Efficacy of rituximab in difficult-to-manage autoimmune hepatitis: Results from the International Autoimmune Hepatitis Group.
dc.contributor.author | Than, Nwe Ni | |
dc.contributor.author | Hodson, James | |
dc.contributor.author | Schmidt-Martin, Daniel | |
dc.contributor.author | Taubert, Richard | |
dc.contributor.author | Wawman, Rebecca E | |
dc.contributor.author | Botter, Meemee | |
dc.contributor.author | Gautam, Nishant | |
dc.contributor.author | Bock, Kilian | |
dc.contributor.author | Jones, Rebecca | |
dc.contributor.author | Appanna, Gautham D | |
dc.contributor.author | Godkin, Andrew | |
dc.contributor.author | Montano-Loza, Aldo J | |
dc.contributor.author | Lammert, Frank | |
dc.contributor.author | Schramm, Christoph | |
dc.contributor.author | Manns, Michael P | |
dc.contributor.author | Swain, Mark | |
dc.contributor.author | Burak, Kelly W | |
dc.contributor.author | Adams, David H | |
dc.contributor.author | Hirschfield, Gideon M | |
dc.contributor.author | Oo, Ye Htun | |
dc.date.accessioned | 2020-02-20T09:21:43Z | |
dc.date.available | 2020-02-20T09:21:43Z | |
dc.date.issued | 2019-12-01 | |
dc.identifier.citation | JHEP Rep. 2019 Nov 5;1(6):437-445. doi: 10.1016/j.jhepr.2019.10.005. eCollection 2019 Dec. | en_US |
dc.identifier.issn | 2589-5559 | |
dc.identifier.pmid | 32039395 | |
dc.identifier.doi | 10.1016/j.jhepr.2019.10.005 | |
dc.identifier.uri | http://hdl.handle.net/10033/622149 | |
dc.description.abstract | Twenty-two patients with type-1 AIH were included, with a median age of 40 years at diagnosis (range 19-79); 15/22 (68%) were female and 18/22 (82%) were Caucasian. The median period from diagnosis to the end of follow-up in these patients was 11 years (range 3-28). Values of alanine aminotransferase, aspartate aminotransferase and albumin improved significantly following rituximab therapy, and were sustained for up to 2 years (all p ≪0.001). Prednisolone doses were significantly reduced by 12 months post-treatment (p = 0.003), with 13/21 (62%) patients having a dose reduction. Over a median post-treatment follow-up period of 6 years (range 1-10), 5 patients developed AIH flares at a median of 22 months post-treatment, giving an estimated 71% freedom from AIH flare at 2 years. Four of these patients received a second course of treatment, of whom 2 had subsequent further flares. No serious adverse events attributable to rituximab were recorded. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Elsevier | en_US |
dc.rights | Attribution-NonCommercial-ShareAlike 4.0 International | * |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-sa/4.0/ | * |
dc.subject | Autoimmune hepatitis | en_US |
dc.subject | B cell depletion therapy | en_US |
dc.subject | Difficult-to-manage | en_US |
dc.subject | Prednisolone | en_US |
dc.subject | Rituximab | en_US |
dc.title | Efficacy of rituximab in difficult-to-manage autoimmune hepatitis: Results from the International Autoimmune Hepatitis Group. | en_US |
dc.type | Article | en_US |
dc.contributor.department | HZI,Helmholtz-Zentrum für Infektionsforschung GmbH, Inhoffenstr. 7,38124 Braunschweig, Germany. | en_US |
dc.identifier.journal | JHEP Reports | en_US |
refterms.dateFOA | 2020-02-20T09:21:44Z | |
dc.source.journaltitle | JHEP reports (Online) |