Department of Gastroenterology, Hospital Clínic, IDIBAPS, CIBERehd, Barcelona, Spain.
Department of Surgery, Hospital U. Fundación Jiménez Díaz, Madrid, Spain.
Gastroenterology. 2018 Apr;154(5):1334-1342.e4. doi: 10.1053/j.gastro.2017.12.020. Epub 2017 Dec 24.
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.
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).
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.
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.
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。
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)。
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。
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。