Delayed-release oral mesalamine 4.8 g/day (800 mg tablets) compared with 2.4 g/day (400 mg tablets) for the treatment of mildly to moderately active ulcerative colitis: The ASCEND I trial

被引:114
作者
Hanauer, Stephen B. [1 ]
Sandborn, William J. [2 ]
Dallaire, Christian [3 ]
Archambault, Andre [4 ]
Yacyshyn, Bruce [5 ]
Yeh, Chyon [5 ]
Smith-Hall, Nancy [5 ]
机构
[1] Univ Chicago, Med Ctr, Div Gastroenterol, Chicago, IL 60637 USA
[2] Mayo Clin, Div Gastroenterol & Hepatol, Rochester, MN USA
[3] Univ Laval, Quebec City, PQ, Canada
[4] Univ Montreal, Montreal, PQ, Canada
[5] Procter & Gamble Pharmaceut, Mason, OH USA
来源
CANADIAN JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY | 2007年 / 21卷 / 12期
关键词
delayed release; inflammatory bowel disease; mesalamine; ulcerative colitis;
D O I
10.1155/2007/862917
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BACKGROUND: Delayed-release oral mesalamine 2.4 g/day to 4.8 g/day has been shown to be effective in treating mildly to moderately active ulcerative colitis (UC), but it is unknown whether an initial dose of 4.8 g/day is more effective than 2.4 g/day in patients with mildly to moderately active UC and in the subgroup with moderate disease. PATIENTS AND METHODS: A six-week, multicentre, randomized, double-blind, controlled trial assessing the safety and clinical efficacy of a new dose (ASCEND 1) of medication randomly assigned 301 adults with mildly to moderately active UC to delayed-release oral mesalamine 2.4 g/day (400 mg tablet [n=154]) or 4.8 g/day (800 mg tabtet [n=147]). The primary efficacy end point was overall improvement (ie, treatment success), defined as complete remission or response to therapy from baseline to week 6. Primary safety end points were adverse events and laboratory evaluations. Data were also analyzed separately for the prespecified subgroup of patients with moderate UC at baseline. RESULTS: Treatment success was not statistically different between the treatment groups at week 6; 51% of the group (77 of 150) who received delayed-release oral mesalamine 2.4 g/day and 56% of the group (76 of 136) who received 4.8 g/day reached the efficacy end point (P=0.441). Among the moderate disease subgroup, however, the higher initial dose was more effective; 57% of patients (53 of 93) given delayed-release oral mesalamine 2.4 g/day and 72% of patients (55 of 76) given 4.8 g/day achieved treatment success (P=0.0384). Both regimens were well tolerated. CONCLUSIONS: Delayed-release oral mesalamine is an effective and well-tolerated initial therapy in patients with mildly to moderately active UC, and a 4.8 g/day dose may enhance treatment success rates in patients with moderate disease compared with mesalamine 2.4 g/day.
引用
收藏
页码:827 / 834
页数:8
相关论文
共 13 条
[1]  
Bernstein CN, 2006, AM J GASTROENTEROL, V101, P1945
[2]   The epidemiology of inflammatory bowel disease in Canada: A population-based study [J].
Bernstein, Charles N. ;
Wajda, Andre ;
Svenson, Lawrence W. ;
MacKenzie, Adrian ;
Koehoorn, Mieke ;
Jackson, Maureen ;
Fedorak, Richard ;
Israel, David ;
Blanchard, James F. .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2006, 101 (07) :1559-1568
[3]   Guidelines for the management of inflammatory bowel disease in adults [J].
Carter, MJ ;
Lobo, AJ ;
Travis, SPL .
GUT, 2004, 53 :v1-v16
[4]  
HANAUER S, 1993, AM J GASTROENTEROL, V88, P1188
[5]   Delayed-release oral mesalamine at 4.8 g/day (800 mg tablet) for the treatment of moderately active ulcerative colitis: The ASCEND II trial [J].
Hanauer, SB ;
Sandborn, WJ ;
Kornbluth, A ;
Katz, S ;
Safdi, M ;
Woogen, S ;
Regalli, G ;
Yeh, C ;
Smith-Hall, N ;
Ajayi, F .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2005, 100 (11) :2478-2485
[6]   Ulcerative colitis practice guidelines in adults (update): American College of Gastroenterology, Practice Parameters Committee [J].
Kornbluth, A ;
Sachar, DB .
AMERICAN JOURNAL OF GASTROENTEROLOGY, 2004, 99 (07) :1371-1385
[7]   INCIDENCE AND PREVALENCE OF ULCERATIVE-COLITIS IN COPENHAGEN COUNTY FROM 1962 TO 1987 [J].
LANGHOLZ, E ;
MUNKHOLM, P ;
NIELSEN, OH ;
KREINER, S ;
BINDER, V .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1991, 26 (12) :1247-1256
[8]   DISPOSITION OF 5-AMINOSALICYLIC ACID BY OLSALAZINE AND 3 MESALAZINE PREPARATIONS IN PATIENTS WITH ULCERATIVE-COLITIS - COMPARISON OF INTRALUMINAL COLONIC CONCENTRATIONS, SERUM VALUES, AND URINARY-EXCRETION [J].
LAURSEN, LS ;
STOKHOLM, M ;
BUKHAVE, K ;
RASKMADSEN, J ;
LAURITSEN, K .
GUT, 1990, 31 (11) :1271-1276
[9]  
*PROCT GAMBL PHARM, 2005, AS PROD MON
[10]   The pharmacokinetic profiles of oral mesalazine formulations and mesalazine pro-drugs used in the management of ulcerative colitis [J].
Sandborn, WJ ;
Hanauer, SB .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2003, 17 (01) :29-42