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Hacking, S.

Publications and source records attributed to Hacking, S..

2 recordsLinked to original sources

Multicenter self-supervised computational pathology identifies prognostic histomorphological phenotypes in colorectal cancer

H&E whole-slide images capture prognostic information encoded in tumor morphology and the surrounding microenvironment, but these signals remain difficult to extract and interpret at scale. Here, we developed a self-supervised computational pathology framework to predict disease-free survival in colorectal cancer and link model-derived risk to interpretable histomorphology and spatial tumor biology. Using a multicenter developmental cohort spanning colorectal adenomas and invasive colorectal cancer, we trained HPL-PanColon, a self-supervised representation model, to extract tile-level embeddings and identify recurrent histomorphological phenotype clusters across the adenoma-carcinoma spectrum. Compared with general-purpose pathology foundation models, HPL-PanColon yielded representations with reduced institution- and dataset-specific batch effects. We then applied HPL-PanColon to a global survival cohort of 1,024 colorectal cancer patients in a leave-one-institution-out framework, using tile embeddings to train an attention-based survival model and derive the Colon Histomorphology Prognostic Score (CHiPS). CHiPS stratified patients by disease-free survival and provided complementary prognostic information to a UICC TNM-informed clinicopathological model, increasing the c-index from 0.683 to 0.706. Integrating model attention with phenotype assignments traced CHiPS-associated risk to pathologist-recognizable tissue patterns, with high-risk regions enriched for desmoplastic, stromal, and fibroinflammatory morphologies and low-risk regions reflecting tumor-rich epithelial glandular patterns. Spatial transcriptomic analysis further linked high-risk morphologies to fibroblastic, perivascular, myofibroblastic, and immune-reactive tumor microenvironment programs, while low-risk morphologies mapped to epithelial and tumor-enriched regions. These findings establish a scalable framework for interpretable histology-based prognosis and spatial biological discovery in colorectal cancer.

pathology↗

MMR Deficiency Defines Distinct Molecular Subtype of Breast Cancer with Unique Proteomic Networks and Variable Clinical Significance

Mismatch repair (MMR) alterations are important prognostic and predictive biomarkers in a variety of cancer subtypes including colorectal and endometrial. However, in breast cancer (BC), the distinction and clinical significance of MMR is largely unknown. This may be due in part to the fact that genetic alterations in MMR genes are rare, and only seen to occur in around 3% of BCs. In the present study we analyzed TCGA data using a multi-sample protein-protein interactions (PPI) analysis tool, Proteinarium, and showed a distinct separation in the MMR deficient and intact specific networks. MMR deficient tumor specific networks have a highly connected cluster of histone genes, identified by unique PPI. We also found that distribution of MMR deficient breast cancer is more prevalent in HER2-enriched and triple-negative (TN) BC subtypes compared to luminal BCs. Poorer survival was seen in patients with HER2-enriched BCs with MMR deficiency, whereas an improved survival was seen in TNBCs with MMR deficiency. We recommend defining MMR deficient breast cancer by next generation sequencing (NGS) when any somatic mutation is detected in one of the 7 MMR genes found in our study. Our recommendations include labeling patients with variants of undetermined significance (VUS) as MMR deficient supported by findings from distinct clusters of patients based on our network analysis. MMR may have a role in guiding the use of immunotherapy for both TN as well as HER2-enriched BC.

bioinformatics↗