Denosumab (Prolia®) offers a new approach in the treatment of osteoporosis. It decreases bone resorption by inhibiting osteoclast formation, function and survival. The current indication covers osteoporosis in postmenopausal women at increased risk of fracture and men receiving hormonal therapy for prostate cancer.
Osteoporosis is characterised by an imbalance between bone formation and bone resorption. The latter process is performed by osteoclasts and occurs at a higher rate in osteoporosis. Receptor Activator of Nuclear factor-κB Ligand (RANKL) is an essential factor in osteoclast differentiation, activation, and survival. RANKL, a member of the tumor necrosis factor (TNF) superfamily, is expressed on the osteoblast membrane and binds to receptor activator of nuclear factor-κB (RANK, the receptor) on the osteoclast membrane. Osteoprotegerin (OPG) is the endogenous regulator of this RANKL-mediated activation of osteoclasts. OPG is a soluble RANKL binding protein that binds RANKL, preventing it from combining with RANK on the osteoclast membrane and thus inhibiting its action. RANK is a membrane-bound, TNF-like receptor that recognizes RANKL through direct cell-to-cell interaction with osteoblasts.Denosumab is a human monoclonal IgG2 antibody that binds RANKL with high affinity and specificity, preventing interaction with RANK on the osteoclast membrane. Thus it mimics endogenous OPG. By attaching to and blocking RANKL, denosumab inhibits osteoclast differentiation, activation, and
Hypocalcaemia is not a concern during denosumab therapy when patients are adequately supplemented with calcium and vitamin D. Patients with hypocalcaemia and/or chronic kidney disease may develop symptomatic hypocalcaemia upon treatment with denosumab. Therefore, hypocalcaemia should be corrected before therapy and serum calcium concentration monitored. A dental check and treatment if needed may be advised before starting treatment because of a risk of osteonecrosis of the jaw.Because RANKL also has a function in the immune system denosumab could adversely influence infections of the urinary and upper respiratory tracts. Cataracts were observed in men receiving treatment for prostate cancer but a mechanism has not been elucidated and the findings may be coincidental. The development and progression of cataracts will be studied prospectively in planned clinical studies.
EPAR of denosumab.