Actively Recruiting
Tissue Procurement and Natural History Study of Patients With Malignant Mesothelioma
Led by National Cancer Institute (NCI) · Updated on 2026-05-11
1000
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Background: * Malignant mesothelioma is a malignancy arising from the mesothelial cells of the pleura, peritoneum, pericardium, or tunica vaginalis. * Mesothelioma accounts for 0.10% of deaths annually in the United States. Malignant pleural mesothelioma is the most common of these, comprising of 80% of the cases with an annual incidence of about 2,500 in the United States. * The median survival from diagnosis of pleural mesothelioma is approximately 12 months. The majority of patients present with stage III or IV disease with 85-90% of patients considered unresectable at diagnosis. * Peritoneal mesothelioma has a better prognosis than pleural mesothelioma; nevertheless, patients undergoing therapy for peritoneal mesothelioma have few well-studied treatment options due in large part to the rarity of the disease. Objectives: -To allow sample acquisition for use in the study of mesothelioma. Eligibility: * All patients age greater than or equal to 2 years with malignant mesothelioma * Must be able and willing to provide informed consent if 18 or over; parent or guardian must be able and willing to provide consent for patients under the age of 18 Design: * Up to 1000 subjects will be enrolled. * Patients will be followed to determine the course of disease and to record any treatment received for mesothelioma. * Patients will undergo sampling of blood, urine, tumor and abnormal body fluids for tissue banking. * Studies which may be performed on banked material include genetic and genomic studies, establishment of cell cultures and immunologic studies.
CONDITIONS
Official Title
Tissue Procurement and Natural History Study of Patients With Malignant Mesothelioma
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Participants aged 2 years or older with malignant mesothelioma
- Participants aged 18 years or older with thymic carcinoma, pancreatic or biliary adenocarcinoma, lung, gastric, or ovarian cancers
- Confirmed pathological diagnosis of the eligible cancer
- Ability and willingness to provide informed consent (or parent/guardian consent for minors)
You will not qualify if you...
- Active symptomatic major organ disorder increasing biopsy risk, including ischemic heart disease, recent heart attack, congestive heart failure, or lung dysfunction
- Pregnant women
- Active medical or psychological illnesses increasing risk or inability to provide informed consent, as determined by the principal investigator
AI-Screening
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Trial Site Locations
Total: 1 location
1
National Institutes of Health Clinical Center
Bethesda, Maryland, United States, 20892
Actively Recruiting
Research Team
M
Maria Gracia L Agra, R.N.
CONTACT
R
Raffit Hassan, M.D.
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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