Department of Internal Medicine, Chonnam National University Hospital and College of Medicine, Hwasun 58128, Jeollanam-do, South Korea.
Department of Parasitology and Tropical Medicine, Chonnam National University Medical School, Hwasun 58128, Jeollanam-do, South Korea.
World J Gastroenterol. 2021 Nov 14;27(42):7340-7349. doi: 10.3748/wjg.v27.i42.7340.
Immunotherapy has revolutionized the clinical outcomes of intractable cancer patients. Little is known about the intestinal nonpathogenic bacterial composition of hepatocellular carcinoma (HCC) patients treated by immunotherapy.
To determine whether there is a correlation between gut bacterial composition and prognosis in HCC patients.
From September 2019 to March 2020, we prospectively collected fecal samples and examined the gut microbiome of 8 advanced HCC patients treated with nivolumab as a second- or third-line systemic treatment. Fecal samples were collected before the start of immunotherapy. Fecal samples of patients with progression during treatment were collected at the time of progression, and fecal samples of patients who showed good response to nivolumab were collected after 5-7 mo as follow-up. Metagenomic data from 16S ribosomal RNA sequencing were analyzed using CLC Genomics Workbench. Microbiome data were analyzed according to therapeutic response.
All 8 patients were male, of which 6 had underlying chronic hepatitis B. A higher Shannon index was found in the responders than in the non-responders after nivolumab therapy ( = 0.036). The unweighted beta diversity analysis also showed that the overall bacterial community structure and phylogenetic diversity were clearly distinguished according to therapeutic response. There was no significant difference in the diversity or composition of the patient gut microbiome according to the immunotherapy used. Several taxa specific to therapeutic response were designated as follows: sp., and for the non-responders; sp. and for the responders. Of note, a skewed ratio and a low ratio can serve as predictive markers of non-response, whereas the presence of species predicts a good response.
The current presumptive study suggests a potential role for the gut microbiome as a prognostic marker for the response to nivolumab in treatment of HCC patients.
免疫疗法彻底改变了难治性癌症患者的临床预后。对于接受免疫治疗的肝细胞癌(HCC)患者的肠道非病原性细菌组成,知之甚少。
确定肠道细菌组成与 HCC 患者预后之间是否存在相关性。
本研究前瞻性收集了 2019 年 9 月至 2020 年 3 月 8 例接受纳武利尤单抗二线或三线系统治疗的晚期 HCC 患者的粪便样本,并对肠道微生物组进行了检查。免疫治疗开始前采集粪便样本。治疗过程中进展的患者在进展时采集粪便样本,对纳武利尤单抗治疗反应良好的患者在 5-7 个月后采集粪便样本作为随访。使用 CLC Genomics Workbench 分析 16S 核糖体 RNA 测序的宏基因组数据。根据治疗反应分析微生物组数据。
所有 8 例患者均为男性,其中 6 例患有慢性乙型肝炎。纳武利尤单抗治疗后,应答者的 Shannon 指数高于无应答者(=0.036)。未加权 beta 多样性分析也表明,根据治疗反应,整体细菌群落结构和系统发育多样性明显区分。根据使用的免疫疗法,患者肠道微生物组的多样性或组成没有差异。指定了几个与治疗反应相关的特定分类群如下:无应答者为 sp. 和 sp.;应答者为 sp. 和 sp.。值得注意的是,偏度比和低 比可作为无反应的预测标志物,而 种的存在则预示着良好的反应。
目前的初步研究表明,肠道微生物组可能作为预测 HCC 患者接受纳武利尤单抗治疗反应的预后标志物。