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Clinical Trials/NCT00897520
NCT00897520
Completed
Not Applicable

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

ECOG-ACRIN Cancer Research Group0 sites40 target enrollmentJanuary 14, 2008
ConditionsMelanoma (Skin)

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Melanoma (Skin)
Sponsor
ECOG-ACRIN Cancer Research Group
Enrollment
40
Primary Endpoint
Comparison of soluble factors
Status
Completed
Last Updated
8 years ago

Overview

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.

Registry
clinicaltrials.gov
Start Date
January 14, 2008
End Date
January 24, 2010
Last Updated
8 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
ECOG-ACRIN Cancer Research Group
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Comparison of soluble factors

Time Frame: 1 month

Serum sample screening via high throughput protein profiling in patients undergoing therapy

Time Frame: 1 month

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