Status:
COMPLETED
Temozolomide and Thalidomide in Treating Patients With Brain Metastases Secondary to Melanoma
Lead Sponsor:
National Cancer Institute (NCI)
Conditions:
Recurrent Melanoma
Stage IV Melanoma
Eligibility:
All Genders
18+ years
Phase:
PHASE2
Brief Summary
This phase II trial is studying how well giving temozolomide together with thalidomide works in treating patients with brain metastases secondary to melanoma. Drugs used in chemotherapy, such as temoz...
Detailed Description
OBJECTIVES: Primary I. Determine the objective response rate in patients with brain metastases secondary to melanoma treated with temozolomide and thalidomide. Secondary I. Determine the toxic effect...
Eligibility Criteria
Inclusion
- Inclusion Criteria:
- Histologically or cytologically confirmed metastatic melanoma
- Clinical evidence of brain metastases
- At least 1 unidimensionally measurable brain lesion at least 2.0 cm by conventional techniques OR at least 1.0 cm by spiral CT scan or MRI
- The following lesions are not considered measurable:
- Bone lesions
- Leptomeningeal disease
- Ascites
- Pleural/pericardial effusion
- Lymphangitis cutis/pulmonis
- Abdominal masses that are not confirmed and followed by imaging techniques
- Cystic lesions
- Lesions situated in a previously irradiated area, unless new growth is documented
- Performance status - CTC 0-1
- Granulocyte count at least 1,500/mm\^3
- Platelet count at least 100,000/mm\^3
- AST and ALT no greater than 2.5 times upper limit of normal (ULN)
- Lactic dehydrogenase no greater than 2.5 times ULN
- Alkaline phosphatase no greater than 2.5 times ULN
- Creatinine no greater than 2 mg/dL
- No history of active angina
- No history of significant ventricular arrhythmia
- No history of deep vein thrombosis
- No myocardial infarction within the past 6 months
- No acute abnormality by EKG
- No uncontrolled arrhythmia
- No history of pulmonary embolism
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use 1 highly-effective and 1 additional method of contraception for 28 days before, during, and for 4 weeks after study participation
- No known HIV disease
- Thyroid-stimulating hormone normal
- Serum anticonvulsant levels normal (for patients on anticonvulsants)
- No frequent vomiting and/or any other medical condition (e.g., partial bowel obstruction) that would preclude oral medication intake
- No preexisting neuropathy greater than grade 1
- No uncontrolled seizures
- No other concurrent medical condition that would preclude study participation
- At least 4 weeks since prior cytokines
- Biologic agents used as adjuvants, vaccines, and cellular therapies do not require a 4-week washout period
- No concurrent prophylactic filgrastim (G-CSF) or sargramostim (GM-CSF)
- No more than 1 prior chemotherapy regimen
- No prior chemotherapy for brain metastases
- No prior continuous daily temozolomide
- At least 4 weeks since prior chemotherapy (6 weeks for nitrosoureas or mitomycin)
- No other concurrent chemotherapy
- No concurrent hormonal therapy except steroids and hormones administered for non-disease-related conditions (e.g., insulin for diabetes) or for control of intracranial edema from brain metastases
- See Disease Characteristics
- Prior whole brain radiotherapy (WBRT) allowed provided patient has progressive disease in a measurable CNS lesion
- Prior stereotactic radiotherapy allowed provided patient has progressive disease in a measurable CNS lesion
- At least 4 weeks since prior WBRT
- At least 3 weeks since prior stereotactic radiosurgery
- No concurrent radiotherapy
- At least 3 weeks since prior surgical resection
- No concurrent warfarin or heparin products or their derivatives
- No concurrent antiplatelet therapy (e.g., daily aspirin, ibuprofen, or clopidogrel bisulfate)
- No concurrent bisphosphonates (e.g., zoledronate)
Exclusion
Key Trial Info
Start Date :
October 1 2003
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
Estimated Enrollment :
50 Patients enrolled
Trial Details
Trial ID
NCT00072163
Start Date
October 1 2003
Last Update
January 17 2013
Active Locations (1)
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1
Cancer and Leukemia Group B
Chicago, Illinois, United States, 60606