Prospective Evaluation of 68Ga-DOTATATE PET/CT, Octreotide and F-DOPA PET Imaging in Ectopic Cushing Syndrome

Cushing's Syndrome Clinical Trial

Official title:

Prospective Evaluation of 68Ga-DOTATATE PET/CT, Octreotide and F-DOPA PET Imaging in Ectopic Cushing Syndrome

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02019706
• Other study ID #: 140028
• Secondary ID: 14-CH-0028
• Status: Recruiting
• Phase: Phase 2
• Start date: February 12, 2014
• Est. completion date: December 31, 2030

Study information

• Verified date: April 19, 2024
• Source: National Institutes of Health Clinical Center (CC)
• Contact: Raven N McGlotten, R.N.
• Phone: (301) 827-0190
• Email: mcglottenr[@]mail.nih.gov
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Between 10% and 15% of patients with endogenous hypercortisolism (Cushing syndrome) have ectopic (non-pituitary) production of adrenocorticotropin hormone (ACTH) that causes cortisol excess. In approximately 50% of these patients, the tumoral source of ACTH cannot be found initially despite very detailed and extensive imaging, including studies such as computed tomography, magnetic resonance imaging, and octreotide scan (Octreoscan) using the standard dose of indium- 111 pentetreotide ([111In-DTPA-D-Phe]-pentetreotide). The sensitivity and specificity of structurally based imaging studies depends on anatomic alterations and the size of the tumor. In contrast, positron emission tomography (PET) and somatostatin ligand imaging detect pathologic tissue based on physiologic and biochemical processes within the abnormal tissue. This protocol tests the ability of [18F]-L-3,4-dihydroxyphenylalanine (18F-DOPA) PET, and the somatostatin imaging analogue, 68Ga-DOTATATE-PET, to localize the source of ectopic ACTH production.

Description:

Study Description: Between 10% and 15% of patients with endogenous hypercortisolism (Cushing syndrome) have ectopic (non-pituitary) production of adrenocorticotropin hormone (ACTH) that causes cortisol excess. In approximately 50% of these patients, the tumoral source of ACTH cannot be found initially despite very detailed and extensive imaging, including studies such as computed tomography, magnetic resonance imaging, and octreotide scan (Octreoscan) using the standard dose of indium- 111 pentetreotide ([111In-DTPA-D-Phe]-pentetreotide). The sensitivity and specificity of structurally based imaging studies depends on anatomic alterations and the size of the tumor. In contrast, positron emission tomography (PET) and somatostatin ligand imaging detect pathologic tissue based on physiologic and biochemical processes within the abnormal tissue. This protocol tests the ability of [18F]-L-3,4-dihydroxyphenylalanine (18F-DOPA) PET, and the somatostatin imaging analogue, 68Ga-DOTATATE-PET, to localize the source of ectopic ACTH production. Objectives: Primary Objectives: - To determine which imaging technique (F-DOPA PET/CT, 68Ga-DOTATATE PET/CT, standard CT, and/or standard MRI) has the best sensitivity. - To determine if there is a combination of imaging tests with optimal diagnostic accuracy. Secondary Objective: -To evaluate a potential correlation between 18F-DOPA or 68Ga-DOTATATE uptake and the type of tumor, its size, SSTR expression or proliferative activity. Exploratory Objectives: - To evaluate the ability of gated cardiac imaging with CT and MRI to improve the detection of retrocardiac lung lesions. - To determine whether PET scans at an interval of less than one year localize tumors. Endpoints: Primary Endpoint: -Imaging results and pathology of resected tumors Secondary Endpoints: -18F-DOPA or 68Ga-DOTATATE imaging results, tumor pathology, tumor size, proliferative index and SSTR expression. Exploratory Endpoints: - Gated cardiac imaging CT and/or MRI; all other imaging results, tumor pathology. - Imaging results and pathology of resected tumors.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 80
• Est. completion date: December 31, 2030
• Est. primary completion date: December 31, 2030
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

• INCLUSION CRITERIA:

To be eligible to participate in this study, an individual must meet all of the following

criteria:

• 18 - 90 years of age
• Medical history of ectopic Cushing syndrome or diagnosed with the possibility of ectopic Cushing syndrome
• For females of reproductive potential: agreement to use highly effective contraception for at least 2 weeks before any PET scan
• Ability of subject to understand and the willingness to sign a written informed consent document
• Stated willingness to comply with all study procedures and availability for the duration of the study EXCLUSION CRITERIA: An individual who meets any of the following criteria will be excluded from participation

in this study:

• Pregnancy or lactation; the radiation associated with PET and CT scans may be harmful to a developing fetus. Likewise the ingestion of radionuclides in breast milk has an unknown risk to an infant.
• Evidence of severe active infection
• Clinically significantly impaired cardiovascular function, abnormal coagulation in the absence of medically-indicated treatment (PT and PTT elevated by 30% above the normal values), hematopoietic (hematocrit less than 30%, hemoglobin below 10 g/dl, white count below 3000 K/UL, and platelets below 100,000 K/mm^3), hepatic (liver enzymes elevated by 4-fold above normal values), or renal function (plasma creatinine level over 2.1).
• Based on the clinical judgment of the attending physician, other medical problems may prompt exclusion.
• Body weight over 136 kg, which is the limit for the tables used in the scanning areas.
• Combined blood withdrawal during the six weeks preceding the study greater than 450 ml.
• Subjects who previously underwent ten or more F-DOPA PET/CT scans and ten or more DOTATATE scans.

Related Conditions & MeSH terms

• ACTH
• Cushing Syndrome
• Cushing's Syndrome
• Syndrome

Intervention

Radiation:
• DOTATATE PET-CT
68Ga-DOTATATE PET/CT
• F-DOPA PET CT
68Ga-DOTATATE PET/CT
• CT scan
routine CT scan

Diagnostic Test:
• Routine MRI scan
routine 1.5 or 3T MRI scan
• Gated MRI scan
Cardiac gated MRI scan

Drug:
• 68Ga-DOTATATE
68Ga-DOTATATE radioligand
• 18F-DOPA
18F-DOPA radioligand

Locations

Country	Name	City	State
United States	National Institutes of Health Clinical Center	Bethesda	Maryland

Sponsors (1)

Lead Sponsor	Collaborator
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	To determine which imaging technique (F-DOPA PET/CT, 68Ga-DOTATATE PET/CT, CT, and/or MRI) has the best sensitivity.	Subjects will be imaged every 6-12 months until tumor is found	6-12 months
Primary	To determine if there is a combination of imaging tests with optimal diagnostic accuracy.	subjects will be imaged every 6-12 months until tumor is found	6-12 months
Secondary	To evaluate a potential correlation between 18F-DOPA or 68Ga-DOTATATE uptake and the type of tumor, its size, SSTR expression or proliferative activity.		Ongoing

External Links

•   NIH Clinical Center Detailed Web Page