Author:
Masamune Atsushi,Nishimori Isao,Kikuta Kazuhiro,Tsuji Ichiro,Mizuno Nobumasa,Iiyama Tatsuo,Kanno Atsushi,Tachibana Yuichi,Ito Tetsuhide,Kamisawa Terumi,Uchida Kazushige,Hamano Hideaki,Yasuda Hiroaki,Sakagami Junichi,Mitoro Akira,Taguchi Masashi,Kihara Yasuyuki,Sugimoto Hiroyuki,Hirooka Yoshiki,Yamamoto Satoshi,Inui Kazuo,Inatomi Osamu,Andoh Akira,Nakahara Kazuyuki,Miyakawa Hiroyuki,Hamada Shin,Kawa Shigeyuki,Okazaki Kazuichi,Shimosegawa Tooru
Abstract
ObjectiveCorticosteroid has been established as the standard therapy for autoimmune pancreatitis (AIP), but the requirement for maintenance corticosteroid therapy is controversial. We conducted a randomised controlled trial to clarify the efficacy of maintenance corticosteroid therapy in patients with AIP.DesignWe conducted a multicentre, tertiary setting, randomised controlled trial. After the induction of remission with the initial oral prednisolone (PSL) treatment, maintenance therapy with PSL at 5–7.5 mg/day was continued for 3 years or withdrawn at 26 weeks. The primary endpoint was relapse-free survival over 3 years and the secondary endpoint was serious corticosteroid-related complications. All analyses were performed on an intention-to-treat basis.ResultsBetween April 2009 and March 2012, 49 patients with AIP were randomly assigned to the maintenance therapy group (n=30) or the cessation group (n=19). Baseline characteristics were not different between the two groups. Relapses occurred within 3 years in 11 out of 19 (57.9%) patients assigned to the cessation group, and in 7 of 30 (23.3%) patients in the maintenance therapy group. The relapse rate over 3 years was significantly lower in the maintenance therapy group than that in the cessation group (p=0.011). The relapse-free survival was significantly longer in the maintenance therapy group than that in the cessation group (p=0.007). No serious corticosteroid-related complications requiring discontinuation of PSL were observed.ConclusionsMaintenance corticosteroid therapy for 3 years may decrease relapses in patients with AIP compared with those who discontinued the therapy at 26 weeks.Trial registration numberUMIN000001818; Results.
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