Denosumab Promising for TDT-Induced Osteoporosis Treatment

Higher percentage increase of L1 to L4 and wrist bone mineral density with DMN, reduction in pain.
Higher percentage increase of L1 to L4 and wrist bone mineral density with DMN, reduction in pain.

HealthDay News — Denosumab (DNM), a fully human monoclonal antibody against the receptor activator of nuclear factor kappa-B ligand (RANKL), may be beneficial for managing transfusion-dependent thalassemia (TDT)-induced osteoporosis, according to a study published online October 31 in Blood Advances.

Ersi Voskaridou, MD, from "Laiko" General Hospital in Athens, Greece, and colleagues randomly assigned patients with TDT-induced osteoporosis to receive 60mg DNM or placebo (32 and 31 patients, respectively) subcutaneously on day zero and day 180 during 12 months of follow-up in a phase 2b clinical trial. 

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The researchers found that compared with the placebo group, the DNM group had a higher percentage increase of L1 to L4 bone mineral density (5.92 ± 5.25% vs 2.92 ± 5.56%; P=.043) and wrist bone mineral density (−0.26 ± 5.31 vs −3.92 ± 8.71%; P=.035). There was no grade 3 or 4 toxicity. Pain scores were reduced in the DNM group and were not altered in the placebo group. Between baseline and the 12th month, DNM showed a significant reduction of soluble RANKL (sRANKL), sRANKL/osteoprotegerin ratio, C-telopeptide of collagen type 1, tartrate-resistant acid phosphatase isoform-5b, and bone-specific alkaline phosphatase.

"Not only is denosumab associated with improved bone health and reduced pain, but its ease of administration may very well make this drug superior to bisphosphonates for the treatment of osteoporosis in patients with TDT and osteoporosis," a coauthor said in a statement.

The study was funded by Amgen, the manufacturer of denosumab.

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