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Clinical Trials/NCT00899002
NCT00899002
Withdrawn
Not Applicable

Molecular Analysis of Liver Cancer

ConditionsLiver Cancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Liver Cancer
Sponsor
Vanderbilt-Ingram Cancer Center
Primary Endpoint
Identification of proteomic profiles and molecular pathways involved in tumor progression
Status
Withdrawn
Last Updated
13 years ago

Overview

Brief Summary

RATIONALE: Studying samples of tumor tissue from patients with cancer in the laboratory may help doctors learn more about changes that occur in DNA and identify biomarkers related to cancer.

PURPOSE: This laboratory study is looking at biomarkers in stored tumor samples from younger patients with liver cancer.

Detailed Description

OBJECTIVES: * To characterize, at a molecular level, archived samples of tissue from young patients with fibrolamellar carcinoma and hepatocellular carcinoma in non-cirrhotic livers matched for age and sex. * To perform genomic analysis on these tissue samples using array comparative genomic hybridization. * To perform targeted gene mutation analysis on these samples by PCR. * To perform proteomic profiling on fixed tissues in these samples by various proteomic methods, including IHC and mass spectrometry. * To look for association between molecular aberrations and clinicopathologic features in these samples. OUTLINE: Archived tissue samples are collected from the pathology department at Vanderbilt University Medical Center and from the Mayo Clinic in Rochester, Minnesota. Tissue samples are analyzed by genomic analysis using array comparative genomic hybridization, target gene mutation analysis by PCR, and proteomic profiling on fixed tissues using various proteomic methods, including IHC and mass spectrometry. Samples are also examined for association between molecular aberrations and clinicopathologic features found in each disease. Clinical patient data (i.e., age, sex, race, date of diagnosis, risk factors, histology, surgical staging, follow-ups, date of death, and adjuvant therapy) are also collected.

Registry
clinicaltrials.gov
Start Date
July 2007
End Date
May 2009
Last Updated
13 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Laura W. Goff, MD

Assistant Professor of Medicine, Medical Oncologist

Vanderbilt-Ingram Cancer Center

Eligibility Criteria

Inclusion Criteria

  • DISEASE CHARACTERISTICS:
  • Diagnosis of fibrolamellar carcinoma or hepatocellular carcinoma in a non-cirrhotic liver
  • Archived tumor specimens available for analysis from Vanderbilt University or Mayo Clinic

Exclusion Criteria

  • Not specified
  • PATIENT CHARACTERISTICS:
  • Not specified
  • PRIOR CONCURRENT THERAPY:
  • Not specified

Outcomes

Primary Outcomes

Identification of proteomic profiles and molecular pathways involved in tumor progression

Time Frame: After collection of tissue samples

Genomic analysis, targeted gene mutation analysis, immunohistochemistry, and mass spectrometry will be employed to identify proteomic profiles and specific molecular pathways involved in tumor progression of fibrolamellar carcinoma and hepatocellular carcinoma

Secondary Outcomes

  • Association between fibrolamellar carcinoma and hepatocellular carcinoma in terms of molecular aberrations and clinicopathologic features(After molecular analysis of tissue and after collection of clinicopathologic data)

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