Guan Xiuwen, Ma Fei, Sun Xiaoying, Li Chunxiao, Li Lixi, Liang Fang, Li Shaochuan, Yi Zongbi, Liu Binliang, Xu Binghe
Department of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
State Key Laboratory of Molecular Oncology, Chinese Academy of Medical Sciences, Beijing, China.
Front Oncol. 2020 Jul 7;10:902. doi: 10.3389/fonc.2020.00902. eCollection 2020.
Low-dose metronomic chemotherapy can achieve disease control with reduced toxicity compared to conventional chemotherapy in maximum tolerated dose. Characterizing the gut microbiota of cancer patients under different dosage regimens may describe a new role of gut microbiota associated with drug efficacy. Therefore, we evaluated the composition and the function of gut microbiome associated with metronomic capecitabine compared to conventional dosage. The fecal samples of HER2-negative metastatic breast cancer patients treated with capecitabine as maintenance chemotherapy were collected and analyzed by 16S ribosome RNA gene sequencing. A total of 15 patients treated with metronomic capecitabine were compared to 16 patients under a conventional dose. The unweighted-unifrac index of the metronomic group was statistically significantly lower than that of the routine group ( = 0.025). Besides that, the Bray-Curtis distance-based redundancy analysis illustrated that the microbial genera between the two groups can be separated partly. Nine Kyoto Encyclopedia of Genes and Genomes (KEGG) modules were enriched in the metronomic group, while no KEGG modules were significantly enriched in the routine group. Moreover, univariate and multivariate analyses suggested that the median progression-free survival (PFS) was significantly shorter in patients with the gut microbial composition of (9.2 vs. 32.7 months, = 0.004), while the patients with had a significantly prolonged PFS than those without (32.7 vs. 12.9 months, = 0.013). The proof-of-principle study suggested that the gut microbiota of patients receiving metronomic chemotherapy was different in terms of diversity, composition, and function from those under conventional chemotherapy, and the presence of specific bacterial species may act as microbial markers associated with drug resistance monitoring and prognostic evaluation.
与最大耐受剂量的传统化疗相比,低剂量节拍化疗可在降低毒性的情况下实现疾病控制。描绘不同剂量方案下癌症患者的肠道微生物群可能会揭示肠道微生物群与药物疗效相关的新作用。因此,我们评估了与节拍性卡培他滨相比,传统剂量下肠道微生物组的组成和功能。收集了接受卡培他滨维持化疗的HER2阴性转移性乳腺癌患者的粪便样本,并通过16S核糖体RNA基因测序进行分析。将15例接受节拍性卡培他滨治疗的患者与16例接受传统剂量治疗的患者进行比较。节拍组的非加权组间距离指数在统计学上显著低于常规组(P = 0.025)。除此之外,基于Bray-Curtis距离的冗余分析表明,两组之间的微生物属可以部分分离。节拍组中富集了9个京都基因与基因组百科全书(KEGG)模块,而常规组中没有KEGG模块显著富集。此外,单因素和多因素分析表明,肠道微生物组为[具体微生物组成情况未给出]的患者中位无进展生存期(PFS)显著缩短(9.2个月对32.7个月,P = 0.004),而有[具体微生物组成情况未给出]的患者PFS比没有的患者显著延长(32.7个月对12.9个月,P = 0.013)。原理验证研究表明,接受节拍化疗患者的肠道微生物群在多样性、组成和功能方面与接受传统化疗的患者不同,特定细菌种类的存在可能作为与耐药性监测和预后评估相关的微生物标志物。