Division of Gastroenterology, University of Alberta, Edmonton, AB, Canada.
Division of Gastroenterology, University of Alberta, Edmonton, AB, Canada.
Lancet Gastroenterol Hepatol. 2021 Apr;6(4):282-291. doi: 10.1016/S2468-1253(21)00007-8. Epub 2021 Feb 23.
Faecal microbiota transplantation (FMT) is highly effective for recurrent Clostridioides difficile infection but has inherent risks. Microbial Ecosystem Therapeutic 2 (MET-2) is an oral encapsulated formulation of 40 lyophilised bacterial species initially isolated from stool of a healthy donor, but subsequently manufactured independently of donors, eliminating potential risks introduced by changes in donor health. The aim of this study was to determine MET-2 activity, safety, and tolerability.
This phase 1, open-label, single-group feasibility study was done in Alberta, Canada. The main inclusion criteria were mild to moderate C difficile infection and at least one episode of C difficile infection recurrence (ie, two episodes of C difficile infection) within 12 months. Initial daily treatment was ten oral capsules for 2 days, then three capsules for 8 days. If C difficile infection recurred, a higher dose was offered: 20 capsules for 2 days, then three capsules for 8 days. Patients were followed for adverse events and C difficile infection recurrence up to day 130. The primary outcome was absence of C difficile infection recurrence (fewer than three unformed bowel movements in 24 h persisting for at least 2 days) at day 40 by intention-to-treat analysis. Secondary outcomes were mortality or hospitalisation due to C difficile infection, infections attributed to treatment, nausea, abdominal pain, vomiting, or diarrhoea during treatment, quality of life (C difficile Health Related Quality of Life Questionnaire) before and after treatment, and engrafted MET-2 bacteria in patient stool. Absence of C difficile infection recurrence at day 130 was an exploratory outcome. This study is registered with ClinicalTrials.gov, NCT02865616 FINDINGS: Between Sept 19, 2018, and Feb 28, 2020, we enrolled 19 adult patients with at least two episodes of mild to moderate C difficile infection (median age 65 years [IQR 56-67]; 12 women [63%], seven men [37%]). Recurrent C difficile infection was absent at day 40 in 15 (79%) of 19 patients after initial treatment, increasing to 18 (95%) 40 days after retreatment. No mortality associated with C difficile infection, infections associated with MET-2 treatment, or other serious adverse events were observed. The most common self-limited, mild to moderate symptoms reported during treatment were diarrhoea in 12 (63%) of 19 patients and abdominal cramps in 12 (63%). After MET-2 treatment, quality of life improved significantly, as did alpha diversity in stool microbial composition (p=1·93×10). MET-2 associated taxa were found in greater abundance in most patients after treatment compared with baseline. 16 (84%) of 19 patients did not have recurrence of C difficile infection by day 130.
MET-2 appears to be safe, efficacious, and well tolerated among patients with recurrent C difficile infection. Results must be validated in controlled studies.
NuBiyota.
粪便微生物群移植(FMT)对复发性艰难梭菌感染非常有效,但存在固有风险。微生物生态治疗 2 号(MET-2)是一种口服封装制剂,包含 40 种冻干细菌,最初从健康供体的粪便中分离出来,但随后独立于供体制造,消除了供体健康变化带来的潜在风险。本研究旨在确定 MET-2 的活性、安全性和耐受性。
这是一项在加拿大艾伯塔省进行的 1 期、开放标签、单组可行性研究。主要纳入标准为轻度至中度艰难梭菌感染,且在 12 个月内至少有一次复发性艰难梭菌感染(即两次艰难梭菌感染)。初始每日治疗为连续 2 天口服 10 粒胶囊,然后连续 8 天口服 3 粒胶囊。如果艰难梭菌感染复发,会提供更高的剂量:连续 2 天口服 20 粒胶囊,然后连续 8 天口服 3 粒胶囊。患者在第 130 天之前接受不良事件和艰难梭菌感染复发的随访。主要结局是意向治疗分析中第 40 天无艰难梭菌感染复发(24 小时内无成形粪便少于 3 次,持续至少 2 天)。次要结局是因艰难梭菌感染导致的死亡率或住院、归因于治疗的感染、治疗期间的恶心、腹痛、呕吐或腹泻、治疗前后的艰难梭菌健康相关生活质量问卷(CD-HRQoL)评分以及患者粪便中定植的 MET-2 细菌。第 130 天无艰难梭菌感染复发是一项探索性结局。本研究在 ClinicalTrials.gov 注册,NCT02865616。
2018 年 9 月 19 日至 2020 年 2 月 28 日,我们纳入了 19 名至少有两次轻度至中度艰难梭菌感染的成年患者(中位年龄 65 岁[IQR 56-67];12 名女性[63%],7 名男性[37%])。19 名患者中,初始治疗后第 40 天 15 名(79%)患者无复发性艰难梭菌感染,第 40 天接受再次治疗后 18 名(95%)患者无复发性艰难梭菌感染。未观察到与艰难梭菌感染、与 MET-2 治疗相关的感染或其他严重不良事件相关的死亡率。治疗期间最常见的自限性、轻度至中度症状是 19 名患者中的 12 名(63%)腹泻和 12 名(63%)腹痛。接受 MET-2 治疗后,生活质量显著改善,粪便微生物组成的 alpha 多样性也有所改善(p=1·93×10)。与基线相比,治疗后大多数患者的 MET-2 相关菌群丰度更高。第 130 天,19 名患者中有 16 名(84%)未复发艰难梭菌感染。
MET-2 似乎在复发性艰难梭菌感染患者中安全、有效且耐受良好。结果必须在对照研究中得到验证。
NuBiyota。