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2026-06-22 PubMed

Denosumab and Zoledronate Cost-Effective for Osteoporosis in Chinese Postmenopausal Women at Specific FRAX Thresholds

Cost-effectiveness thresholds for initiating osteoporosis treatment in postmenopausal women in China: a microsimulation analysis based on real-world data.

Background

Osteoporosis is a prevalent condition in postmenopausal women, significantly increasing the risk of debilitating fractures. Current treatment guidelines often rely on fracture risk assessment tools like FRAX® to guide intervention. However, the cost-effectiveness of various osteoporosis treatments can differ substantially across regions due to varying drug prices, healthcare costs, and willingness-to-pay thresholds. In China, there's a critical need to establish drug-specific, cost-effective FRAX® thresholds to optimize treatment initiation, ensuring both clinical benefit and economic sustainability for the healthcare system and patients.

Study Design

Researchers employed a validated Markov microsimulation model to evaluate the lifetime costs and quality-adjusted life years (QALYs) for no treatment versus alendronate, zoledronate, denosumab, and teriparatide in Chinese postmenopausal women. Baseline patient characteristics and risk factor distribution were derived from China's largest national osteoporosis survey. The analysis adopted a societal perspective, using a willingness-to-pay threshold of USD 13,000 per QALY gained, which aligns with one times China's GDP per capita. The model simulated outcomes across various age groups and 10-year major osteoporotic fracture probabilities.

Results

The microsimulation analysis revealed distinct cost-effectiveness thresholds for different osteoporosis treatments. Denosumab emerged as cost-effective at a 10-year major osteoporotic fracture probability of 7%. Zoledronate also reached cost-effectiveness, but at a higher 10-year major osteoporotic fracture probability of 12%. Notably, neither alendronate nor teriparatide achieved cost-effectiveness at any FRAX probability evaluated within the model. For denosumab, the cost-effective threshold for 10-year major osteoporotic fracture probability varied with age, ranging from 5% to 12%, increasing from 51 to 65 years and then declining in older women. For zoledronate, thresholds were 8% at 51-55 years, 12% at 71-75 years, and 8.5% at 76-80 years. This age-dependent variability highlights the nuanced economic considerations for treatment initiation.

Denosumab was the most cost-effective treatment, reaching favorable thresholds at a 10-year major osteoporotic fracture probability of 7%.

Key Findings

  • Denosumab became cost-effective at a 10-year major osteoporotic fracture probability of 7%.
  • Zoledronate became cost-effective at a 10-year major osteoporotic fracture probability of 12%.
  • Alendronate and teriparatide did not reach cost-effectiveness at any FRAX probability evaluated.
  • Denosumab's cost-effective threshold varied with age, from 5% to 12%.
  • Zoledronate's cost-effective thresholds were 8% at 51-55 years and 12% at 71-75 years.

Why It Matters

This study provides crucial, real-world evidence for guiding osteoporosis treatment decisions in China, moving beyond generic guidelines to drug-specific, cost-effective thresholds. For clinicians and policymakers, these findings suggest that denosumab and zoledronate should be prioritized based on their economic value at specific fracture risk levels, particularly for postmenopausal women. This could lead to more personalized and economically sound treatment protocols, potentially improving patient outcomes by ensuring access to effective therapies while optimizing healthcare resource allocation. The age-dependent thresholds also underscore the importance of considering individual patient profiles, not just a single FRAX score, when initiating therapy. This research offers a framework for developing more refined national guidelines.


denosumab zoledronate alendronate teriparatide osteoporosis postmenopausal
Source: pubmed:42329508 · Ingested 2026-06-22 · Digest: gemini-2.5-flash