Epidemiologic Study of Hepatocellular Carcinoma in the US

Sponsor
Stanford University (Other)
Overall Status
Completed
CT.gov ID
NCT02358070
Collaborator
(none)
45
1
17.1
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Study Details

Study Description

Brief Summary

The purpose of this study is:
  • to investigate the risk factors of HCC among Americans with focus on lifestyle factors and energy balance.

  • to identify single nucleotide polymorphisms (SNPs) and haplotypes that are associated with HCC risk through a genome-wide search.

  • to assess if genetic susceptibility differs by hepatitis virus infection or lifestyle factors, and to explore if there are interplays or effect modifications between genetic factors and viral infection or lifestyle factors.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    45 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Cross-Sectional
    Official Title:
    Epidemiologic Study of Hepatocellular Carcinoma in the US
    Actual Study Start Date :
    Apr 1, 2015
    Actual Primary Completion Date :
    Sep 1, 2016
    Actual Study Completion Date :
    Sep 1, 2016

    Arms and Interventions

    Arm Intervention/Treatment
    HCC group

    control group

    Outcome Measures

    Primary Outcome Measures

    1. Lifetime physical activity [20 years]

      Lifetime physical activity will be measured by collecting data on major types of physical activity separately and by determining frequency, intensity, and duration of each activity using a combined modification of Friedenreich's lifetime physical activity questionnaire and Kriska's past year physical activity questionnaires.

    2. Energy intake [20 years]

      A modified Food Frequency questionnaire based on one developed by Dr. Alan Kristal from the Fred Hutchinson Cancer Research Center (FHCRC) in Seattle will capture energy intake by differentiating low-fat food options from higher-fat counterparts.

    3. Lifestyle factors [20 years]

      Structured questionnaires will be used to elicit information on demographic, anthropometric, and socioeconomic factors, long-term use of medications, medical history, and family history of cancer, cigarette smoking and alcohol consumption, physical activity, and dietary habits. Additional information unrelated to liver cancer will be included in the questionnaire to help assess possible recall bias.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    35 Years to 84 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria for HCC cases:
    • a diagnosis of primary liver cancer (excluding secondary tumors)

    • a diagnosis of hepatocellular carcinoma if histology is available (excluding those diagnosed in intrahepatic bile duct, bile canals, biliary passages, canaliculi, gall duct and gallbladder)

    • a diagnosis of hepatocellular carcinoma with or without microscopic evaluation (including those diagnosed with clinical evidence, lab tests and direct visualization or radiographic and other imaging evidence)

    • a histology of primary hepatocellular carcinoma when the patients had a prior diagnosis of other forms of cancer (excluding those who had no histological diagnosis of hepatocellular carcinoma while having a prior history of other cancer;

    • age at diagnosis between 35 and 84 years

    • living in Connecticut, New Jersey, New York, or Hawaii for at least a year as regular residents.

    Exclusion Criteria for HCC cases:
    • uncertain diagnoses or classification of malignancy, such as unknown origin

    • a diagnosis of primary tumors in other organs, not in the liver

    • unable to communicate well enough in English or Spanish

    • having medical conditions, such as mental disorders, that prevent the subject from providing reasonably comprehensible information or from being able to give informed consent.

    • diagnosed at age <35 years or >84 years

    • temporary residents of New Jersey, Connecticut, New York, or Hawaii

    Inclusion Criteria for control subjects:
    • age between 35 and 84 years

    • living in New Jersey or Connecticut for at least a year as regular residents

    • able to communicate well in English or Spanish

    • having no medical conditions, such as mental disorders, that prevent them from providing adequately comprehensible information

    • potential subjects with a previous history of cancer are eligible.

    Exclusion Criteria for control subjects:
    • age < 35 years or > 84 years

    • temporary residents of New Jersey or Connecticut

    • unable to speak English or Spanish

    • cannot provide adequately comprehensible information

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Stanford Liver Transplant Clinic Stanford California United States 94305

    Sponsors and Collaborators

    • Stanford University

    Investigators

    • Principal Investigator: Mindie Nguyen, MD, Stanford University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Stanford University
    ClinicalTrials.gov Identifier:
    NCT02358070
    Other Study ID Numbers:
    • HEP0049
    First Posted:
    Feb 6, 2015
    Last Update Posted:
    Mar 24, 2020
    Last Verified:
    Mar 1, 2020
    Keywords provided by Stanford University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 24, 2020