Energy Balance & Weight Loss in Craniopharyngioma-related or Other Hypothalamic Tumors in Hypothalamic Obesity

Hypothalamic Obesity Clinical Trial

— ECHO  

Official title:

Glucagon-Like Peptide-1 Agonist Effects on Energy Balance in Hypothalamic Obesity

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02664441
• Other study ID #: R01DK104936-01A1
• Status: Completed
• Phase: Phase 3
• Start date: March 2016
• Est. completion date: July 31, 2020

Study information

• Verified date: May 2022
• Source: Seattle Children's Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The proposed multicenter study will test the effect of glucagon-like peptide (GLP)-1 agonist exenatide once weekly extended-release (ExQW, Bydureon®) on clinical outcomes and metabolic parameters in a double-blind, placebo-controlled 36 week randomized trial with an 18 week open label extension. Following baseline testing, 48 patients will be randomly assigned with equal allocation to ExQW or matching placebo injection for 36 weeks, followed by an 18 week open label extension during which all patients receive ExQW. Changes of weight status, body composition, free-living total daily energy expenditure (EE) by doubly labeled water (DLW), activity by acetimetry, energy intake (questionnaires and food diary), as well as glucose tolerance and hormonal parameters of energy homeostasis and insulin resistance will be assessed before treatment and at the end of the placebo-controlled phase (week 36). Activity, metabolic outcomes, energy intake will be also assessed at study week 18 (mid treatment of randomized study), as well as week 54 (end of open label treatment).

Description:

Excessive weight gain and its cardiometabolic sequela are frequent complications of hypothalamic tumors, a condition known as hypothalamic obesity (HO). Most tumors in this region are craniopharyngiomas (CP),1 which constitute 5-9% of childhood brain tumors. Patients with CP typically become obese and have more features of the metabolic syndrome compared to matched controls. Overall, a 3-19-fold higher cardiovascular mortality had been reported, and a recent nationwide population-based study in Sweden demonstrated increased rates for cerebral infarction (7-fold), death due to cerebrovascular diseases (5-fold), and type 2 diabetes mellitus (6-fold) in CP patients in comparison to the general population. Thus, early and effective management of obesity is vital for this population, which is more resistant to treatment than uncomplicated obesity. Recognized risk factors for severe obesity include large hypothalamic tumors or lesions affecting several medial and posterior hypothalamic nuclei that impact satiety signaling pathways. Structural damage in these nuclei often lead to uncontrolled appetite, rapid weight gain, central insulin and leptin resistance, decreased sympathetic activity, low energy expenditure (EE), and increased energy storage in adipose tissue. Recently, the investigators developed a semi-quantitative assessment of hypothalamic damage on brain magnetic resonance imaging (MRI) to predict the risk for HO development in CP.

Previous results of treating HO with a glucagon-like-peptide-1 receptor agonist (GLP1RA) in rats and humans provide promising proof-of-principle data to support this current randomized clinical trial. The primary hypothesis of this study is that drugs causing weight loss via intact hindbrain signaling pathways offer a desperately needed option for treatment of HO, even in very obese HO subjects with severe hypothalamic damage. Induction of weight loss by GLP1RAs is believed to be related to multiple mechanisms involving the gastrointestinal tract, vagus nerve, and the brain leading to increased satiety. Peripheral administration of GLP-1 or GLP1RA reduces blood glucose and energy intake in humans and rodents, and long-term treatment results in loss of body weight. Critically, the investigators do not know whether GLP1RA treatment affects EE and activity, or whether the site and size of brain lesions affect responses to GLP1RA treatment.

The investigators' previous clinical studies of the GLP1RA exenatide in obese adolescents and adults have generated the critical safety and efficacy data needed to design a clinical trial. In a pilot study conducted at Children's Hospitals and Clinics of MN, pretreatment hyperphagia was associated with BMI reduction. Using these data, the investigators have designed a prospective, multicenter trial that will examine the effects of GLP1RA on BMI, cardiovascular disease (CVD) risk factors, energy homeostasis and other factors in subjects with HO secondary to CP.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 42
• Est. completion date: July 31, 2020
• Est. primary completion date: March 16, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 10 Years to 25 Years

Eligibility

Inclusion Criteria:

• Age 10-25 years at time of enrollment

• Diagnosis of hypothalamic obesity with age- and sex adjusted BMI = 95% or BMI =30 kg/m² if over 18 y

• History of craniopharyngioma or another tumor located in the hypothalamic area

• Hypothalamic lesion documented by neuroradiology

• = 6 months post-surgical or radiation treatment

• Weight stable or increasing over 3 months prior to screening visit

• Stable hormone replacement for at least 3 months prior to screening visit

Exclusion Criteria:

• Renal impairment (GFR<60 ml/min/1.73m² using the Schwarz formula)

• History of gastroparesis; pancreatitis or gallstones (unless status post cholecystectomy)

• Family history of multiple endocrine neoplasia type 2 or familial medullary thyroid carcinoma metabolic disorders

• Any insulin-treated diabetes mellitus, poorly controlled type 2 diabetes (HbA1c = 10%), or any other chronic serious medical conditions such as cardiovascular disease, malignancy or hematologic disorder, complicated syndromic disorder, or psychiatric disorders (schizophrenia, major depression, history of suicide attempts)

• Calcitonin >50 mg/L at screening

• Initiation of weight loss medications within 3 months of screening visit

• Previous donation of blood >10% of estimated blood volume within 3 months prior study

• Current warfarin use

• Current use of any other GLP1 receptor agonist

• Untreated thyroid disorder or adrenal insufficiency

• History of bariatric surgery or planned bariatric surgery until end of study

• Pregnancy, lactation or expectation to conceive during study period

• Subject unlikely to adhere to study procedures in opinion of investigator

• Subject with contraindication to neuroimaging by MRI

Related Conditions & MeSH terms

• Hypothalamic Obesity
• Obesity

Intervention

Drug:
• Exenatide
Weekly injections of active drug.
• placebo
Weekly placebo injections

Locations

Country	Name	City	State
United States	Children's Hospitals adn Clinics of Minnesota	Minneapolis	Minnesota
United States	Vanderbilt University School of Medicine	Nashville	Tennessee
United States	Seattle Childrens	Seattle	Washington

Sponsors (3)

Lead Sponsor	Collaborator
Seattle Children's Hospital	Children's Hospitals and Clinics of Minnesota, Vanderbilt University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Percent Change of Body Mass Index (BMI) as Calculated by the Formula: Body Weight in kg Divided by Height in Meters².	Percent change of body mass index (BMI), as calculated by the formula: body weight in kg divided by height in meters², between baseline and the end of the 36-week randomized drug treatment phase.	From baseline to 36 weeks
Secondary	Changes in Body Composition as Assessed by Body Fat Mass Using Dual Energy X-ray Absorptiometry (DEXA)	Body composition change between baseline and the end of the 36-week randomized drug treatment phase assessed by dual energy x-ray absorptiometry (DEXA) and expressed as the change in adipose tissue mass.	At baseline and 36 weeks
Secondary	Changes in Fat and Total Calorie Intake Assessed by Free Buffet Meal Analysis.	Changes in fat and total calorie intake during free buffet meals assessed at baseline and after 36-weeks of study drug treatment.; The buffet meal is an objective measure of satiety as it assesses food intake and choice after a caloric preload. A standardized test meal preload provided 20% of estimated daily caloric requirements,based on the Schofield-HW equation. The purpose of the test meal is to ensure that study participants are in an equally fed state. Ninety minutes later, an ad libitum buffet meal was served consisting of a wide variety of food items and more than the child's estimated daily calorie requirements will be offered (5,000 kcal). Children had access to the buffet for 30 min, after which calorie intake and composition of consumed foods was measured by weighing back uneaten food.	From baseline to 36 weeks
Secondary	Changes in Fasting Glucose	Change in fasting blood glucose between baseline and the end of the 36-week randomized drug treatment phase.	From baseline to 36 weeks
Secondary	Changes in HDL Cholesterol and Triglycerides Assessed by Fasting Lipids	Change in fasting HDL cholesterol and triglycerides between baseline and the end of the 36-week randomized drug treatment phase.	From baseline to 36 weeks
Secondary	Changes in Inflammation Assessed by C-reactive Protein (CRP)	Change in C-reactive protein (CRP) between baseline and the end of the 36-week randomized drug treatment phase.	From baseline to 36 weeks
Secondary	Changes of Insulin Resistance Assessed by Homeostasis Model Assessment of Insulin Resistance (HOMA-IR)	Changes of insulin resistance estimated by the homeostasis model assessment of insulin resistance (HOMA-IR) using the formula HOMA-IR = insulin [mU/l] x glucose [mmol/l]) / 22.5 where both insulin and glucose values are obtained from a fasting blood sample.	From baseline to 36 weeks
Secondary	Changes of Circulating Leptin Levels	Change in circulating leptin between baseline and the end of the 36-week randomized drug treatment phase.	From baseline to 36 weeks
Secondary	Changes of Energy Expenditure Assessed by Doubly Labeled Water Analysis	Total energy expenditure in the free-living environment was measured using doubly labeled water which estimates carbon dioxide production by measuring the elimination of the tracers deuterium (²H) and oxygen-18 (¹8O) from the body. These measures are used to determine the average daily rate of carbon dioxide production which is then used to calculate total energy expenditure using an equation from Weir and an assumed food quotient (0.85).	Baseline and 36 weeks
Secondary	Changes of Energy Intake Assessed by Automated Self-Administered 24-Hour Dietary Recall (ASA24-Kids)	Self-reported daily energy intake was assessed by Automated Self-Administered 24-Hour Dietary Recall (ASA24-Kids, http://appliedresearch.cancer.gov/tools/instruments/asa24/), a web-based diet assessment tool that allows 24-hour diet recall using branded food items.	Baseline and 36 weeks
Secondary	Changes in Glucose 120 Minutes Following an Oral Glucose Tolerance Test	Change in blood glucose measures 120 minutes post-glucose bolus during an oral glucose tolerance test between baseline and the end of the 36-week randomized drug treatment phase.	From baseline to 36 weeks