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This study evaluates the drugs Dacarbazine and Interferon Alfa-2b in patients with uveal melanoma (cancer of the eye's uvea) whose tumors show genetic imbalance (monosomy 3 and/or 8q amplification). It included patients who had adequate primary therapy. It was a Phase 2 study and has been completed.
The summary above is a plain-language rendering of the official record. The original English title is shown for reference.
Criteria are reproduced from the ClinicalTrials.gov record in the original English. Only the trial team can determine eligibility.
Inclusion * Patients must have a diagnosis, either cytologic or histologic, of melanoma of the iris, ciliary body and/or choroid * Patient's tumor must exhibit monosomy 3 and/or 8q amplification as determined by karyotype, comparative genomic hybridization (CGH), polymerase chain reaction (PCR)-based microsatellite, and/or Fluorescence in situ Hybridization (FISH) analysis; tissue or cells for analysis can be obtained at enucleation, resection, or by fine needle aspirate (FNA). * Patients must have undergone adequate primary therapy; this can include enucleation, brachytherapy, proton beam radiotherapy, stereotactic irradiation, trans-scleral local resection, transretinal resection or diode laser thermotherapy * Patients must have had chest X-ray and hepatic ultrasound or other imaging methods such as CT or MRI to eliminate distant disease * Patients must have a performance status (ECOG) of \< 2 * Patients must be entered within 56 days of completing primary therapy * White blood count (WBC) ≥ 3.0 x 10\^9/L * Neutrophils ≥ 1.5 x 10\^9/L * Platelets ≥ 100 x 10\^9/L * international normalized ratio (INR) and partial thromboplastin time (PTT) \< 1.5 x upper limit of normal * Hemoglobin ≥ 10 gm/100 ml * Creatinine ≤ 2 mg/dl * Bilirubin (total) ≤ 1.5 mg/dl * Alanine transaminase (ALT) ≤ 1.5 x upper limit of normal * Alkaline phosphatase ≤ 1.5 x upper limit of normal * Aspartate aminotransferase (AST) ≤ 1.5 x upper limit of normal * Patients must not have received any other systemic therapy for melanoma * Women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control) prior to study entry and for the duration of study participation; should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately * All patients must be informed of the investigational nature of this study and must provide written informed consent in accordance with institutional and federal guidelines; a copy of the informed consent document signed by the patient must be given to the patient Exclusion * Patients with metastasis * Patients that are pregnant or breastfeeding * Patients may not be receiving any other investigational agents * Patients with a history of immunodeficiency or autoimmune diseases are not eligible; patients requiring therapy with corticosteroids or other immunosuppressives are not eligible; patients requiring ongoing replacement therapy with physiologic doses of corticosteroids will be eligible. * Patients with uncontrolled intercurrent illness including, but not limited to ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements are not eligible * Patients who are known to be positive for HIV or Hepatitis B Surface Antigen (HepBAg) * No patient may have had a malignancy other than a malignant melanoma, with the following exceptions: basal or squamous cell carcinomas of the skin; carcinoma in-situ of the uterine cervix; any malignancy treated with curative intent and in complete remission for \> 3 years * Patients with organ allografts