Department of Medical Oncology, Catalan Institute of Oncology, Barcelona, Spain.
Division of Medical Oncology and Haematology, Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Br J Cancer. 2024 Jun;130(12):1936-1942. doi: 10.1038/s41416-024-02701-y. Epub 2024 May 7.
Gut microbiome modulation to boost antitumor immune responses is under investigation.
ROMA-2 evaluated the microbial ecosystem therapeutic (MET)-4 oral consortia, a mixture of cultured human stool-derived immune-responsiveness associated bacteria, given with chemoradiation (CRT) in HPV-related oropharyngeal cancer patients. Co-primary endpoints were safety and changes in stool cumulative MET-4 taxa relative abundance (RA) by 16SRNA sequencing. Stools and plasma were collected pre/post-MET-4 intervention for microbiome and metabolome analysis.
Twenty-nine patients received ≥1 dose of MET-4 and were evaluable for safety: drug-related adverse events (AEs) occurred in 13/29 patients: all grade 1-2 except one grade 3 (diarrhea). MET-4 was discontinued early in 7/29 patients due to CRT-induced toxicity, and in 1/29 due to MET-4 AEs. Twenty patients were evaluable for ecological endpoints: there was no increase in stool MET-4 RA post-intervention but trended to increase in stage III patients (p = 0.06). MET-4 RA was higher in stage III vs I-II patients at week 4 (p = 0.03) and 2-month follow-up (p = 0.01), which correlated with changes in plasma and stool targeted metabolomics.
ROMA-2 did not meet its primary ecologic endpoint, as no engraftment was observed in the overall cohort. Exploratory findings of engraftment in stage III patients warrants further investigation of microbiome interventions in this subgroup.
调节肠道微生物组以增强抗肿瘤免疫反应正在研究中。
ROMA-2 评估了微生物生态治疗(MET)-4 口服菌群,这是一种由培养的人类粪便衍生的免疫反应相关细菌组成的混合物,与 HPV 相关的口咽癌患者的放化疗(CRT)联合使用。主要终点是安全性和 16SRNA 测序评估的粪便累积 MET-4 分类群相对丰度(RA)的变化。在 MET-4 干预前后采集粪便和血浆进行微生物组和代谢组分析。
29 例患者接受了≥1 剂 MET-4 并可评估安全性:13/29 例患者发生药物相关不良事件(AE):均为 1-2 级,仅 1 例为 3 级(腹泻)。7/29 例患者因 CRT 诱导的毒性而提前停用 MET-4,1/29 例患者因 MET-4 相关 AE 而停用。20 例患者可评估生态终点:干预后粪便 MET-4 RA 无增加趋势,但 III 期患者有增加趋势(p=0.06)。第 4 周(p=0.03)和 2 个月随访时(p=0.01),III 期患者的 MET-4 RA 高于 I-II 期患者,与血浆和粪便靶向代谢组学的变化相关。
ROMA-2 未达到其主要的生态终点,因为在整个队列中未观察到定植。III 期患者定植的探索性发现提示需要进一步研究该亚组的微生物组干预措施。