Withdrawal of Immunosuppression in Crohn's Disease Treated With Scheduled Infliximab Maintenance: A Randomized Trial
Background & Aims: The benefit to risk ratio of concomitant immunosuppressives with scheduled infliximab (IFX) maintenance therapy for Crohn's disease is an issue of debate. We aimed to study the influence of immunosuppressives discontinuation in patients in remission with combination thera...
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Veröffentlicht in: | Gastroenterology (New York, N.Y. 1943) N.Y. 1943), 2008-06, Vol.134 (7), p.1861-1868 |
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creator | Van Assche, Gert Magdelaine–Beuzelin, Charlotte D'Haens, Geert Baert, Filip Noman, Maja Vermeire, Séverine Ternant, David Watier, Hervé Paintaud, Gilles Rutgeerts, Paul |
description | Background & Aims: The benefit to risk ratio of concomitant immunosuppressives with scheduled infliximab (IFX) maintenance therapy for Crohn's disease is an issue of debate. We aimed to study the influence of immunosuppressives discontinuation in patients in remission with combination therapy in an open-label, randomized, controlled trial. Methods: Patients with controlled disease ≥6 months after the start of IFX (5 mg/kg intravenously) combined with immunosuppressives were randomized to continue (Con) or to interrupt (Dis) immunosuppressives, while all patients received scheduled IFX maintenance therapy for 104 weeks. Primary end point was the proportion of patients who required a decrease in IFX dosing interval or stopped IFX therapy. Secondary end points included IFX trough levels, safety, and mucosal healing. Results: A similar proportion (24/40, 60% Con) and (22/40, 55% Dis) of patients needed a change in IFX dosing interval or stopped IFX therapy (11/40 Con, 9/40 Dis). C-reactive protein (CRP) was higher and IFX trough levels were lower in the Dis group (Dis: CRP, 2.8 mg/L; interquartile range [IQR], 1.0–8.0; Con: CRP, 1.6 mg/L; IQR, 1.0–5.6, P < .005; trough IFX: Dis: 1.65 μg/mL; IQR, 0.54–3.68; Con: 2.87 μg/mL; IQR, 1.35–4.72, P < .0001). Low IFX trough levels correlated with increased CRP and clinical score. Mucosal ulcers were absent at week 104 in 64% (Con) and 61% (Dis) of evaluated patients with ongoing response to IFX. Conclusions: Continuation of immunosuppressives beyond 6 months offers no clear benefit over scheduled IFX monotherapy but is associated with higher median IFX trough and decreased CRP levels. The impact of these observations on long-term outcomes needs to be explored further. |
doi_str_mv | 10.1053/j.gastro.2008.03.004 |
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We aimed to study the influence of immunosuppressives discontinuation in patients in remission with combination therapy in an open-label, randomized, controlled trial. Methods: Patients with controlled disease ≥6 months after the start of IFX (5 mg/kg intravenously) combined with immunosuppressives were randomized to continue (Con) or to interrupt (Dis) immunosuppressives, while all patients received scheduled IFX maintenance therapy for 104 weeks. Primary end point was the proportion of patients who required a decrease in IFX dosing interval or stopped IFX therapy. Secondary end points included IFX trough levels, safety, and mucosal healing. Results: A similar proportion (24/40, 60% Con) and (22/40, 55% Dis) of patients needed a change in IFX dosing interval or stopped IFX therapy (11/40 Con, 9/40 Dis). C-reactive protein (CRP) was higher and IFX trough levels were lower in the Dis group (Dis: CRP, 2.8 mg/L; interquartile range [IQR], 1.0–8.0; Con: CRP, 1.6 mg/L; IQR, 1.0–5.6, P < .005; trough IFX: Dis: 1.65 μg/mL; IQR, 0.54–3.68; Con: 2.87 μg/mL; IQR, 1.35–4.72, P < .0001). Low IFX trough levels correlated with increased CRP and clinical score. Mucosal ulcers were absent at week 104 in 64% (Con) and 61% (Dis) of evaluated patients with ongoing response to IFX. Conclusions: Continuation of immunosuppressives beyond 6 months offers no clear benefit over scheduled IFX monotherapy but is associated with higher median IFX trough and decreased CRP levels. The impact of these observations on long-term outcomes needs to be explored further.</description><identifier>ISSN: 0016-5085</identifier><identifier>EISSN: 1528-0012</identifier><identifier>DOI: 10.1053/j.gastro.2008.03.004</identifier><identifier>PMID: 18440315</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject><![CDATA[Adult ; Anti-Inflammatory Agents - administration & dosage ; Anti-Inflammatory Agents - adverse effects ; Anti-Inflammatory Agents - pharmacokinetics ; Antibodies, Monoclonal - administration & dosage ; Antibodies, Monoclonal - adverse effects ; Antibodies, Monoclonal - pharmacokinetics ; Azathioprine - administration & dosage ; Belgium ; C-Reactive Protein - metabolism ; Crohn Disease - drug therapy ; Crohn Disease - metabolism ; Crohn Disease - pathology ; Drug Administration Schedule ; Drug Therapy, Combination ; Female ; France ; Gastroenterology and Hepatology ; Gastrointestinal Agents - administration & dosage ; Gastrointestinal Agents - adverse effects ; Gastrointestinal Agents - pharmacokinetics ; Human health and pathology ; Humans ; Hépatology and Gastroenterology ; Immunosuppressive Agents - administration & dosage ; Infliximab ; Infusions, Intravenous ; Intestinal Mucosa - drug effects ; Intestinal Mucosa - pathology ; Life Sciences ; Male ; Mercaptopurine - administration & dosage ; Methotrexate - administration & dosage ; Middle Aged ; Prospective Studies ; Treatment Outcome]]></subject><ispartof>Gastroenterology (New York, N.Y. 1943), 2008-06, Vol.134 (7), p.1861-1868</ispartof><rights>AGA Institute</rights><rights>2008 AGA Institute</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c520t-b0b3dc78e905de2fff06c16e2308619990b71cac3038ee38f1b157d9af940e813</citedby><cites>FETCH-LOGICAL-c520t-b0b3dc78e905de2fff06c16e2308619990b71cac3038ee38f1b157d9af940e813</cites><orcidid>0000-0003-4020-4545 ; 0000-0002-2139-4171 ; 0000-0003-0158-1356</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0016508508004356$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18440315$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-00616945$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Van Assche, Gert</creatorcontrib><creatorcontrib>Magdelaine–Beuzelin, Charlotte</creatorcontrib><creatorcontrib>D'Haens, Geert</creatorcontrib><creatorcontrib>Baert, Filip</creatorcontrib><creatorcontrib>Noman, Maja</creatorcontrib><creatorcontrib>Vermeire, Séverine</creatorcontrib><creatorcontrib>Ternant, David</creatorcontrib><creatorcontrib>Watier, Hervé</creatorcontrib><creatorcontrib>Paintaud, Gilles</creatorcontrib><creatorcontrib>Rutgeerts, Paul</creatorcontrib><title>Withdrawal of Immunosuppression in Crohn's Disease Treated With Scheduled Infliximab Maintenance: A Randomized Trial</title><title>Gastroenterology (New York, N.Y. 1943)</title><addtitle>Gastroenterology</addtitle><description>Background & Aims: The benefit to risk ratio of concomitant immunosuppressives with scheduled infliximab (IFX) maintenance therapy for Crohn's disease is an issue of debate. We aimed to study the influence of immunosuppressives discontinuation in patients in remission with combination therapy in an open-label, randomized, controlled trial. Methods: Patients with controlled disease ≥6 months after the start of IFX (5 mg/kg intravenously) combined with immunosuppressives were randomized to continue (Con) or to interrupt (Dis) immunosuppressives, while all patients received scheduled IFX maintenance therapy for 104 weeks. Primary end point was the proportion of patients who required a decrease in IFX dosing interval or stopped IFX therapy. Secondary end points included IFX trough levels, safety, and mucosal healing. Results: A similar proportion (24/40, 60% Con) and (22/40, 55% Dis) of patients needed a change in IFX dosing interval or stopped IFX therapy (11/40 Con, 9/40 Dis). C-reactive protein (CRP) was higher and IFX trough levels were lower in the Dis group (Dis: CRP, 2.8 mg/L; interquartile range [IQR], 1.0–8.0; Con: CRP, 1.6 mg/L; IQR, 1.0–5.6, P < .005; trough IFX: Dis: 1.65 μg/mL; IQR, 0.54–3.68; Con: 2.87 μg/mL; IQR, 1.35–4.72, P < .0001). Low IFX trough levels correlated with increased CRP and clinical score. Mucosal ulcers were absent at week 104 in 64% (Con) and 61% (Dis) of evaluated patients with ongoing response to IFX. Conclusions: Continuation of immunosuppressives beyond 6 months offers no clear benefit over scheduled IFX monotherapy but is associated with higher median IFX trough and decreased CRP levels. The impact of these observations on long-term outcomes needs to be explored further.</description><subject>Adult</subject><subject>Anti-Inflammatory Agents - administration & dosage</subject><subject>Anti-Inflammatory Agents - adverse effects</subject><subject>Anti-Inflammatory Agents - pharmacokinetics</subject><subject>Antibodies, Monoclonal - administration & dosage</subject><subject>Antibodies, Monoclonal - adverse effects</subject><subject>Antibodies, Monoclonal - pharmacokinetics</subject><subject>Azathioprine - administration & dosage</subject><subject>Belgium</subject><subject>C-Reactive Protein - metabolism</subject><subject>Crohn Disease - drug therapy</subject><subject>Crohn Disease - metabolism</subject><subject>Crohn Disease - pathology</subject><subject>Drug Administration Schedule</subject><subject>Drug Therapy, Combination</subject><subject>Female</subject><subject>France</subject><subject>Gastroenterology and Hepatology</subject><subject>Gastrointestinal Agents - administration & dosage</subject><subject>Gastrointestinal Agents - adverse effects</subject><subject>Gastrointestinal Agents - pharmacokinetics</subject><subject>Human health and pathology</subject><subject>Humans</subject><subject>Hépatology and Gastroenterology</subject><subject>Immunosuppressive Agents - administration & dosage</subject><subject>Infliximab</subject><subject>Infusions, Intravenous</subject><subject>Intestinal Mucosa - drug effects</subject><subject>Intestinal Mucosa - pathology</subject><subject>Life Sciences</subject><subject>Male</subject><subject>Mercaptopurine - administration & dosage</subject><subject>Methotrexate - administration & dosage</subject><subject>Middle Aged</subject><subject>Prospective Studies</subject><subject>Treatment Outcome</subject><issn>0016-5085</issn><issn>1528-0012</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkk-P0zAQxSMEYsvCN0DIJxCHhnEcpw6HlaryZysVIbFFHC3HmVAXxy52srB8ehylAokLp5Gt33szmjdZ9pRCToGzV8f8q4pD8HkBIHJgOUB5L1tQXoglAC3uZ4tUqiUHwS-yRzEeAaBmgj7MLqgoS2CUL7LhixkObVA_lCW-I9u-H52P4-kUMEbjHTGObII_uBeRvDERVUSyD6gGbMkkJTf6gO1o03PrOmt-ml415IMybkCnnMbXZE0-Kdf63vxK0D4YZR9nDzplIz4518vs87u3-831cvfx_Xaz3i01L2BYNtCwVq8E1sBbLLqug0rTCgsGoqJ1XUOzolppBkwgMtHRhvJVW6uuLgEFZZfZy9n3oKw8hTRauJNeGXm93snpD6CiVV3y24l9PrOn4L-PGAfZm6jRWuXQj1GuaFXxGiCB5Qzq4GMM2P1xpiCnZORRzsnIKRkJLLUpk-zZ2X9semz_is5RJOBqBjBt5NZgkFEbTBtsTUA9yNab_3X410Bb44xW9hveYTz6Mbi0bUllLCTIm-k6puMAMal5xX4DAja2Fw</recordid><startdate>20080601</startdate><enddate>20080601</enddate><creator>Van Assche, Gert</creator><creator>Magdelaine–Beuzelin, Charlotte</creator><creator>D'Haens, Geert</creator><creator>Baert, Filip</creator><creator>Noman, Maja</creator><creator>Vermeire, Séverine</creator><creator>Ternant, David</creator><creator>Watier, Hervé</creator><creator>Paintaud, Gilles</creator><creator>Rutgeerts, Paul</creator><general>Elsevier Inc</general><general>Elsevier</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>1XC</scope><orcidid>https://orcid.org/0000-0003-4020-4545</orcidid><orcidid>https://orcid.org/0000-0002-2139-4171</orcidid><orcidid>https://orcid.org/0000-0003-0158-1356</orcidid></search><sort><creationdate>20080601</creationdate><title>Withdrawal of Immunosuppression in Crohn's Disease Treated With Scheduled Infliximab Maintenance: A Randomized Trial</title><author>Van Assche, Gert ; Magdelaine–Beuzelin, Charlotte ; D'Haens, Geert ; Baert, Filip ; Noman, Maja ; Vermeire, Séverine ; Ternant, David ; Watier, Hervé ; Paintaud, Gilles ; Rutgeerts, Paul</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c520t-b0b3dc78e905de2fff06c16e2308619990b71cac3038ee38f1b157d9af940e813</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Adult</topic><topic>Anti-Inflammatory Agents - administration & dosage</topic><topic>Anti-Inflammatory Agents - adverse effects</topic><topic>Anti-Inflammatory Agents - pharmacokinetics</topic><topic>Antibodies, Monoclonal - administration & dosage</topic><topic>Antibodies, Monoclonal - adverse effects</topic><topic>Antibodies, Monoclonal - pharmacokinetics</topic><topic>Azathioprine - administration & dosage</topic><topic>Belgium</topic><topic>C-Reactive Protein - metabolism</topic><topic>Crohn Disease - drug therapy</topic><topic>Crohn Disease - metabolism</topic><topic>Crohn Disease - pathology</topic><topic>Drug Administration Schedule</topic><topic>Drug Therapy, Combination</topic><topic>Female</topic><topic>France</topic><topic>Gastroenterology and Hepatology</topic><topic>Gastrointestinal Agents - administration & dosage</topic><topic>Gastrointestinal Agents - adverse effects</topic><topic>Gastrointestinal Agents - pharmacokinetics</topic><topic>Human health and pathology</topic><topic>Humans</topic><topic>Hépatology and Gastroenterology</topic><topic>Immunosuppressive Agents - administration & dosage</topic><topic>Infliximab</topic><topic>Infusions, Intravenous</topic><topic>Intestinal Mucosa - drug effects</topic><topic>Intestinal Mucosa - pathology</topic><topic>Life Sciences</topic><topic>Male</topic><topic>Mercaptopurine - administration & dosage</topic><topic>Methotrexate - administration & dosage</topic><topic>Middle Aged</topic><topic>Prospective Studies</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Van Assche, Gert</creatorcontrib><creatorcontrib>Magdelaine–Beuzelin, Charlotte</creatorcontrib><creatorcontrib>D'Haens, Geert</creatorcontrib><creatorcontrib>Baert, Filip</creatorcontrib><creatorcontrib>Noman, Maja</creatorcontrib><creatorcontrib>Vermeire, Séverine</creatorcontrib><creatorcontrib>Ternant, David</creatorcontrib><creatorcontrib>Watier, Hervé</creatorcontrib><creatorcontrib>Paintaud, Gilles</creatorcontrib><creatorcontrib>Rutgeerts, Paul</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>Hyper Article en Ligne (HAL)</collection><jtitle>Gastroenterology (New York, N.Y. 1943)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Van Assche, Gert</au><au>Magdelaine–Beuzelin, Charlotte</au><au>D'Haens, Geert</au><au>Baert, Filip</au><au>Noman, Maja</au><au>Vermeire, Séverine</au><au>Ternant, David</au><au>Watier, Hervé</au><au>Paintaud, Gilles</au><au>Rutgeerts, Paul</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Withdrawal of Immunosuppression in Crohn's Disease Treated With Scheduled Infliximab Maintenance: A Randomized Trial</atitle><jtitle>Gastroenterology (New York, N.Y. 1943)</jtitle><addtitle>Gastroenterology</addtitle><date>2008-06-01</date><risdate>2008</risdate><volume>134</volume><issue>7</issue><spage>1861</spage><epage>1868</epage><pages>1861-1868</pages><issn>0016-5085</issn><eissn>1528-0012</eissn><abstract>Background & Aims: The benefit to risk ratio of concomitant immunosuppressives with scheduled infliximab (IFX) maintenance therapy for Crohn's disease is an issue of debate. We aimed to study the influence of immunosuppressives discontinuation in patients in remission with combination therapy in an open-label, randomized, controlled trial. Methods: Patients with controlled disease ≥6 months after the start of IFX (5 mg/kg intravenously) combined with immunosuppressives were randomized to continue (Con) or to interrupt (Dis) immunosuppressives, while all patients received scheduled IFX maintenance therapy for 104 weeks. Primary end point was the proportion of patients who required a decrease in IFX dosing interval or stopped IFX therapy. Secondary end points included IFX trough levels, safety, and mucosal healing. Results: A similar proportion (24/40, 60% Con) and (22/40, 55% Dis) of patients needed a change in IFX dosing interval or stopped IFX therapy (11/40 Con, 9/40 Dis). C-reactive protein (CRP) was higher and IFX trough levels were lower in the Dis group (Dis: CRP, 2.8 mg/L; interquartile range [IQR], 1.0–8.0; Con: CRP, 1.6 mg/L; IQR, 1.0–5.6, P < .005; trough IFX: Dis: 1.65 μg/mL; IQR, 0.54–3.68; Con: 2.87 μg/mL; IQR, 1.35–4.72, P < .0001). Low IFX trough levels correlated with increased CRP and clinical score. Mucosal ulcers were absent at week 104 in 64% (Con) and 61% (Dis) of evaluated patients with ongoing response to IFX. Conclusions: Continuation of immunosuppressives beyond 6 months offers no clear benefit over scheduled IFX monotherapy but is associated with higher median IFX trough and decreased CRP levels. The impact of these observations on long-term outcomes needs to be explored further.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>18440315</pmid><doi>10.1053/j.gastro.2008.03.004</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-4020-4545</orcidid><orcidid>https://orcid.org/0000-0002-2139-4171</orcidid><orcidid>https://orcid.org/0000-0003-0158-1356</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adult Anti-Inflammatory Agents - administration & dosage Anti-Inflammatory Agents - adverse effects Anti-Inflammatory Agents - pharmacokinetics Antibodies, Monoclonal - administration & dosage Antibodies, Monoclonal - adverse effects Antibodies, Monoclonal - pharmacokinetics Azathioprine - administration & dosage Belgium C-Reactive Protein - metabolism Crohn Disease - drug therapy Crohn Disease - metabolism Crohn Disease - pathology Drug Administration Schedule Drug Therapy, Combination Female France Gastroenterology and Hepatology Gastrointestinal Agents - administration & dosage Gastrointestinal Agents - adverse effects Gastrointestinal Agents - pharmacokinetics Human health and pathology Humans Hépatology and Gastroenterology Immunosuppressive Agents - administration & dosage Infliximab Infusions, Intravenous Intestinal Mucosa - drug effects Intestinal Mucosa - pathology Life Sciences Male Mercaptopurine - administration & dosage Methotrexate - administration & dosage Middle Aged Prospective Studies Treatment Outcome |
title | Withdrawal of Immunosuppression in Crohn's Disease Treated With Scheduled Infliximab Maintenance: A Randomized Trial |
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