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
Hauptverfasser: Van Assche, Gert, Magdelaine–Beuzelin, Charlotte, D'Haens, Geert, Baert, Filip, Noman, Maja, Vermeire, Séverine, Ternant, David, Watier, Hervé, Paintaud, Gilles, Rutgeerts, Paul
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container_end_page 1868
container_issue 7
container_start_page 1861
container_title Gastroenterology (New York, N.Y. 1943)
container_volume 134
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 &lt; .005; trough IFX: Dis: 1.65 μg/mL; IQR, 0.54–3.68; Con: 2.87 μg/mL; IQR, 1.35–4.72, P &lt; .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 &amp; 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 &lt; .005; trough IFX: Dis: 1.65 μg/mL; IQR, 0.54–3.68; Con: 2.87 μg/mL; IQR, 1.35–4.72, P &lt; .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. 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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 &amp; 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 &amp; dosage</subject><subject>Methotrexate - administration &amp; 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 &amp; dosage</topic><topic>Anti-Inflammatory Agents - adverse effects</topic><topic>Anti-Inflammatory Agents - pharmacokinetics</topic><topic>Antibodies, Monoclonal - administration &amp; dosage</topic><topic>Antibodies, Monoclonal - adverse effects</topic><topic>Antibodies, Monoclonal - pharmacokinetics</topic><topic>Azathioprine - administration &amp; 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 &amp; 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 &amp; 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 &amp; dosage</topic><topic>Methotrexate - administration &amp; 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 &amp; 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 &lt; .005; trough IFX: Dis: 1.65 μg/mL; IQR, 0.54–3.68; Con: 2.87 μg/mL; IQR, 1.35–4.72, P &lt; .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. 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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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