Literature DB >> 29329484

Effects of Teriparatide Compared with Risedronate on the Risk of Fractures in Subgroups of Postmenopausal Women with Severe Osteoporosis: The VERO Trial.

Piet Geusens1, Fernando Marin2, David L Kendler3, Luis A Russo4, Cristiano Af Zerbini5, Salvatore Minisola6, Jean Jacques Body7, Eric Lespessailles8, Susan L Greenspan9, Alicia Bagur10, Jan J Stepan11, Péter Lakatos12, Enrique Casado13, Rüdiger Moericke14, Pedro López-Romero2, Astrid Fahrleitner-Pammer15.   

Abstract

The 2-year, randomized, double-blind, active-controlled fracture endpoint VERO study included postmenopausal women with established osteoporosis, who had at least 2 moderate or 1 severe baseline vertebral fractures (VFx), and bone mineral density (BMD) T-score ≤-1.5. Patients were treated with either s.c. daily teriparatide 20 μg or oral weekly risedronate 35 mg. As previously reported, the risk of new VFx and clinical fractures (a composite of clinical VFx and nonvertebral fragility fractures [NVFFx]) was statistically significantly reduced with teriparatide compared with risedronate. Here we present the prospectively planned subgroup analyses of fracture data across subgroups, which were predefined by the following baseline characteristics: age, number and severity of prevalent VFx, prevalent nonvertebral fractures (NVFx), glucocorticoid use, prior osteoporosis drugs, recent bisphosphonate use, clinical VFx in the year before study entry, and baseline BMD. Heterogeneity of the treatment effect on the primary endpoint (new VFx), and the four key secondary endpoints (including clinical fractures and NVFFx) were investigated by logistic and Cox proportional hazards regression models. A total of 1360 women were randomized and treated (680 per group). Mean age was 72.1 years, mean (SD) number of prevalent VFx was 2.7 (2.1), 55.4% had a BMD T-score <-2.5, 36.5% had a recent clinical VFx, 28.3% had a prior major NVFx, 43.2% were osteoporosis drug-naïve, 39.3% were recent bisphosphonate users, and 9.3% were taking glucocorticoids at a prednisone-equivalent dose of >5 mg/d. For most fracture endpoints, the risk reduction of teriparatide versus risedronate did not significantly differ in any of the subgroups analyzed (treatment-by-subgroup interaction p > 0.1), with most subgroups mirroring results from the total study population. In conclusion, in postmenopausal women with severe osteoporosis, the antifracture efficacy of teriparatide compared with risedronate was consistent in a wide range of patient settings, including treatment-naïve and previously treated patients.
© 2018 The Authors. Journal of Bone and Mineral Research Published by Wiley Periodicals Inc. © 2018 The Authors. Journal of Bone and Mineral Research Published by Wiley Periodicals, Inc.

Entities:  

Keywords:  BISPHOSPHONATES; POSTMENOPAUSAL OSTEOPOROSIS; SUBGROUP ANALYSIS; TERIPARATIDE; VERTEBRAL FRACTURES

Mesh:

Substances:

Year:  2018        PMID: 29329484     DOI: 10.1002/jbmr.3384

Source DB:  PubMed          Journal:  J Bone Miner Res        ISSN: 0884-0431            Impact factor:   6.741


  19 in total

Review 1.  The next step after anti-osteoporotic drug discontinuation: an up-to-date review of sequential treatment.

Authors:  Núria Guañabens; María Jesús Moro-Álvarez; Enrique Casado; Josep Blanch-Rubió; Carlos Gómez-Alonso; Guillermo Martínez Díaz-Guerra; Javier Del Pino-Montes; Carmen Valero Díaz de Lamadrid; Pilar Peris; Manuel Muñoz-Torres
Journal:  Endocrine       Date:  2019-04-08       Impact factor: 3.633

Review 2.  Current Status of Bone-Forming Therapies for the Management of Osteoporosis.

Authors:  Anne Sophie Koldkjær Sølling; Torben Harsløf; Bente Langdahl
Journal:  Drugs Aging       Date:  2019-07       Impact factor: 3.923

3.  Denosumab, raloxifene, romosozumab and teriparatide to prevent osteoporotic fragility fractures: a systematic review and economic evaluation.

Authors:  Sarah Davis; Emma Simpson; Jean Hamilton; Marrissa Martyn-St James; Andrew Rawdin; Ruth Wong; Edward Goka; Neil Gittoes; Peter Selby
Journal:  Health Technol Assess       Date:  2020-06       Impact factor: 4.014

Review 4.  Risedronate for the primary and secondary prevention of osteoporotic fractures in postmenopausal women.

Authors:  George A Wells; Shu-Ching Hsieh; Carine Zheng; Joan Peterson; Peter Tugwell; Wenfei Liu
Journal:  Cochrane Database Syst Rev       Date:  2022-05-03

Review 5.  Anabolic Agents for Postmenopausal Osteoporosis: How Do You Choose?

Authors:  Felicia Cosman; David W Dempster
Journal:  Curr Osteoporos Rep       Date:  2021-02-26       Impact factor: 5.096

Review 6.  Which treatment to prevent an imminent fracture?

Authors:  Iconaru Laura; Baleanu Felicia; Charles Alexia; Mugisha Aude; Benoit Florence; Surquin Murielle; Karmali Rafik; Body Jean-Jacques; Bergmann Pierre
Journal:  Bone Rep       Date:  2021-07-09

7.  Patient Preferences for Biologic and Biosimilar Osteoporosis Treatments in Colombia.

Authors:  Peita L Graham-Clarke; Brett Hauber; Marco Boeri; Felice Leonardi; Russel T Burge; Maria Fernandez; Antje Tockhorn-Heidenreich; Sandra Florez
Journal:  Patient Prefer Adherence       Date:  2020-06-23       Impact factor: 2.711

Review 8.  Anabolic treatments for osteoporosis in postmenopausal women.

Authors:  Neelam Hassan; Celia L Gregson; Jon H Tobias
Journal:  Fac Rev       Date:  2021-05-05

Review 9.  Cardiovascular Safety of Antifracture Medications in Patients With Osteoporosis: A Narrative Review of Evidence From Randomized Studies.

Authors:  Alexander J Rodríguez; Bo Abrahamsen
Journal:  JBMR Plus       Date:  2021-06-23

10.  Comparison between teriparatide and bisphosphonates for improving bone mineral density in postmenopausal osteoporosis patients: A meta-analysis.

Authors:  Guiyong Fan; Qun Zhao; Pei Lu; Hao Chen; Wei Tan; Weixiao Guo; Chaoqun Liu; Jinlian Liu
Journal:  Medicine (Baltimore)       Date:  2020-04       Impact factor: 1.817

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