Evaluation of correlation between dose and clinical outcomes in subcutaneous immunoglobulin replacement therapy
Summary The importance of serum immunoglobulin (Ig)G concentration in IgG replacement therapy for primary immunodeficiency diseases is established in certain settings. Generally, IgG is infused via the intravenous (IVIG) or subcutaneous (SCIG) route. For IVIG infusion, published data demonstrate tha...
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Veröffentlicht in: | Clinical and experimental immunology 2012-08, Vol.169 (2), p.172-181 |
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creator | Orange, J. S. Belohradsky, B. H. Berger, M. Borte, M. Hagan, J. Jolles, S. Wasserman, R. L. Baggish, J. S. Saunders, R. Grimbacher, B. |
description | Summary
The importance of serum immunoglobulin (Ig)G concentration in IgG replacement therapy for primary immunodeficiency diseases is established in certain settings. Generally, IgG is infused via the intravenous (IVIG) or subcutaneous (SCIG) route. For IVIG infusion, published data demonstrate that higher IgG doses and trough levels provide patients with improved protection from infection. The same conclusions are not yet accepted for SCIG; data from two recent Phase III studies and a recent post‐hoc analysis, however, suggest the same correlation between higher SCIG dose and serum IgG concentration and decreased incidence of infection seen with IVIG. Other measures of clinical efficacy have not been considered similarly. Thus, combined analyses of these and other published SCIG studies were performed; a full comparison of the 13 studies was, however, limited by non‐standardized definitions and reporting. Despite these limitations, our analyses indicate that certain clinical outcomes improve at higher SCIG doses and associated higher serum IgG concentrations, and suggest that there might be opportunity to improve patient outcomes via SCIG dose adjustment. |
doi_str_mv | 10.1111/j.1365-2249.2012.04594.x |
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The importance of serum immunoglobulin (Ig)G concentration in IgG replacement therapy for primary immunodeficiency diseases is established in certain settings. Generally, IgG is infused via the intravenous (IVIG) or subcutaneous (SCIG) route. For IVIG infusion, published data demonstrate that higher IgG doses and trough levels provide patients with improved protection from infection. The same conclusions are not yet accepted for SCIG; data from two recent Phase III studies and a recent post‐hoc analysis, however, suggest the same correlation between higher SCIG dose and serum IgG concentration and decreased incidence of infection seen with IVIG. Other measures of clinical efficacy have not been considered similarly. Thus, combined analyses of these and other published SCIG studies were performed; a full comparison of the 13 studies was, however, limited by non‐standardized definitions and reporting. Despite these limitations, our analyses indicate that certain clinical outcomes improve at higher SCIG doses and associated higher serum IgG concentrations, and suggest that there might be opportunity to improve patient outcomes via SCIG dose adjustment.</description><identifier>ISSN: 0009-9104</identifier><identifier>EISSN: 1365-2249</identifier><identifier>DOI: 10.1111/j.1365-2249.2012.04594.x</identifier><identifier>PMID: 22774992</identifier><identifier>CODEN: CEXIAL</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Analytical, structural and metabolic biochemistry ; Bacterial Infections - etiology ; Biological and medical sciences ; Clinical outcomes ; dose ; Fundamental and applied biological sciences. Psychology ; Humans ; IgG replacement therapy ; Immune system ; Immunization, Passive - adverse effects ; Immunodeficiencies ; Immunodeficiencies. Immunoglobulinopathies ; immunoglobulin ; Immunoglobulin G - administration & dosage ; Immunoglobulin G - blood ; Immunologic Deficiency Syndromes - complications ; Immunologic Deficiency Syndromes - therapy ; Immunopathology ; Infusions, Subcutaneous ; Medical research ; Medical sciences ; Original ; primary immunodeficiency ; subcutaneous ; Treatment Outcome</subject><ispartof>Clinical and experimental immunology, 2012-08, Vol.169 (2), p.172-181</ispartof><rights>2012 The Authors. Clinical and Experimental Immunology © 2012 British Society for Immunology</rights><rights>2015 INIST-CNRS</rights><rights>2012 The Authors. Clinical and Experimental Immunology © 2012 British Society for Immunology.</rights><rights>2012 The Authors. Clinical and Experimental Immunology © 2012 British Society for Immunology 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c6314-6030f5dfdcf4284610720be63c34f0421c8e8048cd8eb82367926f838cfc5d513</citedby><cites>FETCH-LOGICAL-c6314-6030f5dfdcf4284610720be63c34f0421c8e8048cd8eb82367926f838cfc5d513</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3406377/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3406377/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26116713$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22774992$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Orange, J. S.</creatorcontrib><creatorcontrib>Belohradsky, B. H.</creatorcontrib><creatorcontrib>Berger, M.</creatorcontrib><creatorcontrib>Borte, M.</creatorcontrib><creatorcontrib>Hagan, J.</creatorcontrib><creatorcontrib>Jolles, S.</creatorcontrib><creatorcontrib>Wasserman, R. L.</creatorcontrib><creatorcontrib>Baggish, J. S.</creatorcontrib><creatorcontrib>Saunders, R.</creatorcontrib><creatorcontrib>Grimbacher, B.</creatorcontrib><title>Evaluation of correlation between dose and clinical outcomes in subcutaneous immunoglobulin replacement therapy</title><title>Clinical and experimental immunology</title><addtitle>Clin Exp Immunol</addtitle><description>Summary
The importance of serum immunoglobulin (Ig)G concentration in IgG replacement therapy for primary immunodeficiency diseases is established in certain settings. Generally, IgG is infused via the intravenous (IVIG) or subcutaneous (SCIG) route. For IVIG infusion, published data demonstrate that higher IgG doses and trough levels provide patients with improved protection from infection. The same conclusions are not yet accepted for SCIG; data from two recent Phase III studies and a recent post‐hoc analysis, however, suggest the same correlation between higher SCIG dose and serum IgG concentration and decreased incidence of infection seen with IVIG. Other measures of clinical efficacy have not been considered similarly. Thus, combined analyses of these and other published SCIG studies were performed; a full comparison of the 13 studies was, however, limited by non‐standardized definitions and reporting. Despite these limitations, our analyses indicate that certain clinical outcomes improve at higher SCIG doses and associated higher serum IgG concentrations, and suggest that there might be opportunity to improve patient outcomes via SCIG dose adjustment.</description><subject>Analytical, structural and metabolic biochemistry</subject><subject>Bacterial Infections - etiology</subject><subject>Biological and medical sciences</subject><subject>Clinical outcomes</subject><subject>dose</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>IgG replacement therapy</subject><subject>Immune system</subject><subject>Immunization, Passive - adverse effects</subject><subject>Immunodeficiencies</subject><subject>Immunodeficiencies. Immunoglobulinopathies</subject><subject>immunoglobulin</subject><subject>Immunoglobulin G - administration & dosage</subject><subject>Immunoglobulin G - blood</subject><subject>Immunologic Deficiency Syndromes - complications</subject><subject>Immunologic Deficiency Syndromes - therapy</subject><subject>Immunopathology</subject><subject>Infusions, Subcutaneous</subject><subject>Medical research</subject><subject>Medical sciences</subject><subject>Original</subject><subject>primary immunodeficiency</subject><subject>subcutaneous</subject><subject>Treatment Outcome</subject><issn>0009-9104</issn><issn>1365-2249</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>EIF</sourceid><recordid>eNqNkk1v1DAQhiMEotvCX0CWEBKXLP6OcwCpWi2lUiUucLYcx26zcuzFjtvuv8chy_Jxqi_2aJ55NeN3qgoguEblfNitEeGsxpi2awwRXkPKWrp-fFatTonn1QpC2NYtgvSsOk9pV0LOOX5ZnWHcNLRt8aoK23vlspqG4EGwQIcYjVvCzkwPxnjQh2SA8j3QbvCDVg6EPOkwmgQGD1LudJ6UNyGXeByzD7cudLmwIJq9U9qMxk9gujNR7Q-vqhdWuWReH--L6vvn7bfNl_rm69X15vKm1pwgWnNIoGW97bWlWFCOYINhZzjRhFpIMdLCCEiF7oXpBCa8aTG3gghtNesZIhfVp0V3n7vR9Lq0EJWT-ziMKh5kUIP8N-OHO3kb7iWhkJOmKQLvjwIx_MgmTXIckjbOLaNKBIlgrYAYPwHFApIygCjo2__QXcjRl5-QiFEmOKMtK5RYKB1DStHYU98IynkB5E7OPsvZZzkvgPy1APKxlL75e-5T4W_HC_DuCKhUvLRReT2kPxxHiDeIFO7jwj0Mzhye3IDcbK_nF_kJfm7Npg</recordid><startdate>201208</startdate><enddate>201208</enddate><creator>Orange, J. S.</creator><creator>Belohradsky, B. H.</creator><creator>Berger, M.</creator><creator>Borte, M.</creator><creator>Hagan, J.</creator><creator>Jolles, S.</creator><creator>Wasserman, R. L.</creator><creator>Baggish, J. S.</creator><creator>Saunders, R.</creator><creator>Grimbacher, B.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><general>Oxford University Press</general><general>Blackwell Science Inc</general><scope>24P</scope><scope>IQODW</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>7T5</scope><scope>7U9</scope><scope>H94</scope><scope>M7N</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201208</creationdate><title>Evaluation of correlation between dose and clinical outcomes in subcutaneous immunoglobulin replacement therapy</title><author>Orange, J. S. ; Belohradsky, B. H. ; Berger, M. ; Borte, M. ; Hagan, J. ; Jolles, S. ; Wasserman, R. L. ; Baggish, J. S. ; Saunders, R. ; Grimbacher, B.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c6314-6030f5dfdcf4284610720be63c34f0421c8e8048cd8eb82367926f838cfc5d513</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Analytical, structural and metabolic biochemistry</topic><topic>Bacterial Infections - etiology</topic><topic>Biological and medical sciences</topic><topic>Clinical outcomes</topic><topic>dose</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>IgG replacement therapy</topic><topic>Immune system</topic><topic>Immunization, Passive - adverse effects</topic><topic>Immunodeficiencies</topic><topic>Immunodeficiencies. Immunoglobulinopathies</topic><topic>immunoglobulin</topic><topic>Immunoglobulin G - administration & dosage</topic><topic>Immunoglobulin G - blood</topic><topic>Immunologic Deficiency Syndromes - complications</topic><topic>Immunologic Deficiency Syndromes - therapy</topic><topic>Immunopathology</topic><topic>Infusions, Subcutaneous</topic><topic>Medical research</topic><topic>Medical sciences</topic><topic>Original</topic><topic>primary immunodeficiency</topic><topic>subcutaneous</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Orange, J. S.</creatorcontrib><creatorcontrib>Belohradsky, B. H.</creatorcontrib><creatorcontrib>Berger, M.</creatorcontrib><creatorcontrib>Borte, M.</creatorcontrib><creatorcontrib>Hagan, J.</creatorcontrib><creatorcontrib>Jolles, S.</creatorcontrib><creatorcontrib>Wasserman, R. L.</creatorcontrib><creatorcontrib>Baggish, J. S.</creatorcontrib><creatorcontrib>Saunders, R.</creatorcontrib><creatorcontrib>Grimbacher, B.</creatorcontrib><collection>Wiley Online Library Open Access</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Clinical and experimental immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Orange, J. S.</au><au>Belohradsky, B. H.</au><au>Berger, M.</au><au>Borte, M.</au><au>Hagan, J.</au><au>Jolles, S.</au><au>Wasserman, R. L.</au><au>Baggish, J. S.</au><au>Saunders, R.</au><au>Grimbacher, B.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of correlation between dose and clinical outcomes in subcutaneous immunoglobulin replacement therapy</atitle><jtitle>Clinical and experimental immunology</jtitle><addtitle>Clin Exp Immunol</addtitle><date>2012-08</date><risdate>2012</risdate><volume>169</volume><issue>2</issue><spage>172</spage><epage>181</epage><pages>172-181</pages><issn>0009-9104</issn><eissn>1365-2249</eissn><coden>CEXIAL</coden><abstract>Summary
The importance of serum immunoglobulin (Ig)G concentration in IgG replacement therapy for primary immunodeficiency diseases is established in certain settings. Generally, IgG is infused via the intravenous (IVIG) or subcutaneous (SCIG) route. For IVIG infusion, published data demonstrate that higher IgG doses and trough levels provide patients with improved protection from infection. The same conclusions are not yet accepted for SCIG; data from two recent Phase III studies and a recent post‐hoc analysis, however, suggest the same correlation between higher SCIG dose and serum IgG concentration and decreased incidence of infection seen with IVIG. Other measures of clinical efficacy have not been considered similarly. Thus, combined analyses of these and other published SCIG studies were performed; a full comparison of the 13 studies was, however, limited by non‐standardized definitions and reporting. Despite these limitations, our analyses indicate that certain clinical outcomes improve at higher SCIG doses and associated higher serum IgG concentrations, and suggest that there might be opportunity to improve patient outcomes via SCIG dose adjustment.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>22774992</pmid><doi>10.1111/j.1365-2249.2012.04594.x</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analytical, structural and metabolic biochemistry Bacterial Infections - etiology Biological and medical sciences Clinical outcomes dose Fundamental and applied biological sciences. Psychology Humans IgG replacement therapy Immune system Immunization, Passive - adverse effects Immunodeficiencies Immunodeficiencies. Immunoglobulinopathies immunoglobulin Immunoglobulin G - administration & dosage Immunoglobulin G - blood Immunologic Deficiency Syndromes - complications Immunologic Deficiency Syndromes - therapy Immunopathology Infusions, Subcutaneous Medical research Medical sciences Original primary immunodeficiency subcutaneous Treatment Outcome |
title | Evaluation of correlation between dose and clinical outcomes in subcutaneous immunoglobulin replacement therapy |
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