Cong Jing, Zhang Yuguang, Xue Yadong, Zhang Chuantao, Xu Mingjin, Liu Dong, Zhang Ruiyan, Zhu Hua
College of Marine Science and Biological Engineering, Qingdao University of Science and Technology, Qingdao, China.
Key Laboratory of Forest Ecology, Environment of State Forestry Administration, Institute of Forestry Ecology, Environment and Protection, Chinese Academy of Forestry, Beijing, China.
Front Microbiol. 2020 Nov 10;11:583525. doi: 10.3389/fmicb.2020.583525. eCollection 2020.
Osimertinib contributes to the higher efficacy and few intestinal side effects in non-small cell lung cancer (NSCLC) patients with T790M mutation. Previous studies has reported that intestinal microbiota play important roles in drug efficacy and toxicity. However, we have known less about the changes of intestinal microbiota in response to osimertinib therapy. In this pilot study, we used longitudinal sampling with 6 weeks sampling collection intervals for about 1 year to model intestinal microbial changes based on the 16S rRNA genes sequencing in fecal samples from NSCLC patients in response to osimertinib therapy. The results showed that there was no significantly different on the intestinal microbial composition at the phylum, family, and genus level among NSCLC patients with different treatment cycles ( > 0.05). There were no significant differences in alpha diversity characterized by the richness, Shannon diversity, and phylogenetic diversity based on the Welch's -test among NSCLC patients in response to osimertinib therapy ( > 0.05). However, the dissimilarity test and principal coordination analysis showed a few differences among NSCLC patients. The intestinal microbial markers were changed in post-therapy (, , and ) compared to that in pre-therapy (). Furthermore, the phylogenetic molecular ecological networks (MENs) were influenced by osimertinib therapy based on the module number, link number, and module taxa composition of the first six groups. Overall, it indicated that osimertinib therapy changed the intestinal microbiota to some extent, though not completely. In all, this pilot study provides an understanding of changes of intestinal microbiota from NSCLC patients in response to osimertinib therapy. No complete changes in intestinal microbiota seem to be closely linked with the few intestinal side effects and higher efficacy in response to osimertinib therapy.
奥希替尼对携带T790M突变的非小细胞肺癌(NSCLC)患者疗效更佳且肠道副作用较少。既往研究报道肠道微生物群在药物疗效和毒性方面发挥重要作用。然而,我们对奥希替尼治疗后肠道微生物群的变化了解较少。在这项初步研究中,我们以6周的采样间隔进行纵向采样,持续约1年,基于对NSCLC患者粪便样本中16S rRNA基因测序来模拟肠道微生物变化,以了解奥希替尼治疗后的情况。结果显示,不同治疗周期的NSCLC患者在门、科和属水平的肠道微生物组成无显著差异(>0.05)。基于威尔科克森检验,接受奥希替尼治疗的NSCLC患者在以丰富度、香农多样性和系统发育多样性为特征的α多样性方面无显著差异(>0.05)。然而,差异检验和主坐标分析显示NSCLC患者之间存在一些差异。与治疗前相比,治疗后肠道微生物标志物发生了变化(、和)。此外,基于前六组的模块数量、连接数量和模块分类群组成,系统发育分子生态网络(MENs)受到奥希替尼治疗的影响。总体而言,这表明奥希替尼治疗在一定程度上改变了肠道微生物群,尽管并不完全。总之,这项初步研究让我们了解了NSCLC患者肠道微生物群对奥希替尼治疗的反应变化。肠道微生物群没有完全改变似乎与奥希替尼治疗时较少的肠道副作用和较高的疗效密切相关。