Natural Killer Cell Therapy (UD TGFbetai NK Cells) and Temozolomide for the Treatment of Stage IV Melanoma Metastatic to the Brain

Inclusion Criteria:

Histologically confirmed melanoma with stage IV disease
Radiologically confirmed brain metastasis (n >= 1) with at least one measurable central nervous system (CNS) lesion >= 10 mm on T1-weighted gadolinium enhanced magnetic resonance imaging (MRI) and unequivocal evidence of progression
No indication for stereotactic radiotherapy
At least 4 weeks from any anticancer treatment (cytotoxic chemotherapy, signal transduction inhibitors, immunotherapy or radiation)
Absolute neutrophil count (ANC) 1 x 10^9/L
Platelets > 100,000/L
Hemoglobin (Hgb) >= 10 g/dL
Creatinine =< 1.5 x upper limit of normal (ULN)
Albumin >= 2.5 g/dL
Serum bilirubin < 1.5 x ULN unless due to Gilbert's syndrome
Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) < 5 x ULN if documented liver metastases or < 3 X ULN without liver metastasis
> 18 years old (y/o)
Eastern Cooperative Oncology Group (ECOG) performance status of 0-2
Females of reproductive age must agree to the use of an effective contraceptive method while on treatment, beginning 2 weeks before the first dose of investigational product and for 28 days after the final dose of investigational product for women. Males able to father a child must practice adequate methods of contraception or completely abstain from intercourse from the first dose of investigational treatment until one week after the final dose of investigational treatment
Women of childbearing potential must have a negative serum pregnancy test within 14 days of enrollment and/or urine pregnancy test 48 hours prior to the administration of the first study treatment
Patient information and written informed consent form signed

Exclusion Criteria:

Planned or concurrent systemic treatment or radiation therapy
If requiring corticosteroids for cerebral edema, patients must be on a stable dose. Lowest dose of steroids needed to control CNS edema is recommended. Doses above 4 mg daily need to be cleared by principal investigator (PI) of the study
Known contra-indication to MRI
Patients with non-melanoma malignancies are excluded unless a complete remission has been achieved at least 3 years prior to study entry and no additional therapy is required or anticipated during the study period (exceptions include: non-melanoma skin cancers, in situ bladder cancer, in situ gastric cancer, in situ colon cancers, in situ cervical cancers/dysplasia, or in situ breast carcinoma)

Patients with other concurrent severe and/or uncontrolled medical disease which could compromise participation in the study, such as:

Active infection
Current active hepatic or renal disease
Pregnant women, women who are likely to become pregnant or are breastfeeding
Patients with significantly altered mental status prohibiting the understanding of the study or with psychological, familial, sociological, or geographical conditions potentially hampering ability to consent, compliance with the study protocol, and follow-up schedule; those conditions should be discussed with the patient before remigration in the trial
Patients who received any other investigational drugs within the 30 days prior to screening visit
Leptomeningeal metastases diagnosed by MRI
Inclusion in another therapeutic protocol within 30 days
If steroids are necessary to control symptoms related to CNS metastases, patients should be on the lowest dose of steroids necessary to control symptoms