Genetic Analysis of Birt Hogg-Dube Syndrome and Characterization of Predisposition to Kidney Cancer
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|ClinicalTrials.gov Identifier: NCT00033137|
Recruitment Status : Recruiting
First Posted : April 8, 2002
Last Update Posted : May 19, 2020
This study will investigate the genetic cause of Birt Hogg-Dube (BHD) syndrome and the relationship of this disorder to kidney cancer. BHD is a rare inherited condition characterized by papules, or bumps benign tumors involving hair follicles on the head and neck. People with BHD are at increased risk of developing kidney cancer. Scientists have identified the chromosome (strand of genetic material in the cell nucleus) that contains the BHD gene and the region of the gene on the chromosome. This study will try to learn more about:
- The characteristics and type of kidney tumors associated with BHD
- The risk of kidney cancer in people with BHD
- Whether more than one gene causes BHD
- The genetic mutations (changes) responsible for BHD
Patients with known or suspected Birt Hogg-Dube syndrome, and their family members, may be eligible for this study. Candidates will be screened with a family history and review of medical records, including pathology reports for tumors, and films of computed tomography (CT) and magnetic resonance imaging (MRI) scans.
Participants may undergo various tests and procedures, including the following:
- Physical examination
- Review of personal and family history with a cancer doctor, cancer nurses, kidney surgeon, and genetic counselor
- Chest and other x-rays
- Ultrasound (imaging study using sound waves)
- MRI (imaging study using radiowaves and a magnetic field)
- CT scans of the chest and abdomen (imaging studies using radiation)
- Blood tests for blood chemistries and genetic testing
- Skin evaluation, including a skin biopsy (surgical removal of a small skin tissue sample for microscopic evaluation)
- Cheek swab or mouthwash to collect cells for genetic analysis
- Lung function studies
- Medical photography of skin lesions
These tests will be done on an outpatient basis in either one day or over 3 to 4 days. When the studies are complete, participants will receive counseling about the findings and recommendations. Patients with kidney lesions may be asked to return periodically, such as every 3 to 36 months, based on their individual condition, to document the rate of progression of the lesions.
|Condition or disease|
|Kidney Neoplasms Kidney Cancer Pneumothorax FLCN Protien, Human|
- BHD is a rare, autosomal dominantly inherited disorder which confers susceptibility to develop multifocal, bilateral renal cancer, spontaneous pneumothorax and fibrofolliculomas.
- BHD is caused by mutations in the BHD gene located on Chromosome17
- Defining the genetic and biochemical pathways leading to renal tumorigenesis in BHD may lead to the development of new molecularly targeted drugs.
- To define the types and characteristics (including patterns of growth) of renal cancer associated with BHD
- To determine the risk of renal cancer, lung cysts and fibrofolliculomas in patients with BHD
- To define the natural history of BHD related renal tumors
- To determine if other genes contribute to BHD
- Identify genotype / phenotype correlations
Patients with phenotype or genotype suggestive of Birt Hogg Dube, such as:
- Patients with histologically confirmed fibrofolliculomas,
- Patients with clinical evidence of multiple skin papules consistent with fibrofolliculomas, and a family history of spontaneous pneumothorax or kidney cancer
- A relative (related by blood or marriage) of a patient with a confirmed or suspected diagnosis of BHD
- Patients with a known germline BHD mutation
- These rare families will be recruited to genetically confirm diagnosis, determine size and location of renal tumors, size at presentation, growth rate and metastatic potential of renal tumors.
- Genetic testing will be offered to gain appreciation of the effect of mutations the BHD gene and to assess the relative activity of various germline and somatic mutations.
- We will determine if there is a relationship between mutation and disease phenotype.
|Study Type :||Observational|
|Estimated Enrollment :||800 participants|
|Official Title:||The Birt Hogg-Dube Syndrome: Identification of the Disease Gene and Characterization of the Predisposition of Renal Cancer|
|Actual Study Start Date :||May 13, 2002|
A relative of a patient with a confirmed or suspected diagnosis of BHD (related by blood or marriage)
Patients with phenotype or genotype suggestive of Birt Hogg Dub(SqrRoot)(Copyright) and/or Renal tumor histology consistent with BHD
- Define types and characteristics (including patterns of growth) of renal cancer associated with BHD. [ Time Frame: Ongoing ]Collection of blood, tissue & urine for Identification of the Disease Gene, and Characterization of the disposition to Renal Cancer
- Determine risk of renal cancer, lung cysts and fibrofollicullomas in patients with BHD. [ Time Frame: Ongoing ]Collection of blood, tissue & urine for Identification of the Disease Gene, and Characterization of the disposition to Renal Cancer
- Define the natural history of BHD related renal tumors. [ Time Frame: Ongoing ]Collection of blood, tissue & urine for Identification of the Disease Gene, and Characterization of the disposition to Renal Cancer
- Determine if other genes contribute to BHD. [ Time Frame: Ongoing ]
- Identify genotype / phenotype correlations. [ Time Frame: Ongoing ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00033137
|Contact: W. Marston Linehan, M.D.||(240) email@example.com|
|United States, Maryland|
|National Institutes of Health Clinical Center, 9000 Rockville Pike||Recruiting|
|Bethesda, Maryland, United States, 20892|
|Contact: For more information at the NIH Clinical Center contact National Cancer Institute Referral Office (888) NCI-1937|
|Principal Investigator:||W. Marston Linehan, M.D.||National Cancer Institute (NCI)|