Long-term safety profile of belimumab plus standard therapy in patients with systemic lupus erythematosus
Objective To evaluate the safety profile of long‐term belimumab therapy combined with standard therapy for systemic lupus erythematosus (SLE) in patients with active disease. Methods Patients who were randomized to receive intravenous placebo or belimumab 1, 4, or 10 mg/kg, plus standard therapy, an...
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creator | Merrill, Joan T. Ginzler, Ellen M. Wallace, Daniel J. McKay, James D. Lisse, Jeffrey R. Aranow, Cynthia Wellborne, Frank R. Burnette, Michael Condemi, John Zhong, Z. John Pineda, Lilia Klein, Jerry Freimuth, William W. |
description | Objective
To evaluate the safety profile of long‐term belimumab therapy combined with standard therapy for systemic lupus erythematosus (SLE) in patients with active disease.
Methods
Patients who were randomized to receive intravenous placebo or belimumab 1, 4, or 10 mg/kg, plus standard therapy, and completed the initial 52‐week double‐blind treatment period were then allowed to enter a 24‐week open‐label extension phase. During the extension period, patients in the belimumab group either received the same dose or were switched to 10 mg/kg and patients in the placebo group were switched to belimumab 10 mg/kg. Patients who achieved a satisfactory response during the 24‐week extension period were allowed to participate in the long‐term continuation study of monthly belimumab 10 mg/kg. Adverse events (AEs) and abnormal laboratory results were analyzed per 100 patient‐years in 1‐year intervals.
Results
Of the 364 patients who completed the 52‐week double‐blind treatment period, 345 entered the 24‐week extension, and 296 continued treatment with belimumab in the long‐term continuation study. Safety data through 4 years of belimumab exposure (1,165 cumulative patient‐years) are reported. Incidence rates of AEs, severe/serious AEs, infusion reactions, infections, malignancies, grades 3/4 laboratory abnormalities, and discontinuations due to AEs were stable or declined during 4‐year belimumab exposure. The most common AEs included arthralgia, upper respiratory tract infection, headache, fatigue, and nausea. Serious infusion reactions were rare: only 1 occurred during the 4‐year followup period. Rates of serious infection decreased from 5.9/100 patient‐years to 3.4/100 patient‐years, and no specific type of infection predominated.
Conclusion
Belimumab added to standard therapy was generally well‐tolerated over the 4‐year treatment period in patients with SLE, which suggests that belimumab can be administered long term with an acceptable safety profile. |
doi_str_mv | 10.1002/art.34564 |
format | Article |
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To evaluate the safety profile of long‐term belimumab therapy combined with standard therapy for systemic lupus erythematosus (SLE) in patients with active disease.
Methods
Patients who were randomized to receive intravenous placebo or belimumab 1, 4, or 10 mg/kg, plus standard therapy, and completed the initial 52‐week double‐blind treatment period were then allowed to enter a 24‐week open‐label extension phase. During the extension period, patients in the belimumab group either received the same dose or were switched to 10 mg/kg and patients in the placebo group were switched to belimumab 10 mg/kg. Patients who achieved a satisfactory response during the 24‐week extension period were allowed to participate in the long‐term continuation study of monthly belimumab 10 mg/kg. Adverse events (AEs) and abnormal laboratory results were analyzed per 100 patient‐years in 1‐year intervals.
Results
Of the 364 patients who completed the 52‐week double‐blind treatment period, 345 entered the 24‐week extension, and 296 continued treatment with belimumab in the long‐term continuation study. Safety data through 4 years of belimumab exposure (1,165 cumulative patient‐years) are reported. Incidence rates of AEs, severe/serious AEs, infusion reactions, infections, malignancies, grades 3/4 laboratory abnormalities, and discontinuations due to AEs were stable or declined during 4‐year belimumab exposure. The most common AEs included arthralgia, upper respiratory tract infection, headache, fatigue, and nausea. Serious infusion reactions were rare: only 1 occurred during the 4‐year followup period. Rates of serious infection decreased from 5.9/100 patient‐years to 3.4/100 patient‐years, and no specific type of infection predominated.
Conclusion
Belimumab added to standard therapy was generally well‐tolerated over the 4‐year treatment period in patients with SLE, which suggests that belimumab can be administered long term with an acceptable safety profile.</description><identifier>ISSN: 0004-3591</identifier><identifier>ISSN: 2326-5191</identifier><identifier>EISSN: 1529-0131</identifier><identifier>EISSN: 2326-5205</identifier><identifier>DOI: 10.1002/art.34564</identifier><identifier>PMID: 22674457</identifier><identifier>CODEN: ARHEAW</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adrenal Cortex Hormones - therapeutic use ; Adult ; Antibodies, Monoclonal - adverse effects ; Antibodies, Monoclonal - therapeutic use ; Antibodies, Monoclonal, Humanized ; Biological and medical sciences ; Diseases of the osteoarticular system ; Double-Blind Method ; Drug therapy ; Drug Therapy, Combination ; Female ; Humans ; Immunomodulators ; Immunosuppressive Agents - adverse effects ; Immunosuppressive Agents - therapeutic use ; Infections ; Lupus ; Lupus Erythematosus, Systemic - drug therapy ; Male ; Medical sciences ; Middle Aged ; Patients ; Pharmacology. Drug treatments ; Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis ; Treatment Outcome</subject><ispartof>Arthritis & rheumatology (Hoboken, N.J.), 2012-10, Vol.64 (10), p.3364-3373</ispartof><rights>Copyright © 2012 by the American College of Rheumatology</rights><rights>2014 INIST-CNRS</rights><rights>Copyright © 2012 by the American College of Rheumatology.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4214-a89fa6f7b2cc6fcd7421d53211de6c769462a19d2e869a323e9ad69c3892ef8a3</citedby><cites>FETCH-LOGICAL-c4214-a89fa6f7b2cc6fcd7421d53211de6c769462a19d2e869a323e9ad69c3892ef8a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fart.34564$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fart.34564$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,782,786,1419,27931,27932,45581,45582</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26635596$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22674457$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Merrill, Joan T.</creatorcontrib><creatorcontrib>Ginzler, Ellen M.</creatorcontrib><creatorcontrib>Wallace, Daniel J.</creatorcontrib><creatorcontrib>McKay, James D.</creatorcontrib><creatorcontrib>Lisse, Jeffrey R.</creatorcontrib><creatorcontrib>Aranow, Cynthia</creatorcontrib><creatorcontrib>Wellborne, Frank R.</creatorcontrib><creatorcontrib>Burnette, Michael</creatorcontrib><creatorcontrib>Condemi, John</creatorcontrib><creatorcontrib>Zhong, Z. John</creatorcontrib><creatorcontrib>Pineda, Lilia</creatorcontrib><creatorcontrib>Klein, Jerry</creatorcontrib><creatorcontrib>Freimuth, William W.</creatorcontrib><creatorcontrib>LBSL02/99 Study Group</creatorcontrib><creatorcontrib>on behalf of the LBSL02/99 Study Group</creatorcontrib><title>Long-term safety profile of belimumab plus standard therapy in patients with systemic lupus erythematosus</title><title>Arthritis & rheumatology (Hoboken, N.J.)</title><addtitle>Arthritis & Rheumatism</addtitle><description>Objective
To evaluate the safety profile of long‐term belimumab therapy combined with standard therapy for systemic lupus erythematosus (SLE) in patients with active disease.
Methods
Patients who were randomized to receive intravenous placebo or belimumab 1, 4, or 10 mg/kg, plus standard therapy, and completed the initial 52‐week double‐blind treatment period were then allowed to enter a 24‐week open‐label extension phase. During the extension period, patients in the belimumab group either received the same dose or were switched to 10 mg/kg and patients in the placebo group were switched to belimumab 10 mg/kg. Patients who achieved a satisfactory response during the 24‐week extension period were allowed to participate in the long‐term continuation study of monthly belimumab 10 mg/kg. Adverse events (AEs) and abnormal laboratory results were analyzed per 100 patient‐years in 1‐year intervals.
Results
Of the 364 patients who completed the 52‐week double‐blind treatment period, 345 entered the 24‐week extension, and 296 continued treatment with belimumab in the long‐term continuation study. Safety data through 4 years of belimumab exposure (1,165 cumulative patient‐years) are reported. Incidence rates of AEs, severe/serious AEs, infusion reactions, infections, malignancies, grades 3/4 laboratory abnormalities, and discontinuations due to AEs were stable or declined during 4‐year belimumab exposure. The most common AEs included arthralgia, upper respiratory tract infection, headache, fatigue, and nausea. Serious infusion reactions were rare: only 1 occurred during the 4‐year followup period. Rates of serious infection decreased from 5.9/100 patient‐years to 3.4/100 patient‐years, and no specific type of infection predominated.
Conclusion
Belimumab added to standard therapy was generally well‐tolerated over the 4‐year treatment period in patients with SLE, which suggests that belimumab can be administered long term with an acceptable safety profile.</description><subject>Adrenal Cortex Hormones - therapeutic use</subject><subject>Adult</subject><subject>Antibodies, Monoclonal - adverse effects</subject><subject>Antibodies, Monoclonal - therapeutic use</subject><subject>Antibodies, Monoclonal, Humanized</subject><subject>Biological and medical sciences</subject><subject>Diseases of the osteoarticular system</subject><subject>Double-Blind Method</subject><subject>Drug therapy</subject><subject>Drug Therapy, Combination</subject><subject>Female</subject><subject>Humans</subject><subject>Immunomodulators</subject><subject>Immunosuppressive Agents - adverse effects</subject><subject>Immunosuppressive Agents - therapeutic use</subject><subject>Infections</subject><subject>Lupus</subject><subject>Lupus Erythematosus, Systemic - drug therapy</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Patients</subject><subject>Pharmacology. Drug treatments</subject><subject>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</subject><subject>Treatment Outcome</subject><issn>0004-3591</issn><issn>2326-5191</issn><issn>1529-0131</issn><issn>2326-5205</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10V1rFDEUBuAgit1WL_wDEhBBL6bNxySZXNaiW2FRqBW9C2cziU2dryYZ2vn3RndbQfAqJDznJHkPQi8oOaaEsBOI-ZjXQtaP0IoKpitCOX2MVoSQuuJC0wN0mNJ12TIu-FN0wJhUdS3UCoXNOPyosos9TuBdXvAURx86h0ePt64L_dzDFk_dnHDKMLQQW5yvXIRpwWHAE-TghpzwbchXOC0puz5Y3M1TKXBxKbSHPKY5PUNPPHTJPd-vR-jrh_eXZ-fV5vP649npprI1o3UFjfYgvdoya6W3rSqnreCM0tZJq6SuJQOqW-YaqYEz7jS0UlveaOZ8A_wIvdn1LR-5mV3Kpg_Juq6DwY1zMpQ0tFGM8abQV__Q63GOQ3mdoYIqorUWuqi3O2XjmFJ03kwx9BCX0sr8zt-U_M2f_It9ue84b3vXPsj7wAt4vQeQLHQ-wmBD-uuk5EJoWdzJzt2WWSz_v9GcXlzeX13tKkKZwd1DBcSfRiquhPn2aW2-X-j1uy_k3FD-CwP5rEk</recordid><startdate>201210</startdate><enddate>201210</enddate><creator>Merrill, Joan T.</creator><creator>Ginzler, Ellen M.</creator><creator>Wallace, Daniel J.</creator><creator>McKay, James D.</creator><creator>Lisse, Jeffrey R.</creator><creator>Aranow, Cynthia</creator><creator>Wellborne, Frank R.</creator><creator>Burnette, Michael</creator><creator>Condemi, John</creator><creator>Zhong, Z. John</creator><creator>Pineda, Lilia</creator><creator>Klein, Jerry</creator><creator>Freimuth, William W.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</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>7QL</scope><scope>7QP</scope><scope>7T5</scope><scope>7TM</scope><scope>7U7</scope><scope>C1K</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>201210</creationdate><title>Long-term safety profile of belimumab plus standard therapy in patients with systemic lupus erythematosus</title><author>Merrill, Joan T. ; Ginzler, Ellen M. ; Wallace, Daniel J. ; McKay, James D. ; Lisse, Jeffrey R. ; Aranow, Cynthia ; Wellborne, Frank R. ; Burnette, Michael ; Condemi, John ; Zhong, Z. John ; Pineda, Lilia ; Klein, Jerry ; Freimuth, William W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4214-a89fa6f7b2cc6fcd7421d53211de6c769462a19d2e869a323e9ad69c3892ef8a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adrenal Cortex Hormones - therapeutic use</topic><topic>Adult</topic><topic>Antibodies, Monoclonal - adverse effects</topic><topic>Antibodies, Monoclonal - therapeutic use</topic><topic>Antibodies, Monoclonal, Humanized</topic><topic>Biological and medical sciences</topic><topic>Diseases of the osteoarticular system</topic><topic>Double-Blind Method</topic><topic>Drug therapy</topic><topic>Drug Therapy, Combination</topic><topic>Female</topic><topic>Humans</topic><topic>Immunomodulators</topic><topic>Immunosuppressive Agents - adverse effects</topic><topic>Immunosuppressive Agents - therapeutic use</topic><topic>Infections</topic><topic>Lupus</topic><topic>Lupus Erythematosus, Systemic - drug therapy</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Patients</topic><topic>Pharmacology. Drug treatments</topic><topic>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Merrill, Joan T.</creatorcontrib><creatorcontrib>Ginzler, Ellen M.</creatorcontrib><creatorcontrib>Wallace, Daniel J.</creatorcontrib><creatorcontrib>McKay, James D.</creatorcontrib><creatorcontrib>Lisse, Jeffrey R.</creatorcontrib><creatorcontrib>Aranow, Cynthia</creatorcontrib><creatorcontrib>Wellborne, Frank R.</creatorcontrib><creatorcontrib>Burnette, Michael</creatorcontrib><creatorcontrib>Condemi, John</creatorcontrib><creatorcontrib>Zhong, Z. John</creatorcontrib><creatorcontrib>Pineda, Lilia</creatorcontrib><creatorcontrib>Klein, Jerry</creatorcontrib><creatorcontrib>Freimuth, William W.</creatorcontrib><creatorcontrib>LBSL02/99 Study Group</creatorcontrib><creatorcontrib>on behalf of the LBSL02/99 Study Group</creatorcontrib><collection>Istex</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>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Arthritis & rheumatology (Hoboken, N.J.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Merrill, Joan T.</au><au>Ginzler, Ellen M.</au><au>Wallace, Daniel J.</au><au>McKay, James D.</au><au>Lisse, Jeffrey R.</au><au>Aranow, Cynthia</au><au>Wellborne, Frank R.</au><au>Burnette, Michael</au><au>Condemi, John</au><au>Zhong, Z. John</au><au>Pineda, Lilia</au><au>Klein, Jerry</au><au>Freimuth, William W.</au><aucorp>LBSL02/99 Study Group</aucorp><aucorp>on behalf of the LBSL02/99 Study Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Long-term safety profile of belimumab plus standard therapy in patients with systemic lupus erythematosus</atitle><jtitle>Arthritis & rheumatology (Hoboken, N.J.)</jtitle><addtitle>Arthritis & Rheumatism</addtitle><date>2012-10</date><risdate>2012</risdate><volume>64</volume><issue>10</issue><spage>3364</spage><epage>3373</epage><pages>3364-3373</pages><issn>0004-3591</issn><issn>2326-5191</issn><eissn>1529-0131</eissn><eissn>2326-5205</eissn><coden>ARHEAW</coden><abstract>Objective
To evaluate the safety profile of long‐term belimumab therapy combined with standard therapy for systemic lupus erythematosus (SLE) in patients with active disease.
Methods
Patients who were randomized to receive intravenous placebo or belimumab 1, 4, or 10 mg/kg, plus standard therapy, and completed the initial 52‐week double‐blind treatment period were then allowed to enter a 24‐week open‐label extension phase. During the extension period, patients in the belimumab group either received the same dose or were switched to 10 mg/kg and patients in the placebo group were switched to belimumab 10 mg/kg. Patients who achieved a satisfactory response during the 24‐week extension period were allowed to participate in the long‐term continuation study of monthly belimumab 10 mg/kg. Adverse events (AEs) and abnormal laboratory results were analyzed per 100 patient‐years in 1‐year intervals.
Results
Of the 364 patients who completed the 52‐week double‐blind treatment period, 345 entered the 24‐week extension, and 296 continued treatment with belimumab in the long‐term continuation study. Safety data through 4 years of belimumab exposure (1,165 cumulative patient‐years) are reported. Incidence rates of AEs, severe/serious AEs, infusion reactions, infections, malignancies, grades 3/4 laboratory abnormalities, and discontinuations due to AEs were stable or declined during 4‐year belimumab exposure. The most common AEs included arthralgia, upper respiratory tract infection, headache, fatigue, and nausea. Serious infusion reactions were rare: only 1 occurred during the 4‐year followup period. Rates of serious infection decreased from 5.9/100 patient‐years to 3.4/100 patient‐years, and no specific type of infection predominated.
Conclusion
Belimumab added to standard therapy was generally well‐tolerated over the 4‐year treatment period in patients with SLE, which suggests that belimumab can be administered long term with an acceptable safety profile.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>22674457</pmid><doi>10.1002/art.34564</doi><tpages>10</tpages></addata></record> |
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subjects | Adrenal Cortex Hormones - therapeutic use Adult Antibodies, Monoclonal - adverse effects Antibodies, Monoclonal - therapeutic use Antibodies, Monoclonal, Humanized Biological and medical sciences Diseases of the osteoarticular system Double-Blind Method Drug therapy Drug Therapy, Combination Female Humans Immunomodulators Immunosuppressive Agents - adverse effects Immunosuppressive Agents - therapeutic use Infections Lupus Lupus Erythematosus, Systemic - drug therapy Male Medical sciences Middle Aged Patients Pharmacology. Drug treatments Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis Treatment Outcome |
title | Long-term safety profile of belimumab plus standard therapy in patients with systemic lupus erythematosus |
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