Colon Cancer Clinical Trial
Identification of New Colorectal Cancer Genes
Summary
The purpose of this study is to define new genes for family risks of developing colon cancer.
Full Description
Colorectal cancer is one of the most significant causes of cancer morbidity and mortality in the United States. In 1997, approximately 130,000 men and woman were diagnosed with colorectal cancer (fourth most common cancer site) and approximately 55,000 died of this disease (second most common cause of cancer deaths); (Cancer Facts & Figures, 1997).
Genetic factors clearly contribute to the etiology of colorectal cancer. Because there is evidence to suggest genetically determined susceptibility to colorectal cancer exists in a proportion of newly diagnosed cases each year, we are conducting a study to identify new genes that are associated with an increased susceptibility to familial colorectal cancer by analysis of families with a clustering of colorectal cancers.
Eligibility Criteria
Inclusion Criteria:
Age 18 years or greater
Able to provide informed consent
Any family in which a minimum of two first-degree relatives either are, or have previously been, affected with primary colorectalcancer. These "minimum inclusion criteria" must be met within three generations of the proband or kindreds in which colorectal cancer and lymphoma or renal cell cancer are present or in kindreds in which lymphoma alone or lymphoma and renal cell cancer are present
Exclusion Criteria:
Age less than 18 years
Family not at increased risk for familial colorectal cancer (see Section 4.1)
Family with a hereditary polyposis syndrome (e.g. classic FAP)
Not able to provide informed consent
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There is 1 Location for this study
New York New York, 10065, United States
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