Clinical Trials Directory

Trials / Terminated

TerminatedNCT01348698

Evaluation of Molecular Markers in Adrenal Tumors

Evaluation of Diagnostic and Prognostic Molecular Markers in Adrenal Neoplasm

Status
Terminated
Phase
Study type
Observational
Enrollment
74 (actual)
Sponsor
National Cancer Institute (NCI) · NIH
Sex
All
Age
18 Years – 90 Years
Healthy volunteers
Not accepted

Summary

Background: \- Tumors of the adrenal gland are common. Most of them are not cancerous. However, there are no tests that can accurately tell which adrenal tumors are cancerous and which are not. The only way to tell is to remove the tumor with surgery and then examine it. Researchers have been using new methods to study samples of adrenal tissue. These methods may help identify whether the cells are or may become cancerous without an operation. This information will help doctors determine which tumors will need to be removed. Objectives: \- To collect adrenal tumor tissue biopsy samples in order to study and evaluate new methods that may help identify cancerous or precancerous cells. Eligibility: \- Individuals at least 18 years of age who have an adrenal tumor that may or may not be cancerous. Design: * Participants will be screened with a physical examination, medical history, blood and urine tests, and imaging studies. * Participants will be examined to determine whether they have a specific type of adrenal tumor (pheochromocytoma). * Participants whose tumor does not secrete hormones will have a tumor biopsy to collect tissue for study. * Participants who have a large tumor or one that secretes hormones will have standard surgery to remove the tumor. Tissue will be collected for study. * Researchers will examine the collected tissue. They will try to determine whether the cells are cancerous or may become cancerous. * Participants will be asked to return to the National Institutes of Health Clinical Center every year for about 5 years. During these visits they will have imaging studies, lab tests, and a physical examination.

Detailed description

Background: * Adrenal neoplasms are common and are incidentally discovered in 4-10% of abdominal imaging studies. * The majority of adrenal incidentalomas are cortical adenoma. * Many patients with nonfunctioning adrenal incidentalomas undergo adrenalectomy to exclude a cancer diagnosis. * There are no reliable clinical, radiographic or laboratory studies that accurately distinguish between localized benign and malignant adrenal neoplasm. * This protocol is designed to determine the feasibility and accuracy of using novel molecular markers of malignant adrenal neoplasm in fine needle aspiration (FNA) biopsy and surgically resected samples. Objectives: * Primary Objectives: * To evaluate the feasibility of molecular testing in adrenal neoplasm FNA biopsy samples. * To determine the accuracy of novel diagnostic molecular markers in clinical adrenal FNA biopsy and surgically resected samples. * Secondary Objectives: * To analyze the gene expression level relative to disease-free survival and overall survival in patients with adrenocortical carcinoma Eligibility: * An individual with an adrenal neoplasm greater than 2cm in size * Age greater than or equal to 18 years * Adults must be able to understand and sign the informed consent document Design: * Prospective observational study. * Demographic, clinical, laboratory and pathologic data will be collected for each patient participant. Data will be securely stored in a computerized database. * Patients will have biochemical testing to determine if their adrenal neoplasm is functioning or nonfunctioning. * After their initial on-study evaluation, patients who are found to have a nonfunctioning adrenal tumor with a low risk of malignancy will be re-screened every year for 5 years with non-invasive imaging studies. * Treatment of patients with an adrenal neoplasm will be performed based on standard clinical practice. * Projected accrual will be 50 patients per year for a total of 10 years. Thus, we anticipate accruing 500 patients on this protocol.

Conditions

Interventions

TypeNameDescription
PROCEDURETumor tissue biopsyParticipants whose tumor does not secrete hormones will have a tumor biopsy to collect tissue for the study.
PROCEDURESurgeryParticipants who have a large tumor or one that secretes hormones will have standard surgery to remove the tumor. Tissue will be collected for study.

Timeline

Start date
2011-05-04
Primary completion
2018-01-12
Completion
2018-01-12
First posted
2011-05-05
Last updated
2018-11-26
Results posted
2018-11-26

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01348698. Inclusion in this directory is not an endorsement.