Symptom Improvement of ulceRative colitis after an Induction dose of UStekinumab in Japanese clinical practice (SIRIUS), measured using patient-reported outcomes: a prospective observational study

BMJ Open. 2022 May 4;12(5):e060081. doi: 10.1136/bmjopen-2021-060081.

Abstract

Introduction: Ulcerative colitis (UC) is an idiopathic, chronic inflammatory disease of the large intestine. Ustekinumab is a monoclonal antibody against the p40 subunit of interleukin-12 and interleukin-23 and has proven efficacy in inducing and maintaining remission in adult patients with moderate-to-severe UC. In the Symptom Improvement of ulceRative colitis after an Induction dose of Ustekinumab study, we will document the initial treatment response (daily patient-reported outcomes for 8 weeks from first infusion) and treatment patterns of patients wih UC receiving an induction dose of ustekinumab in the real-world setting in Japan. We will also investigate the relationship between the treatment response at week 8 and early indicators of response and determine patient factors that may define the appropriate dosing interval for maintenance therapy.

Methods and analysis: For this single-arm, prospective observational study at 24 centres in Japan with a follow-up period of 16/20 weeks, we aim to recruit 140 patients with moderate-to-severe UC between July 2021 and July 2022. All surveys will be conducted in Japanese and patient-reported outcomes relating to rectal bleeding, stool frequency, abdominal pain, nocturnal diarrhoea, tenesmus and perception of UC symptoms will be recorded using a smartphone application, where the patients can enter their initial response to ustekinumab induction therapy on a daily basis. Dosing intervals and the reasons for selecting this interval, and concomitant medications taken during treatment with ustekinumab will be collected by a physician questionnaire at the end of the study. On completion of primary end point (8-week patient-reported outcomes) data collection, results will be reported sequentially.

Ethics and dissemination: The study has been approved by the ethics committee of each facility involved and the Institutional Review Board of the non-profit organisation MINS.

Trial registration number: UMIN000043753, NCT04963725.

Keywords: gastroenterology; health informatics; inflammatory bowel disease; protocols & guidelines.

Publication types

  • Observational Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Colitis, Ulcerative* / drug therapy
  • Humans
  • Japan
  • Patient Reported Outcome Measures
  • Remission Induction
  • Treatment Outcome
  • Ustekinumab* / adverse effects
  • Ustekinumab* / therapeutic use

Substances

  • Ustekinumab

Associated data

  • ClinicalTrials.gov/NCT04963725
  • UMIN-CTR/UMIN000043753