Analysis of the Gut Microbiota: An Emerging Source of Biomarkers for Immune Checkpoint Blockade Therapy in Non-Small Cell Lung Cancer

• Published in: Cancers 2021-05, Vol.13 (11), p.2514
• Main Authors: Zhang, Feiyu, Ferrero, Macarena, Dong, Ning, D’Auria, Giuseppe, Reyes-Prieto, Mariana, Herreros-Pomares, Alejandro, Calabuig-Fariñas, Silvia, Duréndez, Elena, Aparisi, Francisco, Blasco, Ana, García, Clara, Camps, Carlos, Jantus-Lewintre, Eloisa, Sirera, Rafael
• Format: Article
• Language: English
• Subjects: Antibiotics; Biomarkers; Cancer immunotherapy; Clinical outcomes; Consortia; Dendritic cells; Disease; DNA sequencing; Immune checkpoint; Immunoregulation; Immunotherapy; Intestinal microflora; Lung cancer; Microbiota; Microorganisms; Multivariate analysis; Mutation; Non-small cell lung carcinoma; Patients; PD-1 protein; PD-L1 protein; Ribosomal DNA; Small cell lung carcinoma; Toxicity; Tumors
• ISSN: 2072-6694; 2072-6694
• DOI: 10.3390/cancers13112514

Background: The human gut harbors around 1013–1014 microorganisms, collectively referred to as gut microbiota. Recent studies have found that the gut microbiota may have an impact on the interaction between immune regulation and anti-cancer immunotherapies. Methods: In order to characterize the diversity and composition of commensal microbiota and its relationship with response to immune checkpoint blockade (ICB), 16S ribosomal DNA (rDNA) sequencing was performed on 69 stool samples from advanced non-small cell lung cancer (NSCLC) patients prior to treatment with ICB. Results: The use of antibiotics and ICB-related skin toxicity were significantly associated with reduced gut microbiota diversity. However, antibiotics (ATB) usage was not related to low ICB efficacy. Phascolarctobacterium was enriched in patients with clinical benefit and correlated with prolonged progression-free survival, whereas Dialister was more represented in patients with progressive disease, and its higher relative abundance was associated with reduced progression-free survival and overall survival, with independent prognostic value in multivariate analysis. Conclusions: Our results corroborate the relation between the baseline gut microbiota composition and ICB clinical outcomes in advanced NSCLC patients, and provide novel potential predictive and prognostic biomarkers for immunotherapy in NSCLC.