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

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

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02019706
Enrollment
80
Registered
2013-12-24
Start date
2014-02-12
Completion date
2030-12-31
Last updated
2026-04-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

ACTH, Cushing's Syndrome

Keywords

DOTATATE, Cushing's Syndrome, Hypercortisolism

Brief 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.

Detailed 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.

Interventions

RADIATIONDOTATATE PET-CT

68Ga-DOTATATE PET/CT

RADIATIONF-DOPA PET CT

68Ga-DOTATATE PET/CT

RADIATIONCT scan

routine CT scan

DIAGNOSTIC_TESTRoutine MRI scan

routine 1.5 or 3T MRI scan

DIAGNOSTIC_TESTGated MRI scan

Cardiac gated MRI scan

68Ga-DOTATATE radioligand

18F-DOPA radioligand

Sponsors

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

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* 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.

Design outcomes

Primary

MeasureTime frameDescription
To determine which imaging technique (F-DOPA PET/CT, 68Ga-DOTATATE PET/CT, CT, and/or MRI) has the best sensitivity.6-12 monthsSubjects will be imaged every 6-12 months until tumor is found
To determine if there is a combination of imaging tests with optimal diagnostic accuracy.6-12 monthssubjects will be imaged every 6-12 months until tumor is found

Secondary

MeasureTime frame
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

Countries

United States

Contacts

CONTACTRaven N McGlotten, R.N.
mcglottenr@mail.nih.gov(301) 827-0190
CONTACTLynnette K Nieman, M.D.
niemanl@mail.nih.gov(301) 496-8935
PRINCIPAL_INVESTIGATORLynnette K Nieman, M.D.

National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 3, 2026