• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

肠道微生物群对日本晚期非小细胞肺癌有反应患者中免疫检查点抑制剂疗效的作用

The role of the gut microbiome on the efficacy of immune checkpoint inhibitors in Japanese responder patients with advanced non-small cell lung cancer.

作者信息

Katayama Yuki, Yamada Tadaaki, Shimamoto Takayuki, Iwasaku Masahiro, Kaneko Yoshiko, Uchino Junji, Takayama Koichi

机构信息

Department of Pulmonary Medicine, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kyoto, Japan.

出版信息

Transl Lung Cancer Res. 2019 Dec;8(6):847-853. doi: 10.21037/tlcr.2019.10.23.

DOI:10.21037/tlcr.2019.10.23
PMID:32010563
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6976345/
Abstract

BACKGROUND

Cancer immunotherapy is being developed as a promising alternative for advanced non-small cell lung cancer (NSCLC). However, novel biomarkers are required to select patients that will benefit from treatment with immune checkpoint inhibitors (ICIs) for a long period of time. The gut microbiome is expected to be a promising biomarker of ICI response owing to the regulation of the immune status within the host.

METHODS

In this retrospective study, we included 17 Japanese patients with advanced NSCLC who were treated with ICIs for >3 months in our hospital. Fecal samples obtained from the patients during ICI treatment were analyzed by 16S ribosomal RNA gene sequencing. We examined the correlation between the diversity of the gut microbiome and treatment with ICIs.

RESULTS

Several bacterial species were more abundant in ICI responders than in non-responders. Patients with abundant Lactobacillus and Clostridium tended to have a longer time to treatment failure (TTF) after receiving ICI than those with a lower abundance.

CONCLUSIONS

In conclusion, the composition of the gut microbiome is associated with better clinical benefits from ICI treatment in Japanese patients with NSCLC. A further large-scale study is warranted to validate the composition of the gut microbiome as a novel clinical factor influencing the response to ICIs for an extended time in NSCLC.

摘要

背景

癌症免疫疗法正被开发为晚期非小细胞肺癌(NSCLC)的一种有前景的替代疗法。然而,需要新的生物标志物来筛选能长期从免疫检查点抑制剂(ICI)治疗中获益的患者。由于宿主内免疫状态的调节,肠道微生物群有望成为ICI反应的一种有前景的生物标志物。

方法

在这项回顾性研究中,我们纳入了17例在我院接受ICI治疗超过3个月的日本晚期NSCLC患者。对ICI治疗期间从患者获取的粪便样本进行16S核糖体RNA基因测序分析。我们研究了肠道微生物群多样性与ICI治疗之间的相关性。

结果

几种细菌种类在ICI反应者中比在无反应者中更为丰富。乳酸杆菌和梭菌丰富的患者在接受ICI治疗后比那些丰度较低的患者往往有更长的至治疗失败时间(TTF)。

结论

总之,在日本NSCLC患者中,肠道微生物群的组成与ICI治疗带来的更好临床获益相关。有必要进行进一步的大规模研究,以验证肠道微生物群的组成作为一种新的临床因素在NSCLC中对ICI反应产生长期影响。

相似文献

1
The role of the gut microbiome on the efficacy of immune checkpoint inhibitors in Japanese responder patients with advanced non-small cell lung cancer.肠道微生物群对日本晚期非小细胞肺癌有反应患者中免疫检查点抑制剂疗效的作用
Transl Lung Cancer Res. 2019 Dec;8(6):847-853. doi: 10.21037/tlcr.2019.10.23.
2
Chronological analysis of the gut microbiome for efficacy of atezolizumab-based immunotherapy in non-small cell lung cancer: Protocol for a multicenter prospective observational study.基于 atezolizumab 的免疫疗法治疗非小细胞肺癌疗效的肠道微生物组的时间分析:一项多中心前瞻性观察研究方案。
Thorac Cancer. 2022 Oct;13(19):2829-2833. doi: 10.1111/1759-7714.14640. Epub 2022 Sep 5.
3
Fluctuations in Gut Microbiome Composition During Immune Checkpoint Inhibitor Therapy.免疫检查点抑制剂治疗期间肠道微生物群组成的波动
World J Oncol. 2023 Jun;14(3):178-187. doi: 10.14740/wjon1587. Epub 2023 Jun 11.
4
Impact of bowel movement condition on immune checkpoint inhibitor efficacy in patients with advanced non-small cell lung cancer.排便状况对晚期非小细胞肺癌患者免疫检查点抑制剂疗效的影响。
Thorac Cancer. 2019 Mar;10(3):526-532. doi: 10.1111/1759-7714.12969. Epub 2019 Jan 21.
5
Cancer Cachexia among Patients with Advanced Non-Small-Cell Lung Cancer on Immunotherapy: An Observational Study with Exploratory Gut Microbiota Analysis.免疫治疗的晚期非小细胞肺癌患者的癌症恶病质:一项探索性肠道微生物群分析的观察性研究
Cancers (Basel). 2022 Nov 2;14(21):5405. doi: 10.3390/cancers14215405.
6
Interaction of bacterial genera associated with therapeutic response to immune checkpoint PD-1 blockade in a United States cohort.美国队列中与免疫检查点 PD-1 阻断治疗反应相关的细菌属的相互作用。
Genome Med. 2022 Mar 29;14(1):35. doi: 10.1186/s13073-022-01037-7.
7
Gut microbiome affects the response to immunotherapy in non-small cell lung cancer.肠道微生物组影响非小细胞肺癌对免疫治疗的反应。
Thorac Cancer. 2024 May;15(14):1149-1163. doi: 10.1111/1759-7714.15303. Epub 2024 Apr 4.
8
The Gut Microbiome and Cancer Immunotherapy: Can We Use the Gut Microbiome as a Predictive Biomarker for Clinical Response in Cancer Immunotherapy?肠道微生物群与癌症免疫疗法:我们能否将肠道微生物群用作癌症免疫疗法临床反应的预测生物标志物?
Cancers (Basel). 2021 Sep 27;13(19):4824. doi: 10.3390/cancers13194824.
9
The Gut Microbiome Associates with Immune Checkpoint Inhibition Outcomes in Patients with Advanced Non-Small Cell Lung Cancer.肠道微生物组与晚期非小细胞肺癌患者免疫检查点抑制剂治疗结局相关。
Cancer Immunol Res. 2020 Oct;8(10):1243-1250. doi: 10.1158/2326-6066.CIR-20-0196. Epub 2020 Jul 27.
10
The Gut Microbiome from a Biomarker to a Novel Therapeutic Strategy for Immunotherapy Response in Patients with Lung Cancer.肠道微生物组:从生物标志物到肺癌患者免疫治疗反应的新型治疗策略。
Curr Oncol. 2023 Oct 24;30(11):9406-9427. doi: 10.3390/curroncol30110681.

引用本文的文献

1
Microbiome meets immunotherapy: unlocking the hidden predictors of immune checkpoint inhibitors.微生物组与免疫疗法相遇:揭开免疫检查点抑制剂的隐藏预测指标
NPJ Biofilms Microbiomes. 2025 Sep 2;11(1):180. doi: 10.1038/s41522-025-00819-2.
2
Non-small Cell Lung Cancer, Immunotherapy and the Influence of Gut Microbiome.非小细胞肺癌、免疫疗法与肠道微生物群的影响
Curr Microbiol. 2025 Jul 29;82(9):419. doi: 10.1007/s00284-025-04408-6.
3
Gut microbiota shapes cancer immunotherapy responses.肠道微生物群塑造癌症免疫治疗反应。
NPJ Biofilms Microbiomes. 2025 Jul 25;11(1):143. doi: 10.1038/s41522-025-00786-8.
4
Chemoimmunotherapy Outcomes and Prognostic Factors in Patients with Advanced, Low PD-L1-Expressing Non-Small Cell Lung Cancer.晚期、低程序性死亡配体1(PD-L1)表达的非小细胞肺癌患者的化疗免疫治疗结果及预后因素
Cancer Res Commun. 2025 Jul 1;5(7):1203-1214. doi: 10.1158/2767-9764.CRC-25-0157.
5
Beyond the tumor: the gut microbiome as a key player in immunotherapy efficacy and resistance.肿瘤之外:肠道微生物群在免疫治疗疗效和耐药性中起关键作用
Naunyn Schmiedebergs Arch Pharmacol. 2025 Jun 3. doi: 10.1007/s00210-025-04315-4.
6
Gut microbes and immunotherapy for non-small cell lung cancer: a systematic review.肠道微生物与非小细胞肺癌的免疫治疗:一项系统综述
Front Oncol. 2025 May 8;15:1518474. doi: 10.3389/fonc.2025.1518474. eCollection 2025.
7
Optimizing Cancer Treatment Through Gut Microbiome Modulation.通过调节肠道微生物群优化癌症治疗
Cancers (Basel). 2025 Apr 7;17(7):1252. doi: 10.3390/cancers17071252.
8
[Intestinal Flora Dysregulation and Lung Cancer: 
Mechanism Analysis and Clinical Application].[肠道菌群失调与肺癌:机制分析及临床应用]
Zhongguo Fei Ai Za Zhi. 2025 Jan 20;28(1):69-74. doi: 10.3779/j.issn.1009-3419.2025.106.02.
9
The gut microbiome and cancer response to immune checkpoint inhibitors.肠道微生物群与癌症对免疫检查点抑制剂的反应
J Clin Invest. 2025 Feb 3;135(3):e184321. doi: 10.1172/JCI184321.
10
Gut microbiota in cancer initiation, development and therapy.肠道微生物群在癌症的起始、发展和治疗中的作用
Sci China Life Sci. 2024 Dec 30. doi: 10.1007/s11427-024-2831-x.

本文引用的文献

1
The Diversity of Gut Microbiome is Associated With Favorable Responses to Anti-Programmed Death 1 Immunotherapy in Chinese Patients With NSCLC.肠道微生物组的多样性与中国 NSCLC 患者对抗 PD-1 免疫治疗的良好反应相关。
J Thorac Oncol. 2019 Aug;14(8):1378-1389. doi: 10.1016/j.jtho.2019.04.007. Epub 2019 Apr 23.
2
Bilophila wadsworthia aggravates high fat diet induced metabolic dysfunctions in mice.脆弱拟杆菌加剧高脂饮食诱导的小鼠代谢功能紊乱。
Nat Commun. 2018 Jul 18;9(1):2802. doi: 10.1038/s41467-018-05249-7.
3
The commensal microbiome is associated with anti-PD-1 efficacy in metastatic melanoma patients.共生微生物群与转移性黑色素瘤患者的抗PD-1疗效相关。
Science. 2018 Jan 5;359(6371):104-108. doi: 10.1126/science.aao3290.
4
Gut microbiome influences efficacy of PD-1-based immunotherapy against epithelial tumors.肠道微生物组影响基于 PD-1 的免疫疗法对上皮性肿瘤的疗效。
Science. 2018 Jan 5;359(6371):91-97. doi: 10.1126/science.aan3706. Epub 2017 Nov 2.
5
Gut microbiome modulates response to anti-PD-1 immunotherapy in melanoma patients.肠道微生物群调节黑色素瘤患者对抗PD-1免疫疗法的反应。
Science. 2018 Jan 5;359(6371):97-103. doi: 10.1126/science.aan4236. Epub 2017 Nov 2.
6
Atezolizumab versus docetaxel in patients with previously treated non-small-cell lung cancer (OAK): a phase 3, open-label, multicentre randomised controlled trial.阿特珠单抗对比多西他赛用于既往治疗过的非小细胞肺癌患者(OAK):一项3期、开放标签、多中心随机对照试验
Lancet. 2017 Jan 21;389(10066):255-265. doi: 10.1016/S0140-6736(16)32517-X. Epub 2016 Dec 13.
7
Mucosal Prevalence and Interactions with the Epithelium Indicate Commensalism of spp.黏膜患病率及与上皮细胞的相互作用表明某物种的共生关系
Front Microbiol. 2016 Oct 26;7:1706. doi: 10.3389/fmicb.2016.01706. eCollection 2016.
8
Biomarkers for the Clinical Use of PD-1/PD-L1 Inhibitors in Non-Small-Cell Lung Cancer: A Review.PD-1/PD-L1 抑制剂在非小细胞肺癌临床应用中的生物标志物:综述。
JAMA Oncol. 2016 Sep 1;2(9):1217-22. doi: 10.1001/jamaoncol.2016.0639.
9
Pembrolizumab versus docetaxel for previously treated, PD-L1-positive, advanced non-small-cell lung cancer (KEYNOTE-010): a randomised controlled trial.帕博利珠单抗对比多西他赛用于治疗后 PD-L1 阳性的、晚期非小细胞肺癌(KEYNOTE-010):一项随机对照试验。
Lancet. 2016 Apr 9;387(10027):1540-1550. doi: 10.1016/S0140-6736(15)01281-7. Epub 2015 Dec 19.
10
Nivolumab versus Docetaxel in Advanced Nonsquamous Non-Small-Cell Lung Cancer.纳武利尤单抗对比多西他赛治疗晚期非鳞状非小细胞肺癌
N Engl J Med. 2015 Oct 22;373(17):1627-39. doi: 10.1056/NEJMoa1507643. Epub 2015 Sep 27.