Effect of Anti-IL5, Anti-IL5R, Anti-IL13 Therapy on Asthma Exacerbations: A Network Meta-analysis
Background Several new treatments for severe asthma have become available in the last decade; yet, little data exist to guide their use in specific patient populations. Objective A network meta-analysis was conducted comparing the efficacy of FDA-approved monoclonal antibody therapies in preventing...
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Veröffentlicht in: | Lung 2020-02, Vol.198 (1), p.95-103 |
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description | Background
Several new treatments for severe asthma have become available in the last decade; yet, little data exist to guide their use in specific patient populations.
Objective
A network meta-analysis was conducted comparing the efficacy of FDA-approved monoclonal antibody therapies in preventing exacerbations in patients with severe eosinophilic asthma.
Methods
PubMed and Ovid were searched from inception until July 2019 for randomized controlled trials that studied the efficacy of benralizumab, dupilumab, mepolizumab, and reslizumab, in preventing acute exacerbations of asthma. Studies were included if they reported data for patients with severe eosinophilic asthma (defined in this meta-analysis as absolute eosinophil count ≥ 250 cells/μL). Annualized rate ratios for asthma exacerbations (during treatment) were calculated and converted to log rate ratios. Direct and indirect treatment estimates (for inter-drug differences) were analyzed using frequentist network meta-analysis methodology in R and treatments were ranked based on
P
-scores.
Results
In total, nine studies were included in the final analysis. Network meta-analysis revealed that all drugs were superior to placebo in preventing rates of asthma exacerbation in the study population and no inter-drug differences existed. Dupilumab was found to have the greatest magnitudes of effect on decreasing log rate ratio of asthma exacerbation based on
P
-score (0.83).
Conclusion
Benralizumab, dupilumab, mepolizumab, and reslizumab are all associated with decreased asthma exacerbations in patients with eosinophilic asthma, with no significant inter-drug differences. |
doi_str_mv | 10.1007/s00408-019-00310-8 |
format | Article |
fullrecord | <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9136642</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A614362632</galeid><sourcerecordid>A614362632</sourcerecordid><originalsourceid>FETCH-LOGICAL-c648t-d62622f59e57678ca6598b90c7e71ca9182eaf4562ad555a68596115b38477d83</originalsourceid><addsrcrecordid>eNp9kl-L1DAUxYMo7rj6BXyQgiA-mDV_mjT1QSjLqAujgqzPIZPeTru2yZi06nx7M9t12IFB8pBL7u8eyLkHoeeUXFBCireRkJwoTGiJCeGUYPUALWjOGaaFIA_RgvCcYpagM_QkxhtCaCGpeIzOOFVlnlOyQGbZNGDHzDdZ5cYOX63Em0P17VBSnl23EMx2l3mXVXFsB5Mt_xgLYW3Gzrv4LquyLzD-9uFH9hlGg40z_S528Sl61Jg-wrO7-xx9_7C8vvyEV18_Xl1WK2xlrkZcSyYZa0QJopCFskaKUq1LYgsoqDUlVQxMkwvJTC2EMFKJUlIq1lzlRVErfo7ez7rbaT1AbcGNwfR6G7rBhJ32ptPHHde1euN_6ZJyKXOWBF7fCQT_c4I46qGLFvreOPBT1IxzRhQRZZ7QlzO6MT3ozjU-Kdo9riuZNpD-wveC-AS1AZeM7L2DpkvPR_zFCT6dGobOnhx4dW-gBdOPbfT9dLuQY5DNoA0-xgDNwRZK9D5Les6STlnSt1nSe0Nf3Df0MPIvPAngMxBTy20g6Bs_hbT2-D_Zv_pSzuI</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2332080594</pqid></control><display><type>article</type><title>Effect of Anti-IL5, Anti-IL5R, Anti-IL13 Therapy on Asthma Exacerbations: A Network Meta-analysis</title><source>MEDLINE</source><source>Springer Nature - Complete Springer Journals</source><creator>Ramonell, Richard P. ; Iftikhar, Imran H.</creator><creatorcontrib>Ramonell, Richard P. ; Iftikhar, Imran H.</creatorcontrib><description>Background
Several new treatments for severe asthma have become available in the last decade; yet, little data exist to guide their use in specific patient populations.
Objective
A network meta-analysis was conducted comparing the efficacy of FDA-approved monoclonal antibody therapies in preventing exacerbations in patients with severe eosinophilic asthma.
Methods
PubMed and Ovid were searched from inception until July 2019 for randomized controlled trials that studied the efficacy of benralizumab, dupilumab, mepolizumab, and reslizumab, in preventing acute exacerbations of asthma. Studies were included if they reported data for patients with severe eosinophilic asthma (defined in this meta-analysis as absolute eosinophil count ≥ 250 cells/μL). Annualized rate ratios for asthma exacerbations (during treatment) were calculated and converted to log rate ratios. Direct and indirect treatment estimates (for inter-drug differences) were analyzed using frequentist network meta-analysis methodology in R and treatments were ranked based on
P
-scores.
Results
In total, nine studies were included in the final analysis. Network meta-analysis revealed that all drugs were superior to placebo in preventing rates of asthma exacerbation in the study population and no inter-drug differences existed. Dupilumab was found to have the greatest magnitudes of effect on decreasing log rate ratio of asthma exacerbation based on
P
-score (0.83).
Conclusion
Benralizumab, dupilumab, mepolizumab, and reslizumab are all associated with decreased asthma exacerbations in patients with eosinophilic asthma, with no significant inter-drug differences.</description><identifier>ISSN: 0341-2040</identifier><identifier>EISSN: 1432-1750</identifier><identifier>DOI: 10.1007/s00408-019-00310-8</identifier><identifier>PMID: 31894410</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Anti-Asthmatic Agents - therapeutic use ; Antibodies, Monoclonal, Humanized - therapeutic use ; Asthma ; Asthma - drug therapy ; Asthma - immunology ; Asthma - physiopathology ; Diagnosis ; Disease Progression ; Eosinophilia - drug therapy ; Eosinophilia - immunology ; Eosinophilia - physiopathology ; Eosinophils ; Health aspects ; Humans ; Interleukin-13 - antagonists & inhibitors ; Interleukin-4 Receptor alpha Subunit - antagonists & inhibitors ; Interleukin-5 - antagonists & inhibitors ; Interleukin-5 Receptor alpha Subunit - antagonists & inhibitors ; Interleukins ; Medicine ; Medicine & Public Health ; Network Meta-Analysis ; Pneumology/Respiratory System ; Randomized Controlled Trials as Topic ; Secondary Prevention</subject><ispartof>Lung, 2020-02, Vol.198 (1), p.95-103</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2020</rights><rights>COPYRIGHT 2020 Springer</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c648t-d62622f59e57678ca6598b90c7e71ca9182eaf4562ad555a68596115b38477d83</citedby><cites>FETCH-LOGICAL-c648t-d62622f59e57678ca6598b90c7e71ca9182eaf4562ad555a68596115b38477d83</cites><orcidid>0000-0001-5102-5193</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00408-019-00310-8$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00408-019-00310-8$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,776,780,881,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31894410$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ramonell, Richard P.</creatorcontrib><creatorcontrib>Iftikhar, Imran H.</creatorcontrib><title>Effect of Anti-IL5, Anti-IL5R, Anti-IL13 Therapy on Asthma Exacerbations: A Network Meta-analysis</title><title>Lung</title><addtitle>Lung</addtitle><addtitle>Lung</addtitle><description>Background
Several new treatments for severe asthma have become available in the last decade; yet, little data exist to guide their use in specific patient populations.
Objective
A network meta-analysis was conducted comparing the efficacy of FDA-approved monoclonal antibody therapies in preventing exacerbations in patients with severe eosinophilic asthma.
Methods
PubMed and Ovid were searched from inception until July 2019 for randomized controlled trials that studied the efficacy of benralizumab, dupilumab, mepolizumab, and reslizumab, in preventing acute exacerbations of asthma. Studies were included if they reported data for patients with severe eosinophilic asthma (defined in this meta-analysis as absolute eosinophil count ≥ 250 cells/μL). Annualized rate ratios for asthma exacerbations (during treatment) were calculated and converted to log rate ratios. Direct and indirect treatment estimates (for inter-drug differences) were analyzed using frequentist network meta-analysis methodology in R and treatments were ranked based on
P
-scores.
Results
In total, nine studies were included in the final analysis. Network meta-analysis revealed that all drugs were superior to placebo in preventing rates of asthma exacerbation in the study population and no inter-drug differences existed. Dupilumab was found to have the greatest magnitudes of effect on decreasing log rate ratio of asthma exacerbation based on
P
-score (0.83).
Conclusion
Benralizumab, dupilumab, mepolizumab, and reslizumab are all associated with decreased asthma exacerbations in patients with eosinophilic asthma, with no significant inter-drug differences.</description><subject>Anti-Asthmatic Agents - therapeutic use</subject><subject>Antibodies, Monoclonal, Humanized - therapeutic use</subject><subject>Asthma</subject><subject>Asthma - drug therapy</subject><subject>Asthma - immunology</subject><subject>Asthma - physiopathology</subject><subject>Diagnosis</subject><subject>Disease Progression</subject><subject>Eosinophilia - drug therapy</subject><subject>Eosinophilia - immunology</subject><subject>Eosinophilia - physiopathology</subject><subject>Eosinophils</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Interleukin-13 - antagonists & inhibitors</subject><subject>Interleukin-4 Receptor alpha Subunit - antagonists & inhibitors</subject><subject>Interleukin-5 - antagonists & inhibitors</subject><subject>Interleukin-5 Receptor alpha Subunit - antagonists & inhibitors</subject><subject>Interleukins</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Network Meta-Analysis</subject><subject>Pneumology/Respiratory System</subject><subject>Randomized Controlled Trials as Topic</subject><subject>Secondary Prevention</subject><issn>0341-2040</issn><issn>1432-1750</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kl-L1DAUxYMo7rj6BXyQgiA-mDV_mjT1QSjLqAujgqzPIZPeTru2yZi06nx7M9t12IFB8pBL7u8eyLkHoeeUXFBCireRkJwoTGiJCeGUYPUALWjOGaaFIA_RgvCcYpagM_QkxhtCaCGpeIzOOFVlnlOyQGbZNGDHzDdZ5cYOX63Em0P17VBSnl23EMx2l3mXVXFsB5Mt_xgLYW3Gzrv4LquyLzD-9uFH9hlGg40z_S528Sl61Jg-wrO7-xx9_7C8vvyEV18_Xl1WK2xlrkZcSyYZa0QJopCFskaKUq1LYgsoqDUlVQxMkwvJTC2EMFKJUlIq1lzlRVErfo7ez7rbaT1AbcGNwfR6G7rBhJ32ptPHHde1euN_6ZJyKXOWBF7fCQT_c4I46qGLFvreOPBT1IxzRhQRZZ7QlzO6MT3ozjU-Kdo9riuZNpD-wveC-AS1AZeM7L2DpkvPR_zFCT6dGobOnhx4dW-gBdOPbfT9dLuQY5DNoA0-xgDNwRZK9D5Les6STlnSt1nSe0Nf3Df0MPIvPAngMxBTy20g6Bs_hbT2-D_Zv_pSzuI</recordid><startdate>20200201</startdate><enddate>20200201</enddate><creator>Ramonell, Richard P.</creator><creator>Iftikhar, Imran H.</creator><general>Springer US</general><general>Springer</general><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>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-5102-5193</orcidid></search><sort><creationdate>20200201</creationdate><title>Effect of Anti-IL5, Anti-IL5R, Anti-IL13 Therapy on Asthma Exacerbations: A Network Meta-analysis</title><author>Ramonell, Richard P. ; Iftikhar, Imran H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c648t-d62622f59e57678ca6598b90c7e71ca9182eaf4562ad555a68596115b38477d83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Anti-Asthmatic Agents - therapeutic use</topic><topic>Antibodies, Monoclonal, Humanized - therapeutic use</topic><topic>Asthma</topic><topic>Asthma - drug therapy</topic><topic>Asthma - immunology</topic><topic>Asthma - physiopathology</topic><topic>Diagnosis</topic><topic>Disease Progression</topic><topic>Eosinophilia - drug therapy</topic><topic>Eosinophilia - immunology</topic><topic>Eosinophilia - physiopathology</topic><topic>Eosinophils</topic><topic>Health aspects</topic><topic>Humans</topic><topic>Interleukin-13 - antagonists & inhibitors</topic><topic>Interleukin-4 Receptor alpha Subunit - antagonists & inhibitors</topic><topic>Interleukin-5 - antagonists & inhibitors</topic><topic>Interleukin-5 Receptor alpha Subunit - antagonists & inhibitors</topic><topic>Interleukins</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Network Meta-Analysis</topic><topic>Pneumology/Respiratory System</topic><topic>Randomized Controlled Trials as Topic</topic><topic>Secondary Prevention</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ramonell, Richard P.</creatorcontrib><creatorcontrib>Iftikhar, Imran H.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Lung</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ramonell, Richard P.</au><au>Iftikhar, Imran H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effect of Anti-IL5, Anti-IL5R, Anti-IL13 Therapy on Asthma Exacerbations: A Network Meta-analysis</atitle><jtitle>Lung</jtitle><stitle>Lung</stitle><addtitle>Lung</addtitle><date>2020-02-01</date><risdate>2020</risdate><volume>198</volume><issue>1</issue><spage>95</spage><epage>103</epage><pages>95-103</pages><issn>0341-2040</issn><eissn>1432-1750</eissn><abstract>Background
Several new treatments for severe asthma have become available in the last decade; yet, little data exist to guide their use in specific patient populations.
Objective
A network meta-analysis was conducted comparing the efficacy of FDA-approved monoclonal antibody therapies in preventing exacerbations in patients with severe eosinophilic asthma.
Methods
PubMed and Ovid were searched from inception until July 2019 for randomized controlled trials that studied the efficacy of benralizumab, dupilumab, mepolizumab, and reslizumab, in preventing acute exacerbations of asthma. Studies were included if they reported data for patients with severe eosinophilic asthma (defined in this meta-analysis as absolute eosinophil count ≥ 250 cells/μL). Annualized rate ratios for asthma exacerbations (during treatment) were calculated and converted to log rate ratios. Direct and indirect treatment estimates (for inter-drug differences) were analyzed using frequentist network meta-analysis methodology in R and treatments were ranked based on
P
-scores.
Results
In total, nine studies were included in the final analysis. Network meta-analysis revealed that all drugs were superior to placebo in preventing rates of asthma exacerbation in the study population and no inter-drug differences existed. Dupilumab was found to have the greatest magnitudes of effect on decreasing log rate ratio of asthma exacerbation based on
P
-score (0.83).
Conclusion
Benralizumab, dupilumab, mepolizumab, and reslizumab are all associated with decreased asthma exacerbations in patients with eosinophilic asthma, with no significant inter-drug differences.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>31894410</pmid><doi>10.1007/s00408-019-00310-8</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-5102-5193</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Anti-Asthmatic Agents - therapeutic use Antibodies, Monoclonal, Humanized - therapeutic use Asthma Asthma - drug therapy Asthma - immunology Asthma - physiopathology Diagnosis Disease Progression Eosinophilia - drug therapy Eosinophilia - immunology Eosinophilia - physiopathology Eosinophils Health aspects Humans Interleukin-13 - antagonists & inhibitors Interleukin-4 Receptor alpha Subunit - antagonists & inhibitors Interleukin-5 - antagonists & inhibitors Interleukin-5 Receptor alpha Subunit - antagonists & inhibitors Interleukins Medicine Medicine & Public Health Network Meta-Analysis Pneumology/Respiratory System Randomized Controlled Trials as Topic Secondary Prevention |
title | Effect of Anti-IL5, Anti-IL5R, Anti-IL13 Therapy on Asthma Exacerbations: A Network Meta-analysis |
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