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Western Osteoporosis Alliance Clinical Practice Series: Treat-to-Target for Osteoporosis - 25/11/19

Doi : 10.1016/j.amjmed.2019.04.044 
E. Michael Lewiecki, MD a, , David L. Kendler, MD b, K. Shawn Davison, PhD c, David A. Hanley, MD d, Steven T. Harris, MD e, Michael R. McClung, MD f, g, Paul D. Miller, MD h
a New Mexico Clinical Research & Osteoporosis Center, Albuquerque, NM 
b Department of Medicine (Endocrinology), University of British Columbia, Vancouver, Canada 
c A Priori Medical Sciences, Inc., Victoria, British Columbia, Canada 
d Departments of Medicine, Community Health Sciences, and Oncology, Cumming School of Medicine and McCaig Institute for Bone and Joint Health Cumming School of Medicine, The University of Calgary, Calgary, Alberta, Canada 
e University of California, San Francisco, CA 
f Oregon Osteoporosis Center and Oregon Health & Science University, Portland, OR 
g Mary MacKillop Institute for Health Research, Australian Catholic University, Melbourne, Victoria, Australia 
h Colorado Center for Bone Research, Lakewood, CO 

Requests for reprints should be addressed to E. Michael Lewiecki, MD, Director, New Mexico Clinical Research & Osteoporosis Center, Director, Bone Health TeleECHO, UNM Health Sciences Center, 300 Oak St. NE, Albuquerque, NM 87106.UNM Health Sciences Center300 Oak St. NEAlbuquerqueNM87106

Abstract

Patients often start treatment to reduce fracture risk because of a bone mineral density T-score consistent with osteoporosis (≤ −2.5). Others with a T-score above −2.5 may be treated when there is a history of fragility fracture or when a fracture risk algorithm categorizes them as having a high risk for fracture. It is common to initiate therapy with a generic oral bisphosphonate, unless contraindicated, and continue therapy if the patient is responding as assessed by stability or an increase in bone mineral density. However, some patients may respond well to an oral bisphosphonate, yet remain with an unacceptably high risk for fracture. Recognition of this occurrence has led to the development of an alternative strategy: treat-to-target. This involves identifying a biological marker (treatment target) that represents an acceptable fracture risk and then initiating treatment with an agent likely to reach this target. If the patient is on a path to reaching the target with initial therapy, treatment is continued. If it appears the target will not be reached with initial therapy, treatment is changed to an agent more likely to achieve the goal.

El texto completo de este artículo está disponible en PDF.

Keywords : Bone mineral density, Bone turnover markers, Osteoporosis, Goal, Treatment target


Esquema


 Funding: None.
 Conflicts of Interest: EML has received no direct income from potentially conflicting entities in the past year. His employer, New Mexico Clinical Research & Osteoporosis Center, has received research grants from Radius, Amgen, Mereo, Bindex; income for service on scientific advisory boards or consulting for Amgen, Radius, Alexion, Sandoz, Samsung Bioepis; service on speakers’ bureaus for Radius, Alexion; project development for University of New Mexico; and royalties from UpToDate for sections on DXA, fracture risk assessment, and prevention of osteoporosis. He is a board member of the National Osteoporosis Foundation, International Society for Clinical Densitometry, and Osteoporosis Foundation of New Mexico. DLK has received institutional grant/research support and speaking honoraria from Amgen, Pfizer, Astrazenica, and Eli Lilly. KSD has received speaking honoraria from Amgen. DAH has received institutional grant/research support and speaking honoraria from Amgen and Eli Lilly. STH has received speaker honoraria from Amgen, Eli Lilly, and Radius Health. MRM has received consulting fees from Amgen and speaking honoraria from Amgen and Radius Health. PDM has received scientific research grants from Amgen, Radius Health, Regeneron, Ultragenyx, National Bone Health Alliance, Immunodiagnostics, and Roche Diagnostics and serves on the Scientific Advisory Boards of Amgen, Radius Health, Ultragenyx, National Bone Health Alliance, and Sandoz.
 Authorship: All authors had access to the data and a role in writing this manuscript.


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Vol 132 - N° 11

P. e771-e777 - novembre 2019 Regresar al número
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