Authors: Antony Gitau, Martyna Borak, Bjørn-Jostein Singstad, Martin Paulson, Karl Thomas Hjelmervik, Ola Marius Lysaker, Veralia Gabriela Sanchez
Organizations: Faculty of Technology, Natural Sciences and Maritime Sciences, University of South-Eastern Norway, Borre, Norway · Center for Cancer and Blood Diseases, Vestfold Hospital Trust, Tønsberg, Norway · Faculty of Biomedical Engineering, Silesian University of Technology, Zabrze, Poland · Department of Radiology, Vestfold Hospital Trust, Tønsberg, Norway
Whole-slide image (WSI) report generation requires recognizing spatially distributed pathological features and organizing them into a coherent diagnostic narrative. Although direct vision-to-text models can yield fluent reports, they obscure the contributions and failure modes of visual recognition, structured reasoning, and language generation. We propose a decomposed framework in which frozen Virchow2 tile embeddings are aggregated by multiple-instance learning (MIL) classification heads that answer organ-specific diagnostic questions. An organ-conditioned graph constrains the assembly of these answers into a structured reasoning chain, which a language model realizes as a pathology report. On the REG2026 held-out set of 2,028 slides, the proposed workflow achieved a chain-Jaccard score of 0.702. Performance fell to 0.420 without graph-based chain construction, 0.398 when the organ-specific graphs were replaced by a single organ-agnostic graph, and 0.371 when the language model constructed the chain freely from MIL predictions. Using the same report generator, graph-structured chains improved the report score from 0.330 to 0.495. On 350 external TCGA WSIs spanning the seven REG organs without fine-tuning, the expected organ graph was selected in 64.0% of cases and ranked among the top three in 86.6%. Providing the correct organ graph increased agreement with coarse TCGA primary-diagnosis labels from 61.8% to 92.6%, identifying organ routing as a main bottleneck under domain shift. Overall, organ-conditioned, graph-constrained chain assembly improves structured reasoning and report generation while enabling stage-specific error localization.
Figures & tables
Figure 1: Overview of the proposed framework. The WSI is densely divided into non-overlapping 224×224 pixel candidate tiles. Tiles are retained when at least 50% of their pixels have a mean RGB intensity below 220, and up to 128 retained tissue tiles are uniformly and randomly sampled during training and inference. A frozen Virchow2 encoder transforms these tiles into an embedding bag used by an organ MIL classifier, which selects the organ-specific reasoning graph, and organ–question-specific MIL classifiers, which predict answers to successive graph questions. Graph-guided reasoning organizes these predictions into a structured question–answer chain, which Qwen2.5-1.5B-Instruct with LoRA converts into the final pathology report.
Organ
n
Full
Canon
Shuf
Majority
Heads
No organ
Free-form
Bladder
153
0.678
0.616
0.318
0.512
0.547
0.457
0.490
Breast
442
0.633
0.510
0.236
0.484
0.349
0.403
0.313
Cervix
162
0.737
0.733
0.390
0.640
0.562
0.359
0.448
Colon
399
0.690
0.552
0.337
0.426
0.425
0.378
0.370
Lung
188
0.773
0.734
0.374
0.632
0.510
0.391
0.410
Prostate
333
0.738
0.479
0.363
0.401
0.391
0.476
0.391
Table 1: Per-organ reasoning performance on the held-out set; all values report chain-Jaccard. Canon uses modal-answer transitions, whereas Shuf permutes answer-to-transition mappings within branching nodes.
Question category
Nodes
Occurrences
Accuracy
Error share
Grading / quantification
22
3,689
0.686
38.0%
Diagnosis / subtype
49
7,437
0.849
36.9%
Presence / extent
68
8,274
0.942
15.9%
Workflow / schema
31
7,252
0.963
8.8%
Rare findings
5
83
0.867
0.4%
Total
175
26,735
–
100%
Table 2: Post-hoc category-level analysis of question-node errors on the held-out set. Error share denotes the proportion of all incorrect question-level predictions attributable to each category.
Organ
n
Route
Expected organ in top 3
Weak concordance
Oracle-organ concordance
Bladder
50
11/50 (0.220)
29/50 (0.580)
8/42 (0.190)
30/42 (0.714)
Breast
50
42/50 (0.840)
49/50 (0.980)
37/49 (0.755)
44/49 (0.898)
Cervix
50
17/50 (0.340)
33/50 (0.660)
15/49 (0.306)
47/49 (0.959)
Colon
50
38/50 (0.760)
50/50 (1.000)
35/50 (0.700)
45/50 (0.900)
Lung
50
47/50 (0.940)
50/50 (1.000)
47/50 (0.940)
50/50 (1.000)
Prostate
50
46/50 (0.920)
48/50 (0.960)
45/50 (0.900)
49/50 (0.980)
Table 3: External evaluation on 350 TCGA diagnostic WSIs, with 50 slides per organ. Route denotes top-1 organ-routing accuracy and Top-3 indicates whether the expected organ was among the three highest-ranked predictions. Weak concordance measures agreement with coarse GDC primary-diagnosis labels; Oracle reports concordance when the expected organ graph is provided.
Whole slide image (WSI) analysis is central to computational pathology, with multiple instance learning (MIL) emerging as the standard pipeline for slide-level diagnosis. However, conventional approaches formulate WSI diagnosis as a flat classification task over discrete labels, contradicting the inherently hierarchical, coarse-to-fine nature of clinical reasoning. Although recent hierarchical classifiers and vision-language models (VLMs) have sought to address this structural gap, they either fail to capture semantic continuity between related diagnoses or suffer from unconstrained text generation that produces taxonomic hallucinations and parent-child label violations. To address these limitations, we propose TaxoMIL, a taxonomy-constrained framework that reformulates WSI diagnosis as a multi-granularity text generation task. TaxoMIL utilizes a dual-head Transformer decoder to generate coarse- and fine-level diagnostic text, and introduces taxonomy-guided objectives that explicitly structure the label embedding space and strictly ground slide-level visual representations within the clinical taxonomy. Extensive experiments across three diverse WSI datasets demonstrate that TaxoMIL consistently outperforms state-of-the-art MIL classifiers and VLM-based generative methods, yielding accurate and hierarchy-aware diagnostic predictions. The code is released at https://github.com/QuIIL/TaxoMIL
Chaeyeon Lee, Khang Nguyen Quoc, Jinsol Song +3
School of Electrical Engineering, Korea University, Seoul, Republic of Korea · Department of Hospital Pathology, The Catholic University of Korea College of Medicine, Seoul, Republic of Korea
Whole-slide images (WSIs) present a fundamental challenge for computational pathology due to their extreme resolution, multi-scale heterogeneity, and the requirement for clinically reliable interpretation. Although recent pathology foundation models have enabled fluent report generation, they often lack clinical grounding, failing to accurately represent key diagnostic concepts and relationships observed by pathologists. This limitation arises from the difficulty of integrating heterogeneous visual evidence spanning fine-grained cellular patterns, slide-level tissue architecture, and high-level diagnostic concepts, while maintaining interpretability and clinical coherence. Here we present SCOUT: Semantic Context-aware mOdality fUsion Transformer, a context-aware concept-grounded multimodal framework for pathology report generation that enables progressive conditioning of image representations by global slide information and explicit diagnostic concepts. The method integrates local histological patterns, whole-slide context, and expert-curated semantic descriptors within a unified learning paradigm, allowing visual features to be dynamically refined throughout the encoding process. By combining depth-aware contextual modulation with adaptive multimodal fusion during text generation, the framework produces clinically coherent reports while preserving complementarity across representational scales. Using CONCH1.5 features, we evaluate SCOUT against WSI-Caption, HistGen, and BiGen on TCGA-BRCA, MICCAI REG, and HistAI. SCOUT achieves the best BLEU-1 to BLEU-4 and METEOR scores on all datasets, plus the best ROUGE-L on TCGA-BRCA and MICCAI REG. On TCGA-BRCA, it reaches 0.436/0.303/0.202/0.156 BLEU-1/2/3/4 and 0.204 METEOR; on REG 2025, it achieves 0.865/0.834/0.805/0.780 and 0.568. These results support progressive contextual conditioning for grounded pathology report generation.
Generating clinically useful pathology reports for pathology cases from whole-slide images (WSIs) is challenging due to gigapixel resolution, long visual-token sequences, and the complexity of case-level reasoning, where a single case may contain multiple WSIs with heterogeneous tissues and ambiguous findings. We present a simple token-efficient vision--language model for case-level synoptic report generation that remains practical under constrained GPU memory. Our architecture follows a minimal three-component design: a frozen pathology patch encoder, a lightweight two-layer MLP vision-language aligner, and a large language model decoder, with an explicit WSI marker token to separate slides within a case. Training proceeds in two supervised stages: (1) aligner-only WSI captioning using heterogeneous WSI-text pairs, and (2) case-level supervised fine-tuning on case-report pairs for structured report generation. To reduce sequence length, we represent each slide using 512×512 patches at 5× magnification, which reduces the average sequence length by up to 64× times compared to the commonly used 20× patches. Combined with efficient training techniques, we enable practical training with only half a NVIDIA H100 GPU. Across both training stages, our approach achieves high ROUGE-L/METEOR/BLEU-4 scores while being substantially more efficient in memory and runtime. In AI-based evaluations, our model is consistently preferred over strong baselines. Extensive ablations characterize performance-efficiency trade-offs and identify simple choices that improve robustness in multi-WSI settings. Overall, this work provides a strong, reproducible baseline for efficient pathology report generation, lowering the barrier to multi-WSI VLM research under limited compute.
Zhiyuan Yang, Jiahao Cheng, Vincent Quoc-Huy Trinh +1
Department of Computer Science and Software Engineering (CSSE), Concordia University, Montreal, Canada · Axe Cancer, Centre de recherche du CHUM, Université de Montréal, Montreal, Canada · Institut de recherche en immunologie et cancérologie (IRIC), Université de Montréal