Cost-effectiveness intervention thresholds for romosozumab and teriparatide in the treatment of osteoporosis in the UK

Osteoporos Int. 2024 Dec;35(12):2183-2193. doi: 10.1007/s00198-024-07251-w. Epub 2024 Oct 4.

Abstract

Sequential romosozumab-to-alendronate or sequential teriparatide-to-alendronate can be a cost-effective treatment option for postmenopausal women at very high risk of fracture.

Purpose: To estimate the 10-year probability of a major osteoporotic fracture (MOF) at which sequential treatment with romosozumab or teriparatide followed by alendronate, compared with alendronate alone, becomes cost-effective in a UK setting.

Methods: A microsimulation model with a Markov structure was used to simulate fractures, costs, and quality-adjusted life years (QALYs), in women receiving sequential treatment with either romosozumab or teriparatide followed by alendronate, compared with alendronate alone. Patients aged 50 to 90 years with a recent MOF, hip or spine fracture were followed from the start of a 5-year treatment until the age of 100 years or death. The analysis had a healthcare perspective. Efficacy of romosozumab, teriparatide and alendronate was derived from phase III randomised controlled trials. Resource use and unit costs were derived from the literature. Cost-effectiveness intervention threshold (CEIT), defined as the 10-year probability of a major osteoporotic fracture at which treatment becomes cost-effective, was compared with clinically appropriate intervention thresholds for bone-forming treatment in women with very high fracture risk as recommended by the UK National Osteoporosis Guideline Group (NOGG).

Results: The base case analysis showed that sequential romosozumab-to-alendronate treatment was cost-effective from a 10-year MOF probability of 18-35% and above depending on age and site of sentinel fracture at a willingness to pay (WTP) of £30,000. For teriparatide-to-alendronate, treatment was cost-effective at a 10-year MOF probability of 27-57%. The results were sensitive to pricing of the drugs but relatively insensitive to treatment duration, romosozumab persistence assumptions, and site of sentinel fracture. The CEITs for romosozumab-to-alendronate treatment were lower than the clinical thresholds from the age of 70 years meaning that treatment could be considered both cost-effective and aligned with the NOGG treatment guidelines. By contrast, for teriparatide-to-alendronate the CEITs were higher than the clinical thresholds irrespective of age. However, cost-effective scenarios were found in the presence of strong clinical risk factors in addition to a recent sentinel fracture.

Conclusion: The results of this study indicate that sequential romosozumab-to-alendronate or teriparatide-to-alendronate treatment can be a cost-effective treatment option for postmenopausal women at very high risk of fracture.

Keywords: Cost-effectiveness; Economic evaluation; FRAX; Intervention thresholds; Markov microsimulation model; Osteoporosis; Recent fracture.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Alendronate* / administration & dosage
  • Alendronate* / economics
  • Alendronate* / therapeutic use
  • Antibodies, Monoclonal* / administration & dosage
  • Antibodies, Monoclonal* / economics
  • Antibodies, Monoclonal* / therapeutic use
  • Bone Density Conservation Agents* / administration & dosage
  • Bone Density Conservation Agents* / economics
  • Bone Density Conservation Agents* / therapeutic use
  • Cost-Benefit Analysis*
  • Drug Administration Schedule
  • Drug Costs* / statistics & numerical data
  • Drug Therapy, Combination
  • Female
  • Humans
  • Markov Chains*
  • Middle Aged
  • Models, Econometric
  • Osteoporosis, Postmenopausal* / drug therapy
  • Osteoporosis, Postmenopausal* / economics
  • Osteoporotic Fractures* / economics
  • Osteoporotic Fractures* / prevention & control
  • Quality-Adjusted Life Years*
  • Teriparatide* / administration & dosage
  • Teriparatide* / economics
  • Teriparatide* / therapeutic use
  • United Kingdom

Substances

  • Teriparatide
  • Bone Density Conservation Agents
  • romosozumab
  • Alendronate
  • Antibodies, Monoclonal