TY - JOUR
T1 - Middle-term prognosis in patients with ulcerative colitis who achieved clinical and endoscopic remission by budesonide rectal foam
AU - ESCORT study Group
AU - Naganuma, Makoto
AU - Hirai, Fumihito
AU - Kobayashi, Kiyonori
AU - Watanabe, Kenji
AU - Takeuchi, Ken
AU - Aoyama, Nobuo
AU - Nozawa, Hiroshi
AU - Motoya, Satoshi
AU - Ohmori, Toshihide
AU - Harada, Akio
AU - Nagai, Yushi
AU - Abe, Takayuki
AU - Yamada, Yoji
AU - Inagaki, Katsutoshi
AU - Shimizu, Naoki
AU - Kanai, Takanori
AU - Watanabe, Mamoru
AU - Tanaka, Shinji
AU - Arai, Takehiro
AU - Kishi, Masahiro
AU - Watanabe, Chiyuki
AU - Sakata, Yasuhisa
AU - Ashida, Toshifumi
AU - Maemoto, Atsuo
AU - Sai, Souken
AU - Kitano, Atsuo
AU - Sameshima, Yukinori
AU - Yokoyama, Kaoru
AU - Kobayashi, Taku
AU - Suekane, Takehisa
AU - Matsuda, Koichiro
AU - Obata, Hirozumi
AU - Fujiya, Mikihiro
AU - Shirai, Takayuki
AU - Tominaga, Keiichi
AU - Takedatsu, Hidetoshi
AU - Suzuki, Ryouichi
N1 - Funding Information:
This work was funded by EA Pharma Co. and Kissei Pharmaceutical Co., Ltd. The commercial affiliates provided support in the form of salaries for authors [YY,KI and NS]. The specific roles of these authors are articulated in the Author Contributions section. The funders had no additional role in the study design, data collection and analysis, or decision to publish.
Publisher Copyright:
© 2019 Naganuma et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PY - 2019/8/1
Y1 - 2019/8/1
N2 - Background Budesonide foam is effective in inducing clinical remission in ulcerative colitis (UC) patients with active proctosigmoiditis. The aim of this study was to evaluate the duration of remission and predictors of relapse in UC patients who achieved clinical remission and mucosal healing by 6-week treatment with topical budesonide. Methods This is a retrospective, observational, multicenter study with a 2-year follow-up period. UC patients who were treated with budesonide foam in phase 2 or phase 3 clinical trials and achieved both clinical remission and mucosal healing were enrolled. Results Among 84 patients who met the eligibility criteria, 60 participated in the study. Eighteen of the 60 patients (30.0%; 95% confidence interval [CI]: 18.9–43.2) experienced no relapse (i.e., maintenance of remission) during the 2-year follow-up period. The median relapse-free survival time was 0.82 years (95% CI: 0.51–1.52). Of 37 patients with a Mayo endoscopic subscore of 0 after inducing remission with budesonide foam, 25 (67.6%) relapsed within 2 years. Patients with a disease duration of <1 year experienced a worse clinical outcome than patients with a disease duration of >5 years, and the hazard ratio was 2.38 (95% CI: 1.04–5.45). Conclusion This is the first study to evaluate the short- to middle-term prognosis in UC patients who achieved mucosal healing with topical preparations. After inducing remission by budesonide foam, treatment for maintaining remissions and strict follow-up may be needed for patients with shorter disease duration.
AB - Background Budesonide foam is effective in inducing clinical remission in ulcerative colitis (UC) patients with active proctosigmoiditis. The aim of this study was to evaluate the duration of remission and predictors of relapse in UC patients who achieved clinical remission and mucosal healing by 6-week treatment with topical budesonide. Methods This is a retrospective, observational, multicenter study with a 2-year follow-up period. UC patients who were treated with budesonide foam in phase 2 or phase 3 clinical trials and achieved both clinical remission and mucosal healing were enrolled. Results Among 84 patients who met the eligibility criteria, 60 participated in the study. Eighteen of the 60 patients (30.0%; 95% confidence interval [CI]: 18.9–43.2) experienced no relapse (i.e., maintenance of remission) during the 2-year follow-up period. The median relapse-free survival time was 0.82 years (95% CI: 0.51–1.52). Of 37 patients with a Mayo endoscopic subscore of 0 after inducing remission with budesonide foam, 25 (67.6%) relapsed within 2 years. Patients with a disease duration of <1 year experienced a worse clinical outcome than patients with a disease duration of >5 years, and the hazard ratio was 2.38 (95% CI: 1.04–5.45). Conclusion This is the first study to evaluate the short- to middle-term prognosis in UC patients who achieved mucosal healing with topical preparations. After inducing remission by budesonide foam, treatment for maintaining remissions and strict follow-up may be needed for patients with shorter disease duration.
UR - http://www.scopus.com/inward/record.url?scp=85070589565&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85070589565&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0220413
DO - 10.1371/journal.pone.0220413
M3 - Article
C2 - 31381615
AN - SCOPUS:85070589565
SN - 1932-6203
VL - 14
JO - PloS one
JF - PloS one
IS - 8
M1 - e0220413
ER -