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Doubling the infliximab dose versus halving the infusion intervals in Crohn's disease patients with loss of response

dc.contributor.authorKatz, Lioren_US
dc.contributor.authorGisbert, Javier P.en_US
dc.contributor.authorManoogian, Bethen_US
dc.contributor.authorLin, Kirken_US
dc.contributor.authorSteenholdt, Casperen_US
dc.contributor.authorMantzaris, Gerassimos J.en_US
dc.contributor.authorAtreja, Ashishen_US
dc.contributor.authorRon, Yuliaen_US
dc.contributor.authorSwaminath, Arunen_US
dc.contributor.authorShah, Somalen_US
dc.contributor.authorHart, Ailsaen_US
dc.contributor.authorLakatos, Peter Laszloen_US
dc.contributor.authorEllul, Pierreen_US
dc.contributor.authorIsraeli, Eranen_US
dc.contributor.authorSvendsen, Mads Naundrupen_US
dc.contributor.authorvan der Woude, C. Jannekeen_US
dc.contributor.authorKatsanos, Konstantinos H.en_US
dc.contributor.authorYun, Lauraen_US
dc.contributor.authorTsianos, Epameinondas V.en_US
dc.contributor.authorNathan, Torbenen_US
dc.contributor.authorAbreu, Mariaen_US
dc.contributor.authorDotan, Irisen_US
dc.contributor.authorLashner, Breten_US
dc.contributor.authorBrynskov′, Jornen_US
dc.contributor.authorTerdiman, Jonathan P.en_US
dc.contributor.authorHiggins, Peter D.Ren_US
dc.contributor.authorChaparro, Mariaen_US
dc.contributor.authorBen‐horin, Shomronen_US
dc.date.accessioned2012-11-07T17:04:23Z
dc.date.available2014-01-07T14:51:07Zen_US
dc.date.issued2012-11en_US
dc.identifier.citationKatz, Lior; Gisbert, Javier P.; Manoogian, Beth; Lin, Kirk; Steenholdt, Casper; Mantzaris, Gerassimos J.; Atreja, Ashish; Ron, Yulia; Swaminath, Arun; Shah, Somal; Hart, Ailsa; Lakatos, Peter Laszlo; Ellul, Pierre; Israeli, Eran; Svendsen, Mads Naundrup; van der Woude, C. Janneke; Katsanos, Konstantinos H.; Yun, Laura; Tsianos, Epameinondas V.; Nathan, Torben; Abreu, Maria; Dotan, Iris; Lashner, Bret; Brynskov′, Jorn ; Terdiman, Jonathan P.; Higgins, Peter D.R; Chaparro, Maria; Ben‐horin, Shomron (2012). "Doubling the infliximab dose versus halving the infusion intervals in Crohn's disease patients with loss of response ." Inflammatory Bowel Diseases 18(11): 2026-2033. <http://hdl.handle.net/2027.42/94222>en_US
dc.identifier.issn1078-0998en_US
dc.identifier.issn1536-4844en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/94222
dc.description.abstractBackground: Intensifying infliximab therapy is often practiced in Crohn's disease (CD) patients losing response to the drug but there are no data if halving the interval is superior to doubling the dose. We aimed to assess the efficacy of infliximab dose intensification by interval‐halving compared with dose‐doubling. Methods: A multicenter retrospective study of CD patients losing response to infliximab was undertaken. The clinical outcome of patients whose infusion intervals were halved (5 mg/kg/4 weeks) was compared with patients treated by dose‐doubling (10 mg/kg/8 weeks). Results: In all, 168 patients were included from 18 centers in Europe, USA, and Israel. Of these, 112 were intensified by dose‐doubling and 56 received interval‐halving strategy. Early response to dose‐escalation was experienced by 86/112 (77%) patients in the dose‐doubling group compared with 37/56 patients (66%) in the interval‐halving group (odds ratio [OR] 1.7, 95% confidence interval [CI] 0.8–3.4, P = 0.14). Sustained clinical response at 12 months postescalation was maintained in 50% of patients in the dose‐doubling group compared with 39% in the interval‐halving group (OR 1.5, 95% CI 0.8–2.9, P = 0.2). On multivariate analysis, predictors of long‐term response to escalation were a nonsmoking status, CD diagnosis between 16–40 years of age, and normal C‐reactive protein (CRP). Conclusions: Dose intensification leads to a sustained regained response in 47% of CD patients who lost response to standard infliximab dose, but halving the infusion intervals is probably not superior to dose‐doubling. Given the costs and patient inconvenience incurred by an additional infusion visit, the dose‐doubling strategy may be preferable to the interval‐halving strategy. (Inflamm Bowel Dis 2012;)en_US
dc.publisherWiley Subscription Services, Inc., A Wiley Companyen_US
dc.subject.otherCrohn's Diseaseen_US
dc.subject.otherInfliximaben_US
dc.subject.otherInflammatory Bowel Diseaseen_US
dc.titleDoubling the infliximab dose versus halving the infusion intervals in Crohn's disease patients with loss of responseen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelInternal Medicine and Specialtiesen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumUniversity of Michigan Medical Center, Ann Arbor, USAen_US
dc.contributor.affiliationother1st Department of Medicine, Semmelweis University, Budapest, Hungaryen_US
dc.contributor.affiliationotherGastroenterology Department, Sheba Medical Center, Tel Hashomer, Tel‐Aviv University, Israelen_US
dc.contributor.affiliationotherHospital Universitario de La Princesa, Instituto de Investigación Sanitaria Princesa (IP) and Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD), Madrid, Spainen_US
dc.contributor.affiliationotherDivision of Gastroenterology, Department of Medicine, University of California San Francisco, San Francisco, USAen_US
dc.contributor.affiliationotherDepartment of Medical Gastroenterology, Herlev Hospital, University of Copenhagen, Denmarken_US
dc.contributor.affiliationother1st Department of Gastroenterology, Evangelismos Hospital, Athens, Greeceen_US
dc.contributor.affiliationotherCenter for Inflammatory Bowel Disease at Cleveland Clinic, Digestive Diseases Institute in Cleveland, Ohio, USAen_US
dc.contributor.affiliationotherDivision of Gastroenterology, Tel‐Aviv Medical Center, Israelen_US
dc.contributor.affiliationotherDivision of Gastroenterology, Columbia university Presbyterian hospital, New‐York, New‐York, USAen_US
dc.contributor.affiliationotherUniversity of Miami Miller School of Medicine, Miami, Florida, USAen_US
dc.contributor.affiliationotherSt. Marks Hospital, London, United Kingdomen_US
dc.contributor.affiliationotherGastroenterology Department, Mater Dei Hospital, Msida, Maltaen_US
dc.contributor.affiliationotherGastroenterology Department, Hadassah Medical Center, Jerusalem, Israelen_US
dc.contributor.affiliationotherMedicinsk afdeling Vejle, Sygehus Hospital, Denmarken_US
dc.contributor.affiliationotherErasmus Medical Center, Rotterdam The Netherlandsen_US
dc.contributor.affiliationotherHepato‐Gastroenterology Unit, 1st Department of Internal Medicine, Medical School of Ioannina, Ionnina, Greeceen_US
dc.contributor.affiliationotherNorthwestern University Feinberg School of Medicine, Chicago, Illinois, USAen_US
dc.contributor.affiliationotherGastroenterology Department, Sheba Medical Center, Tel Hashomer 52621, Israelen_US
dc.identifier.pmid22294554en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/94222/1/22902_ftp.pdf
dc.identifier.doi10.1002/ibd.22902en_US
dc.identifier.sourceInflammatory Bowel Diseasesen_US
dc.identifier.citedreferenceRutgeerts P, Sandborn WJ, Feagan BG, et al. Infliximab for induction and maintenance therapy for ulcerative colitis. N Engl J Med. 2005; 353: 2462 – 2476en_US
dc.identifier.citedreferenceLichtenstein GR, Yan S, Bala M, et al. Infliximab maintenance treatment reduces hospitalizations, surgeries, and procedures in fistulizing Crohn's disease. Gastroenterology. 2005; 128: 862 – 869.en_US
dc.identifier.citedreferenceHanauer S, Feagan B, Lichtenshtein G, et al. Maintenance infliximab for Crohn's disease: the ACCENT 1 randomized trial. Lancet. 2002; 359: 1541 – 1549.en_US
dc.identifier.citedreferencePariente B, Pineton de Chambrun G, Desroches M, et al. Clinical value of measuring trough levels and human anti‐chimeric antibodies in patients with inflammatory bowel disease who lost response to infliximab therapy. J Crohn Colitis. 2011; 5: S111 – 112.en_US
dc.identifier.citedreferenceAfif W, Loftus EV, Faubion WA, et al. Clinical utility of measuring Infliximab and human anti‐chimeric antibody concentrations in patients with inflammatory bowel disease. Am J Gastroenterol. 2010; 105: 1133 – 1139.en_US
dc.identifier.citedreferenceVermeire S, Noman M, Van Assche G, et al. Effectiveness of concomitant immunosuppressive therapy in suppressing the formation of antibodies to infliximab in Crohn's disease. Gut. 2007; 56: 1226 – 1231.en_US
dc.identifier.citedreferenceBaert F, Noman M, Vermeire S, et al. Influence of immunogenicity on the long‐term efficacy of Infliximab in Crohn's disease. N Engl J Med. 2003; 348: 601 – 608.en_US
dc.identifier.citedreferenceBen‐Horin S, Yavzori M, Katz L, et al. The immunogenic part of infliximab lies within the Fab fragment, but measurement of antibodies against the intact Infliximab molecule shows superior clinical usefulness. Gut. 2011; 60: 41 – 48.en_US
dc.identifier.citedreferenceKaplan GG, Hur C, Korzenik J, Sands BE. Infliximab dose escalation vs. initiation of adalimumab for loss of response in Crohn's disease: a cost‐effectiveness analysis. Aliment Pharmacol Ther. 2007; 26: 1509 – 1520.en_US
dc.identifier.citedreferenceSandborn WJ, Abreu MT, D'Haens G, et al. Certolizumab pegol in patients with moderate to severe Crohn's disease and secondary failure to infliximab. Clin Gastroenterol Hepatol. 2010; 8: 688 – 695.en_US
dc.identifier.citedreferenceSandborn WJ, Colombel JF, Schreiber S, et al. Dosage adjustment during long‐term adalimumab treatment for Crohn's disease: clinical efficacy and pharmacoeconomics. Inflamm Bowel Dis. 2011; 17: 141 – 151.en_US
dc.identifier.citedreferenceRequeiro M, Siemanowski B, Kip K, et al. Infliximab dose intensification in Crohn's disease. Inflamm Bowel Dis. 2007; 13: 1093 – 1099.en_US
dc.identifier.citedreferenceSchnitzler F, Fidder H, Ferrante M, et al. Long‐term outcome of treatment with infliximab in 614 patients with Crohn's disease: results from a single‐centre cohort. Gut. 2009; 58: 492 – 500.en_US
dc.identifier.citedreferenceKopylov U, Mantzaris GJ, Katsanos KH, et al. The efficacy of shortening the dosing interval to once every six weeks in Crohn's patients losing response to maintenance dose of Infliximab. Aliment Pharmacol Ther. 2011; 33: 349 – 357.en_US
dc.identifier.citedreferenceSt. Clair EW, Wagner CL, Fasanmade AA, et al. The relationship of serum infliximab concentrations to clinical improvement in rheumatoid arthritis. Arthritis Rheum. 2002; 46: 1451 – 1459.en_US
dc.identifier.citedreferenceGisbert JP, Panes J. Loss of response and requirement of infliximab dose intensification in Crohn's disease: a review. Am J Gastroenterol. 2009; 104: 760 – 767.en_US
dc.identifier.citedreferenceBen‐Horin S, Chowers Y. Review article: loss of response to anti‐TNF treatments in Crohn's disease. Aliment Pharmacol Ther. 2011; 33: 987 – 995.en_US
dc.identifier.citedreferenceHanauer SB, Wagner CL, Bala M, et al. Incidence and importance of antibody responses to infliximab after maintenance or episodic treatment in Crohn's disease. Clin Gastroenterol Hepatol. 2004; 2: 542 – 553.en_US
dc.identifier.citedreferenceRutgeerts P, Feagan BG, Lichtenstein GR, et al. Comparison of scheduled and episodic treatment strategies of infliximab in Crohn's disease. Gastroenterology. 2004; 126: 402 – 413.en_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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