Literature DB >> 25707611

The Effect of Discontinuing Treatment With Blosozumab: Follow-up Results of a Phase 2 Randomized Clinical Trial in Postmenopausal Women With Low Bone Mineral Density.

Christopher P Recknor1, Robert R Recker2, Charles T Benson3, Deborah A Robins3, Alan Y Chiang3, Jahangir Alam3, Leijun Hu3, Toshio Matsumoto4, Hideaki Sowa5, John H Sloan3, Robert J Konrad3, Bruce H Mitlak3, Adrien A Sipos3.   

Abstract

Administration of blosozumab, a humanized monoclonal antibody that binds sclerostin, increases bone formation and bone mineral density (BMD) in postmenopausal women with low BMD. To evaluate the effect of discontinuing blosozumab, we studied women enrolled in a 1-year randomized, placebo-controlled phase 2 trial for an additional year after they completed treatment. Of the 120 women initially enrolled in the study, 106 women completed treatment and continued into follow-up; 88 women completed 1 year of follow-up. At the beginning of follow-up, groups remained balanced for age, race, and body mass index, but lumbar spine and total hip BMD were increased in prior blosozumab groups, reflecting an anabolic treatment effect. At the end of follow-up, 1 year after discontinuing treatment, lumbar spine BMD remained significantly greater than placebo in women initially treated with blosozumab 270 mg every 2 weeks (Q2W) and blosozumab 180 mg Q2W (6.9% and 3.6% above baseline, respectively). Total hip BMD also declined after discontinuation of treatment but at 1 year after treatment remained significantly greater than placebo in women initially treated with blosozumab 270 mg Q2W and blosozumab 180 mg Q2W (3.9% and 2.6% above baseline, respectively). During follow-up, median serum P1NP was not consistently different between the prior blosozumab groups and placebo. A similar pattern was apparent for median serum C-terminal telopeptide of type 1 collagen (CTx) levels, with more variability. Mean serum total sclerostin concentration increased with blosozumab, indicating target engagement, and declined to baseline after discontinuation. There were no adverse events considered related to prior treatment with blosozumab. Anti-drug antibodies generally declined in patients who had detectable levels during prior treatment. These findings support the continued study of blosozumab as an anabolic therapy for treatment of osteoporosis.
© 2015 American Society for Bone and Mineral Research.

Entities:  

Keywords:  ANABOLICS; BLOSOZUMAB; DXA; OSTEOPOROSIS; SCLEROSTIN ANTIBODY

Mesh:

Substances:

Year:  2015        PMID: 25707611     DOI: 10.1002/jbmr.2489

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


  29 in total

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Authors:  Nilsson Holguin
Journal:  Clin Orthop Relat Res       Date:  2016-01-12       Impact factor: 4.176

Review 2.  Bone repair with skeletal stem cells: rationale, progress to date and clinical application.

Authors:  Elena A Jones; Peter V Giannoudis; Dimitrios Kouroupis
Journal:  Ther Adv Musculoskelet Dis       Date:  2016-04-01       Impact factor: 5.346

Review 3.  Role and mechanism of action of sclerostin in bone.

Authors:  Jesus Delgado-Calle; Amy Y Sato; Teresita Bellido
Journal:  Bone       Date:  2016-10-12       Impact factor: 4.398

Review 4.  New anabolic therapies for osteoporosis.

Authors:  Salvatore Minisola; Cristiana Cipriani; Marco Occhiuto; Jessica Pepe
Journal:  Intern Emerg Med       Date:  2017-08-05       Impact factor: 3.397

5.  N-cadherin Regulation of Bone Growth and Homeostasis Is Osteolineage Stage-Specific.

Authors:  Francesca Fontana; Cynthia L Hickman-Brecks; Valerie S Salazar; Leila Revollo; Grazia Abou-Ezzi; Susan K Grimston; Sung Yeop Jeong; Marcus Watkins; Manuela Fortunato; Yael Alippe; Daniel C Link; Gabriel Mbalaviele; Roberto Civitelli
Journal:  J Bone Miner Res       Date:  2017-03-29       Impact factor: 6.741

6.  Single dose of bisphosphonate preserves gains in bone mass following cessation of sclerostin antibody in Brtl/+ osteogenesis imperfecta model.

Authors:  Joseph E Perosky; Basma M Khoury; Terese N Jenks; Ferrous S Ward; Kai Cortright; Bethany Meyer; David K Barton; Benjamin P Sinder; Joan C Marini; Michelle S Caird; Kenneth M Kozloff
Journal:  Bone       Date:  2016-09-15       Impact factor: 4.398

Review 7.  Exploiting the WNT Signaling Pathway for Clinical Purposes.

Authors:  Mark L Johnson; Robert R Recker
Journal:  Curr Osteoporos Rep       Date:  2017-06       Impact factor: 5.096

8.  Low Dose of Bisphosphonate Enhances Sclerostin Antibody-Induced Trabecular Bone Mass Gains in Brtl/+ Osteogenesis Imperfecta Mouse Model.

Authors:  Diana Olvera; Rachel Stolzenfeld; Joan C Marini; Michelle S Caird; Kenneth M Kozloff
Journal:  J Bone Miner Res       Date:  2018-05-07       Impact factor: 6.741

Review 9.  Anabolic Therapy for the Treatment of Osteoporosis in Childhood.

Authors:  Leanne M Ward; Frank Rauch
Journal:  Curr Osteoporos Rep       Date:  2018-06       Impact factor: 5.096

Review 10.  Sclerostin antibodies in osteoporosis: latest evidence and therapeutic potential.

Authors:  Michael R McClung
Journal:  Ther Adv Musculoskelet Dis       Date:  2017-08-29       Impact factor: 5.346

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