Effect of Extended MMX Mesalamine Therapy for Acute, Mild-to-Moderate Ulcerative Colitis

被引:58
作者
Kamm, Michael A. [1 ,2 ,3 ]
Lichtenstein, Gary R. [4 ]
Sandborn, William J. [5 ]
Schreiber, Stefan [6 ]
Lees, Kirstin [7 ]
Barrett, Karen [8 ]
Joseph, Raymond [7 ]
机构
[1] St Vincent Hosp, Univ Dept Med, Melbourne, Vic 3065, Australia
[2] Univ Melbourne, Melbourne, Vic, Australia
[3] Univ London Imperial Coll Sci Technol & Med, London, England
[4] Univ Penn, Div Gastroenterol, Philadelphia, PA 19104 USA
[5] Mayo Clin, Inflammatory Bowel Dis Clin, Rochester, MN USA
[6] Univ Kiel, Dept Med 1, Kiel, Germany
[7] Shire Pharmaceut Inc, Wayne, PA USA
[8] Shire Pharmaceut Inc, Basingstoke, Hants, England
关键词
inflammatory bowel disease; ulcerative colitis; 5-aminosalicyclic acid; mesalamine; Multi Matrix System; 5-AMINOSALICYLIC ACID; DOUBLE-BLIND; REMISSION; ENEMAS; ADULTS; NONADHERENCE; BALSALAZIDE; GUIDELINES; INDUCTION; TRIAL;
D O I
10.1002/ibd.20580
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Many patients with ulcerative colitis (UC) respond to mesalamine therapy within 8 weeks. Those not achieving remission after 8 weeks are often treated with steroids or other immunosuppressive therapies. This study aimed to determine the effect of 8 weeks' high-dose MMX mesalamine extension therapy in patients with active, mild-to-moderate UC who had previously failed to achieve complete remission in 2 phase III, double-blind, placebo-controlled studies of MMX mesalamine (SPD476-301 and -302). Methods: Patients with active, mild-to-moderate UC who did not achieve clinical and endoscopic remission after <= 8 weeks' treatment with MMX mesalamine (2.4 or 4.8 g/day), ASACOL (R) (mesalamine) delayed-release tablets 2.4 g/day, or placebo in the phase III Studies received MMX mesalamine 4.8 g/day for 8 weeks. The aim was to assess remission at week 8. defined as a total modified UC Disease Activity Index score of <= 1, calculated as: scores of 0 for rectal bleeding and stool frequency, a combined Physician's Global Assessment score and sigmoidoscopy score of <= 1, no mucosal friability and a >= 1 point reduction from baseline in sigmoidoscopy score. Results: Overall, 304 patients who entered this acute extension were evaluated; 59.5% achieved remission at week 8. Remission rates were similar irrespective of prior treatment in the initial acute phase III Studies. Conclusions: Most patients with mild-to-moderate UC who fail to achieve remission with up to 8 weeks' initial mesalamine therapy can achieve clinical and endoscopic remission following a further 8 weeks' treatment with high-dose MMX mesalamine therapy, thereby avoiding step-up therapy.
引用
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页码:1 / 8
页数:8
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