Safety of denosumab in postmenopausal women with osteoporosis or low bone mineral density: a meta-analysis

The aim of this meta-analysis was to assess the safety of denosumab in postmenopausal women with osteoporosis or low bone mineral density (BMD). Safety of denosumab was compared with placebo or bisphosphonates. A systematic literature search without language restriction was conducted up to January,...

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Veröffentlicht in:International journal of clinical and experimental pathology 2014-01, Vol.7 (5), p.2113-2122
Hauptverfasser: Zhou, Zhenyu, Chen, Chen, Zhang, Jun, Ji, Xinran, Liu, Lifeng, Zhang, Guichun, Cao, Xuecheng, Wang, Pingshan
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container_issue 5
container_start_page 2113
container_title International journal of clinical and experimental pathology
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creator Zhou, Zhenyu
Chen, Chen
Zhang, Jun
Ji, Xinran
Liu, Lifeng
Zhang, Guichun
Cao, Xuecheng
Wang, Pingshan
description The aim of this meta-analysis was to assess the safety of denosumab in postmenopausal women with osteoporosis or low bone mineral density (BMD). Safety of denosumab was compared with placebo or bisphosphonates. A systematic literature search without language restriction was conducted up to January, 2014. The RevMan 5.1 software was used for statistical analysis. A total of 11 English literatures were eventually identified. The pooled data in the overall analysis revealed that there was no significant difference when compared denosumab with placebo or bisphosphonates in any adverse events (AAE) (RR=0.99, 95% CI=0.98-1.01, p=0.29), serious adverse event (SAE) (RR=1.05, 95% CI=0.98-1.13, p=0.18), neoplasm/cancer (RR=1.14, 95% CI=0.95-1.37, p=0.16) and deaths (RR=0.77, 95% CI=0.57-1.04, p=0.09). However, significant differences were found when compared denosumab with placebo or bisphosphonates in SAE related to infection (RR=1.23, 95% CI=1.00-1.52, p=0.05) and non-vertebral fracture (RR=0.86, 95% CI=0.74-1.00, p=0.05). Subgroup analysis was performed by the type of drugs which was used in the control group. The results of subgroup analysis did not demonstrate the differences between denosumab and bisphosphonates in SAE related to infection (RR=1.13, 95% CI=0.63-2.03) and non-vertebral fracture (RR=1.31, 95% CI=0.87-1.98). Compared to placebo, denosumab treatment significantly decreased the risk of non-vertebral fracture but increased the risk of SAE related to infection in the postmenopausal women with osteoporosis or low BMD. However, no difference between the safety of denosumab and bisphosphonates was found.
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Safety of denosumab was compared with placebo or bisphosphonates. A systematic literature search without language restriction was conducted up to January, 2014. The RevMan 5.1 software was used for statistical analysis. A total of 11 English literatures were eventually identified. The pooled data in the overall analysis revealed that there was no significant difference when compared denosumab with placebo or bisphosphonates in any adverse events (AAE) (RR=0.99, 95% CI=0.98-1.01, p=0.29), serious adverse event (SAE) (RR=1.05, 95% CI=0.98-1.13, p=0.18), neoplasm/cancer (RR=1.14, 95% CI=0.95-1.37, p=0.16) and deaths (RR=0.77, 95% CI=0.57-1.04, p=0.09). However, significant differences were found when compared denosumab with placebo or bisphosphonates in SAE related to infection (RR=1.23, 95% CI=1.00-1.52, p=0.05) and non-vertebral fracture (RR=0.86, 95% CI=0.74-1.00, p=0.05). Subgroup analysis was performed by the type of drugs which was used in the control group. The results of subgroup analysis did not demonstrate the differences between denosumab and bisphosphonates in SAE related to infection (RR=1.13, 95% CI=0.63-2.03) and non-vertebral fracture (RR=1.31, 95% CI=0.87-1.98). Compared to placebo, denosumab treatment significantly decreased the risk of non-vertebral fracture but increased the risk of SAE related to infection in the postmenopausal women with osteoporosis or low BMD. 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The results of subgroup analysis did not demonstrate the differences between denosumab and bisphosphonates in SAE related to infection (RR=1.13, 95% CI=0.63-2.03) and non-vertebral fracture (RR=1.31, 95% CI=0.87-1.98). Compared to placebo, denosumab treatment significantly decreased the risk of non-vertebral fracture but increased the risk of SAE related to infection in the postmenopausal women with osteoporosis or low BMD. 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Chen, Chen ; Zhang, Jun ; Ji, Xinran ; Liu, Lifeng ; Zhang, Guichun ; Cao, Xuecheng ; Wang, Pingshan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p266t-6785e00dd1c102c3e9438d566a15d9de9d038b1ad64ef6998e85c03c308e20cc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Age Factors</topic><topic>Antibodies, Monoclonal, Humanized - adverse effects</topic><topic>Antibodies, Monoclonal, Humanized - therapeutic use</topic><topic>Bone Density - drug effects</topic><topic>Bone Density Conservation Agents - adverse effects</topic><topic>Bone Density Conservation Agents - therapeutic use</topic><topic>Chi-Square Distribution</topic><topic>Denosumab</topic><topic>Female</topic><topic>Humans</topic><topic>Odds Ratio</topic><topic>Original</topic><topic>Osteoporosis, Postmenopausal - diagnosis</topic><topic>Osteoporosis, Postmenopausal - drug therapy</topic><topic>Osteoporosis, Postmenopausal - physiopathology</topic><topic>Osteoporotic Fractures - diagnosis</topic><topic>Osteoporotic Fractures - physiopathology</topic><topic>Osteoporotic Fractures - prevention &amp; control</topic><topic>Risk Assessment</topic><topic>Risk Factors</topic><topic>Sex Factors</topic><topic>Treatment Outcome</topic><toplevel>online_resources</toplevel><creatorcontrib>Zhou, Zhenyu</creatorcontrib><creatorcontrib>Chen, Chen</creatorcontrib><creatorcontrib>Zhang, Jun</creatorcontrib><creatorcontrib>Ji, Xinran</creatorcontrib><creatorcontrib>Liu, Lifeng</creatorcontrib><creatorcontrib>Zhang, Guichun</creatorcontrib><creatorcontrib>Cao, Xuecheng</creatorcontrib><creatorcontrib>Wang, Pingshan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>International journal of clinical and experimental pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhou, Zhenyu</au><au>Chen, Chen</au><au>Zhang, Jun</au><au>Ji, Xinran</au><au>Liu, Lifeng</au><au>Zhang, Guichun</au><au>Cao, Xuecheng</au><au>Wang, Pingshan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Safety of denosumab in postmenopausal women with osteoporosis or low bone mineral density: a meta-analysis</atitle><jtitle>International journal of clinical and experimental pathology</jtitle><addtitle>Int J Clin Exp Pathol</addtitle><date>2014-01-01</date><risdate>2014</risdate><volume>7</volume><issue>5</issue><spage>2113</spage><epage>2122</epage><pages>2113-2122</pages><eissn>1936-2625</eissn><abstract>The aim of this meta-analysis was to assess the safety of denosumab in postmenopausal women with osteoporosis or low bone mineral density (BMD). Safety of denosumab was compared with placebo or bisphosphonates. A systematic literature search without language restriction was conducted up to January, 2014. The RevMan 5.1 software was used for statistical analysis. A total of 11 English literatures were eventually identified. The pooled data in the overall analysis revealed that there was no significant difference when compared denosumab with placebo or bisphosphonates in any adverse events (AAE) (RR=0.99, 95% CI=0.98-1.01, p=0.29), serious adverse event (SAE) (RR=1.05, 95% CI=0.98-1.13, p=0.18), neoplasm/cancer (RR=1.14, 95% CI=0.95-1.37, p=0.16) and deaths (RR=0.77, 95% CI=0.57-1.04, p=0.09). However, significant differences were found when compared denosumab with placebo or bisphosphonates in SAE related to infection (RR=1.23, 95% CI=1.00-1.52, p=0.05) and non-vertebral fracture (RR=0.86, 95% CI=0.74-1.00, p=0.05). Subgroup analysis was performed by the type of drugs which was used in the control group. The results of subgroup analysis did not demonstrate the differences between denosumab and bisphosphonates in SAE related to infection (RR=1.13, 95% CI=0.63-2.03) and non-vertebral fracture (RR=1.31, 95% CI=0.87-1.98). Compared to placebo, denosumab treatment significantly decreased the risk of non-vertebral fracture but increased the risk of SAE related to infection in the postmenopausal women with osteoporosis or low BMD. However, no difference between the safety of denosumab and bisphosphonates was found.</abstract><cop>United States</cop><pub>e-Century Publishing Corporation</pub><pmid>24966919</pmid><tpages>10</tpages></addata></record>
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subjects Age Factors
Antibodies, Monoclonal, Humanized - adverse effects
Antibodies, Monoclonal, Humanized - therapeutic use
Bone Density - drug effects
Bone Density Conservation Agents - adverse effects
Bone Density Conservation Agents - therapeutic use
Chi-Square Distribution
Denosumab
Female
Humans
Odds Ratio
Original
Osteoporosis, Postmenopausal - diagnosis
Osteoporosis, Postmenopausal - drug therapy
Osteoporosis, Postmenopausal - physiopathology
Osteoporotic Fractures - diagnosis
Osteoporotic Fractures - physiopathology
Osteoporotic Fractures - prevention & control
Risk Assessment
Risk Factors
Sex Factors
Treatment Outcome
title Safety of denosumab in postmenopausal women with osteoporosis or low bone mineral density: a meta-analysis
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