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Distinct Functional Metagenomic Markers Predict the Responsiveness to Anti-PD-1 Therapy in Chinese Non-Small Cell Lung Cancer Patients

BACKGROUND: Programmed death 1 (PD-1) and the ligand of PD-1 (PD-L1) are central targets for immune-checkpoint therapy (ICT) blocking immune evasion-related pathways elicited by tumor cells. A number of PD-1 inhibitors have been developed, but the efficacy of these inhibitors varies considerably and...

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Autores principales: Fang, Chao, Fang, Wenfeng, Xu, Liqin, Gao, Fangfang, Hou, Yong, Zou, Hua, Ma, Yuxiang, Moll, Janne Marie, Yang, Yunpeng, Wang, Dan, Huang, Yan, Ren, Huahui, Zhao, Hongyun, Qin, Shishang, Zhong, Huanzi, Li, Junhua, Liu, Sheng, Yang, Huanming, Wang, Jian, Brix, Susanne, Kristiansen, Karsten, Zhang, Li
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9069064/
https://www.ncbi.nlm.nih.gov/pubmed/35530307
http://dx.doi.org/10.3389/fonc.2022.837525
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author Fang, Chao
Fang, Wenfeng
Xu, Liqin
Gao, Fangfang
Hou, Yong
Zou, Hua
Ma, Yuxiang
Moll, Janne Marie
Yang, Yunpeng
Wang, Dan
Huang, Yan
Ren, Huahui
Zhao, Hongyun
Qin, Shishang
Zhong, Huanzi
Li, Junhua
Liu, Sheng
Yang, Huanming
Wang, Jian
Brix, Susanne
Kristiansen, Karsten
Zhang, Li
author_facet Fang, Chao
Fang, Wenfeng
Xu, Liqin
Gao, Fangfang
Hou, Yong
Zou, Hua
Ma, Yuxiang
Moll, Janne Marie
Yang, Yunpeng
Wang, Dan
Huang, Yan
Ren, Huahui
Zhao, Hongyun
Qin, Shishang
Zhong, Huanzi
Li, Junhua
Liu, Sheng
Yang, Huanming
Wang, Jian
Brix, Susanne
Kristiansen, Karsten
Zhang, Li
author_sort Fang, Chao
collection PubMed
description BACKGROUND: Programmed death 1 (PD-1) and the ligand of PD-1 (PD-L1) are central targets for immune-checkpoint therapy (ICT) blocking immune evasion-related pathways elicited by tumor cells. A number of PD-1 inhibitors have been developed, but the efficacy of these inhibitors varies considerably and is typically below 50%. The efficacy of ICT has been shown to be dependent on the gut microbiota, and experiments using mouse models have even demonstrated that modulation of the gut microbiota may improve efficacy of ICT. METHODS: We followed a Han Chinese cohort of 85 advanced non-small cell lung cancer (NSCLC) patients, who received anti-PD-1 antibodies. Tumor biopsies were collected before treatment initiation for whole exon sequencing and variant detection. Fecal samples collected biweekly during the period of anti-PD-1 antibody administration were used for metagenomic sequencing. We established gut microbiome abundance profiles for identification of significant associations between specific microbial taxa, potential functionality, and treatment responses. A prediction model based on random forest was trained using selected markers discriminating between the different response groups. RESULTS: NSCLC patients treated with antibiotics exhibited the shortest survival time. Low level of tumor-mutation burden and high expression level of HLA-E significantly reduced progression-free survival. We identified metagenomic species and functional pathways that differed in abundance in relation to responses to ICT. Data on differential enrichment of taxa and predicted microbial functions in NSCLC patients responding or non-responding to ICT allowed the establishment of random forest algorithm-adopted models robustly predicting the probability of whether or not a given patient would benefit from ICT. CONCLUSIONS: Overall, our results identified links between gut microbial composition and immunotherapy efficacy in Chinese NSCLC patients indicating the potential for such analyses to predict outcome prior to ICT.
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spelling pubmed-90690642022-05-05 Distinct Functional Metagenomic Markers Predict the Responsiveness to Anti-PD-1 Therapy in Chinese Non-Small Cell Lung Cancer Patients Fang, Chao Fang, Wenfeng Xu, Liqin Gao, Fangfang Hou, Yong Zou, Hua Ma, Yuxiang Moll, Janne Marie Yang, Yunpeng Wang, Dan Huang, Yan Ren, Huahui Zhao, Hongyun Qin, Shishang Zhong, Huanzi Li, Junhua Liu, Sheng Yang, Huanming Wang, Jian Brix, Susanne Kristiansen, Karsten Zhang, Li Front Oncol Oncology BACKGROUND: Programmed death 1 (PD-1) and the ligand of PD-1 (PD-L1) are central targets for immune-checkpoint therapy (ICT) blocking immune evasion-related pathways elicited by tumor cells. A number of PD-1 inhibitors have been developed, but the efficacy of these inhibitors varies considerably and is typically below 50%. The efficacy of ICT has been shown to be dependent on the gut microbiota, and experiments using mouse models have even demonstrated that modulation of the gut microbiota may improve efficacy of ICT. METHODS: We followed a Han Chinese cohort of 85 advanced non-small cell lung cancer (NSCLC) patients, who received anti-PD-1 antibodies. Tumor biopsies were collected before treatment initiation for whole exon sequencing and variant detection. Fecal samples collected biweekly during the period of anti-PD-1 antibody administration were used for metagenomic sequencing. We established gut microbiome abundance profiles for identification of significant associations between specific microbial taxa, potential functionality, and treatment responses. A prediction model based on random forest was trained using selected markers discriminating between the different response groups. RESULTS: NSCLC patients treated with antibiotics exhibited the shortest survival time. Low level of tumor-mutation burden and high expression level of HLA-E significantly reduced progression-free survival. We identified metagenomic species and functional pathways that differed in abundance in relation to responses to ICT. Data on differential enrichment of taxa and predicted microbial functions in NSCLC patients responding or non-responding to ICT allowed the establishment of random forest algorithm-adopted models robustly predicting the probability of whether or not a given patient would benefit from ICT. CONCLUSIONS: Overall, our results identified links between gut microbial composition and immunotherapy efficacy in Chinese NSCLC patients indicating the potential for such analyses to predict outcome prior to ICT. Frontiers Media S.A. 2022-04-21 /pmc/articles/PMC9069064/ /pubmed/35530307 http://dx.doi.org/10.3389/fonc.2022.837525 Text en Copyright © 2022 Fang, Fang, Xu, Gao, Hou, Zou, Ma, Moll, Yang, Wang, Huang, Ren, Zhao, Qin, Zhong, Li, Liu, Yang, Wang, Brix, Kristiansen and Zhang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Fang, Chao
Fang, Wenfeng
Xu, Liqin
Gao, Fangfang
Hou, Yong
Zou, Hua
Ma, Yuxiang
Moll, Janne Marie
Yang, Yunpeng
Wang, Dan
Huang, Yan
Ren, Huahui
Zhao, Hongyun
Qin, Shishang
Zhong, Huanzi
Li, Junhua
Liu, Sheng
Yang, Huanming
Wang, Jian
Brix, Susanne
Kristiansen, Karsten
Zhang, Li
Distinct Functional Metagenomic Markers Predict the Responsiveness to Anti-PD-1 Therapy in Chinese Non-Small Cell Lung Cancer Patients
title Distinct Functional Metagenomic Markers Predict the Responsiveness to Anti-PD-1 Therapy in Chinese Non-Small Cell Lung Cancer Patients
title_full Distinct Functional Metagenomic Markers Predict the Responsiveness to Anti-PD-1 Therapy in Chinese Non-Small Cell Lung Cancer Patients
title_fullStr Distinct Functional Metagenomic Markers Predict the Responsiveness to Anti-PD-1 Therapy in Chinese Non-Small Cell Lung Cancer Patients
title_full_unstemmed Distinct Functional Metagenomic Markers Predict the Responsiveness to Anti-PD-1 Therapy in Chinese Non-Small Cell Lung Cancer Patients
title_short Distinct Functional Metagenomic Markers Predict the Responsiveness to Anti-PD-1 Therapy in Chinese Non-Small Cell Lung Cancer Patients
title_sort distinct functional metagenomic markers predict the responsiveness to anti-pd-1 therapy in chinese non-small cell lung cancer patients
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9069064/
https://www.ncbi.nlm.nih.gov/pubmed/35530307
http://dx.doi.org/10.3389/fonc.2022.837525
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