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Romosozumab or alendronate for fracture prevention in East Asian patients: a subanalysis of the phase III, randomized ARCH study.
Lau, E M C; Dinavahi, R; Woo, Y C; Wu, C-H; Guan, J; Maddox, J; Tolman, C; Yang, W; Shin, C S.
Afiliação
  • Lau EMC; Hong Kong Orthopaedic and Osteoporosis Center for Treatment and Research, 6th Floor, Tower 2, New World Tower, 18 Queen's Road Central, Hong Kong, Hong Kong. edith.lau@hkosc.org.
  • Dinavahi R; Amgen, Inc., Thousand Oaks, CA, USA.
  • Woo YC; Department of Medicine, University of Hong Kong, Queen Mary Hospital, 102 Pok Fu Lam Road, Pok Fu Lam, Hong Kong.
  • Wu CH; Department of Family Medicine, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Sheng Li Road, Tainan, Taiwan.
  • Guan J; UCB Pharma, Brussels, Belgium.
  • Maddox J; Amgen, Inc., Thousand Oaks, CA, USA.
  • Tolman C; Amgen Asia Holding Ltd, One Island East, 18 Westlands Rd, Quarry Bay, Hong Kong.
  • Yang W; Amgen, Inc., Thousand Oaks, CA, USA.
  • Shin CS; Department of Internal Medicine, Seoul National University College of Medicine, Seoul, South Korea.
Osteoporos Int ; 31(4): 677-685, 2020 Apr.
Article em En | MEDLINE | ID: mdl-32047951
Romosozumab, a sclerostin antibody, exerts dual effect to increase bone formation and decrease bone resorption. Among high-risk postmenopausal East Asian women, romosozumab followed by alendronate was associated with lower incidences of fractures vs alendronate alone. Romosozumab demonstrates potential to address an unmet need in osteoporosis management in Asia. INTRODUCTION: Romosozumab, a sclerostin antibody, exerts dual effect to increase bone formation and decrease bone resorption. The global ARCH study demonstrated superiority of romosozumab followed by alendronate in reducing fracture risk in high-risk postmenopausal osteoporotic women vs alendronate alone. We report outcomes among ARCH East Asian patients. METHODS: In ARCH, 4093 postmenopausal osteoporotic women with fragility fracture were randomized 1:1 to monthly romosozumab 210 mg or weekly alendronate 70 mg for 12 months, both followed by open-label alendronate. Primary endpoints were incidence of new vertebral fracture (VF) at 24 months and clinical fracture at primary analysis (confirmed fractures in ≥ 330 patients and all patients had opportunity to attend month 24 visit). This post hoc analysis was not powered to detect fracture-rate differences. RESULTS: This analysis included 275 patients from Hong Kong, Korea, and Taiwan. Romosozumab followed by alendronate reduced risk of new VFs at 24 months by 60% (P = 0.11) and clinical fractures at primary analysis by 44% (P = 0.15) vs alendronate alone. Romosozumab followed by alendronate significantly increased mean bone mineral density at 24 months from baseline by a further 9.0%, 3.3%, and 3.0% at the lumbar spine, total hip, and femoral neck vs alendronate alone. Adverse event (AE) rates, including positively adjudicated serious cardiovascular AEs (1.6% vs 1.4% at 12 months for romosozumab vs alendronate), were similar across treatment groups. CONCLUSIONS: Consistent with the global analysis, romosozumab followed by alendronate was associated with lower incidences of new vertebral, clinical, non-vertebral, and hip fractures vs alendronate alone among East Asian patients.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Osteoporose Pós-Menopausa / Alendronato / Fraturas Ósseas / Conservadores da Densidade Óssea / Anticorpos Monoclonais Tipo de estudo: Clinical_trials Limite: Aged / Female / Humans País como assunto: Asia Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Osteoporose Pós-Menopausa / Alendronato / Fraturas Ósseas / Conservadores da Densidade Óssea / Anticorpos Monoclonais Tipo de estudo: Clinical_trials Limite: Aged / Female / Humans País como assunto: Asia Idioma: En Ano de publicação: 2020 Tipo de documento: Article