Docetaxel and Vinorelbine Plus Sargramostim in Metastatic Malignant Melanoma
Metastatic Melanoma

About this trial
This is an interventional treatment trial for Metastatic Melanoma focused on measuring Metastatic Melanoma
Eligibility Criteria
Inclusion Criteria: Age greater than or equal to 18 Karnofsky Performance Status (KFS) of greater than or equal to 70 Laboratory values (performed in 14 days, inclusive prior to study drug administration): Absolute neutrophil count (ANC) >1500/mm3 Platelet count >100,000/mm3 Hemoglobin > 10 g/dl Blood urea nitrogen (BUN) and serum creatinine < 0.5 times the upper limit of laboratory normal Total and direct bilirubin < 1.5 times the upper limit of laboratory normal Serum glutamic-oxaloacetic transaminase (SGOT) and Serum glutamic pyruvic transaminase(SGPT) < 3 times the upper limit of laboratory normal Alkaline phosphatase < 3 times upper limit of laboratory normal Life expectancy of greater than 12 weeks Written informed consent Exclusion Criteria: No recovery from all active toxicities of prior therapies Surgery within 1 week prior to study drug administration, providing acute surgical toxicity is resolved Subjects within acute infection treated with intravenous antibiotics Frequent vomiting or medical condition that could interfere with oral medication intake (e.g., partial bowel obstruction) Concurrent malignancies at other sites with the exception of surgically cured carcinoma in situ (CIS ) of the cervix, basal or squamous cell carcinoma of the skin, and prior malignancies which have not required anit-tumor treatment within the preceding 24 months Known HIV-positivity or AIDS-related illness Women of childbearing potential who are not using an effective method of contraception (eligible patients must have a negative urine pregnancy test 24 hours prior to administration of study drug and be practicing medically approved contraceptive precautions) Men who do not use an effective method of contraception. Chemotherapy within four weeks prior to study drug administration or biologic therapy/immunotherapy within two weeks prior to study drug administration Completion of radiation therapy, interstitial brachytherapy, or radiosurgery within 4 weeks prior to study drug administration (patients with brain metastases from melanoma must have completed radiotherapy to the brain at least 3 weeks before study commences) Bone metastases as sole reason for Stage IV disease Karnofsky Performance Status of less than or equal to 60
Sites / Locations
- Chao Family Comprehensive Cancer Center
Arms of the Study
Arm 1
Experimental
Docetaxel & Vinorelbine + Sargramostim
Docetaxel, Vinorelbine, and Sargramostim