Romosozumab or alendronate for fracture prevention in East Asian patients: a subanalysis of the phase III, randomized ARCH study
Summary 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 demonstrate...
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Veröffentlicht in: | Osteoporosis international 2020-04, Vol.31 (4), p.677-685 |
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description | Summary
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. |
doi_str_mv | 10.1007/s00198-020-05324-0 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7075830</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2377614150</sourcerecordid><originalsourceid>FETCH-LOGICAL-c474t-5e4c678c904513ab3588f566f77e2ab7bab9872d29eb73be64a7015fe65b2ed53</originalsourceid><addsrcrecordid>eNp9kU9rFDEYxoModq1-AQ8S8OLBafN3MvEgLEu1C4VCUfAW3sxkuikzyZrMFLYnP7pZt7bqwVMIz-958r55EHpNyQklRJ1mQqhuKsJIRSRnoiJP0IIKziuma_kULYjmqtKCfjtCL3K-IcWktXqOjjgjQmlJF-jHVRxjjnfzCBbHhGFwoUsxwORwX-59gnaak8Pb5G5dmHwM2Ad8BnnCy-wh4C1Mvgj5AwacZwsBhl32GcceT5vi20B2eL1ev8cJQhdHf-c6vLxaneM8zd3uJXrWw5Ddq_vzGH39dPZldV5dXH5er5YXVSuUmCrpRFurptVESMrBctk0vazrXinHwCoLVjeKdUw7q7h1tQBFqOxdLS1zneTH6OMhdzvb0XVtGTnBYLbJj5B2JoI3fyvBb8x1vDWKKNlwUgLe3Qek-H12eTKjz60bBgguztkwLgUVWqi6oG__QW_inMrH7Cmlaiqo3AeyA9WmmHNy_cMwlJh9weZQsCkFm18Fm73pzZ9rPFh-N1oAfgBykcK1S49v_yf2J-AOssI</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2377614150</pqid></control><display><type>article</type><title>Romosozumab or alendronate for fracture prevention in East Asian patients: a subanalysis of the phase III, randomized ARCH study</title><source>MEDLINE</source><source>Springer Nature - Complete Springer Journals</source><creator>Lau, E. M. C. ; Dinavahi, R. ; Woo, Y. C. ; Wu, C.-H. ; Guan, J. ; Maddox, J. ; Tolman, C. ; Yang, W. ; Shin, C. S.</creator><creatorcontrib>Lau, E. M. C. ; Dinavahi, R. ; Woo, Y. C. ; Wu, C.-H. ; Guan, J. ; Maddox, J. ; Tolman, C. ; Yang, W. ; Shin, C. S.</creatorcontrib><description>Summary
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.</description><identifier>ISSN: 0937-941X</identifier><identifier>EISSN: 1433-2965</identifier><identifier>DOI: 10.1007/s00198-020-05324-0</identifier><identifier>PMID: 32047951</identifier><language>eng</language><publisher>London: Springer London</publisher><subject>Aged ; Alendronate - therapeutic use ; Alendronic acid ; Antibodies, Monoclonal - therapeutic use ; Bisphosphonates ; Bone Density ; Bone Density Conservation Agents - therapeutic use ; Bone growth ; Bone mineral density ; Bone resorption ; Endocrinology ; Female ; Fractures ; Fractures, Bone - prevention & control ; Hip ; Hong Kong ; Humans ; Medicine ; Medicine & Public Health ; Monoclonal antibodies ; Original ; Original Article ; Orthopedics ; Osteogenesis ; Osteoporosis ; Osteoporosis, Postmenopausal - drug therapy ; Patients ; Post-menopause ; Republic of Korea ; Rheumatology ; SOST protein ; Spine (lumbar) ; Taiwan ; Vertebrae ; Vitamin D</subject><ispartof>Osteoporosis international, 2020-04, Vol.31 (4), p.677-685</ispartof><rights>The Author(s) 2020</rights><rights>Osteoporosis International is a copyright of Springer, (2020). All Rights Reserved. This work is published under https://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c474t-5e4c678c904513ab3588f566f77e2ab7bab9872d29eb73be64a7015fe65b2ed53</citedby><cites>FETCH-LOGICAL-c474t-5e4c678c904513ab3588f566f77e2ab7bab9872d29eb73be64a7015fe65b2ed53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00198-020-05324-0$$EPDF$$P50$$Gspringer$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00198-020-05324-0$$EHTML$$P50$$Gspringer$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32047951$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lau, E. M. C.</creatorcontrib><creatorcontrib>Dinavahi, R.</creatorcontrib><creatorcontrib>Woo, Y. C.</creatorcontrib><creatorcontrib>Wu, C.-H.</creatorcontrib><creatorcontrib>Guan, J.</creatorcontrib><creatorcontrib>Maddox, J.</creatorcontrib><creatorcontrib>Tolman, C.</creatorcontrib><creatorcontrib>Yang, W.</creatorcontrib><creatorcontrib>Shin, C. S.</creatorcontrib><title>Romosozumab or alendronate for fracture prevention in East Asian patients: a subanalysis of the phase III, randomized ARCH study</title><title>Osteoporosis international</title><addtitle>Osteoporos Int</addtitle><addtitle>Osteoporos Int</addtitle><description>Summary
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.</description><subject>Aged</subject><subject>Alendronate - therapeutic use</subject><subject>Alendronic acid</subject><subject>Antibodies, Monoclonal - therapeutic use</subject><subject>Bisphosphonates</subject><subject>Bone Density</subject><subject>Bone Density Conservation Agents - therapeutic use</subject><subject>Bone growth</subject><subject>Bone mineral density</subject><subject>Bone resorption</subject><subject>Endocrinology</subject><subject>Female</subject><subject>Fractures</subject><subject>Fractures, Bone - prevention & control</subject><subject>Hip</subject><subject>Hong Kong</subject><subject>Humans</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Monoclonal antibodies</subject><subject>Original</subject><subject>Original Article</subject><subject>Orthopedics</subject><subject>Osteogenesis</subject><subject>Osteoporosis</subject><subject>Osteoporosis, Postmenopausal - drug therapy</subject><subject>Patients</subject><subject>Post-menopause</subject><subject>Republic of Korea</subject><subject>Rheumatology</subject><subject>SOST protein</subject><subject>Spine (lumbar)</subject><subject>Taiwan</subject><subject>Vertebrae</subject><subject>Vitamin D</subject><issn>0937-941X</issn><issn>1433-2965</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kU9rFDEYxoModq1-AQ8S8OLBafN3MvEgLEu1C4VCUfAW3sxkuikzyZrMFLYnP7pZt7bqwVMIz-958r55EHpNyQklRJ1mQqhuKsJIRSRnoiJP0IIKziuma_kULYjmqtKCfjtCL3K-IcWktXqOjjgjQmlJF-jHVRxjjnfzCBbHhGFwoUsxwORwX-59gnaak8Pb5G5dmHwM2Ad8BnnCy-wh4C1Mvgj5AwacZwsBhl32GcceT5vi20B2eL1ev8cJQhdHf-c6vLxaneM8zd3uJXrWw5Ddq_vzGH39dPZldV5dXH5er5YXVSuUmCrpRFurptVESMrBctk0vazrXinHwCoLVjeKdUw7q7h1tQBFqOxdLS1zneTH6OMhdzvb0XVtGTnBYLbJj5B2JoI3fyvBb8x1vDWKKNlwUgLe3Qek-H12eTKjz60bBgguztkwLgUVWqi6oG__QW_inMrH7Cmlaiqo3AeyA9WmmHNy_cMwlJh9weZQsCkFm18Fm73pzZ9rPFh-N1oAfgBykcK1S49v_yf2J-AOssI</recordid><startdate>20200401</startdate><enddate>20200401</enddate><creator>Lau, E. M. C.</creator><creator>Dinavahi, R.</creator><creator>Woo, Y. C.</creator><creator>Wu, C.-H.</creator><creator>Guan, J.</creator><creator>Maddox, J.</creator><creator>Tolman, C.</creator><creator>Yang, W.</creator><creator>Shin, C. S.</creator><general>Springer London</general><general>Springer Nature B.V</general><scope>C6C</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7RV</scope><scope>7TS</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20200401</creationdate><title>Romosozumab or alendronate for fracture prevention in East Asian patients: a subanalysis of the phase III, randomized ARCH study</title><author>Lau, E. M. C. ; Dinavahi, R. ; Woo, Y. C. ; Wu, C.-H. ; Guan, J. ; Maddox, J. ; Tolman, C. ; Yang, W. ; Shin, C. S.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c474t-5e4c678c904513ab3588f566f77e2ab7bab9872d29eb73be64a7015fe65b2ed53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Aged</topic><topic>Alendronate - therapeutic use</topic><topic>Alendronic acid</topic><topic>Antibodies, Monoclonal - therapeutic use</topic><topic>Bisphosphonates</topic><topic>Bone Density</topic><topic>Bone Density Conservation Agents - therapeutic use</topic><topic>Bone growth</topic><topic>Bone mineral density</topic><topic>Bone resorption</topic><topic>Endocrinology</topic><topic>Female</topic><topic>Fractures</topic><topic>Fractures, Bone - prevention & control</topic><topic>Hip</topic><topic>Hong Kong</topic><topic>Humans</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Monoclonal antibodies</topic><topic>Original</topic><topic>Original Article</topic><topic>Orthopedics</topic><topic>Osteogenesis</topic><topic>Osteoporosis</topic><topic>Osteoporosis, Postmenopausal - drug therapy</topic><topic>Patients</topic><topic>Post-menopause</topic><topic>Republic of Korea</topic><topic>Rheumatology</topic><topic>SOST protein</topic><topic>Spine (lumbar)</topic><topic>Taiwan</topic><topic>Vertebrae</topic><topic>Vitamin D</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lau, E. M. C.</creatorcontrib><creatorcontrib>Dinavahi, R.</creatorcontrib><creatorcontrib>Woo, Y. C.</creatorcontrib><creatorcontrib>Wu, C.-H.</creatorcontrib><creatorcontrib>Guan, J.</creatorcontrib><creatorcontrib>Maddox, J.</creatorcontrib><creatorcontrib>Tolman, C.</creatorcontrib><creatorcontrib>Yang, W.</creatorcontrib><creatorcontrib>Shin, C. S.</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Physical Education Index</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Osteoporosis international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lau, E. M. C.</au><au>Dinavahi, R.</au><au>Woo, Y. C.</au><au>Wu, C.-H.</au><au>Guan, J.</au><au>Maddox, J.</au><au>Tolman, C.</au><au>Yang, W.</au><au>Shin, C. S.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Romosozumab or alendronate for fracture prevention in East Asian patients: a subanalysis of the phase III, randomized ARCH study</atitle><jtitle>Osteoporosis international</jtitle><stitle>Osteoporos Int</stitle><addtitle>Osteoporos Int</addtitle><date>2020-04-01</date><risdate>2020</risdate><volume>31</volume><issue>4</issue><spage>677</spage><epage>685</epage><pages>677-685</pages><issn>0937-941X</issn><eissn>1433-2965</eissn><abstract>Summary
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.</abstract><cop>London</cop><pub>Springer London</pub><pmid>32047951</pmid><doi>10.1007/s00198-020-05324-0</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Alendronate - therapeutic use Alendronic acid Antibodies, Monoclonal - therapeutic use Bisphosphonates Bone Density Bone Density Conservation Agents - therapeutic use Bone growth Bone mineral density Bone resorption Endocrinology Female Fractures Fractures, Bone - prevention & control Hip Hong Kong Humans Medicine Medicine & Public Health Monoclonal antibodies Original Original Article Orthopedics Osteogenesis Osteoporosis Osteoporosis, Postmenopausal - drug therapy Patients Post-menopause Republic of Korea Rheumatology SOST protein Spine (lumbar) Taiwan Vertebrae Vitamin D |
title | Romosozumab or alendronate for fracture prevention in East Asian patients: a subanalysis of the phase III, randomized ARCH study |
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