Azathioprine or Methotrexate Maintenance for ANCA-Associated Vasculitis
Current standard therapy for Wegener's granulomatosis and microscopic polyangiitis combines corticosteroids and cyclophosphamide to induce remission, followed by a less toxic immunosuppressant. This prospective, open-label, multicenter trial indicated that the safety and efficacy of azathioprin...
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creator | Pagnoux, Christian Mahr, Alfred Hamidou, Mohamed A Boffa, Jean-Jacques Ruivard, Marc Ducroix, Jean-Pierre Kyndt, Xavier Lifermann, François Papo, Thomas Lambert, Marc Le Noach, José Khellaf, Mehdi Merrien, Dominique Puéchal, Xavier Vinzio, Stéphane Cohen, Pascal Mouthon, Luc Cordier, Jean-François Guillevin, Loïc |
description | Current standard therapy for Wegener's granulomatosis and microscopic polyangiitis combines corticosteroids and cyclophosphamide to induce remission, followed by a less toxic immunosuppressant. This prospective, open-label, multicenter trial indicated that the safety and efficacy of azathioprine and methotrexate are similar for maintenance therapy after initial remission in these two conditions.
This trial indicated that the safety and efficacy of azathioprine and methotrexate are similar for maintenance therapy after initial remission in Wegener's granulomatosis and microscopic polyangiitis.
Combined corticosteroid and cyclophosphamide therapy remains the standard care for antineutrophil cytoplasmic antibody (ANCA)–associated vasculitides, despite the potential risk of adverse events, particularly with the long-term use of cyclophosphamide.
1
,
2
Moreover, even after induction with daily oral or pulse intravenous cyclophosphamide therapy, relapse rates remain as high as 15% at 12 months
3
and reach 38% at 30 months.
4
A decisive step in the approach to the treatment of Wegener's granulomatosis and microscopic polyangiitis was the development of a staged induction–maintenance strategy to reduce cumulative exposure to cyclophosphamide. This strategy uses cyclophosphamide to induce remission, followed by a less toxic immunosuppressant. . . . |
doi_str_mv | 10.1056/NEJMoa0802311 |
format | Article |
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This trial indicated that the safety and efficacy of azathioprine and methotrexate are similar for maintenance therapy after initial remission in Wegener's granulomatosis and microscopic polyangiitis.
Combined corticosteroid and cyclophosphamide therapy remains the standard care for antineutrophil cytoplasmic antibody (ANCA)–associated vasculitides, despite the potential risk of adverse events, particularly with the long-term use of cyclophosphamide.
1
,
2
Moreover, even after induction with daily oral or pulse intravenous cyclophosphamide therapy, relapse rates remain as high as 15% at 12 months
3
and reach 38% at 30 months.
4
A decisive step in the approach to the treatment of Wegener's granulomatosis and microscopic polyangiitis was the development of a staged induction–maintenance strategy to reduce cumulative exposure to cyclophosphamide. This strategy uses cyclophosphamide to induce remission, followed by a less toxic immunosuppressant. . . .</description><identifier>ISSN: 0028-4793</identifier><identifier>EISSN: 1533-4406</identifier><identifier>DOI: 10.1056/NEJMoa0802311</identifier><identifier>PMID: 19109574</identifier><identifier>CODEN: NEJMAG</identifier><language>eng</language><publisher>Waltham, MA: Massachusetts Medical Society</publisher><subject>Adult ; Aged ; Antibodies, Antineutrophil Cytoplasmic ; Azathioprine - adverse effects ; Azathioprine - therapeutic use ; Biological and medical sciences ; Clinical trials ; Cyclophosphamide - administration & dosage ; Cyclophosphamide - therapeutic use ; Drug Therapy, Combination ; Female ; General aspects ; Glucocorticoids - administration & dosage ; Glucocorticoids - therapeutic use ; Granulomatosis with Polyangiitis - drug therapy ; Granulomatosis with Polyangiitis - immunology ; Humans ; Immunosuppressive Agents - administration & dosage ; Immunosuppressive Agents - adverse effects ; Immunosuppressive Agents - therapeutic use ; Kaplan-Meier Estimate ; Male ; Medical research ; Medical sciences ; Methotrexate - adverse effects ; Methotrexate - therapeutic use ; Methylprednisolone - administration & dosage ; Methylprednisolone - therapeutic use ; Middle Aged ; Prednisone - administration & dosage ; Prednisone - therapeutic use ; Prospective Studies ; Pulse Therapy, Drug ; Remission Induction ; Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis ; Vasculitis - drug therapy ; Vasculitis - immunology ; Young Adult</subject><ispartof>The New England journal of medicine, 2008-12, Vol.359 (26), p.2790-2803</ispartof><rights>Copyright © 2008 Massachusetts Medical Society. All rights reserved.</rights><rights>2009 INIST-CNRS</rights><rights>2008 Massachusetts Medical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c535t-dfe8b4b4e6a01f44e41e94920dd8c78ed1e4c51ee78c40b1ac23e971991e6af23</citedby><cites>FETCH-LOGICAL-c535t-dfe8b4b4e6a01f44e41e94920dd8c78ed1e4c51ee78c40b1ac23e971991e6af23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.nejm.org/doi/pdf/10.1056/NEJMoa0802311$$EPDF$$P50$$Gmms$$H</linktopdf><linktohtml>$$Uhttps://www.nejm.org/doi/full/10.1056/NEJMoa0802311$$EHTML$$P50$$Gmms$$H</linktohtml><link.rule.ids>314,776,780,2746,2747,26080,27901,27902,52357,54039</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20966482$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19109574$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Pagnoux, Christian</creatorcontrib><creatorcontrib>Mahr, Alfred</creatorcontrib><creatorcontrib>Hamidou, Mohamed A</creatorcontrib><creatorcontrib>Boffa, Jean-Jacques</creatorcontrib><creatorcontrib>Ruivard, Marc</creatorcontrib><creatorcontrib>Ducroix, Jean-Pierre</creatorcontrib><creatorcontrib>Kyndt, Xavier</creatorcontrib><creatorcontrib>Lifermann, François</creatorcontrib><creatorcontrib>Papo, Thomas</creatorcontrib><creatorcontrib>Lambert, Marc</creatorcontrib><creatorcontrib>Le Noach, José</creatorcontrib><creatorcontrib>Khellaf, Mehdi</creatorcontrib><creatorcontrib>Merrien, Dominique</creatorcontrib><creatorcontrib>Puéchal, Xavier</creatorcontrib><creatorcontrib>Vinzio, Stéphane</creatorcontrib><creatorcontrib>Cohen, Pascal</creatorcontrib><creatorcontrib>Mouthon, Luc</creatorcontrib><creatorcontrib>Cordier, Jean-François</creatorcontrib><creatorcontrib>Guillevin, Loïc</creatorcontrib><creatorcontrib>French Vasculitis Study Group</creatorcontrib><title>Azathioprine or Methotrexate Maintenance for ANCA-Associated Vasculitis</title><title>The New England journal of medicine</title><addtitle>N Engl J Med</addtitle><description>Current standard therapy for Wegener's granulomatosis and microscopic polyangiitis combines corticosteroids and cyclophosphamide to induce remission, followed by a less toxic immunosuppressant. This prospective, open-label, multicenter trial indicated that the safety and efficacy of azathioprine and methotrexate are similar for maintenance therapy after initial remission in these two conditions.
This trial indicated that the safety and efficacy of azathioprine and methotrexate are similar for maintenance therapy after initial remission in Wegener's granulomatosis and microscopic polyangiitis.
Combined corticosteroid and cyclophosphamide therapy remains the standard care for antineutrophil cytoplasmic antibody (ANCA)–associated vasculitides, despite the potential risk of adverse events, particularly with the long-term use of cyclophosphamide.
1
,
2
Moreover, even after induction with daily oral or pulse intravenous cyclophosphamide therapy, relapse rates remain as high as 15% at 12 months
3
and reach 38% at 30 months.
4
A decisive step in the approach to the treatment of Wegener's granulomatosis and microscopic polyangiitis was the development of a staged induction–maintenance strategy to reduce cumulative exposure to cyclophosphamide. This strategy uses cyclophosphamide to induce remission, followed by a less toxic immunosuppressant. . . .</description><subject>Adult</subject><subject>Aged</subject><subject>Antibodies, Antineutrophil Cytoplasmic</subject><subject>Azathioprine - adverse effects</subject><subject>Azathioprine - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Clinical trials</subject><subject>Cyclophosphamide - administration & dosage</subject><subject>Cyclophosphamide - therapeutic use</subject><subject>Drug Therapy, Combination</subject><subject>Female</subject><subject>General aspects</subject><subject>Glucocorticoids - administration & dosage</subject><subject>Glucocorticoids - therapeutic use</subject><subject>Granulomatosis with Polyangiitis - drug therapy</subject><subject>Granulomatosis with Polyangiitis - immunology</subject><subject>Humans</subject><subject>Immunosuppressive Agents - administration & dosage</subject><subject>Immunosuppressive Agents - adverse effects</subject><subject>Immunosuppressive Agents - therapeutic use</subject><subject>Kaplan-Meier Estimate</subject><subject>Male</subject><subject>Medical research</subject><subject>Medical sciences</subject><subject>Methotrexate - adverse effects</subject><subject>Methotrexate - therapeutic use</subject><subject>Methylprednisolone - administration & dosage</subject><subject>Methylprednisolone - therapeutic use</subject><subject>Middle Aged</subject><subject>Prednisone - administration & dosage</subject><subject>Prednisone - therapeutic use</subject><subject>Prospective Studies</subject><subject>Pulse Therapy, Drug</subject><subject>Remission Induction</subject><subject>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</subject><subject>Vasculitis - drug therapy</subject><subject>Vasculitis - immunology</subject><subject>Young Adult</subject><issn>0028-4793</issn><issn>1533-4406</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp1kDFPwzAQhS0EoqUwsqIIiTHgs53EHqOqFFBbFmCNHOeipmqSYicS8OsxakTFwC033Hfv6T1CLoHeAo3iu9XsadlqKinjAEdkDBHnoRA0PiZjSpkMRaL4iJw5t6F-QKhTMgIFVEWJGJN5-qW7ddXubNVg0Npgid267Sx-6A6Dpa6aDhvdGAxKf0xX0zRMnWtN5c9F8Kad6bdVV7lzclLqrcOLYU_I6_3sZfoQLp7nj9N0EZqIR11YlChzkQuMNYVSCBSASihGi0KaRGIBKEwEiIk0guagDeOoElAK_EvJ-IRc73V3tn3v0XXZpu1t4y0zxrgCEcvEQ-EeMrZ1zmKZ-Xi1tp8Z0OyntexPa56_GkT7vMbiQA81eeBmAHxgvS2tb6RyvxyjKo6FZAeurl3W4Kb-x_AbyKh_vg</recordid><startdate>20081225</startdate><enddate>20081225</enddate><creator>Pagnoux, Christian</creator><creator>Mahr, Alfred</creator><creator>Hamidou, Mohamed A</creator><creator>Boffa, Jean-Jacques</creator><creator>Ruivard, Marc</creator><creator>Ducroix, Jean-Pierre</creator><creator>Kyndt, Xavier</creator><creator>Lifermann, François</creator><creator>Papo, Thomas</creator><creator>Lambert, Marc</creator><creator>Le Noach, José</creator><creator>Khellaf, Mehdi</creator><creator>Merrien, Dominique</creator><creator>Puéchal, Xavier</creator><creator>Vinzio, Stéphane</creator><creator>Cohen, Pascal</creator><creator>Mouthon, Luc</creator><creator>Cordier, Jean-François</creator><creator>Guillevin, Loïc</creator><general>Massachusetts Medical Society</general><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>0TZ</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BEC</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K0Y</scope><scope>LK8</scope><scope>M0R</scope><scope>M0T</scope><scope>M1P</scope><scope>M2M</scope><scope>M2O</scope><scope>M2P</scope><scope>M7P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope></search><sort><creationdate>20081225</creationdate><title>Azathioprine or Methotrexate Maintenance for ANCA-Associated Vasculitis</title><author>Pagnoux, Christian ; Mahr, Alfred ; Hamidou, Mohamed A ; Boffa, Jean-Jacques ; Ruivard, Marc ; Ducroix, Jean-Pierre ; Kyndt, Xavier ; Lifermann, François ; Papo, Thomas ; Lambert, Marc ; Le Noach, José ; Khellaf, Mehdi ; Merrien, Dominique ; Puéchal, Xavier ; Vinzio, Stéphane ; Cohen, Pascal ; Mouthon, Luc ; Cordier, Jean-François ; Guillevin, Loïc</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c535t-dfe8b4b4e6a01f44e41e94920dd8c78ed1e4c51ee78c40b1ac23e971991e6af23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antibodies, Antineutrophil Cytoplasmic</topic><topic>Azathioprine - adverse effects</topic><topic>Azathioprine - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Clinical trials</topic><topic>Cyclophosphamide - administration & dosage</topic><topic>Cyclophosphamide - therapeutic use</topic><topic>Drug Therapy, Combination</topic><topic>Female</topic><topic>General aspects</topic><topic>Glucocorticoids - administration & dosage</topic><topic>Glucocorticoids - therapeutic use</topic><topic>Granulomatosis with Polyangiitis - drug therapy</topic><topic>Granulomatosis with Polyangiitis - immunology</topic><topic>Humans</topic><topic>Immunosuppressive Agents - administration & dosage</topic><topic>Immunosuppressive Agents - adverse effects</topic><topic>Immunosuppressive Agents - therapeutic use</topic><topic>Kaplan-Meier Estimate</topic><topic>Male</topic><topic>Medical research</topic><topic>Medical sciences</topic><topic>Methotrexate - adverse effects</topic><topic>Methotrexate - therapeutic use</topic><topic>Methylprednisolone - administration & dosage</topic><topic>Methylprednisolone - therapeutic use</topic><topic>Middle Aged</topic><topic>Prednisone - administration & dosage</topic><topic>Prednisone - therapeutic use</topic><topic>Prospective Studies</topic><topic>Pulse Therapy, Drug</topic><topic>Remission Induction</topic><topic>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</topic><topic>Vasculitis - drug therapy</topic><topic>Vasculitis - immunology</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Pagnoux, Christian</creatorcontrib><creatorcontrib>Mahr, Alfred</creatorcontrib><creatorcontrib>Hamidou, Mohamed A</creatorcontrib><creatorcontrib>Boffa, Jean-Jacques</creatorcontrib><creatorcontrib>Ruivard, Marc</creatorcontrib><creatorcontrib>Ducroix, Jean-Pierre</creatorcontrib><creatorcontrib>Kyndt, Xavier</creatorcontrib><creatorcontrib>Lifermann, François</creatorcontrib><creatorcontrib>Papo, Thomas</creatorcontrib><creatorcontrib>Lambert, Marc</creatorcontrib><creatorcontrib>Le Noach, José</creatorcontrib><creatorcontrib>Khellaf, Mehdi</creatorcontrib><creatorcontrib>Merrien, Dominique</creatorcontrib><creatorcontrib>Puéchal, Xavier</creatorcontrib><creatorcontrib>Vinzio, Stéphane</creatorcontrib><creatorcontrib>Cohen, Pascal</creatorcontrib><creatorcontrib>Mouthon, Luc</creatorcontrib><creatorcontrib>Cordier, Jean-François</creatorcontrib><creatorcontrib>Guillevin, Loïc</creatorcontrib><creatorcontrib>French Vasculitis Study Group</creatorcontrib><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>Pharma and Biotech Premium PRO</collection><collection>Proquest Nursing & Allied Health Source</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>British Nursing Database</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>eLibrary</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>New England Journal of Medicine</collection><collection>ProQuest Biological Science Collection</collection><collection>Consumer Health Database</collection><collection>Healthcare Administration Database</collection><collection>Medical Database</collection><collection>ProQuest Psychology</collection><collection>Research Library</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><jtitle>The New England journal of medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Pagnoux, Christian</au><au>Mahr, Alfred</au><au>Hamidou, Mohamed A</au><au>Boffa, Jean-Jacques</au><au>Ruivard, Marc</au><au>Ducroix, Jean-Pierre</au><au>Kyndt, Xavier</au><au>Lifermann, François</au><au>Papo, Thomas</au><au>Lambert, Marc</au><au>Le Noach, José</au><au>Khellaf, Mehdi</au><au>Merrien, Dominique</au><au>Puéchal, Xavier</au><au>Vinzio, Stéphane</au><au>Cohen, Pascal</au><au>Mouthon, Luc</au><au>Cordier, Jean-François</au><au>Guillevin, Loïc</au><aucorp>French Vasculitis Study Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Azathioprine or Methotrexate Maintenance for ANCA-Associated Vasculitis</atitle><jtitle>The New England journal of medicine</jtitle><addtitle>N Engl J Med</addtitle><date>2008-12-25</date><risdate>2008</risdate><volume>359</volume><issue>26</issue><spage>2790</spage><epage>2803</epage><pages>2790-2803</pages><issn>0028-4793</issn><eissn>1533-4406</eissn><coden>NEJMAG</coden><abstract>Current standard therapy for Wegener's granulomatosis and microscopic polyangiitis combines corticosteroids and cyclophosphamide to induce remission, followed by a less toxic immunosuppressant. This prospective, open-label, multicenter trial indicated that the safety and efficacy of azathioprine and methotrexate are similar for maintenance therapy after initial remission in these two conditions.
This trial indicated that the safety and efficacy of azathioprine and methotrexate are similar for maintenance therapy after initial remission in Wegener's granulomatosis and microscopic polyangiitis.
Combined corticosteroid and cyclophosphamide therapy remains the standard care for antineutrophil cytoplasmic antibody (ANCA)–associated vasculitides, despite the potential risk of adverse events, particularly with the long-term use of cyclophosphamide.
1
,
2
Moreover, even after induction with daily oral or pulse intravenous cyclophosphamide therapy, relapse rates remain as high as 15% at 12 months
3
and reach 38% at 30 months.
4
A decisive step in the approach to the treatment of Wegener's granulomatosis and microscopic polyangiitis was the development of a staged induction–maintenance strategy to reduce cumulative exposure to cyclophosphamide. This strategy uses cyclophosphamide to induce remission, followed by a less toxic immunosuppressant. . . .</abstract><cop>Waltham, MA</cop><pub>Massachusetts Medical Society</pub><pmid>19109574</pmid><doi>10.1056/NEJMoa0802311</doi><tpages>14</tpages></addata></record> |
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subjects | Adult Aged Antibodies, Antineutrophil Cytoplasmic Azathioprine - adverse effects Azathioprine - therapeutic use Biological and medical sciences Clinical trials Cyclophosphamide - administration & dosage Cyclophosphamide - therapeutic use Drug Therapy, Combination Female General aspects Glucocorticoids - administration & dosage Glucocorticoids - therapeutic use Granulomatosis with Polyangiitis - drug therapy Granulomatosis with Polyangiitis - immunology Humans Immunosuppressive Agents - administration & dosage Immunosuppressive Agents - adverse effects Immunosuppressive Agents - therapeutic use Kaplan-Meier Estimate Male Medical research Medical sciences Methotrexate - adverse effects Methotrexate - therapeutic use Methylprednisolone - administration & dosage Methylprednisolone - therapeutic use Middle Aged Prednisone - administration & dosage Prednisone - therapeutic use Prospective Studies Pulse Therapy, Drug Remission Induction Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis Vasculitis - drug therapy Vasculitis - immunology Young Adult |
title | Azathioprine or Methotrexate Maintenance for ANCA-Associated Vasculitis |
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