A new oral delivery system for 5-ASA: Preliminary clinical findings for MMx

被引:117
作者
Prantera, C [1 ]
Viscido, A
Biancone, L
Francavilla, A
Giglio, L
Campieri, M
机构
[1] Azienda Osped S Camillo Orlanini, Div Gastroenterol, Rome, Italy
[2] Univ Roma La Sapienza, Dept Gastroenterol, Rome, Italy
[3] Univ Roma Tor Vergata, Dept Gastroenterol, Rome, Italy
[4] Univ Bari, Dept Gastroenterol, I-70124 Bari, Italy
[5] Policlin S Orsola, Bologna, Italy
关键词
5-aminosalicyclic acid; 5-aminosalicyclic acid multi-matrix; left-sided ulcerative colitis; mesalamine;
D O I
10.1097/01.MIB.0000158386.25660.1e
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Multi-matrix (MMx), a new delivery system for mesalazine. seems to release 5-aminosalicyclic acid (5-ASA) preferentially in the sigmoid colon. This Study had 2 objectives: (1) to evaluate the therapeutic response to MMx in patients with active left-sided disease and (2) to gain additional insights as to how the therapy would compare with topical 5-ASA. Methods: Patients received either 1.2 g of 5-ASA MMx three times per day plus placebo enema or 4, of 5-ASA enema Plus placebo tablets for 8 weeks. The primary endpoint was clinical remission (clinical activity index <= 4) at 8 weeks. Secondary endpoints were endoscopic and histologic remissions. Results: Seventy-nine patients were enrolled. Clinical remission rates at 4 and 8 weeks were 57.5% and 60.0% for patients treated with MMx and 68.4% and 50.0% for patients randomized to 5-ASA enemas, respectively (95% confidence interval for the difference at 8 weeks, - 12 to + 32). Endoscopic remission was achieved by 45.0% of patients on 5-ASA MMx and by 36.8% of those on enema, whereas 15.0% and 8% of patients, respectively, showed histologic remission. Compliance was 97.0% for oral and 87.5% for topical therapy. In the enema group, compliance was 88.0% for the patients in remission and 65.5% for those with active disease. Conclusions: Preliminary studies suggest that similar rates for induction of remission can be expected from 5-ASA enemas and MMx for patients with left-sided Ulcerative colitis.
引用
收藏
页码:421 / 427
页数:7
相关论文
共 27 条
[1]  
Ardizzone S, 1999, ITAL J GASTROENTEROL, V31, P677
[2]   Gastrointestinal transit and 5-ASA release from a new mesalazine extended-release formulation [J].
Brunner, M ;
Assandri, R ;
Kletter, K ;
Tschurlovits, M ;
Corrado, ME ;
Villa, R ;
Eichler, HG ;
Müller, M .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2003, 17 (03) :395-402
[3]   BETTER QUALITY OF THERAPY WITH 5-ASA COLONIC FOAM IN ACTIVE ULCERATIVE-COLITIS - A MULTICENTER COMPARATIVE TRIAL WITH 5-ASA ENEMA [J].
CAMPIERI, M ;
PAOLUZI, P ;
DALBASIO, G ;
BRUNETTI, G ;
PERA, A ;
BARBARA, L .
DIGESTIVE DISEASES AND SCIENCES, 1993, 38 (10) :1843-1850
[4]  
Cohen RD, 2000, AM J GASTROENTEROL, V95, P1263
[5]   CLINICAL-PATTERNS, NATURAL-HISTORY, AND PROGRESSION OF ULCERATIVE-COLITIS - A LONG-TERM FOLLOW-UP OF 1116 PATIENTS [J].
FARMER, RG ;
EASLEY, KA ;
RANKIN, GB .
DIGESTIVE DISEASES AND SCIENCES, 1993, 38 (06) :1137-1146
[6]  
Farrokhyar F, 1999, GASTROENTEROLOGY, V116, pA711
[7]   HISTOLOGIC AND COLONOSCOPIC ASSESSMENT OF DISEASE EXTENSION IN ULCERATIVE-COLITIS [J].
FLOREN, CH ;
BENONI, C ;
WILLEN, R .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1987, 22 (04) :459-462
[8]   Renal tubular injury is present in acute inflammatory bowel disease prior to the introduction of drug therapy [J].
Fraser, JS ;
Muller, AF ;
Smith, DJ ;
Newman, DJ ;
Lamb, EJ .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2001, 15 (08) :1131-1137
[9]  
Gionchetti P, 1999, ALIMENT PHARM THERAP, V13, P381
[10]   Medication Nonadherence and the outcomes of patients with quiescent ulcerative colitis [J].
Kane, S ;
Huo, DZ ;
Aikens, J ;
Hanauer, S .
AMERICAN JOURNAL OF MEDICINE, 2003, 114 (01) :39-43