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Efficacy and safety of infliximab induction therapy in Crohn's Disease in Central Europe - a Hungarian nationwide observational study

Authors :
Simon László
Hunyady Béla
Altorjay István
Döbrönte Zoltán
Zeher Margit
Rácz István
Balázs Csaba
Barta Zsolt
Lakatos László
Gelley András
Szabó Andrea
Jakab Zsolt
Papp Mária
Palatka Károly
Rumi György
Czimmer József
Salamon Ágnes
Czeglédi Zsófia
Szamosi Tamás
Molnár Tamás
Horváth Gábor
Lakatos Péter L
Miheller Pál
Papp János
Banai János
Nagy Ferenc
Lonovics János
Újszászy László
Műzes Györgyi
Herszényi László
Tulassay Zsolt
Source :
BMC Gastroenterology, Vol 9, Iss 1, p 66 (2009)
Publication Year :
2009
Publisher :
BMC, 2009.

Abstract

Abstract Background Infliximab (IFX) has proven to be an effective addition to the therapeutic arsenal for refractory, fistulizing, and steroid dependent Crohn's disease (CD), with efficacy in the induction and maintenance of clinical remission of CD. Our objective in this study is to report the nationwide, multicenter experience with IFX induction therapy for CD in Hungary. Methods During a 6-year-period, beginning in 2000, a total of 363 CD patients were treated with IFX as induction therapy (5 mg/kg IFX infusions given at week 0, 2 and 6) at eleven centers in Hungary in this observational study. Data analysis included patient demographics, important disease parameters and the outcome of IFX induction therapy. Results Three hundred and sixty three patients (183 women and 180 men) were treated with IFX since 2000. Mean age was 33.5 ± 11.2 years and the mean duration of disease was 6.7 ± 6.1 years. The population included 114 patients (31.4%) with therapy-refractory CD, 195 patients (53.7%) with fistulas, 16 patients (4.4%) with both therapy-refractory CD and fistulas, and 26 patients (7.2%) with steroid dependent CD. Overall response rate was 86.2% (313/363). A higher response rate was observed in patients with shorter disease duration (p = 0.05, OR:0.54, 95%CI:0.29-0.99) and concomitant immunosuppressant therapy (p = 0.05, OR: 2.03, 95%CI:0.165-0.596). Concomitant steroid treatment did not enhance the efficacy of IFX induction therapy. Adverse events included 34 allergic reactions (9.4%), 17 delayed type hypersensitivity (4.7%), 16 infections (4.4%), and 3 malignancies (0.8%). Conclusion IFX was safe and effective treatment in this cohort of Hungarian CD patients. Based on our experience co-administration of immunosuppressant therapy is suggested in patients receiving IFX induction therapy. However, concomitant steroid treatment did not enhanced the efficacy of IFX induction therapy.

Details

Language :
English
ISSN :
1471230X
Volume :
9
Issue :
1
Database :
Directory of Open Access Journals
Journal :
BMC Gastroenterology
Publication Type :
Academic Journal
Accession number :
edsdoj.2c91456f849e4af695bf7eab8d6766de
Document Type :
article
Full Text :
https://doi.org/10.1186/1471-230X-9-66