Searchable abstracts of presentations at key conferences in endocrinology
Endocrine Abstracts (2014) 35 P155 | DOI: 10.1530/endoabs.35.P155

ECE2014 Poster Presentations Calcium and Vitamin D metabolism (68 abstracts)

Denosumab increases bone mineral density in primary hyperparathyroidism treated with Cinacalcet

José Manuel Quesada Gómez & Concepción Muñoz Jiménez


IMIBIC, Córdoba/Andalucía, Spain.


Cinacalcet decreases and normalizes serum calcium levels across a broad severity range of primary hyperparathyroidism (PHPT), slightly reduces parathyroid hormone levels which generally remains elevated, whereas it has no effect on bone mineral density (BMD). Therefore, when administering Cinacalcet to a patient with PHPT, concomitant treatment with an anti-catabolic drug should be considered.

An open-labeled, prospective trial was conducted in 30 patients with PHPT with Cinacalcet treatment (contraindications to surgery: comorbidities, high surgical risk and age, clinical judgment of inappropriate parathyroid surgery (PTx): negative parathyroid imaging, persistent or relapsing PHPT after PTx- and refusal of PTx), to determine whether denosumab, maintains or improves BMD in patients with PHPT after a year of treatment.

PHPT patients with low BMD were treated with Cinacalcet (Mimpara, Amgen; titrated dose), 25-OH vitamin D (Hidroferol, Faes) and denosumab (Prolia, Amgen) 60 mg s.c. injections given every 6 months. Serum calcium, phosphorous PTH, and bone turnover markers were evaluates every 3 months. BMD was measured at the lumbar spine (LS) and total femur (TF) by dual-energy X-ray absorptiometry baseline and after 12 months of treatment.

The treatment normalized calcium, phosphorous, and 25(OH)D serum levels and urinary calcium excretion. Bone turnover markers remained suppressed for the duration of the trial. The treatment was also associated with a significant increase after 12 months in vs baseline in LS BMD: 3.7% (P: 0.0001) and in TF BMD: 1.854% (P: 0.03).

Denosumab associated to Cinacalcet is an excellent therapeutic option to normalize serum calcium and to treat the metabolic bone-disease in patients with PHPT who do not meet criteria for surgical treatment.

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