Should Prolia (denosumab) be discontinued and Evenity (romosozumab) started in a 70-year-old smoker with osteoporosis and a T score of -2.8 in the distal ulnar and radial bones?

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Management of Osteoporosis in a 70-Year-Old Smoker with Distal Radius Osteoporosis

Prolia (denosumab) should be continued rather than switching to Evenity (romosozumab) in this 70-year-old smoker with osteoporosis who has shown improvement and stability in femoral neck, total hip, and lumbar spine BMD measurements on Prolia.

Assessment of Current Treatment Response

  • The patient has demonstrated positive response to Prolia with:

    • Improved BMD at femoral neck, total hip, and lumbar spine between 2022-2024
    • Stable BMD at these sites in 2025
    • Only the newly measured distal ulnar and radial sites show a T-score of -2.8
  • This pattern suggests that Prolia is effectively treating the central skeletal sites (spine and hip) which are most associated with serious fracture outcomes 1

Rationale for Continuing Prolia

  1. Treatment is working at critical fracture sites:

    • Hip and spine are the most clinically significant sites for fracture risk assessment and treatment monitoring 1
    • Improvement and stabilization at these sites indicates successful treatment
  2. Age and risk factors:

    • At 70 years of age with smoking history, the patient has significant risk factors for osteoporosis 1
    • Denosumab has shown efficacy in geriatric populations with no need for dose adjustment 2
  3. Distal radius findings:

    • The distal radius T-score of -2.8 is newly measured and doesn't necessarily indicate treatment failure
    • According to ACR guidelines, the primary monitoring sites for osteoporosis treatment are the lumbar spine and hip 1

Concerns with Switching to Evenity

  1. Cardiovascular risk:

    • Evenity carries a boxed warning for increased risk of major adverse cardiac events 3
    • This is particularly concerning in a 70-year-old smoker who likely has elevated baseline cardiovascular risk
  2. Limited treatment duration:

    • Romosozumab is limited to a 12-month course 3, 4
    • Would require sequential therapy with an antiresorptive agent afterward 1, 5
  3. Rebound concerns:

    • Switching from Prolia without appropriate sequential therapy can lead to rapid bone loss and increased vertebral fracture risk 1

Recommended Approach

  1. Continue Prolia (denosumab):

    • Maintain current 6-month dosing schedule
    • Ensure adequate calcium and vitamin D supplementation 1
  2. Address modifiable risk factors:

    • Strongly encourage smoking cessation as this is a significant risk factor for osteoporosis 1
    • Recommend weight-bearing exercise if not contraindicated
  3. Monitoring plan:

    • Continue regular DXA scans to monitor BMD at central sites (hip and spine)
    • Consider vertebral fracture assessment (VFA) if not recently performed 1
    • Monitor for potential side effects of long-term denosumab therapy

Special Considerations

  • If the patient were to discontinue Prolia in the future, a sequential therapy plan would be essential to prevent rebound bone loss 1
  • If a fragility fracture occurs while on Prolia, or if BMD significantly decreases at central sites, then reassessment of therapy would be warranted 1

The evidence strongly supports continuing a medication that is showing effectiveness at the most clinically significant skeletal sites rather than switching to a medication with higher cardiovascular risk and limited treatment duration in this 70-year-old smoker.

References

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

Research

Romosozumab Treatment in Postmenopausal Women with Osteoporosis.

The New England journal of medicine, 2016

Research

One Year of Romosozumab Followed by Two Years of Denosumab Maintains Fracture Risk Reductions: Results of the FRAME Extension Study.

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2019

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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