Glioma Clinical Trial
Official title:
EGF Polymorphisms and Gliomagenesis
This study will examine tissue from gliomas (a type of brain tumor) removed during surgery
for gene mutations, or changes, thought to be involved in tumor formation and growth. One
common gene mutation causes the receptor for a protein called epidermal growth factor (EGF)
to be in an active state all of the time, allowing uncontrolled cell growth that can lead to
tumor formation. This study will analyze blood and tumor tissue samples from patients with
gliomas for:
- Changes in the EGF gene in the tumor
- Changes in other genes, such as that for the EGF receptor (EGFR)
- Changes in levels of EGF and EGFR, and in other proteins and genes that respond to
changes in the levels of these proteins in the tumor
- Changes in the EGF gene and protein in the blood
The study will also determine if production of EGF and EGFR obtained from glioma and from
blood cells derived from the tumor can be altered in the laboratory to grow indefinitely in
culture.
Patients between 18 and 75 years of age with a brain tumor that requires surgical treatment
may be eligible for this study.
Participants will be admitted to the NIH Clinical Center for about 3 to 10 days. They will
have a physical and neurological examination, blood and urine tests, other tests, if
medically necessary, and will be evaluated and prepared for surgery. During surgery, as much
of the tumor as possible will be removed. A small amount of the tumor tissue will be
collected for this study. No tissue will be removed for this study that would not otherwise
have been removed. Some of the tissue will be used to culture glioma cells and the rest will
be frozen and stored for examination, as described above. If any normal-appearing brain
tissue is removed during surgery in order to enhance safety in removing the tumor, the
normal tissue will be studied as well. Brain tissue that appears normal will not be removed
strictly for research.
During surgery and the day after surgery, a blood sample will be drawn from a catheter
(plastic tube) that was placed in an artery or vein for surgery. If catheters are no longer
in place, blood will be drawn through a needle in a vein.
| Status | Completed |
| Enrollment | 344 |
| Est. completion date | November 2004 |
| Est. primary completion date | |
| Accepts healthy volunteers | No |
| Gender | Both |
| Age group | N/A and older |
| Eligibility |
INCLUSION CRITERIA: Radiographic evidence of a primary glial neoplasm of the CNS (WHO grade II-IV) or any patient with known primary neoplasms of the CNS. Medically indicated diagnostic and/or therapeutic tumor resection. Informed consent from patient, age 18 or older to 75 years of age. Females of child-bearing capacity: Pregnant women will be entered into the study for tumor collection, but blood will not be drawn at the time of surgery. Six weeks or more after the completion of pregnancy, these women will be contacted and 10cc (2 tsp) of blood will be collected for genotyping. No racial or ethnic group or gender is excluded. EXCLUSION CRITERIA: Inability to provide informed consent prior to surgery. Medical conditions that cannot be corrected prior to surgery that would be standard contraindications for neurosurgery. |
N/A
| Country | Name | City | State |
|---|---|---|---|
| United States | National Institute of Neurological Disorders and Stroke (NINDS) | Bethesda | Maryland |
| Lead Sponsor | Collaborator |
|---|---|
| National Institute of Neurological Disorders and Stroke (NINDS) |
United States,
Burdick JS, Chung E, Tanner G, Sun M, Paciga JE, Cheng JQ, Washington K, Goldenring JR, Coffey RJ. Treatment of Ménétrier's disease with a monoclonal antibody against the epidermal growth factor receptor. N Engl J Med. 2000 Dec 7;343(23):1697-701. — View Citation
Groenen LC, Nice EC, Burgess AW. Structure-function relationships for the EGF/TGF-alpha family of mitogens. Growth Factors. 1994;11(4):235-57. Review. — View Citation
Laurence DJ, Gusterson BA. The epidermal growth factor. A review of structural and functional relationships in the normal organism and in cancer cells. Tumour Biol. 1990;11(5):229-61. Review. — View Citation
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