Anaplastic Lymphoma Kinase Gene Rearrangement in Children and Young Adults With Mesothelioma.
Idrees Mian, Zied Abdullaev, Betsy Morrow...
https://pubmed.ncbi.nlm.nih.gov/31783178/Actively Recruiting
Led by National Cancer Institute (NCI) · Updated on 2026-08-07
1000
Participants Needed
1
Research Sites
N/A
Total Duration
Malignant mesothelioma is a cancer originating from mesothelial cells in areas such as the pleura and peritoneum, accounting for a small percentage of deaths annually in the United States. This condition, especially pleural mesothelioma, often presents at advanced stages with limited treatment options. The study also focuses on other cancers that express mesothelin, including thymic carcinoma, pancreatic, biliary, lung, gastric, and ovarian cancers, aiming to collect samples for research purposes. Participants include those aged 2 years and older with malignant mesothelioma and those 18 years and older with other mesothelin-expressing cancers. The study involves collecting samples of blood, urine, tumor tissue, and abnormal body fluids for tissue banking. These samples will support various research activities such as genetic and genomic studies, cell culture establishment, and immunologic analysis. During the study, participants will be followed to observe the course of their disease and any treatments they receive. The research team will collect and store biological samples to advance understanding of mesothelioma and related cancers. The primary outcome is ongoing sample acquisition. Participation may last several years as the disease course is monitored, with no intervention or treatment provided as part of this observational study.
CONDITIONS
Tissue Procurement and Natural History Study of Patients With Malignant Mesothelioma
M
Maria Gracia L Agra, R.N.
R
Raffit Hassan, M.D.
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here
National Cancer Institute (NCI)
Lead Sponsor
You may qualify if you...
You will not qualify if you...
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Ongoing throughout participation
Participants provide blood, urine, tumor, and abnormal body fluid samples for tissue banking. They are followed over time to monitor disease progression and record any treatments received.
Regular visits as scheduled for sample collection and assessments
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
Have more questions? Get in touch with our team for quick support
Idrees Mian, Zied Abdullaev, Betsy Morrow...
https://pubmed.ncbi.nlm.nih.gov/31783178/National Cancer Institute (NCI)
Lead Sponsor