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Answering Questions About Vitamin D Supplementation and Sun Exposure in Patients Who Have Undergone Surgery for Stage IB, Stage II, or Stage IIIA Melanoma

Melanoma Lifestyle Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00672321
Enrollment
2774
Registered
2008-05-06
Start date
2007-12-31
Completion date
Unknown
Last updated
2013-08-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Melanoma (Skin)

Keywords

recurrent melanoma, stage IB melanoma, stage II melanoma, stage IIIA melanoma

Brief summary

RATIONALE: Gathering information about vitamin D supplementation and sun exposure in patients with melanoma may help doctors learn more about the disease and find what may affect cancer relapse. PURPOSE: This clinical trial is studying vitamin D supplementation and sun exposure in patients who have undergone surgery for stage IB, stage II, or stage IIIA melanoma.

Detailed description

OBJECTIVES: * To examine the findings of the pilot study, that vitamin D supplementation in combination with vitamin D receptor (VDR) polymorphisms protects from late relapse (after 3 years) in patients who have had melanoma. * To investigate the effects of vitamin D supplement dosage in reducing the risk of late relapse. * To examine if vitamin D supplementation in combination with particular VDR polymorphisms protects from early relapse (before 3 years). * To examine if serum levels of vitamin D correlate with risk of relapse in groups of patients with different VDR polymorphisms. * To examine the effect of vitamin supplementation and VDR status on time to relapse and survival in these patients. * To examine other factors that may affect risk of relapse by assembling a tissue (genomic DNA and serum) resource. * To investigate the effect of exposure to incidental drugs, such as statins, on risk of relapse in these patients. OUTLINE: Patients are stratified according to disease relapse in the past 5 years (yes vs no). Patients are asked to complete a food frequency questionnaire focusing on vitamin D and the following area: supplementation of diet with vitamins/fish oil and duration of use; sun exposure and sunscreen-use per decade prior to and after diagnosis. Patients are also asked to provide a blood sample for serum and DNA analysis. Consenting patients are also tagged with the Office of National Statistics to allow passive follow up. Stored tissue from the patient's primary melanoma may be used to corroborate research findings using immunohistochemistry or studies of gene expression, polymorphism, or mutation.

Interventions

GENETICgene expression analysis
GENETICmutation analysis
GENETICpolymorphism analysis
OTHERlaboratory biomarker analysis
OTHERquestionnaire administration

Sponsors

Leeds Cancer Centre at St. James's University Hospital
Lead SponsorOTHER

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

DISEASE CHARACTERISTICS: * Diagnosed with melanoma * Must meet either of the following conditions: * Resected stage IB, II, or IIIA disease that has relapsed as either stage III or IV disease (cases) * First loco regional and/or visceral relapse (with/without sentinel node biopsy) * No more than 3 months since first relapse * Resected stage IB, II, or IIIA disease that has not relapsed for ≥ 5 years (controls) PATIENT CHARACTERISTICS: * Not specified PRIOR CONCURRENT THERAPY: * See Disease Characteristics

Design outcomes

Primary

MeasureTime frame
Odds ratio (OR) for vitamin D supplementation in relapse
OR for vitamin D supplementation in patients with specific VDR genotypes

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026