Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/33565
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dc.contributor.authorWright, Emily K-
dc.contributor.authorChaparro, Maria-
dc.contributor.authorGionchetti, Paolo-
dc.contributor.authorHamilton, Amy L-
dc.contributor.authorSchulberg, Julien-
dc.contributor.authorGisbert, Javier P-
dc.contributor.authorValerii, Maria Chiara-
dc.contributor.authorRizzello, Fernando-
dc.contributor.authorDe Cruz, Peter P-
dc.contributor.authorPanetta, John C-
dc.contributor.authorEverts-van der Wind, Annelie-
dc.contributor.authorKamm, Michael A-
dc.contributor.authorDervieux, Thierry-
dc.date2023-
dc.date.accessioned2023-08-23T07:20:03Z-
dc.date.available2023-08-23T07:20:03Z-
dc.date.issued2023-08-18-
dc.identifier.citationJournal of Crohn's & Colitis 2023-08-18en_US
dc.identifier.issn1876-4479-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/33565-
dc.description.abstractWe postulated that adalimumab (ADA) drug clearance (CL) may be a more critical determinant of therapeutic outcome than ADA concentration. This was tested in Crohn's disease (CD) patients undergoing ADA maintenance treatment. CD patients from 4 cohorts received ADA induction and started maintenance therapy. Therapeutic outcomes consisted of endoscopic remission (ER), sustained -reactive protein (CRP) based clinical remission (defined as CRP levels below 3 mg/L in the absence of symptoms) and fecal calprotectin (FC) level below 100µg/g. Serum albumin, ADA concentration and anti-drug antibody status were determined using immunochemistry and homogenous mobility shift assay, respectively. CL was determined using a nonlinear mixed effect model with Bayesian priors. Statistical analysis consisted of Mann-Whitney test, and logistic regression with calculation of odds ratio. Repeated event analysis was conducted using a nonlinear mixed effect model. In 237 enrolled patients (median age 40 years, 45% females), median CL was lower in patients achieving ER as compared to those with persistent active endoscopic disease (median 0.247 L/day vs 0.326 L/day, respectively) (p<0.01). There was no significant difference in ADA concentration between patients in endoscopic remission compared to those with recurrence (median 9.3 µg/mL vs 11.7 µg/mL, respectively). Sustained CRP-based clinical remission and FC levels below 100µg/g were generally associated with lower CL and higher ADA concentration. Repeated event analysis confirmed those findings with better performances of CL than concentration in associating with ER and other outcomes. Lower ADA Clearance is associated with an improved clinical outcome for patients with Crohn's disease and may be a superior pharmacokinetic measure than concentration.en_US
dc.language.isoeng-
dc.subjectAdalimumaben_US
dc.subjectClearanceen_US
dc.subjectCrohn’s diseaseen_US
dc.subjectpharmacokineticsen_US
dc.titleAdalimumab Clearance, rather than Trough Level, May Have Greatest Relevance to Crohn's Disease Therapeutic Outcomes Assessed Clinically and Endoscopically.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleJournal of Crohn's & Colitisen_US
dc.identifier.affiliationSt Vincent's Hospital, Melbourne, Australia.en_US
dc.identifier.affiliationHospital Universitario de La Princesa, IIS-Princesa, UAM and CIBEREHD, Madrid, Spain.en_US
dc.identifier.affiliationIBD Unit IRCCS Azienda Ospedaliera Universitaria di Bologna and DIMEC University of Bologna Italy.en_US
dc.identifier.affiliationThe University of Melbourne, Melbourne, Australia.en_US
dc.identifier.affiliationAustin Healthen_US
dc.identifier.affiliationHospital Universitario de La Princesa, IIS-Princesa, UAM and CIBEREHD, Madrid, Spain.en_US
dc.identifier.affiliationIBD Unit IRCCS Azienda Ospedaliera Universitaria di Bologna and DIMEC University of Bologna Italy.en_US
dc.identifier.affiliationAustin Health, Melbourne, Australia.;The University of Melbourne, Melbourne, Australia.en_US
dc.identifier.affiliationSt Jude Children's Research Hospital, Memphis TN, USA.en_US
dc.identifier.affiliationPrometheus Laboratories San Diego, CA, USA.en_US
dc.identifier.affiliationPrometheus Laboratories San Diego, CA, USA.en_US
dc.identifier.doi10.1093/ecco-jcc/jjad140en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-9275-4242en_US
dc.identifier.orcid0000-0002-1627-2057en_US
dc.identifier.orcid0000-0003-2090-3445en_US
dc.identifier.pubmedid37594369-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.languageiso639-1en-
crisitem.author.deptGastroenterology and Hepatology-
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