Abstract 1497P
Background
Lung cancer is a malignancy with extremely high morbidity and mortality, of which non-small cell lung cancer (NSCLC) accounts for about 85%. With the advent of immunotherapy has brought survival benefit to NSCLC patients, some patients still be hard to achieving satisfactory outcomes. The link between gut microbes and immunotherapy is strong, but the role they play in NSCLC immunotherapy is unclear. The aim of this study was to investigate the relationship between gut microbial composition and the efficacy of immunotherapy in NSCLC.
Methods
Patients with advanced NSCLC receiving first-line immunotherapy were enrolled, and fresh stool samples were collected before and after 2 cycles of anti-PD-1 monoclonal antibody treatment for metagenomics sequencing and annotation using the KEGG and MetaCyc databases for subsequent differential flora analysis and functional analysis, and correlated the results with outcomes at 41 months.
Results
A total of 51 patients with advanced NSCLC treated with first-line immunotherapy were included in this study, and the relative abundance of Streptomyces, Corynebacterium, Kineosphaera, and Schaalia genus under the Actinomyces phylum was increased in the R group, and the PFS (progression-free survival time) of patients with high relative abundance of Schaalia and Corynebacterium genus was significantly longer than in those with low relative abundance. Functional analysis revealed reduced levels of glycolysis in the R group and may be due to the enrichment of Schaalia genus. The BMI and fasting glucose values of the patients may be influential factors in the relative abundance of Schaalia genus. In addition, the type of irAE occurrence was also correlated with the composition of gut microbes.
Conclusions
We have newly discovered that Schaalia genus under the Actinobacteria phylum may influence the efficacy of immunotherapy in NSCLC patients by inhibiting the level of glycolysis through affecting the level of PFP. Therefore, Schaalia flora may be a potential marker for predicting the efficacy of immunotherapy in NSCLC patients, and interfering with the levels of Schaalia or PFP is expected to be a new target to enhance the efficacy of immunotherapy in NSCLC patients.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
National Natural Science Foundation of China.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
1523P - Phase II dose optimization results from MOUNTAINEER-02: A study of tucatinib, trastuzumab, ramucirumab, and paclitaxel for HER2+ gastroesophageal cancer (GEC)
Presenter: Mustapha Tehfe
Session: Poster session 21
1524P - First-line TST001 plus capecitabine and oxaliplatin (CAPOX) for advanced G/GEJ cancer with CLDN18.2 positive overall survival data from study transtar102-Cohort C
Presenter: Lin Shen
Session: Poster session 21
1526P - Phase Ib results of bemarituzumab (BEMA)+mfolfox6+nivolumab (NIVO) for advanced gastric/gastroesophageal junction cancer (G/GEJC): Fortitude-102 part 1
Presenter: Zev Wainberg
Session: Poster session 21
1527P - Efficacy and safety of infigratinib in locally advanced or metastatic gastric cancer or gastroesophageal junction adenocarcinoma patients with FGFR2 gene amplification
Presenter: Jiajia Yuan
Session: Poster session 21
1528P - A phase I/II trial investigating safety and efficacy of autologous TAC01-HER2 in relapsed or refractory solid tumors
Presenter: Daniel Olson
Session: Poster session 21
1529P - Tislelizumab plus chemotherapy sequential neo-chemoradiotherapy therapy as total neoadjuvant therapy in locally advanced esophageal squamous cell carcinoma (ETNT)
Presenter: Wenwu He
Session: Poster session 21
1530P - Health-related quality of life (hrqol) in patients with claudin-18 isoform 2-positive (CLDN18.2+) locally advanced (LA) unresectable or metastatic gastric or gastroesophageal junction (mg/GEJ) adenocarcinoma: Results from SPOTLIGHT and GLOW
Presenter: Florian Lordick
Session: Poster session 21
1532P - Phase Ib study of futibatinib plus pembrolizumab in patients with esophageal carcinoma: Updated results of antitumor activity and tolerability results in combination with chemotherapy
Presenter: Shun Yamamoto
Session: Poster session 21