TY - JOUR
T1 - Managing Osteoporosis in Patients on Long-Term Bisphosphonate Treatment
T2 - Report of a Task Force of the American Society for Bone and Mineral Research
AU - Adler, Robert A.
AU - El-Hajj Fuleihan, Ghada
AU - Bauer, Douglas C.
AU - Camacho, Pauline M.
AU - Clarke, Bart L.
AU - Clines, Gregory A.
AU - Compston, Juliet E.
AU - Drake, Matthew T.
AU - Edwards, Beatrice J.
AU - Favus, Murray J.
AU - Greenspan, Susan L.
AU - McKinney, Ross
AU - Pignolo, Robert J.
AU - Sellmeyer, Deborah E.
N1 - Funding Information:
Dr Nelson Watts served as a consultant to the Task Force and gave input on all Task Force documents. In addition, the authors thank international experts for their contributions to various parts of the manuscript: Dr Dennis Black for information, interpretation, and discussions regarding FLEX and HORIZON extension studies; Dr Felicia Cosman for discussions and information regarding the HORIZON study; Dr Richard Eastell for input regarding the usefulness of bone remodeling markers in the context of drug holidays; and the following experts for input regarding the developed algorithm and its applicability worldwide: Drs Peter Ebeling, Akira Itabashi, Aliya Khan, Edith Lau, William Leslie, Ambrish Mithal, and Michael McClung. The authors thank Drs Michael McClung and Marlene Chakhtoura for the Table summarizing approved osteoporosis therapies and antifracture efficacy by sex and skeletal site. The authors thank the following individuals at the American University of Beirut for their assistance in completing Task Force charges: Ms Aida Farha, medical information specialist, Saab Medical Library, for her advice and assistance in designing comprehensive and complex searches of the various medical literature resources and for the provision of select articles; Ms Maya Rahme for running the search and retrieving relevant articles; and Mr Ali Hammoudi for his artwork on the algorithm and Supplemental Appendices. The authors thank members of the ASBMR Professional Practice Committee (Suzanne Jan de Beur [Chair], Douglas Bauer, Jan Bruder, Nuria Guanabens, Eric Hesse, Erik Imel, Deborah Sellmeyer, Emily Stein, Pamela Taxel, and Bo Abrahamsen) for their insightful comments on the final draft of Task Force Report. Special thanks to Douglas Fesler and Kirsten Mills for their continued support throughout the work of the Task Force. Authors’ roles: The original charge came from the ASBMR Professional Practice Committee and was modified by the entire task force. All the drafts were written by the co-chairs with specific input from all of the members of the task force. The entire task force reviewed the manuscript, provided edits, and approved the final draft.
Publisher Copyright:
© 2015 American Society for Bone and Mineral Research.
PY - 2016/1/1
Y1 - 2016/1/1
N2 - Bisphosphonates (BPs) are the most commonly used medications for osteoporosis. This ASBMR report provides guidance on BP therapy duration with a risk-benefit perspective. Two trials provided evidence for long-term BP use. In the Fracture Intervention Trial Long-term Extension (FLEX), postmenopausal women receiving alendronate for 10 years had fewer clinical vertebral fractures than those switched to placebo after 5 years. In the HORIZON extension, women who received 6 annual infusions of zoledronic acid had fewer morphometric vertebral fractures compared with those switched to placebo after 3 years. Low hip T-score, between -2 and -2.5 in FLEX and below -2.5 in HORIZON extension, predicted a beneficial response to continued therapy. Hence, the Task Force suggests that after 5 years of oral BP or 3 years of intravenous BP, reassessment of risk should be considered. In women at high risk, for example, older women, those with a low hip T-score or high fracture risk score, those with previous major osteoporotic fracture, or who fracture on therapy, continuation of treatment for up to 10 years (oral) or 6 years (intravenous), with periodic evaluation, should be considered. The risk of atypical femoral fracture, but not osteonecrosis of the jaw, clearly increases with BP therapy duration, but such rare events are outweighed by vertebral fracture risk reduction in high-risk patients. For women not at high fracture risk after 3 to 5 years of BP treatment, a drug holiday of 2 to 3 years can be considered. The suggested approach for long-term BP use is based on limited evidence, only for vertebral fracture reduction, in mostly white postmenopausal women, and does not replace the need for clinical judgment. It may be applicable to men and patients with glucocorticoid-induced osteoporosis, with some adaptations. It is unlikely that future trials will provide data for formulating definitive recommendations.
AB - Bisphosphonates (BPs) are the most commonly used medications for osteoporosis. This ASBMR report provides guidance on BP therapy duration with a risk-benefit perspective. Two trials provided evidence for long-term BP use. In the Fracture Intervention Trial Long-term Extension (FLEX), postmenopausal women receiving alendronate for 10 years had fewer clinical vertebral fractures than those switched to placebo after 5 years. In the HORIZON extension, women who received 6 annual infusions of zoledronic acid had fewer morphometric vertebral fractures compared with those switched to placebo after 3 years. Low hip T-score, between -2 and -2.5 in FLEX and below -2.5 in HORIZON extension, predicted a beneficial response to continued therapy. Hence, the Task Force suggests that after 5 years of oral BP or 3 years of intravenous BP, reassessment of risk should be considered. In women at high risk, for example, older women, those with a low hip T-score or high fracture risk score, those with previous major osteoporotic fracture, or who fracture on therapy, continuation of treatment for up to 10 years (oral) or 6 years (intravenous), with periodic evaluation, should be considered. The risk of atypical femoral fracture, but not osteonecrosis of the jaw, clearly increases with BP therapy duration, but such rare events are outweighed by vertebral fracture risk reduction in high-risk patients. For women not at high fracture risk after 3 to 5 years of BP treatment, a drug holiday of 2 to 3 years can be considered. The suggested approach for long-term BP use is based on limited evidence, only for vertebral fracture reduction, in mostly white postmenopausal women, and does not replace the need for clinical judgment. It may be applicable to men and patients with glucocorticoid-induced osteoporosis, with some adaptations. It is unlikely that future trials will provide data for formulating definitive recommendations.
KW - BISPHOSPHONATES
KW - DRUG HOLIDAY
KW - LONG TERM-BISPHOSPHONATE USE
KW - OTHER OSTEOPOROSIS THERAPIES
KW - RISK BENEFIT
UR - http://www.scopus.com/inward/record.url?scp=84957609430&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84957609430&partnerID=8YFLogxK
U2 - 10.1002/jbmr.2708
DO - 10.1002/jbmr.2708
M3 - Review article
C2 - 26350171
AN - SCOPUS:84957609430
SN - 0884-0431
VL - 31
SP - 16
EP - 35
JO - Journal of Bone and Mineral Research
JF - Journal of Bone and Mineral Research
IS - 1
ER -