The only known cure for primary hyperparathyroidism is surgical removal of one or more parathyroid glands. Some patients however, do not fulfill criteria for surgery or do not want to undergo a procedure due to fear of the associated risks. Therefore a medical alternative is warranted. This study aims to evaluate the effects of Denosumab alone, and in combination with Cinacalcet, as a medical treatment for patients suffering from primary hyperparathyroidism, with mild osteoporosis. To the best of our knowledge no previously reported randomized controlled trial has investigated the use of denosumab in primary hyperparathyroidism. 60 patients will be enrolled in three different treatment-groups: 20 receiving both Denosumab and Cinacalcet, 20 Denosumab and placebo and 20 placebo and placebo. Patients included do not meet the criteria for, or have no wish for a surgical procedure. By combining the two drugs, this study could possibly contribute to the discovery of a realistic medical alternative to surgery. It is expected that the therapy will be able to both control s-calcium and s-intact parathyroid hormone (iPTH), and simultaneously enhance bone-structure. The therapy thus has the potential of preventing fractures and possibly other long-term effects of primary hyperparathyroidism such as formation of kidney stones, and coronary calcification. Another objective of this project is to investigate whether the combined therapy can facilitate an actual reset of the Calcium-sensing receptor, and thereby de facto cure the disease.
Background/Context: This project deals with medical treatment of primary hyperparathyroidism. The only cure currently available is surgical removal of one or more parathyroid glands, but this option is neither feasible, nor desirable in all patients with the diagnosis. Today a major group of patients are being diagnosed by coincidence with biochemical blood-screening, and are therefore in an asymptomatic state of the disease at the time of diagnosis. Long term studies show that these patients over time often have progression in their disease, and develop complications such as osteoporosis. Thus a medical alternative is warranted. Previous studies have investigated the effects of well known antiresorptive drugs such as bisphosphonates, as well as estrogen-related compounds. These drugs have had effects on particularly bone mineral density (BMD) and biochemical bone-turnover markers, but have been able only transiently to lower blood-calcium levels. Combined with too many unwanted side-effects and a high prevalence of contraindications for a large proportion of the patients needing treatment, these drugs have not provided a realistic alternative to surgery. Treatment today generally follows the international consensus for treatment of asymptomatic patients with primary hyperparathyroidism. Briefly this includes watchful waiting with biannual control-sessions for indication of surgery, screening for kidney stones/nephrolithiasis, osteoporosis and s-calcium - and s-iPTH levels. This randomized controlled trial involves the drugs Cinacalcet og Denosumab. Denosumab has previously been shown to greatly improve BMD, lower s-calcium, lower the rate of bone-turnover and prevent osteoporotic fractures in several populations with different diseases, but has never been tested in a published randomized controlled trial in patients with primary hyperparathyroidism. Cinacalcet has been proved able to lower s-iPTH, lower s-Calcium and thereby relieve symptoms of hypercalcaemia caused by primary hyperparathyroidism. It does not however, lower the rate of bone turnover, and it has not been show to improve BMD. By combining the two drugs, this study could possibly contribute to the discovery of a realistic medical alternative to surgery. It is expected that the therapy will be able to both control s-calcium and s-iPTH, and simultaneously enhance bone-structure. The therapy thus has the potential of preventing fractures and possibly other long-term effects of primary hyperparathyroidism such as formation of kidney stones, and coronary calcification. Another objective of this project is to investigate whether the combined therapy can facilitate an actual reset of the Calcium-sensing receptor, and thereby de facto cure the disease.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
46
Participants in one arm will receive 30 mg cinacalcet each day.
Participants in two arms will receive 60 mg Denosumab biannually.
Participants in two arms will receive one placebo-tablet each day.
Participants in one arm will receive saline injections as placebo for denosumab.
Aalborg University Hospital
Aalborg, Denmark
Change in Lumbar Spine Bone Mineral Density
Change of Bone Mineral Density after one year of treatment from baseline. Measured with Dual-energy X-ray absorptiometry (DXA)-scan.
Time frame: Baseline,one year
Change in Total Hip Bone Mineral Density
Change of Bone Mineral Density after one year of treatment from baseline. Measured with Dual-energy X-ray absorptiometry (DXA)-scan.
Time frame: Baseline,one year
Change in Femoral Neck Bone Mineral Density
Change of Bone Mineral Density after one year of treatment from baseline. Measured with Dual-energy X-ray absorptiometry (DXA)-scan.
Time frame: Baseline,one year
Change in 1/3 Forearm Bone Mineral Density
Change of Bone Mineral Density after one year of treatment from baseline. Measured with Dual-energy X-ray absorptiometry (DXA)-scan.
Time frame: Baseline,one year
Percentage Change in Lumbar Spine Bone Mineral Density
Percentage change of Bone Mineral Density after one year of treatment from baseline. Measured with Dual-energy X-ray absorptiometry (DXA)-scan.
Time frame: Baseline,one year
Percentage Change in Total Hip Bone Mineral Density
Percentage change of Bone Mineral Density after one year of treatment from baseline. Measured with Dual-energy X-ray absorptiometry (DXA)-scan.
Time frame: Baseline,one year
Percentage Change in Femoral Neck Bone Mineral Density
Percentage change of Bone Mineral Density after one year of treatment from baseline. Measured with Dual-energy X-ray absorptiometry (DXA)-scan.
Time frame: Baseline,one year
Percentage Change in 1/3 Forearm Bone Mineral Density
Percentage change of Bone Mineral Density after one year of treatment from baseline. Measured with Dual-energy X-ray absorptiometry (DXA)-scan.
Time frame: Baseline,one year
Change in Volumetric BMD for the Lumbar Spine.
Measured at baseline and after one year by QCT.
Time frame: Baseline, one year
Mean P-calcium During Treatment.
Blood samples were acquired once every 4 weeks for safety-purposes.
Time frame: Monthly up to one year.
Percent Change From Baseline in P-carboxy-terminal Collagen Crosslinks (CTX)
p-CTX, change from baseline at 48 weeks.
Time frame: Change from baseline at 48 weeks reported.
Median Agatstons Score Final
Simultaneously with QCT-measurements coronary calcification was be assessed. Agatston score is a score based on the extent of coronary artery calcification calculated on the amount of plaque observed in a CT scan. A score of zero indicates absence of coronary calcium, 1-10: minimal calcification, 11-100 mild calcification, 101-400 moderate calcification, \>400 severe calcification. Thus the score increases with increasing level of calcification in the coronary vessels.
Time frame: Baseline, one year
Patients With Nephrolithiasis Final Scan.
Number of subjects w. renal stones at final scan.
Time frame: Patients with nephrolithiasis at one year reported.
Patients With Pancreas-calcifications Final Scan.
By QCT.
Time frame: Patients with pancreas-calcifications at one year reported.
Reset of the Calcium Sensing Receptor?
Measured from effect on s-calcium and PTH weeks after termination of IMP
Time frame: 2 weeks after termination of medication.
Vertebral Fracture Assessment - Final Scan
Number of participants with vertebral fractures as assessed by VFA at final scan.
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Time frame: Patients with vertebral fractures at one year reported.
Change MDI-score
Major Depression Inventory (MDI)-score, Baseline, 6 months, one year (week 52)., change between baseline and 1 year reported. The Major Depression Inventory (MDI) is a mood questionnaire developed by the World Health Organization. To calculate the total score, a sum of ten individual items (each with an individual score between 0-5, with 0 indicating absence of a symptom and 5 indicating constant presence of a given symptom) is used. A higher score signifies deeper depression with 50 being the maximum score.
Time frame: Baseline, 6 mths, one year.
Adverse Reactions.
All participants filled in questionnaires regarding symptoms related to the treatment. Results are reported in the Adverse Events section.
Time frame: Monthly up to one year.
Bone Mineral Content
Measured at baseline and after one year at the lumbar spine and distal 1/3 of the non-dominant antebrachii.
Time frame: Baseline, one year
Change in Cortical Width.
Measured at baseline and after one year at the distal non-dominant antebrachii.
Time frame: Baseline, one year.
Change in Volumetric BMD for the Distal Forearm.
Measured at baseline and after one year by QCT.
Time frame: Baseline, one year
Percentage Change in Volumetric BMD for the Lumbar Spine.
Measured at baseline and after one year by QCT.
Time frame: Baseline, one year
Percentage Change in Volumetric BMD for the Distal Forearm.
Measured at baseline and after one year by QCT.
Time frame: Baseline, one year
Mean p-PTH During Treatment.
Blood samples were acquired once every 4 weeks for safety-purposes.
Time frame: Monthly up to one year.
Mean p-Phosphate During Treatment.
Blood samples were acquired once every 4 weeks for safety-purposes.
Time frame: Monthly up to one year.
Percent Change From Baseline in p-N-terminal Propeptide of Type I Procollagen (p-P1NP).
p-P1NP, change from baseline at 48 weeks.
Time frame: Change from baseline at 48 weeks reported.
Percent Change From Baseline in P-osteocalcin.
p-osteocalcin, change from baseline at 48 weeks.
Time frame: Change from baseline at 48 weeks reported.
Percent Change From Baseline in S-bone-specific Alkaline Phosphatase (BAP).
S-Bone specific alkaline phosphatase, change from baseline at 48 weeks.
Time frame: Change from baseline at 48 weeks reported.
Percent Change From Baseline in p-Tartrate-resistant Acid Phosphatase 5b (Trap5b).
P-Trap5b, change from baseline at 48 weeks.
Time frame: Change from baseline at 48 weeks reported.
Percent Change From Baseline in p-Sclerostin.
P-Sclerostin, change from baseline at 48 weeks.
Time frame: Change from baseline at 48 weeks reported.
Percent Change From Baseline in P-fibroblast Growth Factor 23 (FGF23).
P-FGF23 , change from baseline at 48 weeks.
Time frame: Change from baseline at 48 weeks reported.
Changes in p-25-vitamin D
P-25-vitD , change from baseline at 48 weeks.
Time frame: Change from baseline at 48 weeks reported.
Changes in s-1,25-vitamin D
S-1,25-vitD, change from baseline at 48 weeks.
Time frame: Change from baseline at 48 weeks reported.
Patients With Nephrocalcinosis, Final Scan.
Number of subjects w. renal calcifications at final scan.
Time frame: Baseline, one year