Efficacy and Safety of Romosozumab Among Postmenopausal Women With Osteoporosis and Mild-to-Moderate Chronic Kidney Disease.


Journal

Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research
ISSN: 1523-4681
Titre abrégé: J Bone Miner Res
Pays: United States
ID NLM: 8610640

Informations de publication

Date de publication:
08 2022
Historique:
revised: 23 03 2022
received: 02 06 2021
accepted: 21 04 2022
pubmed: 26 4 2022
medline: 11 8 2022
entrez: 25 4 2022
Statut: ppublish

Résumé

Patients with osteoporosis and chronic kidney disease (CKD) are at increased risk of fracture and associated negative outcomes, including increased mortality. The present post hoc analysis of two randomized, multicenter, phase 3 clinical trials-Fracture Study in Postmenopausal Women with Osteoporosis (FRAME) and Active-Controlled Fracture Study in Postmenopausal Women with Osteoporosis at High Risk (ARCH)-investigated the efficacy and safety of romosozumab in postmenopausal women with osteoporosis and mild-to-moderate CKD. The analysis included data from 7147 patients from FRAME and 4077 from ARCH. Eighty-one percent of patients from FRAME and 85% from ARCH had mild or moderate reduction in estimated glomerular filtration rate (eGFR) at baseline, and part of this reduction is likely age related. During the 1-year double-blind phases of the trials, patients received romosozumab 210 mg sc or placebo monthly in FRAME and romosozumab 210 mg sc monthly or alendronate 70 mg po weekly in ARCH. Bone mineral density (BMD) at the lumbar spine, total hip, and femoral neck and vertebral and nonvertebral fractures were assessed at baseline and month 12. In both trials, the least-square mean percent change from baseline BMD was significantly greater in the romosozumab groups versus controls across all kidney function categories at month 12. Romosozumab reduced the relative risk of new vertebral fractures at month 12 among patients with eGFR of 30-59, 60-89, and ≥90 mL/min by 72% (95% confidence interval [CI] 14-91; p = 0.017), 70% (40-85; p < 0.001), and 84% (30-96; p = 0.005), respectively, in FRAME versus placebo, and by 51% (5-75; p = 0.04), 19% (-28 to 49; p = 0.39), and 57% (1-81, p = 0.04), respectively, in ARCH versus alendronate. Incidences of adverse events, asymptomatic decreases in serum calcium, and evolution of kidney function during the studies were similar across all baseline kidney function groups. Romosozumab is an effective treatment option for postmenopausal women with osteoporosis and mild-to-moderate reduction in kidney function, with a similar safety profile across different levels of kidney function. © 2022 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR).

Identifiants

pubmed: 35466448
doi: 10.1002/jbmr.4563
pmc: PMC9544335
doi:

Substances chimiques

Antibodies, Monoclonal 0
Bone Density Conservation Agents 0
romosozumab 3VHF2ZD92J
Alendronate X1J18R4W8P

Types de publication

Clinical Trial, Phase III Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1437-1445

Subventions

Organisme : Amgen
Organisme : Astellas Pharma
Organisme : UCB

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn
Type : CommentIn
Type : CommentIn

Informations de copyright

© 2022 The Authors. Journal of Bone and Mineral Research published by Wiley Periodicals LLC on behalf of American Society for Bone and Mineral Research (ASBMR).

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Auteurs

Paul D Miller (PD)

Colorado Center for Bone Health, Lakewood, CO, USA.

Jonathan D Adachi (JD)

St. Joseph's Healthcare Hamilton, McMaster University, Hamilton, Canada.

Ben-Hur Albergaria (BH)

Federal University of Espirito Santo, Espirito Santo Research and Osteoporosis Center, Vitória, Brazil.

Angela M Cheung (AM)

Department of Medicine, University Health Network, University of Toronto, Toronto, Canada.

Arkadi A Chines (AA)

Amgen Inc., Thousand Oaks, CA, USA.

Evelien Gielen (E)

Gerontology and Geriatrics, Department of Public Health and Primary Care, KU Leuven & Center for Metabolic Bone Diseases, UZ Leuven, Leuven, Belgium.

Bente L Langdahl (BL)

Aarhus University Hospital, Aarhus, Denmark.

Akimitsu Miyauchi (A)

Miyauchi Medical Center, Osaka, Japan.

Mary Oates (M)

Amgen Inc., Thousand Oaks, CA, USA.

Ian R Reid (IR)

University of Auckland, Auckland, New Zealand.

Norma Ruiz Santiago (NR)

Amgen Inc., Thousand Oaks, CA, USA.

Mark Vanderkelen (M)

UCB S.A, Brussels, Belgium.

Zhenxun Wang (Z)

Amgen Inc., Thousand Oaks, CA, USA.

Zhigang Yu (Z)

Amgen Inc., Thousand Oaks, CA, USA.

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Classifications MeSH