This study is NOT currently recruiting participants.
Number
16-C-0151
Sponsoring Institute
National Cancer Institute (NCI)
Recruitment Detail
Type: No longer recruiting/follow-up only Gender: Male & Female Min Age: 18 Years Max Age: N/A
Referral Letter Required
No
Population Exclusion(s)
Children
Keywords
Brain Tumor; Glioma; Astrocytoma; Brain Cancer; Spine Cancer; Natural History
Recruitment Keyword(s)
None
Condition(s)
Brain Cancer; Brain Tumor; Spine Cancer; Spine Tumor; Neoplasm
Investigational Drug(s)
Investigational Device(s)
Intervention(s)
Other: No Treatment
Supporting Site
National Cancer Institute
Brain and spinal cord tumors are uncommon. But they contribute substantially to cancer deaths in the U.S. in children and adults. Little progress has been made in treating brain tumors. Researchers want to learn more about these tumors by studying people who have them.
Objectives:
To understand brain and spinal cord tumors better and uncover areas for further research. Also, to connect people with these tumors to doctors who can help them manage their illness and give them new treatment options.
Design:
Participants will have an initial (baseline) visit. They will have their medical history taken and undergo physical and neurological exams. They will have blood tests. They may have scans (imaging studies) of the nervous system.
If participants have urine or cerebrospinal fluid collected during their regular care, researchers may save some.
Brain tumor tissue from a prior surgery may be studied.
Genomic DNA testing will be done on samples. Results will be linked to participants medical and/or family history.
The number of study visits at NIH will depend on the wishes of participants and their local doctors.
Participants will take a brain tumor survey on a computer. They can take it all at once or in 6 separate sections.
Participants will answer questions about their general well-being. They will answer questions to learn if they have symptoms of depression or anxiety.
Physicians will discuss test results with participants. They will recommend management and treatment options.
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INCLUSION CRITERIA: -Patients (Person with the Disease) -All patients >= 18 years of age with tumors of the CNS (or a history of tumors of the CNS) of interest to the NOB who may be future candidates for another NOB trial. This includes patients with undiagnosed imaging abnormalities in the central nervous system (brain and/or spinal cord) and patients with known genetic syndromes at high risk of developing CNS Cancers. -Patients with tumors of the CNS that are of particular interest to members of the NOB because they pose important clinical and/or scientific questions and/or shed light on important aspects of the disease. -Patients with rare tumors of the CNS (defined as occurring in less than 2,500 patients/year in the United States) who offer an important educational benefit to neuro-oncology trainees and staff. -Ability of subject or Legally Authorized Representative (LAR) to understand and the willingness to sign a written informed consent document. -Caregivers (Informants) -Participants must be able to speak and read in English -Age >= 18 years old -Participant must be able to understand and willing to sign a written consent document -Participants must be a caregiver for Natural History Study participants with the disease addressed above (Patients). Caregivers will be defined as anyone who patients identify as an unpaid close friend or family member who knows them well and who is involved with their day-to-day care. EXCLUSION CRITERIA: None
-Patients (Person with the Disease)
-All patients >= 18 years of age with tumors of the CNS (or a history of tumors of the CNS) of interest to the NOB who may be future candidates for another NOB trial. This includes patients with undiagnosed imaging abnormalities in the central nervous system (brain and/or spinal cord) and patients with known genetic syndromes at high risk of developing CNS Cancers.
-Patients with tumors of the CNS that are of particular interest to members of the NOB because they pose important clinical and/or scientific questions and/or shed light on important aspects of the disease.
-Patients with rare tumors of the CNS (defined as occurring in less than 2,500 patients/year in the United States) who offer an important educational benefit to neuro-oncology trainees and staff.
-Ability of subject or Legally Authorized Representative (LAR) to understand and the willingness to sign a written informed consent document.
-Caregivers (Informants)
-Participants must be able to speak and read in English
-Age >= 18 years old
-Participant must be able to understand and willing to sign a written consent document
-Participants must be a caregiver for Natural History Study participants with the disease addressed above (Patients). Caregivers will be defined as anyone who patients identify as an unpaid close friend or family member who knows them well and who is involved with their day-to-day care.
EXCLUSION CRITERIA:
Principal Investigator
Referral Contact
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