Efficacy of Dose Escalation of Oral 5-Aminosalicylic Acid for Ulcerative Colitis With a Mayo Endoscopic Subscore of 1: An Open Label Randomized Controlled Trial

Author:

Fukuda Tomohiro12ORCID,Aoki Yasuhiro1,Kiyohara Hiroki13ORCID,Yokoyama Ayumi4,Nakazawa Atsushi4,Yoshimatsu Yusuke1,Sugimoto Shinya1ORCID,Nanki Kosaku1,Mikami Yohei1,Fukuhara Kayoko5,Mizuno Shinta1,Sujino Tomohisa6,Mutaguchi Makoto6,Takabayashi Kaoru6,Morohoshi Yuichi2,Hosoda Yasuo7,Ogata Haruhiko6,Iwao Yasushi5,Naganuma Makoto18,Kanai Takanori1

Affiliation:

1. Division of Gastroenterology and Hepatology, Department of Internal Medicine, Keio University School of Medicine , 35 Shinanomachi, Shinjuku-ku, Tokyo, 160-8582 , Japan

2. Department of Gastroenterology, Yokohama Municipal Citizen’s Hospital , Kanagawa , Japan

3. Center for Advanced IBD Research and Treatment, Kitasato University Kitasato Institute Hospital , Tokyo , Japan

4. Department of Gastroenterology, Tokyo Saiseikai Central Hospital , Tokyo , Japan

5. Center for Preventive Medicine, Keio University School of Medicine , Tokyo , Japan

6. Center for Diagnostic and Therapeutic Endoscopy, Keio University School of Medicine , Tokyo , Japan

7. Department of Gastroenterology, National Hospital Organization Saitama Hospital , Saitama , Japan

8. Division of Gastroenterology and Hepatology, The Third Department of Internal Medicine, Kansai Medical University , Osaka , Japan

Abstract

Abstract Background Endoscopic healing is generally defined as Mayo endoscopic subscore (MES) ≤1 in ulcerative colitis (UC). However, patients with an MES of 1 are at higher relapse risk than those with an MES of 0. This study evaluated the therapeutic efficacy of proactive dose escalation of oral 5-aminosalicylic acid (5-ASA) in UC patients with an MES of 1. Methods An open-label, randomized controlled trial was conducted in 5 hospitals between 2018 and 2022. Ulcerative colitis patients in clinical remission under oral 5-ASA therapy and diagnosed as having an MES of 1 were enrolled. Patients receiving maintenance therapy other than 5-ASA and immunomodulator were excluded. Patients were randomly assigned in a 1:1 ratio to receive either a dose-escalated (intervention) or constant dose (control) of 5-ASA. Concomitant immunomodulator was used as the stratification factor in the randomization. The primary end point was relapse within 1 year. The subgroup analysis was stratified for the use of immunomodulators. Results The full analysis set included 79 patients (39 intervention and 40 control). Immunomodulators were used in 20 (25.3%) patients. Relapse was less in the intervention group (15.4%) than the control group (37.5%; P = .026). In the subgroup with concomitant immunomodulators, relapse was also less in the intervention group (10.0%) than the control group (70.0%; P = .020). In patients without immunomodulators, the difference was not significant between 2 groups (intervention, 17.2%; control, 26.7%; P = .53). Conclusions Dose escalation of 5-ASA reduced relapse within 1 year in UC patients in clinical remission with an MES of 1.

Publisher

Oxford University Press (OUP)

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