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Truong Le, T.

Publications and source records attributed to Truong Le, T..

2 recordsLinked to original sources

Deep Learning-Driven Subtype Classification of Colorectal Cancer Using Histopathology Images for Personalized Medicine

AbstractAccurate and timely diagnosis of colorectal cancer (CRC) is essential for effective treatment and better patient outcomes. This study explores the application of deep learning (DL) for automated CRC categories classification using hematoxylin and eosin-stained histopathology (H&E) images. Among the models, ResNet-34 demonstrated a strong balance of performance and complexity, achieving an overall accuracy of 85.04%, with top-2 and top-3 classification accuracies of 96.68% and 99.23%, respectively. ResNet-50 exhibited the highest micro-averaged ROC AUC of 0.9933 and F1-score of 87.51%. Swin Transformer V2 model also showed competitive results, with Swin v2-t-w8 achieving particularly high accuracy in Hyperplasia polyp detection (95.83%) and Adenocarcinoma (93.33%), alongside strong ROC AUCs (0.9926 for Hyperplasia polyp and 0.9864 for Adenocarcinoma), though at the cost of increased computational demands. We further developed a two-stage prediction framework comprising a binary abnormal detection stage followed by a multiclass cancer classifier. This approach substantially improved classification robustness, particularly for underrepresented and morphologically complex classes. Particularly, High-grade dysplasia classification accuracy improved from 53.57% with ResNet-34 to 71.43% in its two-stage extension. These results suggest that moderate-depth architectures can effectively capture the morphological diversity of colorectal cancer stages and provide an interpretable, efficient deep learning-based diagnostic tool to support pathologists.

cancer biology↗

Spatial Transcriptomic Profiling Of Advanced Ovarian Clear Cell Carcinoma Reveals Intra-Tumor Heterogeneity In Epithelial-Mesenchymal Gradient

Intratumoral heterogeneity is intrinsically comprised of molecular alterations of tumor cells and extrinsically from interconnections with microenvironments. This study explores the spatial heterogeneity of ovarian clear cell carcinoma (OCCC), a rare cancer with significance to East Asian women. We profile 21 primary-metastatic tumor pairs in a discovery cohort and 16 tumors in two validation cohorts using spatial transcriptomic (ST) platforms. Our integrative analysis revealed an inverse relationship between OXPHOS and inflammation along the EMT gradient. OCCC cells undergoing partial EMT have metabolic shifts and lose LCN2 expression, possibly via concomitant down-regulation of SOX9. Conversely, LCN2 expression correlated with OXPHOS-enriched tumor signature, low EMT, and better outcomes in OCCC. Single-cell ST profiling using CosMx further identifies nine spatially distinct cancer cell populations including the LCN2-high cancer subclone with a high epithelial score. SOX9 induction could partially restore epithelial-ness in LCN2-low cells suggesting that plasticity in OCCC is achieved via transcriptional reprogramming. Our findings provide further insights into epithelial-mesenchymal plasticity and the adaptive interactions between cancer cells and their microenvironments in OCCC.

cancer biology↗