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

NCT ID: NCT02664441

Last Updated: 2022-05-05

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE3
• Total Enrollment: 42 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2016-03-31
• Study Completion Date: 2020-07-31

Brief 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).

Detailed 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.

Conditions

Hypothalamic Obesity

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Exenatide once weekly extended-release

Injections of glucagon-like peptide (GLP)-1 agonist exenatide once weekly extended-release (Bydureon®) for 36 weeks in randomized intervention followed by 18 weeks open label exenatide once weekly extended-release.

Group Type: ACTIVE_COMPARATOR

Exenatide

Intervention Type: DRUG

Weekly injections of active drug.

Matching placebo

Weekly injections of placebo for 36 weeks followed by 18 weeks open label exenatide once weekly extended-release.

Group Type: PLACEBO_COMPARATOR

placebo

Intervention Type: DRUG

Weekly placebo injections

Interventions

Exenatide

Weekly injections of active drug.

Intervention Type: DRUG

placebo

Weekly placebo injections

Intervention Type: DRUG

Other Intervention Names

Bydureon®

Eligibility Criteria

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

• Minimum Eligible Age: 10 Years
• Maximum Eligible Age: 25 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Children's Hospitals and Clinics of Minnesota

OTHER

Sponsor Role: collaborator

Vanderbilt University

OTHER

Sponsor Role: collaborator

Seattle Children's Hospital

OTHER

Sponsor Role: lead

Responsible Party

Christian L Roth, MD

Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Christian Roth, MD

Role: PRINCIPAL_INVESTIGATOR

Seattle Childrens

Locations

Children's Hospitals adn Clinics of Minnesota

Minneapolis, Minnesota, United States

Vanderbilt University School of Medicine

Nashville, Tennessee, United States

Seattle Childrens

Seattle, Washington, United States

Countries

United States

Provided Documents

Document Type: Study Protocol and Statistical Analysis Plan

View Document

Other Identifiers

R01DK104936-01A1

Identifier Type: NIH

Identifier Source: org_study_id

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