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干细胞治疗(Cx601)对克罗恩病合并复杂性肛旁瘘患者的长期疗效和安全性。

Long-term Efficacy and Safety of Stem Cell Therapy (Cx601) for Complex Perianal Fistulas in Patients With Crohn's Disease.

机构信息

Department of Gastroenterology, Hospital Clínic, IDIBAPS, CIBERehd, Barcelona, Spain.

Department of Surgery, Hospital U. Fundación Jiménez Díaz, Madrid, Spain.

出版信息

Gastroenterology. 2018 Apr;154(5):1334-1342.e4. doi: 10.1053/j.gastro.2017.12.020. Epub 2017 Dec 24.

Abstract

BACKGROUND & AIMS: Therapies for perianal fistulas in patients with Crohn's disease are often ineffective in producing long-term healing. We performed a randomized placebo-controlled trial to determine the long-term efficacy and safety of a single local administration of allogeneic expanded adipose-derived stem cells (Cx601) in patients with Crohn's disease and perianal fistulas.

METHODS

We performed a double-blind study at 49 hospitals in Europe and Israel, comprising 212 patients with Crohn's disease and treatment-refractory, draining, complex perianal fistulas. Patients were randomly assigned (1:1) to groups given a single local injection of 120 million Cx601 cells or placebo (control), in addition to the standard of care. Efficacy endpoints evaluated in the modified intention-to-treat population (randomly assigned, treated, and with 1 or more post-baseline efficacy assessment) at week 52 included combined remission (closure of all treated external openings draining at baseline with absence of collections >2 cm, confirmed by magnetic resonance imaging) and clinical remission (absence of draining fistulas).

RESULTS

The study's primary endpoint, at week 24, was previously reported (combined remission in 51.5% of patients given Cx601 vs 35.6% of controls, for a difference of 15.8 percentage points; 97.5% confidence interval [CI] 0.5-31.2; P = .021). At week 52, a significantly greater proportion of patients given Cx601 achieved combined remission (56.3%) vs controls (38.6%) (a difference of 17.7 percentage points; 95% CI 4.2-31.2; P = .010), and clinical remission (59.2% vs 41.6% of controls, for a difference of 17.6 percentage points; 95% CI 4.1-31.1; P = .013). Safety was maintained throughout week 52; adverse events occurred in 76.7% of patients in the Cx601 group and 72.5% of patients in the control group.

CONCLUSION

In a phase 3 trial of patients with Crohn's disease and treatment-refractory complex perianal fistulas, we found Cx601 to be safe and effective in closing external openings, compared with placebo, after 1 year. ClinicalTrials.gov no: NCT01541579.

摘要

背景与目的

克罗恩病患者的肛周瘘治疗通常无法实现长期愈合。我们进行了一项随机安慰剂对照试验,以确定同种异体扩增脂肪源性干细胞(Cx601)单次局部给药在克罗恩病合并肛周瘘患者中的长期疗效和安全性。

方法

我们在欧洲和以色列的 49 家医院进行了这项双盲研究,纳入了 212 例克罗恩病且经治疗后仍有活动性、有分泌物、复杂的肛周瘘患者。患者以 1:1 的比例随机分为两组,分别接受 1200 万 Cx601 细胞或安慰剂(对照)的单次局部注射,同时接受标准治疗。在修改后的意向治疗人群(随机分配、治疗且有 1 次或更多基线后疗效评估)中,第 52 周的主要疗效终点包括联合缓解(所有基线时接受治疗且有分泌物的瘘管外口闭合,且无>2cm 的蓄积,通过磁共振成像确认)和临床缓解(无活动性瘘管)。

结果

本研究的主要终点(第 24 周)此前已报道过(接受 Cx601 治疗的患者中,联合缓解率为 51.5%,而对照组为 35.6%,差异为 15.8 个百分点;97.5%置信区间[CI]为 0.5-31.2;P=.021)。第 52 周时,接受 Cx601 治疗的患者中达到联合缓解的比例显著更高(56.3%),而对照组为 38.6%(差异为 17.7 个百分点;95%CI 4.2-31.2;P=.010),达到临床缓解的比例也更高(59.2%vs对照组 41.6%,差异为 17.6 个百分点;95%CI 4.1-31.1;P=.013)。第 52 周时安全性仍保持稳定;Cx601 组有 76.7%的患者和对照组有 72.5%的患者出现不良事件。

结论

在一项针对克罗恩病且经治疗后仍有活动性复杂肛周瘘的患者的 3 期试验中,我们发现 Cx601 与安慰剂相比,在 1 年后能更有效地关闭瘘管外口,且安全性良好。临床试验注册:NCT01541579。

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