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Autologous Fecal Microbiota Transplantation for Diversion Colitis

2026年6月23日 更新者:Yongjian Liao

Autologous Fecal Microbiota Transplantation Via the Diverting Stoma Ameliorates Diversion Colitis in Patients With Temporary Ileostomy for Rectal Cancer: A Randomized Controlled Trial With Endoscopic and Histopathological Assessment

Diversion colitis (DC) is a common inflammatory complication in patients with temporary ileostomy after rectal cancer surgery, and no standardized medical treatment exists. This prospective, assessor-blinded, parallel-group, randomized controlled trial evaluated whether autologous fecal microbiota transplantation (auto-FMT) delivered through the diverting stoma ameliorates DC and improves post-reversal outcomes. Sixty-six patients with endoscopically confirmed DC were randomized 1:1 to receive daily auto-FMT (n=33) or saline irrigation (n=33) for four weeks. The primary endpoints are changes from baseline to week 4 in endoscopic (modified Harig score, 0-12) and histopathological (0-9) scores. Secondary endpoints include Wexner incontinence score, quality of life (EORTC QLQ-C30/CR29), inflammatory biomarkers, and safety. The study is designed to test whether auto-FMT produces superior improvements in endoscopic and histopathological severity compared with saline control, and leads to better functional outcomes after stoma reversal.

調査の概要

詳細な説明

Background and Rationale

Diversion colitis frequently develops after fecal stream diversion, affecting most patients whose intestinal continuity remains interrupted for more than three to six months. While stoma reversal is definitive, many patients require prolonged diversion due to adjuvant chemotherapy, poor general condition, or anastomotic healing concerns. Existing medical therapies-including short-chain fatty acid enemas, 5-aminosalicylates, corticosteroids, and probiotics-lack consistent efficacy in randomized trials. Gut microbiota dysbiosis is a central driver of DC; restoring a diverse microbial community via fecal microbiota transplantation represents a rational approach. Autologous FMT using the patient's own stoma effluent avoids pathogen transmission, donor screening, and ethical concerns. However, no prospective RCT has systematically evaluated auto-FMT for DC using endoscopic and histopathological endpoints.

Study Design

Single-center, prospective, assessor-blinded, parallel-group, superiority randomized controlled trial with a 1:1 allocation ratio.

Participants

Adults aged 18-75 years with histopathologically confirmed rectal adenocarcinoma who underwent low anterior resection with temporary loop ileostomy, scheduled for reversal at 3-6 months after primary surgery, and with endoscopic DC (modified Harig score ≥4 at week 4 post-ileostomy). Key exclusion criteria: neoadjuvant chemoradiotherapy, pre-existing inflammatory bowel disease, recent antibiotic or probiotic use, severe organ dysfunction, pregnancy, or lactation.

Interventions

Auto-FMT group: Daily irrigations of autologous fecal microbiota suspension for 4 weeks. Preparation: 50-80 g of fresh stool collected from the patient's stoma bag within 2 hours of passage, homogenized with 500 mL sterile normal saline (0.9% NaCl) pre-warmed to 37°C, stirred, and filtered through two layers of sterile gauze. The filtrate was used within 30 minutes. Irrigation: a 14-16 French Foley catheter inserted 10-15 cm into the efferent limb of the loop ileostomy; suspension infused by gravity drip over 5-10 minutes; patients retained the suspension for at least 30 minutes before evacuation.

Control group: Daily irrigations of 500 mL sterile normal saline (37°C) using the same catheter and technique, with the same retention time.

Outcome Measures

Primary outcomes: Change from baseline to week 4 in endoscopic score (modified Harig score, 0-12) and histopathological score (composite of mucosal atrophy, crypt distortion, and inflammatory infiltrate, 0-9), assessed by blinded reviewers.

Secondary outcomes: Wexner incontinence score at 1, 3, and 6 months after stoma reversal; quality of life (EORTC QLQ-C30 and QLQ-CR29) at baseline, week 4, and 6 months post-reversal; serum hs-CRP, albumin, and fecal calprotectin at baseline and week 4; adverse events (CTCAE v5.0); treatment adherence (≥80% of 28 sessions).

Sample Size

33 patients per group (total 66) to detect a mean endoscopic score reduction difference of 1.5 points (assuming SD 2.0 in auto-FMT group and SD 1.8 in control group), 80% power, two-sided α = 0.05, accounting for a 20% dropout rate.

Statistical Analysis

Primary analysis was intention-to-treat. Change scores were analyzed using ANCOVA with baseline score as covariate. Secondary outcomes: Wexner scores with generalized estimating equations; quality of life with ANCOVA; biomarkers with Mann-Whitney U tests. Missing data were handled with multiple imputation. Two-tailed p < 0.05 was considered significant.

Ethical Approval

The protocol was approved by the Ethics Committee of Lin'an First People's Hospital, Hangzhou (Approval No.: Lin'an First People's Hospital Lun Yan Shen 2022 No.20, dated April 29, 2022). Written informed consent was obtained from all participants. The study followed the Declaration of Helsinki.

研究の種類

介入

入学 (実際)

66

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

    • Zhejiang
      • Hangzhou、Zhejiang、中国、311300
        • Department of Colorectal Surgery, The First People's Hospital of Lin'an District, Hangzhou

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

Inclusion Criteria:

  • Histopathologically confirmed rectal adenocarcinoma.
  • Low anterior resection with temporary loop ileostomy.
  • Age 18-75 years.
  • Scheduled for ileostomy reversal at 3-6 months after primary surgery.
  • Endoscopic confirmation of diversion colitis at week 4 post-ileostomy (modified Harig score ≥4, range 0-12).
  • Written informed consent.

Exclusion Criteria:

  • Neoadjuvant chemoradiotherapy.
  • Pre-existing inflammatory bowel disease, irritable bowel syndrome, or chronic constipation.
  • Previous colorectal surgery (other than index surgery).
  • Active infection requiring systemic antibiotics within 4 weeks before enrollment.
  • Use of probiotics, prebiotics, or antibiotics within 4 weeks before enrollment.
  • Severe organ dysfunction (Child-Pugh B/C cirrhosis, end-stage renal disease).
  • Pregnancy or lactation.
  • Any condition precluding protocol compliance or outcome assessment.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:独身

武器と介入

参加者グループ / アーム
介入・治療
実験的:Autologous Fecal Microbiota Transplantation (auto-FMT)
Daily irrigations of autologous fecal microbiota suspension via the diverting stoma for 4 weeks. Preparation: 50-80 g of fresh stool collected from the patient's stoma bag within 2 hours of passage, homogenized with 500 mL of sterile normal saline (0.9% NaCl) pre-warmed to 37 °C, stirred, and filtered through two layers of sterile gauze. The filtrate is used within 30 minutes. Irrigation: A 14-16 French Foley catheter inserted 10-15 cm into the efferent limb of the loop ileostomy, balloon inflated with 5-8 mL of air. The suspension is infused by gravity drip (bag 40-50 cm above stoma) over 5-10 minutes. Patients retain the suspension for at least 30 minutes before evacuation. Vital signs are monitored for the first 3 days.
Daily irrigation of autologous fecal microbiota suspension via the diverting stoma for 4 weeks.
他の:Saline Irrigation
Daily irrigations of 500 mL sterile normal saline (0.9% NaCl) pre-warmed to 37 °C via the diverting stoma for 4 weeks. A 14-16 French Foley catheter is inserted 10-15 cm into the efferent limb of the loop ileostomy, and the balloon is inflated with 5-8 mL of air. Saline is infused by gravity drip (bag 40-50 cm above stoma) over 5-10 minutes. Patients retain the saline for at least 30 minutes before evacuation.
Daily irrigation of 500 mL sterile normal saline (0.9%) at 37°C via the diverting stoma, using the same catheter and technique as the auto-FMT group.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Change in Endoscopic Score
時間枠:Baseline and Week 4
Change from baseline to week 4 in modified Harig score (0-12), evaluating edema/erythema, loss of vascular pattern, friability/contact bleeding, and erosions/ulcerations (each 0-3). Higher scores indicate more severe inflammation. A blinded colorectal endoscopist performed colonoscopy through the stoma at week 0 and week 4.
Baseline and Week 4
Change in Histopathological Score
時間枠:Baseline and Week 4
Change from baseline to week 4 in composite histopathological score (0-9), assessing mucosal atrophy, crypt distortion, and inflammatory infiltrate (each 0-3). The average score of two blinded gastrointestinal pathologists was used; disagreements (>2 points) were resolved by joint review.
Baseline and Week 4

二次結果の測定

結果測定
メジャーの説明
時間枠
Wexner Incontinence Score
時間枠:Month 1, Month 3, Month 6 post-reversal
Wexner incontinence score (0-20, where 0 = perfect continence, 20 = complete incontinence) assessed at 1, 3, and 6 months after stoma reversal.
Month 1, Month 3, Month 6 post-reversal
Quality of Life - EORTC QLQ-C30 Global Health Status
時間枠:Baseline, Week 4, and Month 6 post-reversal
Global health status / quality of life score from the EORTC QLQ-C30 questionnaire. Higher scores indicate better quality of life.
Baseline, Week 4, and Month 6 post-reversal
Quality of Life - EORTC QLQ-CR29
時間枠:Baseline, Week 4, and Month 6 post-reversal
Disease-specific quality of life assessed by the EORTC QLQ-CR29 module, covering symptoms and functioning domains relevant to colorectal cancer patients.
Baseline, Week 4, and Month 6 post-reversal
Serum hs-CRP Level
時間枠:Baseline and Week 4
High-sensitivity C-reactive protein (hs-CRP) measured in mg/L from serum samples.
Baseline and Week 4
Serum Albumin Level
時間枠:Baseline and Week 4
Albumin concentration measured in g/L from serum samples.
Baseline and Week 4
Fecal Calprotectin Level
時間枠:Baseline and Week 4
Fecal calprotectin concentration measured by ELISA (μg/g), as a biomarker of intestinal inflammation.
Baseline and Week 4
Adverse Events and Treatment Adherence
時間枠:Throughout the 4-week intervention period for adverse events; at end of intervention for adherence
Adverse events graded according to CTCAE v5.0 (incidence, severity, and causality). Treatment adherence defined as completion of ≥80% of 28 scheduled irrigation sessions.
Throughout the 4-week intervention period for adverse events; at end of intervention for adherence

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研究に関する情報を入力する責任者は、自発的にこれらの出版物を提供します。これらは、研究に関連するあらゆるものに関するものである可能性があります。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2022年6月1日

一次修了 (実際)

2025年3月31日

研究の完了 (実際)

2025年9月30日

試験登録日

最初に提出

2026年6月15日

QC基準を満たした最初の提出物

2026年6月23日

最初の投稿 (実際)

2026年6月29日

学習記録の更新

投稿された最後の更新 (実際)

2026年6月29日

QC基準を満たした最後の更新が送信されました

2026年6月23日

最終確認日

2026年6月1日

詳しくは

本研究に関する用語

その他の研究ID番号

  • 2022-YJ-020

個々の参加者データ (IPD) の計画

個々の参加者データ (IPD) を共有する予定はありますか?

はい

IPD プランの説明

De-identified individual participant data underlying the results reported in this manuscript will be made available to researchers who provide a methodologically sound proposal, for the purpose of individual participant data meta-analysis or other approved research. The study protocol, statistical analysis plan, and informed consent form will also be available. Data will be accessible immediately after publication, upon reasonable request to the corresponding author.

IPD 共有サポート情報タイプ

  • STUDY_PROTOCOL
  • ANALYTIC_CODE

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