Sulindac in Preventing Melanoma in Healthy Participants Who Are at Increased Risk of Melanoma

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.

Criteria:

- Healthy participants at risk for developing melanoma and meeting the following
criteria: must have >= 4 large (>= 5 mm and < 15 mm) atypical nevi and have 1 benign
nevus amenable to biopsies

- No histologically confirmed melanoma on the baseline biopsy

- No more than 1 prior cutaneous melanoma

- One prior stage I, IIA, or IIB melanoma allowed provided patients have been off
treatment > 3 months

- Modified dermoscopy score < 4.8

- Karnofsky performance status 80-100%

- ANC >= 1,500/mm^3

- No family history of melanoma involving >= 2 first degree relatives

- Platelets count >= 100,000/mm^3

- Total bilirubin =< 2.0 mg/dL

- AST/ALT =< 2.0 times upper limit of normal

- Creatinine =< 1.5 mg/dL

- Not pregnant or nursing

- Fertile patients must use effective contraception

- More than 6 months since prior and no concurrent tanning bed use or other methods to
promote sun-tanning

- Willing to minimize sunlight exposure by applying sunscreen/sunblock or wearing
clothing to shield skin during outdoor activity during study participation

- Willing or able to limit alcohol consumption to less than 3 servings a week during the
study period

- No frequent, chronic or moderate/severe gastrointestinal (GI) complaints

- Upper GI problems requiring prescription or nonprescription medical remedies for
symptoms of heartburn, dyspepsia, nausea, or abdominal pain > once a week on average

- History of peptic ulcer, occult or gross intestinal bleeding

- No prior allergic reaction to aspirin (unless subsequent dosing with other NSAIDs has
been well tolerated)

- No history of allergic reaction to lidocaine or xylocaine

- No history of allergic reaction (e.g., urticaria, asthma, or rhinitis) or gastric
intolerance attributed to compounds of similar chemical or biological composition to
sulindac

- No invasive cancer or cancer treatment within the past 5 years, except nonmelanoma
skin cancer

- No immunosuppression by medication or disease, including any of the following: AIDS,
oral prednisone, immunosuppressant/immunomodulator (i.e., cyclosporine,
chemotherapeutic agent, or biologic therapy)

- No uncontrolled intercurrent illness

- No ongoing or active infection

- No symptomatic congestive heart failure

- No unstable angina pectoris

- No cardiac arrhythmia

- No psychiatric illness/social situations that would limit compliance with study
requirements

- At least 30 days since prior participation and no concurrent enrollment or planning to
enroll in another clinical trial

- No NSAIDs for more than 5 days per month within the past 3 months and no concurrent
non-study NSAIDs, except low dose aspirin (81 mg/day)

- Willing or able to refrain from herbal medicines, above-standard vitamins, or minerals
during study

- Standard daily multivitamin/mineral supplement (i.e., therapeutic doses of calcium and
vitamin D for osteoporosis) allowed

- No concurrent lithium, phenytoin, or sulfonamides

- WBC >= 3,000/mm^3

- No history of bleeding or clotting disorder

- At least 3 months since prior and no concurrent coumadin or other systemic
anticoagulant other than aspirin