Clinical Trial: Hereditary Gastric Cancer Syndromes: An Integrated Genomic and Clinicopathologic Study of the Predisposition to Gastric Cancer

Study Status: Recruiting
Recruit Status: Recruiting
Study Type: Observational

Official Title: Hereditary Gastric Cancer Syndromes: An Integrated Genomic and Clinicopathologic Study of the Predisposition to Gastric Cancer

Brief Summary:

Background:

Gastric cancers are cancers of the stomach. Hereditary ones are passed from parent to child. Researchers want to gather data about hereditary gastric cancers. They want to learn about changes these cause in the body and about the genes involved.

Objective:

-To gather data about hereditary gastric cancer.

Eligibility:

  • People at least 2 years old with personal or family history with a hereditary gastric cancer.
  • People at least 2 years old with gene changes that lead to such cancer or a lesion that may be hereditary.

Design:

  • Participants will be screened in a separate protocol.

  • Participants will have:

    • Physical exam
    • Medical history
    • Blood tests
    • Scans
    • Photos of skin lesions and other findings
    • Gynecology consultation for women
    • Cheek swab (some participants)
  • For some participants, their relatives will be asked to join the study.
  • Some participants will be asked to allow the study to get stored tissue samples for relatives who have died.
  • Some samples will be sent to outside labs. All person

    Detailed Summary:

    Background:

    • An estimated 1-3% of gastric cancer cases occur within a familial background as part of an inherited cancer syndrome
    • Hereditary Diffuse Gastric Cancer (HDGC) is the most frequent form of familial gastric cancer and has been linked to a germline mutation in the CDH1 gene
    • Gastric Adenocarcinoma and Proximal Polyposis of the Stomach (GAPPS) is a more recently described autosomal dominant syndrome characterized by fundic gland polyposis with antral sparing
    • Other syndromes that predispose to gastric cancer include Li-Fraumeni syndrome, Lynch syndrome, Peutz-Jeghers syndrome, familial adenomatous polyposis syndrome and others

    Objectives:

    - Characterize the natural and clinical histories of hereditary gastric cancer syndromes

    Eligibility:

    - Individuals, and family members, who fulfill clinical criteria for a hereditary gastric cancer syndrome irrespective of previous genetic testing or treatment

    Design:

    • These rare families will be recruited to genetically confirm diagnosis and study the natural history of hereditary gastric cancers
    • Genetic testing will be offered to gain appreciation of the effect of mutations on the relative activity of various germline and somatic mutations.
    • We will determine if there is a relationship between mutation and disease phenotype.

    Sponsor: National Cancer Institute (NCI)

    Current Primary Outcome: Characterization of the natural and clinical histories of hereditary gastric cancer syndromes [ Time Frame: 10 years ]

    Original Primary Outcome: Same as current

    Current Secondary Outcome:

    Original Secondary Outcome:

    Information By: National Institutes of Health Clinical Center (CC)

    Dates:
    Date Received: January 24, 2017
    Date Started: January 11, 2017
    Date Completion: December 31, 2026
    Last Updated: April 21, 2017
    Last Verified: January 23, 2017