Once versus three times daily dosing of oral budesonide for active Crohn's disease: A double-blind, double-dummy, randomised trial

被引:27
作者
Dignass, Axel [1 ]
Stoynov, Simeon [2 ]
Dorofeyev, Andrey E. [3 ]
Grigorieva, Galina A. [4 ]
Tormova, Eva [5 ]
Altorjay, Istvan [6 ]
Tuculanu, Daniel [7 ]
Bunganic, Ivan [8 ]
Pokrotnieks, Juris [9 ]
Kupcinskas, Limas [10 ]
Dilger, Karin [11 ]
Greinwald, Roland [11 ]
Mueller, Ralph [11 ]
机构
[1] Goethe Univ Frankfurt, Agaplesion Markus Krankenhaus, Dept Med 1, D-60431 Frankfurt, Germany
[2] Univ Gen Hosp Act Treatment Tzaritza Yoanna, Gastroenterol Clin, Sofia 1527, Bulgaria
[3] M Gorkyy Donetsk Natl Med Univ, Donetsk City Clin Hosp 3, Dept Gastroenterol, UA-83003 Donetsk, Ukraine
[4] IM Sechenov First Moscow Med State Univ, Conservat Coloproctol Dept, Moscow 119992, Russia
[5] Dist Hosp Mlada Boleslav, Mlada Boleslav 29301 2, Czech Republic
[6] II Sz Belgyogyaszati Klin, DEOEC, H-4012 Debrecen, Hungary
[7] Med Ctr Tuculanu, Timisoara 300158, Romania
[8] Gastro I Sro, Dept Gastroenterol, Presov, Slovakia
[9] Paula Stradina Univ Hosp, Ctr Gastroenterol, LV-1002 Riga, Latvia
[10] Lithuanian Univ Hlth Sci, Dept Gastroenterol, LT-50009 Kaunas, Lithuania
[11] Dr Falk Pharma GmbH, Clin Res & Dev Dept, D-79108 Freiburg, Germany
关键词
Budesonide; Crohn's disease; Clinical remission; Adherence; Dosing; INFLAMMATORY-BOWEL-DISEASE; MODIFIED RELEASE BUDESONIDE; SHORT HEALTH SCALE; OF-LIFE INDEX; ULCERATIVE-COLITIS; SUBJECTIVE HEALTH; MEDICATION; 6-METHYLPREDNISOLONE; NONADHERENCE; VALIDATION;
D O I
10.1016/j.crohns.2014.01.021
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Oral budesonide 9 mg/day represents first-line treatment of mild-to-moderately active ileocolonic Crohn's disease. However, there is no precise recommendation for budesonide dosing due to lack of comparative data. A once-daily (OD) 9 mg dose may improve adherence and thereby efficacy. Methods: An eight-week, double-blind, double-dummy randomised trial compared budesonide 9 mg OD versus 3 mg three-times daily (TID) in patients with mild-to-moderately active ileocolonic Crohn's disease. Primary endpoint was clinical remission defined as CDAI <150 at week 8 (last observation carried forward). Results: The final intent-to-treat population comprised 471 patients (238 [9 mg OD], 233 [3 mg TID]). The confirmatory population for the primary endpoint analysis was the interim per protocol population (n = 377; 188 [9 mg OD], 189 [3 mg TID]), in which the primary endpoint was statistically non-inferior with budesonide 9 mg OD versus 3 mg TID. Clinical remission was achieved in 71.3% versus 75.1%, a difference of -3.9% (95% CI [-14.6%; 6.4%]; p = 0.020 for non-inferiority). The mean (SD) time to remission was 21.9 (13.8) days versus 21.4 (14.6) days with budesonide 9 mg OD versus 3 mg TID, respectively. In a subpopulation of 122 patients with baseline SES-CD ulcer score >= 1, complete mucosa( healing occurred in 32.8% (21/64) on 9 mg OD and 41.4% (24/58) on 3 mg TID; deep remission (mucosal healing and clinical remission) was observed in 26.6% (17/64) and 32.8% (19/58) of patients, respectively. Treatment-emergent suspected adverse drug reactions were reported in 4.6% of 9 mg OD and 4.7% of 3 mg TID patients. Conclusions: Budesonide at the recommended dose of 9 mg/day can be administered OD without impaired efficacy and safety compared to 3 mg TID dosing in mild-to-moderately active Crohn's disease. (C) 2014 European Crohn's and Colitis Organisation. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:970 / 980
页数:11
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