · Interventional
Temozolomide and Vinorelbine in Treating Patients With Recurrent Brain Metastases
A Phase I/II Trial Of Temozolomide And Vinorelbine For Patients With Recurrent Brain Metastases
NCT00026494CI-TRIAL-00020564completedPhase 1 / Phase 2Results postedClinicalTrials.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: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. PURPOSE: Phase I/II trial to study the effectiveness of temozolomide and vinorelbine in treating patients who have recurrent brain metastases.
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 |
|---|---|---|---|
| Metastatic Cancer | Malignant Neoplasm | CURATED_BROADER | 0.78 |
Interventions
Interventions (2)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| temozolomide | Drug | Temozolomide | ALIAS |
| vinorelbine tartrate | Drug | Vinorelbine | ALIAS |
Design
Arms and outcomes
Arms (1)
- type
- EXPERIMENTAL
- label
- Temozolomide and Vinorelbine
- description
- Patients will be treated with vinorelbine on days 1 and 8 of each cycle; temozolomide will be administered on days 1 to 7 and 15 to 21 of each cycle. The dose level of temozolomide will be given at a dose of 150 mg/m2/day. A cycle will be defined as 28 days of treatment.
- interventionNames
- Drug: temozolomide
- Drug: vinorelbine tartrate
Primary outcomes (1)
- measure
- Radiographic Response Assessed by Macdonald Criteria Every 2 Months
- timeFrame
- 2 years
- description
- All patients will have their tumor measurements recorded at baseline and at the time of each MRI scan. Lesions must be measured in two dimensions.
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
Show eligibility criteria text
INCLUSION CRITERIAL: * Age \> or = 18 years. * Karnofsky performance score \> or = 60. * Histopathologic confirmation of the diagnosis of a solid tumor malignancy. The brain metastasis diagnosis per se does not have to be pathologically confirmed if the clinical and neuro radiographic picture is typical. * MRI (or CT if the patient cannot undergo MRI) evidence of evaluable disease in the brain. * Absolute neutrophil count \> or = 1,500/mm³. Platelet count \> or = 100,000/mm³. * Hemoglobin \> or = 10 g/dl. * BUN and serum creatinine both \< 1.5 times upper limit of normal. * Total and direct bilirubin both \< 1.5 times upper limit of normal. * SGOT and SGPT both \< or = 3 times upper limit of normal. * Alkaline phosphatase \< or = 2 times upper limit of normal. * At least two weeks must have elapsed from brain biopsy, craniotomy, or other surgery. * Life expectancy \> or = 8 weeks. * Patient or their legal guardian or legal next-of-kin must provide written informed consent prior to patient's registration on study. * At least four weeks must have elapsed from previous external beam radiation therapy, or eight weeks from stereotactic radiosurgery. * Patients treated with radiosurgery should have evidence of progression at a distant site in the brain, or confirmation of tumor progression by biopsy or PET scan. EXCLUSION CRITERIA: * Previous treatment with temozolomide, dacarbazine or vinorelbine. * Patients who have not recovered from all acute toxicities of prior therapies. * Patients with evidence of leptomeningeal metastases or primary dural metastases. * Patients who are poor medical risks because of nonmalignant systemic disease, as well as those with acute infection requiring treatment with intravenous antibiotics. * Patients whose psychiatric condition would, in the judgment of the principal investigator, make it unlikely that they could adhere to the requirements of the protocol.
References
Publications (1)
- RESULTIwamoto FM, Omuro AM, Raizer JJ, Nolan CP, Hormigo A, Lassman AB, Gavrilovic IT, Abrey LE. A phase II trial of vinorelbine and intensive temozolomide for patients with recurrent or progressive brain metastases. J Neurooncol. 2008 Mar;87(1):85-90. doi: 10.1007/s11060-007-9491-3. Epub 2007 Nov 7. PMID 17987262