Hereditary Leiomyomatosis Renal Cell Cancer - Study of the Genetic Cause and the Predisposition to Renal Cancer
| Status: | Recruiting |
|---|---|
| Conditions: | Cancer, Other Indications, Kidney Cancer |
| Therapuetic Areas: | Oncology, Other |
| Healthy: | No |
| Age Range: | 1 - 100 |
| Updated: | 4/6/2019 |
| Start Date: | December 17, 2002 |
| Contact: | W. Marston Linehan, M.D. |
| Email: | wl3e@nih.gov |
| Phone: | (240) 760-6245 |
Hereditary Leiomyomatosis Renal Cell Cancer (HLRCC): Identification of the Disease Gene and Characterization of the Predisposition to Renal Cancer
This study will investigate what causes hereditary leiomyomatosis renal (kidney) cell cancer,
or HLRCC, and how the disease is related to the development of kidney tumors. Leiomyomas are
benign (non-cancerous) tumors arising from smooth muscle. HLRCC can cause various health
problems. Some people develop red bumps on their skin that can be painful at times. Some
women with HLRCC can develop leiomyomas of the uterus. In some families, people with HLRCC
develop kidney tumors. This study will try to determine:
- What gene changes (mutations) cause HLRCC
- What kind of kidney tumors develop in HLRCC and how they grow
- What the chance is that a person with HLRCC will develop a kidney tumor
People with known or suspected HLRCC (and their family members of any age) may be eligible
for this study. This includes people in families in which one or more members has skin
leiomyoma and kidney cancer; skin leiomyoma and uterine leiomyoma; multiple skin leiomyomas;
kidney cancer and uterine leiomyomas, or kidney cancer consistent with HLRCC, including, but
not limited to, collecting duct or papillary, type II. Candidates will be screened with a
physical examination, family history, and, for affected family members, a review of medical
records, including pathology slides and computed tomography (CT) or magnetic resonance
imaging (MRI) scans.
Participants will undergo tests and procedures that may include the following:
- Review of medical records, x-rays, and tissue slides
- Physical examination and family history
- Skin examination
- Gynecological examination for women
- Interviews with a cancer doctor, cancer nurses, kidney surgeon, and genetic counselor
- Blood tests for:
1. Genetic research to identify the gene responsible for HLRCC
2. Evaluation of liver, kidney, heart, pancreas, and thyroid function
3. Complete blood count and clotting profile
4. Pregnancy test for pre-menopausal women
5. PSA test for prostate cancer in men over age 40
- CT or MRI scans (for participants 15 years of age and older only)
- Skin biopsy (surgical removal of a small sample of skin tissue)
- Cheek swab or mouth rinse to collect cells for genetic analysis
- Medical photographs of lesions
- Questionnaire
When the tests are completed, participants will discuss the results with a doctor and
possibly a genetic nurse or genetic counselor. The genetic findings will not be revealed to
participants because their meaning and implications may not yet be understood. Participants
may be asked to return to NIH from every 3 months to every 3 years, depending on their
condition, for follow-up examinations and tests.
or HLRCC, and how the disease is related to the development of kidney tumors. Leiomyomas are
benign (non-cancerous) tumors arising from smooth muscle. HLRCC can cause various health
problems. Some people develop red bumps on their skin that can be painful at times. Some
women with HLRCC can develop leiomyomas of the uterus. In some families, people with HLRCC
develop kidney tumors. This study will try to determine:
- What gene changes (mutations) cause HLRCC
- What kind of kidney tumors develop in HLRCC and how they grow
- What the chance is that a person with HLRCC will develop a kidney tumor
People with known or suspected HLRCC (and their family members of any age) may be eligible
for this study. This includes people in families in which one or more members has skin
leiomyoma and kidney cancer; skin leiomyoma and uterine leiomyoma; multiple skin leiomyomas;
kidney cancer and uterine leiomyomas, or kidney cancer consistent with HLRCC, including, but
not limited to, collecting duct or papillary, type II. Candidates will be screened with a
physical examination, family history, and, for affected family members, a review of medical
records, including pathology slides and computed tomography (CT) or magnetic resonance
imaging (MRI) scans.
Participants will undergo tests and procedures that may include the following:
- Review of medical records, x-rays, and tissue slides
- Physical examination and family history
- Skin examination
- Gynecological examination for women
- Interviews with a cancer doctor, cancer nurses, kidney surgeon, and genetic counselor
- Blood tests for:
1. Genetic research to identify the gene responsible for HLRCC
2. Evaluation of liver, kidney, heart, pancreas, and thyroid function
3. Complete blood count and clotting profile
4. Pregnancy test for pre-menopausal women
5. PSA test for prostate cancer in men over age 40
- CT or MRI scans (for participants 15 years of age and older only)
- Skin biopsy (surgical removal of a small sample of skin tissue)
- Cheek swab or mouth rinse to collect cells for genetic analysis
- Medical photographs of lesions
- Questionnaire
When the tests are completed, participants will discuss the results with a doctor and
possibly a genetic nurse or genetic counselor. The genetic findings will not be revealed to
participants because their meaning and implications may not yet be understood. Participants
may be asked to return to NIH from every 3 months to every 3 years, depending on their
condition, for follow-up examinations and tests.
Background:
- Hereditary Leiomyomatosis and Renal Cell Cancer (HLRCC) is a rare autosomal dominantly
inherited disorder which confers susceptibility to develop cutaneous and uterine
leiomyomas and renal cell carcinoma.
- HLRCC is caused by mutations in the Krebs cycle enzyme, fumarate hydratase localized on
chromosome 1q42.3-q43.
Objectives:
- Define the risk of developing renal cancer, cutaneous leiomyoma and uterine leiomyoma in
this hereditary cancer syndrome
- Define the types and characteristics (including patterns of growth) of renal cancer
associated with HLRCC.
- Determine the incidence and characteristics of HLRCC-associated fumarate hydratase gene
mutations.
- Determine genotype/phenotype correlations.
- Determine if other genes caused HLRCC.
Eligibility:
-An individual from a family in which one or more family members have:
- Cutaneous leiomyoma and kidney cancer.
- Cutaneous leiomyoma and uterine leiomyoma.
- Multiple cutaneous leiomyoma.
- Kidney cancer and uterine leiomyomata.
- Renal tumor histology consistent with HLRCC including, but not limited to: Collecting
Duct and/ or Papillary, Type II.
Design:
- 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 on the
relative activity of various germline and somatic mutations.
- We will determine if there is a relationship between mutation and disease phenotype.
- Hereditary Leiomyomatosis and Renal Cell Cancer (HLRCC) is a rare autosomal dominantly
inherited disorder which confers susceptibility to develop cutaneous and uterine
leiomyomas and renal cell carcinoma.
- HLRCC is caused by mutations in the Krebs cycle enzyme, fumarate hydratase localized on
chromosome 1q42.3-q43.
Objectives:
- Define the risk of developing renal cancer, cutaneous leiomyoma and uterine leiomyoma in
this hereditary cancer syndrome
- Define the types and characteristics (including patterns of growth) of renal cancer
associated with HLRCC.
- Determine the incidence and characteristics of HLRCC-associated fumarate hydratase gene
mutations.
- Determine genotype/phenotype correlations.
- Determine if other genes caused HLRCC.
Eligibility:
-An individual from a family in which one or more family members have:
- Cutaneous leiomyoma and kidney cancer.
- Cutaneous leiomyoma and uterine leiomyoma.
- Multiple cutaneous leiomyoma.
- Kidney cancer and uterine leiomyomata.
- Renal tumor histology consistent with HLRCC including, but not limited to: Collecting
Duct and/ or Papillary, Type II.
Design:
- 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 on the
relative activity of various germline and somatic mutations.
- We will determine if there is a relationship between mutation and disease phenotype.
- INCLUSION CRITERIA:
Patients with known or suspected Hereditary Leiomyomatosis and Renal Cell Cancer Syndrome
and their family members of any age will be recruited from the dermatology, urology,
oncology, and genetics communities worldwide.
An individual from a family in which one or more family member have:
- Cutaneous leiomyoma and kidney cancer
- Cutaneous leiomyoma and uterine leiomyoma
- Multiple cutaneous leiomyoma
- Kidney cancer and uterine leiomyomata
- Renal tumor histology consistent with HRLRCC including, but not limited to: Collecting
Duct and/or Papillary, Type II
Spouses enrolled primarily for linkage analysis
EXCLUSION CRITERIA:
Persons unable to give informed consent.
We found this trial at
1
site
9000 Rockville Pike
Bethesda, Maryland 20892
Bethesda, Maryland 20892
Phone: (888) NCI-1937
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