Poster
Concordance analysis of AI-powered CD8 quantification and automated CD8 topology with manual histopathological assessment across seven solid tumor types
SITC 2022
Study Background
The degree of CD8+ lymphocyte infiltration into the tumor microenvironment, as well as the distribution of lymphocytes within the tumor and surrounding stroma (inflamed, excluded, or desert immunophenotypes), are key determinants for the potential efficacy of immunotherapy1-3. Thus, accurate characterization of the tumor immune microenvironment is essential. However, manual histopathological assessment of CD8 topology is subject to many challenges, including subjectivity and reproducibility.
We previously developed ML-based models for the identification and quantification of CD8+ lymphocytes6 and topology7 in melanoma. Here, we developed ML-based models for the identification and quantification of CD8+ lymphocytes and CD8 topology classifiers across seven cancer types: urothelial carcinoma (UC), head and neck squamous cell carcinoma (HNSCC), non-small cell lung cancer (NSCLC), gastric cancer (GC), colorectal cancer (CRC), pancreatic cancer (PC), and hepatocellular carcinoma (HCC).
We previously developed ML-based models for the identification and quantification of CD8+ lymphocytes6 and topology7 in melanoma. Here, we developed ML-based models for the identification and quantification of CD8+ lymphocytes and CD8 topology classifiers across seven cancer types: urothelial carcinoma (UC), head and neck squamous cell carcinoma (HNSCC), non-small cell lung cancer (NSCLC), gastric cancer (GC), colorectal cancer (CRC), pancreatic cancer (PC), and hepatocellular carcinoma (HCC).
Authors
Guramare et al.