Vorinostat in Treating Patients With Metastatic or Unresectable Melanoma

Completed · Phase 2

Conditions studied: Ciliary Body and Choroid Melanoma, Medium/Large Size, Extraocular Extension Melanoma, Iris Melanoma, Uveal Melanoma, Recurrent Intraocular Melanoma, Recurrent Melanoma, Stage IV Melanoma

In brief

This phase II trial is studying how well vorinostat works in treating patients with metastatic or unresectable melanoma. Vorinostat may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor.

Key facts

Study ID

NCT00121225

Run by

National Cancer Institute (NCI)

People needed

32

Starts

2005-09-01

Expected to finish

2013-06-01

Last updated by the study team

2019-01-29

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Histologically/cytologically confirmed melanoma that is metastatic/unresectable
• Residual, recurrent, or metastatic disease by radiographic examination. Measurable disease (at least 1 lesion in at least 1 dimension (longest diameter) as >20mm with conventional techniques or >10mm with spiral CT scan, within 4 weeks prior to registration
• No prior therapy or 1 prior treatment (cytokine/chemotherapy/combination) for metastatic disease allowed. Patients should not take valproic acid, another histone deacetylase inhibitor, for at least 2 weeks prior to enrollment. At least 4 weeks from prior therapy to be eligible or 6 weeks if last regimen included BCNU or mitomycin C
• Age>=18 years
• Life expectancy >=3 months.
• ECOG<2 (Karnofsky ≥60%)
• Leukocytes >3,000/mcL
• Absolute neutrophil count >1,500/mcL
• Platelets >100,000/mcL
• Total bilirubin within institutional limits
• AST/ALT≤2.5Xinstitutional ULN
• Creatinine within institutional limits OR creatinine clearance >60mL/min/1.73 m2 if creatinine levels above institutional limits
• Eligibility of patients taking medications with potential to affect activity/PK of Vorinostat will be determined by PI
• Must not use concomitant steroids except topical/inhaled use
• Vorinostat effects on developing human fetus are unknown. Women of childbearing potential (WOCBP) and sexually active males must agree to use accepted/effective contraception method prior to study entry and for duration of the study
• Ability to understand/willingness to sign written informed consent
• Must have paraffin block of tumor tissue available for future studies

You may not qualify if…

• Chemotherapy/radiotherapy within 4 weeks (6 weeks for nitrosoureas or mitomycin C) prior to entering study
• May not be receiving any other investigational agents
• Known brain metastases
• History of allergic reactions attributed to compounds of similar chemical/biologic composition to Vorinostat
• Uncontrolled intercurrent illness including but not limited to ongoing/active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements
• Pregnant women excluded because Vorinostat is a HDAC inhibitor agent with potential for teratogenic or abortifacient effects
• HIV-positive patients receiving combination antiretroviral therapy are ineligible because of potential for PK interactions with Vorinostat

Where it is running

• Fox Chase Cancer Center — Philadelphia, Pennsylvania, United States
• Fox Chase Cancer Center — Rockledge, Pennsylvania, United States
• Juravinski Cancer Centre at Hamilton Health Sciences — Hamilton, Ontario, Canada
• Princess Margaret Hospital Phase 2 Consortium — Toronto, Ontario, Canada
• University Health Network-Princess Margaret Hospital — Toronto, Ontario, Canada

Full record on ClinicalTrials.gov

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