TY - GEN
T1 - AI in neuro-oncology
T2 - 22nd International Conference on Artificial Intelligence in Medicine, AIME 2024
AU - Danaei Mehr, Homay
AU - Noorani, Imran
AU - Rana, Priyanka
AU - Di Ieva, Antonio
AU - Liu, Sidong
PY - 2024
Y1 - 2024
N2 - Glioblastoma (GBM), the most aggressive type of brain cancer, is notorious for its resistance to treatments due to its rapid growth and high degree of heterogeneity. Epidermal Growth Factor Receptor (EGFR) is an important diagnostic, prognostic, and therapeutic biomarker in GBM. The current gold standard diagnosis of EGFR detection relies on immunohistochemistry (IHC), Fluorescence in Situ Hybridization (FISH), and sequencing analysis of surgical samples with a turnaround time of several days to weeks, not to mention the laboratory costs related to the analyses. To improve the efficiency and cost-effectiveness of EGFR detection, we propose an alternative solution based on Whole Slide Image (WSI) and artificial intelligence (AI) methods, specifically multiple instance learning (MIL) frameworks. In this study, we conducted a comprehensive analysis of two public datasets, TCGA and CPTAC, with three MIL frameworks, Clustering Constrained Attention Multiple Instance Learning (CLAM), Double–Tier Feature Distillation Multiple Instance Learning (DTFD), and Transformer-based Correlated MIL for WSI Classification (TransMIL), to predict the EGFR status in GBM. With evaluation using 5–fold cross-validation, the CLAM model achieved 0.736 ± 0.181 and 0.799 ± 0.164 area under the curve (AUC) on TCGA and CPTAC, respectively, outperforming the state-of-the-art model (AUC of 0.71 ± 0.031). This study demonstrates the effectiveness of MIL models in the classification of EGFR biomarkers with a high potential to shift the paradigm from the current gold standard to the more efficient and cheaper WSI and AI workflows.
AB - Glioblastoma (GBM), the most aggressive type of brain cancer, is notorious for its resistance to treatments due to its rapid growth and high degree of heterogeneity. Epidermal Growth Factor Receptor (EGFR) is an important diagnostic, prognostic, and therapeutic biomarker in GBM. The current gold standard diagnosis of EGFR detection relies on immunohistochemistry (IHC), Fluorescence in Situ Hybridization (FISH), and sequencing analysis of surgical samples with a turnaround time of several days to weeks, not to mention the laboratory costs related to the analyses. To improve the efficiency and cost-effectiveness of EGFR detection, we propose an alternative solution based on Whole Slide Image (WSI) and artificial intelligence (AI) methods, specifically multiple instance learning (MIL) frameworks. In this study, we conducted a comprehensive analysis of two public datasets, TCGA and CPTAC, with three MIL frameworks, Clustering Constrained Attention Multiple Instance Learning (CLAM), Double–Tier Feature Distillation Multiple Instance Learning (DTFD), and Transformer-based Correlated MIL for WSI Classification (TransMIL), to predict the EGFR status in GBM. With evaluation using 5–fold cross-validation, the CLAM model achieved 0.736 ± 0.181 and 0.799 ± 0.164 area under the curve (AUC) on TCGA and CPTAC, respectively, outperforming the state-of-the-art model (AUC of 0.71 ± 0.031). This study demonstrates the effectiveness of MIL models in the classification of EGFR biomarkers with a high potential to shift the paradigm from the current gold standard to the more efficient and cheaper WSI and AI workflows.
KW - Multiple Instance Learning
KW - Weakly Supervised Deep Learning
KW - Glioblastoma
KW - EGFR biomarker
KW - Whole Slide Images
UR - http://www.scopus.com/inward/record.url?scp=85206217610&partnerID=8YFLogxK
U2 - 10.1007/978-3-031-66535-6_3
DO - 10.1007/978-3-031-66535-6_3
M3 - Conference proceeding contribution
AN - SCOPUS:85206217610
SN - 9783031665349
T3 - Lecture Notes in Computer Science (including subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics)
SP - 21
EP - 29
BT - Artificial Intelligence in Medicine
A2 - Finkelstein, Joseph
A2 - Moskovitch, Robert
A2 - Parimbelli, Enea
PB - Springer, Springer Nature
CY - Switzerland
Y2 - 9 July 2024 through 12 July 2024
ER -