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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Veröffentlicht in:Arthritis & rheumatology (Hoboken, N.J.) N.J.), 2012-10, Vol.64 (10), p.3364-3373
Hauptverfasser: 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.
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container_end_page 3373
container_issue 10
container_start_page 3364
container_title Arthritis & rheumatology (Hoboken, N.J.)
container_volume 64
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
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John ; Pineda, Lilia ; Klein, Jerry ; Freimuth, William W.</creator><creatorcontrib>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. ; LBSL02/99 Study Group ; on behalf of the LBSL02/99 Study Group</creatorcontrib><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><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. 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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 &amp; rheumatology (Hoboken, N.J.)</title><addtitle>Arthritis &amp; 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 &amp; 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 &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Arthritis &amp; 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 &amp; rheumatology (Hoboken, N.J.)</jtitle><addtitle>Arthritis &amp; 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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