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Blog Archives: Nov 2004 - present
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Criteria for Participation in this Clinical Trial
DISEASE CHARACTERISTICS:
- Any of the following:
- Families with neoplasias of an unusual type, pattern, or number, including breast cancer, or which is consistent with an identified or suspected familial cancer syndrome, including breast and/or ovarian cancer
- Families with a history of any of the following types of syndromes:
- Familial breast/ovarian
- Li-Fraumeni
- Peutz-Jegher
- Cowden
- Families with multiple cases of breast cancer among first- and second-degree relatives
- Families with a history of other cancers that do not fit into a well-characterized syndrome (e.g., multiple occurrences of breast and colorectal cancers)
- Families of an individual with a known mutation in the BRCA1 or BRCA2 gene
- Individuals with a personal history of neoplasia(s) or benign conditions of an unusual type
- Individuals with unusual demographic features, including:
- Young age at onset of disease
- Multiple primary sites
- Rare tumor type of pathologic characteristic
- At least 2 living affected family members are required for known or suspected familial syndromes for which no gene has been identified
- Diagnoses must be verifiable
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