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Dysbiosis of Fecal Microbiota in Chinese Advanced Non-Small-Cell Lung Cancer Patients and its Role in Response to Immunotherapy

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inferredcites →https://doi.org/10.1002/ijc.32003openalex-extracted
Fecal microbiota transplantation in cancer management: Current status and perspectives
inferredcites →https://doi.org/10.1007/s00432-021-03644-0openalex-extracted
Role of lung and gut microbiota on lung cancer pathogenesis
inferredcites →https://doi.org/10.1007/s10482-020-01474-7openalex-extracted
Human gut microbiota/microbiome in health and diseases: a review
inferredcites →https://doi.org/10.1007/s11274-021-03086-3openalex-extracted
Association of gut microbiomes with lung and esophageal cancer: a pilot study
inferredcites →https://doi.org/10.1016/j.ccell.2015.11.010openalex-extracted
Immunotherapy Not Working? Check Your Microbiota
inferredcites →https://doi.org/10.1016/j.chom.2016.07.001openalex-extracted
Gut Microbial Metabolites Fuel Host Antibody Responses
inferredcites →https://doi.org/10.1016/j.critrevonc.2019.102841openalex-extracted
Gut microbiome and response to checkpoint inhibitors in non-small cell lung cancer—A review
inferredcites →https://doi.org/10.1016/j.jtho.2019.04.007openalex-extracted
The Diversity of Gut Microbiome is Associated With Favorable Responses to Anti–Programmed Death 1 Immunotherapy in Chinese Patients With NSCLC
inferredcites →https://doi.org/10.1016/j.jtho.2020.04.028openalex-extracted
Lung Cancer in People’s Republic of China
inferredcites →https://doi.org/10.1016/j.pharmthera.2021.107973openalex-extracted
The gut microbiome and efficacy of cancer immunotherapy
inferredcites →https://doi.org/10.1016/j.psychres.2019.112691openalex-extracted
A review of antibiotics, depression, and the gut microbiome
inferredcites →https://doi.org/10.1038/s41467-021-23265-yopenalex-extracted
Identification of microbial markers across populations in early detection of colorectal cancer
inferredcites →https://doi.org/10.1038/s41575-020-00376-3openalex-extracted
Utilizing the gut microbiome in decompensated cirrhosis and acute-on-chronic liver failure
inferredcites →https://doi.org/10.1038/s41591-021-01655-5openalex-extracted
Intestinal Akkermansia muciniphila predicts clinical response to PD-1 blockade in patients with advanced non-small-cell lung cancer
inferredcites →https://doi.org/10.1038/s41598-020-65792-6openalex-extracted
Impact of pemetrexed chemotherapy on the gut microbiota and intestinal inflammation of patient-lung-derived tumor xenograft (PDX) mouse models
inferredcites →https://doi.org/10.1053/j.gastro.2018.04.001openalex-extracted
Gut Microbiota Promotes Tumor Growth in Mice by Modulating Immune Response
inferredcites →https://doi.org/10.1080/1040841x.2016.1176988openalex-extracted
Gut–lung axis: The microbial contributions and clinical implications
inferredcites →https://doi.org/10.1111/1759-7714.14199openalex-extracted
Intestinal flora characteristics of advanced non‐small cell lung cancer in China and their role in chemotherapy based on metagenomics: A prospective exploratory cohort study
inferredcites →https://doi.org/10.1126/science.aac4255openalex-extracted
Commensal Bifidobacterium promotes antitumor immunity and facilitates anti–PD-L1 efficacy
inferredcites →https://doi.org/10.1126/science.aad1329openalex-extracted
Anticancer immunotherapy by CTLA-4 blockade relies on the gut microbiota
inferredcites →https://doi.org/10.1126/science.aan3706openalex-extracted
Gut microbiome influences efficacy of PD-1–based immunotherapy against epithelial tumors
inferredcites →https://doi.org/10.1126/science.abb5920openalex-extracted
Fecal microbiota transplant promotes response in immunotherapy-refractory melanoma patients
inferredcites →https://doi.org/10.1126/science.abf3363openalex-extracted
Fecal microbiota transplant overcomes resistance to anti–PD-1 therapy in melanoma patients
inferredcites →https://doi.org/10.1667/rr15579.1openalex-extracted
The Intestinal Microbiota Plays as a Protective Regulator Against Radiation Pneumonitis
inferredcites →https://doi.org/10.21037/tlcr.2019.10.23openalex-extracted
The role of the gut microbiome on the efficacy of immune checkpoint inhibitors in Japanese responder patients with advanced non-small cell lung cancer
inferredcites →https://doi.org/10.2217/fon-2019-0783openalex-extracted
Gut microbiota and cancer immunotherapy: prognostic and therapeutic implications
inferredcites →https://doi.org/10.3389/fcimb.2019.00112openalex-extracted
Dysbiosis of the Gut Microbiome in Lung Cancer
inferredcites →https://doi.org/10.3389/fcimb.2021.725284openalex-extracted
Specific Gut Microbiome and Serum Metabolome Changes in Lung Cancer Patients
inferredcites →https://doi.org/10.3390/cancers13194824openalex-extracted
The Gut Microbiome and Cancer Immunotherapy: Can We Use the Gut Microbiome as a Predictive Biomarker for Clinical Response in Cancer Immunotherapy?
inferredcites →https://doi.org/10.7150/ijbs.35980openalex-extracted
Dysbiosis of the Gut Microbiome is associated with Tumor Biomarkers in Lung Cancer
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