Rapid Autopsy and Procurement of Cancer Tissue
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|ClinicalTrials.gov Identifier: NCT01851395|
Recruitment Status : Recruiting
First Posted : May 10, 2013
Last Update Posted : November 4, 2019
- Individuals with cancer of the lung, chest cavity or bladder, as well as patients who have been treated with adoptive cell therapy unfortunately commonly succumb to their disease. Some agree to donate their bodies to cancer research that may help the medical community better understand these diseases. Studies of cancer tumor tissue obtained soon after death may be used to answer questions about the origins, progression, and treatment of cancer. Researchers want to conduct a study that involves planned collection of cancer tumor tissue shortly after death. To do so, they will arrange to provide inpatient hospice care for people with non-small cell lung cancer, bladder cancer or patients who have been treated with adoptive cell therapy.
- To collect cancer tissue biopsy samples as soon as possible after death.
- Individuals who have cancer of the lung, chest cavity or bladder, or those who have been treated with adoptive cell therapy and are planning to receive end-of-life hospice care are eligible to participate.
- Participants will agree to receive inpatient hospice care at the National Institutes of Health Clinical Center. Full details on end-of-life care preference will be acknowledged.
- An autopsy will be performed at the clinical center within 3 hours of death. Tumor tissue will be collected from the primary site of cancer and from any areas of the body to which the cancer has spread.
- Participants will not receive further cancer treatments as part of this study. This is a tissue collection study only.
|Condition or disease|
|Thymus Tumors Adoptive Cellular Therapy Mesothelioma Genitourinary Cancer Lung Cancer|
Show Detailed Description
|Study Type :||Observational|
|Estimated Enrollment :||135 participants|
|Official Title:||A Pilot Study of Inpatient Hospice With Procurement of Tissue on Expiration in Thoracic Malignancies|
|Actual Study Start Date :||December 30, 2013|
|Estimated Primary Completion Date :||March 31, 2024|
|Estimated Study Completion Date :||March 31, 2025|
Patients treated with an adoptive cellular therapy
Patients with genitourinary malignancies
Patients with histologically or cytologically confirmed metastatic NSCLC, SCLC, EPCC, pNET, thymic epithelial tumor (thymoma, thymic carcinoma) or mesothelioma.
- Procurement of primary and metastatic tissue of thoracic malignancies shortly after death in order to investigate tumor heterogeneity [ Time Frame: Death ]Both intratumor and between paired primary and metastatic site, using integrated genomic and proteomic analysis.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01851395
|Contact: Elizabeth Q Akoth||(240) email@example.com|
|Contact: Udayan Guha, M.D.||(240) firstname.lastname@example.org|
|United States, Maryland|
|National Institutes of Health Clinical Center, 9000 Rockville Pike||Recruiting|
|Bethesda, Maryland, United States, 20892|
|Contact: For more information at the NIH Clinical Center contact National Cancer Institute Referral Office 888-624-1937|
|Principal Investigator:||Udayan Guha, M.D.||National Cancer Institute (NCI)|