Department of Gastrointestinal Surgery, Helsinki University Hospital, Helsinki, Finland.
Genome-Scale Biology Research Program, Research Programs Unit, University of Helsinki, Helsinki, Finland.
Inflamm Bowel Dis. 2021 Oct 20;27(11):1766-1772. doi: 10.1093/ibd/izab001.
In ulcerative colitis, a pouchitis is the most common long-term adverse effect after proctocolectomy and ileal pouch-anal anastomosis. Approximately 5% of patients develop chronic antibiotic-dependent or antibiotic-refractory pouchitis without any effective treatment. The aim of this trial was to investigate the efficacy and safety of fecal microbiota transplantation in the treatment of chronic pouchitis.
This was a single-center, double-blinded, parallel group trial comparing donor fecal microbiota transplantation with placebo (autologous transplant) in chronic pouchitis. Twenty-six patients were recruited at the Helsinki University Hospital between December 2017 and August 2018 and were randomly allocated a 1:1 ratio to either donor fecal microbiota transplantation or placebo. The protocol included 2 transplantations into the pouch on weeks 0 and 4, and patients were followed up for 52 weeks.
Nine patients in the intervention group and 8 patients in the placebo group relapsed during the 52-week follow-up, and the relapse-free survival did not differ between the groups (P = 0.183, log-rank; hazard ratio, 1.90 [95% confidence interval, 0.73-4.98; P = 0.190]). In the subgroup analysis of patients using continuous antibiotics before the study, the relapse-free survival was shorter in the intervention group (P = 0.004, log-rank; hazard ratio, 13.08 [95% confidence interval, 1.47-116.60; P = 0.021]). No major adverse effects were reported.
The fecal microbiota transplantation treatment regime used in our study was not effective in the treatment of chronic pouchitis. The safety profile of fecal microbiota transplantation was good.
CLINICALTRIALS.GOV IDENTIFIER: NCT03378921.
在溃疡性结肠炎患者中,直肠结肠切除和回肠储袋肛管吻合术后最常见的长期不良事件是 pouchitis。大约 5%的患者发生慢性抗生素依赖性或抗生素难治性 pouchitis,而没有任何有效的治疗方法。本试验旨在研究粪便微生物群移植在治疗慢性 pouchitis 中的疗效和安全性。
这是一项单中心、双盲、平行组试验,比较了供体粪便微生物群移植与慢性 pouchitis 安慰剂(自体移植)的疗效。2017 年 12 月至 2018 年 8 月期间,赫尔辛基大学医院招募了 26 名患者,并以 1:1 的比例随机分配接受供体粪便微生物群移植或安慰剂。方案包括在第 0 周和第 4 周时向储袋中移植 2 次,随访 52 周。
在 52 周的随访期间,干预组有 9 名患者和安慰剂组有 8 名患者复发,两组的无复发生存率无差异(P = 0.183,对数秩;风险比,1.90 [95%置信区间,0.73-4.98;P = 0.190])。在研究前使用连续抗生素的患者亚组分析中,干预组的无复发生存率较短(P = 0.004,对数秩;风险比,13.08 [95%置信区间,1.47-116.60;P = 0.021])。未报告主要不良事件。
本研究中使用的粪便微生物群移植治疗方案对慢性 pouchitis 的治疗无效。粪便微生物群移植的安全性良好。
NCT03378921。