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Jessica Ng

Publications and source records attributed to Jessica Ng.

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Weakly Supervised Pathology-Informed Representation Learning for PET-Based Content Retrieval of Intra-Tumour Heterogeneity

We propose a weakly supervised 18FFDG PET representation-learning framework for content based medical image retrieval, using H&E derived information during training while preserving PET-only inference. The proposed method was designed to use H&E derived information during training while maintaining PET only inference. A teacher student training strategy was used to learn the PET tumour derived voxel representations, from which global and hotspot conditioned embeddings were generated along with maps of intra tumour heterogeneity in our oesophegeal cancer test case. A progressive ablation strategy was used to evaluate the contribution of different supervision mechanisms. Retrieval performance was assessed across cross-validation folds using metrics including mean average precision, normalised discounted cumulative gain and mean reciprocal rank. Additional analyses evaluated ablation performance, hotspot faithfulness through perturbation/deletion experiments, prototype-specific PET uptake behaviour and indirect patient level concordance between learned PET prototype classes and selected histomic features. Progressive introduction of pathology informed supervision and hotspot modelling improved PET retrieval performance compared with global PET representations and conventional PET baselines. Across the ablation ladder, PET hotspot conditioned representations consistently provided stronger retrieval than global embeddings, indicating that focusing on informative tumour subregions improved sensitivity to intra tumour heterogeneity. Histopathology concordance further showed that the learned classes were not simply high uptake PET regions; instead, they demonstrated distinct heterogeneity in 18F FDG uptake.

cs.CV

Stress-testing cross-cancer generalizability of 3D nnU-Net for PET-CT tumor segmentation: multi-cohort evaluation with novel oesophageal and lung cancer datasets

Robust generalization is essential for deploying deep learning based tumor segmentation in clinical PET-CT workflows, where anatomical sites, scanners, and patient populations vary widely. This study presents the first cross cancer evaluation of nnU-Net on PET-CT, introducing two novel, expert-annotated whole-body datasets. 279 patients with oesophageal cancer (Australian cohort) and 54 with lung cancer (Indian cohort). These cohorts complement the public AutoPET dataset and enable systematic stress-testing of cross domain performance. We trained and tested 3D nnUNet models under three paradigms. Target only (oesophageal), public only (AutoPET), and combined training. For the tested sets, the oesophageal only model achieved the best in-domain accuracy (mean DSC, 57.8) but failed on external Indian lung cohort (mean DSC less than 3.4), indicating severe overfitting. The public only model generalized more broadly (mean DSC, 63.5 on AutoPET, 51.6 on Indian lung cohort) but underperformed in oesophageal Australian cohort (mean DSC, 26.7). The combined approach provided the most balanced results (mean DSC, lung (52.9), oesophageal (40.7), AutoPET (60.9)), reducing boundary errors and improving robustness across all cohorts. These findings demonstrate that dataset diversity, particularly multi demographic, multi center and multi cancer integration, outweighs architectural novelty as the key driver of robust generalization. This work presents the demography based cross cancer deep learning segmentation evaluation and highlights dataset diversity, rather than model complexity, as the foundation for clinically robust segmentation.

eess.IV