Research Center of the Centre Hospitalier de l'Université de Montréal, Montréal (CRCHUM), Montreal, Quebec, Canada.
Hematology-Oncology Division, Department of Medicine, Centre Hospitalier de l'Université de Montréal (CHUM), Montreal, Quebec, Canada.
Nat Med. 2023 Aug;29(8):2121-2132. doi: 10.1038/s41591-023-02453-x. Epub 2023 Jul 6.
Fecal microbiota transplantation (FMT) represents a potential strategy to overcome resistance to immune checkpoint inhibitors in patients with refractory melanoma; however, the role of FMT in first-line treatment settings has not been evaluated. We conducted a multicenter phase I trial combining healthy donor FMT with the PD-1 inhibitors nivolumab or pembrolizumab in 20 previously untreated patients with advanced melanoma. The primary end point was safety. No grade 3 adverse events were reported from FMT alone. Five patients (25%) experienced grade 3 immune-related adverse events from combination therapy. Key secondary end points were objective response rate, changes in gut microbiome composition and systemic immune and metabolomics analyses. The objective response rate was 65% (13 of 20), including four (20%) complete responses. Longitudinal microbiome profiling revealed that all patients engrafted strains from their respective donors; however, the acquired similarity between donor and patient microbiomes only increased over time in responders. Responders experienced an enrichment of immunogenic and a loss of deleterious bacteria following FMT. Avatar mouse models confirmed the role of healthy donor feces in increasing anti-PD-1 efficacy. Our results show that FMT from healthy donors is safe in the first-line setting and warrants further investigation in combination with immune checkpoint inhibitors. ClinicalTrials.gov identifier NCT03772899 .
粪便微生物群移植(FMT)代表了一种克服难治性黑色素瘤患者对免疫检查点抑制剂耐药的潜在策略;然而,FMT 在一线治疗中的作用尚未得到评估。我们在 20 名未经治疗的晚期黑色素瘤患者中进行了一项多中心 I 期试验,将健康供体 FMT 与 PD-1 抑制剂纳武单抗或帕博利珠单抗联合使用。主要终点是安全性。单独进行 FMT 无 3 级不良事件报告。5 名患者(25%)联合治疗出现 3 级免疫相关不良事件。关键次要终点是客观缓解率、肠道微生物组组成变化以及系统免疫和代谢组学分析。客观缓解率为 65%(20 例中有 13 例),包括 4 例(20%)完全缓解。纵向微生物组分析显示,所有患者均从各自供体中定植了菌株;然而,在应答者中,供体和患者微生物组之间的获得相似性仅随时间增加。应答者在 FMT 后经历了免疫原性细菌的富集和有害细菌的丧失。Avatar 小鼠模型证实了健康供体粪便在增加抗 PD-1 疗效中的作用。我们的结果表明,健康供体的 FMT 在一线治疗中是安全的,值得与免疫检查点抑制剂进一步联合研究。ClinicalTrials.gov 标识符:NCT03772899。