Infections in postmenopausal women with osteoporosis treated with denosumab or placebo: coincidence or causal association?
- N. B. WattsAffiliated withBone Health and Osteoporosis Center, College of Medicine, University of Cincinnati Email author
- , C. RouxAffiliated withParis Descartes University Hôpital Cochin
- , J. F. ModlinAffiliated withDartmouth Medical School
- , J. P. BrownAffiliated withCHUQ-CHUL, Laval University
- , A. DanielsAffiliated withAmgen Inc.
- , S. JacksonAffiliated withAmgen Inc.
- , S. SmithAffiliated withAmgen Inc.
- , D. J. ZackAffiliated withAmgen Inc.
- , L. ZhouAffiliated withAmgen Inc.
- and 2 more
- , A. GrauerAffiliated withAmgen Inc.
- , S. FerrariAffiliated withGeneva University Hospital and Faculty of Medicine
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Serious adverse events of infections that occurred in subjects receiving denosumab or placebo in the Fracture Reduction Evaluation of Denosumab in Osteoporosis every 6 Months (FREEDOM) study were examined in detail. Serious adverse events of infections in denosumab subjects had heterogeneous etiology, with no clear clinical pattern to suggest a relationship to time or duration of exposure to denosumab.
Denosumab reduces the risk for new vertebral, hip, and nonvertebral fractures compared with placebo. In the pivotal phase 3 fracture trial (FREEDOM), the overall safety profile and incidence of adverse events including adverse events of infections were similar between groups. Serious adverse events of erysipelas and cellulitis were more frequent in denosumab-treated subjects. In this report, we further evaluate the details of infectious events in FREEDOM to better understand if RANKL inhibition with denosumab influences infection risk.
FREEDOM was an international multicenter, randomized, double-blind, placebo-controlled study in postmenopausal women with osteoporosis randomly assigned to receive placebo (n = 3,906) or denosumab 60 mg every 6 months (n = 3,902). The incidence of adverse events and serious adverse events categorized within the Medical Dictionary for Regulatory Activities system organ class, “Infections and Infestations,” was compared between the placebo and denosumab groups by body systems and preferred terms. The temporal relationship between occurrence of serious adverse events of infections of interest and administration of denosumab was explored.
Serious adverse events of infections involving the gastrointestinal system, renal and urinary system, ear, and endocarditis were numerically higher in the denosumab group compared with placebo, but the number of events was small. No relationship was observed between serious adverse events of infections and timing of administration or duration of exposure to denosumab.
Serious adverse events of infections that occurred with denosumab treatment had heterogeneous etiology, with no clear clinical pattern to suggest a relationship to time or duration of exposure to denosumab.
KeywordsClinical trial Denosumab Infections Postmenopausal osteoporosis RANKL
- Infections in postmenopausal women with osteoporosis treated with denosumab or placebo: coincidence or causal association?
- Open Access
- Available under Open Access This content is freely available online to anyone, anywhere at any time.
Volume 23, Issue 1 , pp 327-337
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- Clinical trial
- Postmenopausal osteoporosis
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- Author Affiliations
- 1. Bone Health and Osteoporosis Center, College of Medicine, University of Cincinnati, 222 Piedmont Avenue, Suite 6300, Cincinnati, OH, 45219, USA
- 2. Paris Descartes University Hôpital Cochin, Paris, France
- 3. Dartmouth Medical School, Lebanon, NH, USA
- 4. CHUQ-CHUL, Laval University, Quebec City, QC, Canada
- 5. Amgen Inc., Thousand Oaks, CA, USA
- 6. Geneva University Hospital and Faculty of Medicine, Geneva, Switzerland