Precancerous Condition Clinical Trial
Official title:
Phase II Trial of Sulindac in Individuals at Increased Risk for Melanoma
This randomized phase II trial is studying how well sulindac works in preventing melanoma in healthy participants who are at increased risk of melanoma. Sulindac may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. It is not yet known whether sulindac is more effective than a placebo in preventing melanoma in individuals with many moles and abnormal moles.
PRIMARY OBJECTIVE:
I. To determine sulindac and metabolite levels in healthy participants with atypical nevi and
benign nevus at increased risk for melanoma treated with sulindac versus placebo.
SECONDARY OBJECTIVES:
I. To assess the effects of sulindac on apoptosis in atypical nevi of these participants.
II. To assess the effects of sulindac on VEGF expression in atypical nevi of these
participants.
III. To assess sulindac and metabolite levels in plasma and its association with drug levels
in the target tissue.
OUTLINE: This is a multicenter study. Participants are randomized to 1 of 2 treatment arms.
ARM I: Participants receive oral sulindac twice daily.
ARM II: Participants receive oral placebo twice daily.
In both arms, treatment continues for 8 weeks in the absence of unacceptable toxicity.
Blood and tissue samples are collected at baseline and/or after completion of study therapy
and analyzed for sulindac and metabolite levels via high performance liquid chromatography
tandem mass spectrometry; the detection of apoptotic cells via TUNEL assay; and VEGF
expression via immunohistochemistry assays.
After completion of study therapy, participants are followed for 2 weeks.
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