Granulocyte/monocyte adsorptive apheresis for the treatment of therapy-refractory chronic active ulcerative colitis

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TitreGranulocyte/monocyte adsorptive apheresis for the treatment of therapy-refractory chronic active ulcerative colitis
Type de publicationJournal Article
Year of Publication2018
AuteursDignass A, Akbar A, Baumgart DC, Bommelaer G, Bouguen G, Cadiot G, Gillessen A, Grimaud J-C, Hart A, Hoque S, Makins R, Michiels C, Moreau J, Premchand P, Ramlow W, Schanz S, Subramanian S, von Tirpitz C, Bonaz B
JournalSCANDINAVIAN JOURNAL OF GASTROENTEROLOGY
Volume53
Pagination442-448
Type of ArticleArticle
ISSN0036-5521
Mots-clésdevices, granulocyte, Inflammatory bowel disease, large intestine, monocyte adsorptive apheresis, Ulcerative Colitis
Résumé

Objectives: Current options for patients with steroid-dependent, chronic-active ulcerative colitis (UC) with insufficient response/intolerance to immunosuppressants (ISs) and/or biologics are limited. The aim of this study was to assess the long-term outcome of granulocyte/monocyte adsorptive (GMA) apheresis (Adacolumn((R))) in this population.Materials and methods: Ninety five adults with steroid-dependent active UC and insufficient response/intolerance to IS and/or TNF inhibitors received 5-8 aphereses in a single induction series of 10 weeks. Endpoints included rates of remission (clinical activity index [CAI]4) at weeks 24 and 48.Results: Of 94 patients (ITT population), remission and response rates were 34.0% and 44.7% at week 24, and 33.0% and 39.4% at week 48. Among 30 patients with prior failure of IS and biologics, 33.3% and 20.0% were in remission at weeks 24 and 48. At both weeks, 19.2% of patients achieved steroid-free remission. Sustained remission or response occurred in 27.7% of patients at 48 weeks. The cumulative colectomy rate at week 96 was 23.4%. Safety was consistent with previous findings.Conclusions: This study confirms findings of the 12-week interim analysis and demonstrates that GMA apheresis provides a safe and beneficial long-term outcome for patients with chronic active UC resistant/intolerant to IS and/or TNF inhibitors.

DOI10.1080/00365521.2018.1447598