Hematopoietic Cell Transplant and Cellular Therapy Program, Massachusetts General Hospital, Boston, MA.
Platform for Innovative Microbiome and Translational Research, Department of Genomic Medicine, The University of Texas MD Anderson Cancer Center, Houston, TX.
Blood Adv. 2024 May 14;8(9):2074-2084. doi: 10.1182/bloodadvances.2024012556.
Disruption of the intestinal microbiome is observed with acute graft-versus-host disease (GVHD) of the lower gastrointestinal (LGI) tract, and fecal microbiota transplantation (FMT) has successfully cured steroid-refractory cases. In this open-label, single-arm, pilot study, third-party, single-donor FMT was administered in combination with systemic corticosteroids to participants with high-risk acute LGI GVHD, with a focus on treatment-naïve cases. Participants were scheduled to receive 1 induction dose (15 capsules per day for 2 consecutive days), followed by 3 weekly maintenance doses, consisting of 15 capsules per dose. The primary end point of the study was feasibility, which would be achieved if ≥80% of participants able to swallow ≥40 of the 75 scheduled capsules. Ten participants (9 treatment-naïve; 1 steroid-refractory) were enrolled and treated. The study met the primary end point, with 9 of 10 participants completing all eligible doses. Organ-specific LGI complete response rate at day 28 was 70%. Initial clinical response was observed within 1 week for all responders, and clinical responses were durable without recurrent LGI GVHD in complete responders. Exploratory analyses suggest that alpha diversity increased after FMT. Although recipient microbiome composition never achieved a high degree of donor similarity, expansion of donor-derived species and increases in tryptophan metabolites and short-chain fatty acids were observed within the first 7 days after FMT. Investigation into the use of microbiome-targeted interventions earlier in the treatment paradigm for acute LGI GVHD is warranted. This trial was registered at www.ClinicalTrials.gov as #NCT04139577.
肠道微生物组的紊乱与急性移植物抗宿主病(GVHD)的下胃肠道(LGI)有关,粪便微生物群移植(FMT)已成功治愈了类固醇难治性病例。在这项开放标签、单臂、试点研究中,对高危急性 LGI GVHD 患者联合全身皮质类固醇给予第三方、单一供体 FMT,重点关注治疗初治病例。患者计划接受 1 次诱导剂量(连续 2 天每天 15 粒胶囊),然后接受 3 次每周维持剂量,每次剂量 15 粒胶囊。研究的主要终点是可行性,如果≥80%的参与者能够吞咽≥75 粒预定胶囊中的 40 粒,则认为达到主要终点。10 名参与者(9 名治疗初治;1 名类固醇难治性)入组并接受治疗。该研究达到了主要终点,10 名参与者中有 9 名完成了所有合格剂量。28 天时,器官特异性 LGI 完全缓解率为 70%。所有应答者均在 1 周内观察到初始临床应答,且在完全应答者中,临床应答持久,无复发性 LGI GVHD。探索性分析表明,FMT 后 alpha 多样性增加。尽管受者微生物组组成从未达到供者相似的高度,但在 FMT 后 7 天内观察到供者衍生物种的扩张以及色氨酸代谢物和短链脂肪酸的增加。值得对急性 LGI GVHD 的治疗模式早期进行微生物组靶向干预的研究。该试验在 www.ClinicalTrials.gov 上注册,编号为#NCT04139577。