The Optimal Dose of 5-Aminosalicylic Acid in Active Ulcerative Colitis: A Dose-Finding Study With Newly Developed Mesalamine

被引:91
作者
Kruis, Wolfgang [1 ]
Bar-Meir, Simon [2 ]
Feher, Janos [3 ]
Mickisch, Oliver
Mlitz, Horst
Faszczyk, Marek [4 ]
Chowers, Yehuda [2 ]
Lengyele, Gabriella [3 ]
Kovacs, Agota [5 ]
Lakatos, Laszlo [6 ]
Stolte, Manfred [7 ]
Vieth, Michael [7 ]
Greinwald, Roland [8 ]
机构
[1] Univ Cologne, Evangel Krankenhaus Kalk, D-51103 Cologne, Germany
[2] Chaim Sheba Med Ctr, Dept Gastroenterol, IL-52621 Tel Hashomer, Israel
[3] Natl Inst Internal Med, Budapest, Hungary
[4] Barzilai Govt Hosp, Ashqelon, Israel
[5] Erzsebet Korhaz Rendelointezet, Budapest, Hungary
[6] Csolnoky Ferenc Korhaz Endoszkopos Szolgalat, Veszprem, Hungary
[7] Klinikum Bayreuth, Inst Pathol, Bayreuth, Germany
[8] Dr Falk Pharma GmbH, Freiburg, Germany
关键词
D O I
10.1053/jcgh.2003.50006
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: 5-Aminosalicylate is the gold standard for inducing remission in patients with mildly to moderately active ulcerative colitis. The optimal dose is as yet not defined. Despite some recent developments, the ideal formulation for 5-aminosalicylic acid is still awaited. A new pellet preparation was designed combining slow and delayed release properties. Aims of the study were to find the optimal dose and to test efficacy and safety of a new 5-aminosalicylic acid formulation. Methods: Three hundred twenty-one patients were included in a double-blind multicenter trial. Inclusion criteria were active ulcerative colitis (Clinical Activity Index [CAI] and Endoscopic Index [EI] according to Rachmilewitz, CAI 6-12; EI >= 4). Three different doses of 5-aminosalicylic acid (0.5 g 3 times a day, 1.0 g 3 times a day, and 1.5 g 3 times a day) were studied for 8 weeks. Results: Clinical remission rate (CAI <= 4) was highest in the 1.0 g 3 times a day group (66 %), 50% in the 0.5 g 3 times a day group, and 55% in the 1.5 g 3 times a day group. Hierarchical testing showed no significance, indicating a lack of dose response across the 3 mesalamine doses. In addition, times to first clinical response were similar: 26.5 days (1.0 g 3 times a day), 27.5 days (0.5 g 3 times a day), and 21.5 days (1.5 g 3 times a day). Endoscopic improvement was better with 1.0 g mesalamine 3 times a day than with 0.5 g 3 times a day, but overall endoscopic and histologic improvement was not different between treatment groups. Baseline activity, duration, and localization of ulcerative colitis did have some influence on the therapeutic activity, but there was no significant interaction with the dose of the study drug. Safety, with special focus on kidney function, was excellent in all 3 groups. Conclusions: There is no significant dose response between mesalamine 1.5 g/day, 3.0 g/day, and 4.5 g/day. The optimal dose to induce remission of ulcerative colitis is 0.5 g 5-aminosalicylic acid 3 times a day. Patients failing with this dose may benefit from an increase of the dose up to 1.0 g 3 times a day, but should also be considered for alternative treatment. A newly developed pellet formulation of 5-aminosalicylic acid has promising efficacy and excellent safety.
引用
收藏
页码:36 / 43
页数:8
相关论文
共 23 条
[1]   COLONIC N-ACETYLATION OF 5-AMINOSALICYLIC ACID IN INFLAMMATORY BOWEL-DISEASE [J].
ALLGAYER, H ;
AHNFELT, NO ;
KRUIS, W ;
KLOTZ, U ;
FRANKHOLMBERG, K ;
SODERBERG, HNA ;
PAUMGARTNER, G .
GASTROENTEROLOGY, 1989, 97 (01) :38-41
[2]  
ALLGAYER H, 1992, GASTROENTEROL CLIN N, V21, P643
[3]  
[Anonymous], CANADIAN J GASTROENT
[4]   CONCENTRATIONS OF 5-ASA AND AC-5-ASA IN HUMAN ILEOCOLONIC BIOPSY HOMOGENATES AFTER ORAL 5-ASA PREPARATIONS [J].
DEVOS, M ;
VERDIEVEL, H ;
SCHOONJANS, R ;
PRAET, M ;
BOGAERT, M ;
BARBIER, F .
GUT, 1992, 33 (10) :1338-1342
[5]   EFFECT OF FOOD-INTAKE ON GASTRIC-EMPTYING OF GASTRIC JUICE-RESISTANT TABLETS AND CAPSULES [J].
EWE, K ;
PRESS, AG ;
OESTREICHER, M .
DEUTSCHE MEDIZINISCHE WOCHENSCHRIFT, 1992, 117 (08) :287-290
[6]  
Ewe K, 1990, GASTROENTEROLOGY, V8, pA350
[7]   Mucosal 5-aminosalicylic acid concentration inversely correlates with severity of colonic inflammation in patients with ulcerative colitis [J].
Frieri, G ;
Giacomelli, R ;
Pimpo, M ;
Palumbo, G ;
Passacantando, A ;
Pantaleoni, G ;
Caprilli, R .
GUT, 2000, 47 (03) :410-414
[8]  
HANAUER S, 1993, AM J GASTROENTEROL, V88, P1188
[9]  
Hussain F, 1996, GASTROENTEROLOGY, V110, pA928
[10]  
Kruis W, 1998, ALIMENT PHARM THER, V12, P707