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

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.

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