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Spots Global Cancer Trial Database for Biomarkers in Patients With High-Risk Melanoma Receiving High-Dose Interferon Therapy

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Trial Identification

Brief Title: Biomarkers in Patients With High-Risk Melanoma Receiving High-Dose Interferon Therapy

Official Title: PILOT-high Throughput-protein Profiling Analysis of Sera Collected From E1694 Patients Undergoing HDI (Arm B)

Study ID: NCT00897520

Conditions

Melanoma (Skin)

Study Description

Brief Summary: RATIONALE: Studying samples of blood from patients with cancer in the laboratory may help doctors identify biomarkers related to cancer and predict how patients will respond to treatment. PURPOSE: This research study is looking at biomarkers in patients with high-risk melanoma receiving high-dose interferon therapy.

Detailed Description: OBJECTIVES: * To screen serum specimens using a high throughput protein profiling platform that tests for the highest number of known biomarkers (detectable by antibodies) that could be predictors of response to interferon treatment, autoimmunity, and disease outcome in patients with high-risk melanoma undergoing high-dose interferon (IFNa2b) therapy . * To compare soluble factors across all patients at each time point (baseline and during therapy). * To compare pre-therapy vs post-therapy serum samples from these patients. * To assess the kinetics of soluble factors' appearance, persistence, and disappearance during the 12 months of therapy. * To assess whether the amount of specific soluble factors in the pre-therapy sample is predictive of response independent of therapy. * To correlate statistically significant factors with S100 and autoimmunity in these patients. * To confirm the data obtained with the Luminex technology. OUTLINE: Patients are stratified according to survival (\< 2 years vs \> 5 years). Blood samples collected from patients enrolled in E-1694 are analyzed using high throughput protein profiling by ELISA to compare changes in levels of putative biomarkers of interferon alfa-2b, including cytokines and paired receptors, chemokines, cell adhesion molecules, metalloproteinases, angiogenic markers, growth factors, soluble receptors, signal transduction molecules, hormones, and other biomarkers of disease and dysregulated immune processes, at baseline and during therapy.

Eligibility

Minimum Age:

Eligible Ages: CHILD, ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Contact Details

Name: Monica Panelli, PhD

Affiliation: University of Pittsburgh

Role: STUDY_CHAIR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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