Abstract 45P
Background
Despite the remarkable efficacy of immune checkpoint inhibitor(ICI)-based immunotherapy in various cancers, it still faces prominent issues such as a limited population benefiting from the treatment. Numerous studies have shown that the gut microbiome can participate in immune modulation. Therefore, utilizing the gut microbiome to accurately predict the effectiveness of immunotherapy, thereby achieving precision diagnosis and treatment, has become a research hotspot.
Methods
Metagenomic sequencing was conducted on stool samples from patients receiving ICIs across three centers. Machine learning techniques were employed for model development, while SHapley Additive explanations (SHAP) were utilized to interpret the models.
Results
Distinct characteristics were observed in the gut microbiome between patients with different responses to ICIs. The areas under the receiver operating characteristic curve (0.81 in the validation cohort) and the precision-recall curve (0.80 in the validation cohort) demonstrated that the gut microbiome signature (GMS) exhibited excellent predictive performance. SHAP analysis identified the top five taxa driving GMS predictions: Anaerobutyricum hallii, Bacteroides eggerthii, Faecalibaculum rodentium, Clostridiales bacterium, and Anaerostipes hadrus. Survival analysis indicated that GMS also has prognostic value, showing significant associations with overall survival (P value < 0.001 for both log-rank test and multivariate Cox analysis) and progression-free survival (P value < 0.001 for log-rank test and P value = 0.008 for multivariate Cox analysis). In the validation cohort, GMS outperformed traditional single gut microbiome biomarkers (P value > 0.05) in terms of predictive performance (P value < 0.05).
Conclusions
The GMS demonstrated excellent performance in predicting responses to ICIs and prognosis, positioning it as a promising new generation of non-invasive biomarkers for evaluating ICIs efficacy. The taxa identified through SHAP analysis may serve as potential targets for enhancing the effectiveness of ICIs.
Legal entity responsible for the study
D-X. Wang.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
7P - ACOX2 disturbs the stability of MRE11-RAD50-NBS1 complex and shapes activated immune tumor microenvironment in clear cell renal cell carcinoma
Presenter: Shiqi Ye
Session: Poster Display session
Resources:
Abstract
9P - CXCR6+PD-1- Tissue Resident memory T cells are associated with poor prognosis in patients with metastatic colorectal cancer
Presenter: Emilien Laloy
Session: Poster Display session
Resources:
Abstract
10P - Tumor-infiltrating lymphocytes and tertiary lymphoid structures in oral cavity squamous cell carcinoma in non-smokers and non-drinkers: Predict clinical outcome
Presenter: Israa Laklouk
Session: Poster Display session
Resources:
Abstract
11P - Tumor-infiltrating lymphocytes on routine H&E staining with automated quantification predict outcomes in resectable non-small cell lung cancer
Presenter: Guus Heuvel
Session: Poster Display session
Resources:
Abstract
12P - Epithelial-mesenchymal transition facilitates response to AXL/PD-1 inhibition in relapsed mesothelioma
Presenter: Essa Baitei
Session: Poster Display session
Resources:
Abstract
14P - Integrated genomic analysis of whole genomes to derive a biomarker of durable response to immunotherapy in melanoma
Presenter: Irene Lobon
Session: Poster Display session
Resources:
Abstract
15P - Verteporfin might potentiate the effects of anti-PD-1 therapy in melanoma-bearing mice model
Presenter: Szonja Kovács
Session: Poster Display session
Resources:
Abstract
16P - Immune checkpoint blockade and HLA-related epistasis in melanoma: Genetic determinants of response and toxicity
Presenter: Martin Little
Session: Poster Display session
Resources:
Abstract
17P - Identification PD-L1-associated lncRNA biomarkers for immunoregulation in ovarian cancer
Presenter: Hee Jung Kim
Session: Poster Display session
Resources:
Abstract
19P - Genetic profiling of early triple-negative breast cancer patients with an indication for neoadjuvant pembrolizumab
Presenter: Bogdan Popescu
Session: Poster Display session
Resources:
Abstract