Automated radiology report generation for multi-sequence brain MRI holds strong promise for alleviating radiologists' workload, yet it remains a demanding problem: brain MRI studies are inherently volumetric, each pulse sequence carries complementary diagnostic information, and annotated data are critically scarce for low-resource clinical languages. Existing brain MRI-report resources are still dominated by English reports, translated clinical text, or datasets adapted from task-specific imaging benchmarks, leaving routine low-resource clinical reporting and heterogeneous multi-sequence MRI protocols insufficiently represented. To bridge this gap, we introduce ViBMR, to the best of our knowledge, the first large-scale multi-sequence brain MRI dataset paired with routine Vietnamese clinical reports, comprising 3,649 patients and 11,875 MRI series across T1, T2, FLAIR, and contrast-enhanced T1 sequences. Building on ViBMR, we establish a comprehensive evaluation setup for brain MRI report generation, covering representative medical vision-language models, multi-sequence inputs, and feature aggregation strategies. The results provide key insights into dataset characteristics and model behavior, while demonstrating the necessity of native low-resource clinical datasets for reliable Vietnamese-origin brain MRI report generation. Our dataset and baseline models will be released for non-commercial research.
https://arxiv.org/abs/2610.29905
Learning across medical imaging modalities requires making use of images without paired text and accommodating new domains while retaining existing representations. We propose a medical vision-language technique built around an expandable bank of modality experts. Its Multiway Transformer combines shared visual computation with deterministically routed feed-forward experts and a separate text pathway. A modality-aware visual tokenizer supplies targets for masked pretraining on 19.4 million unpaired image rows across seven modalities; contrastive alignment then uses 3.23 million image-text pairs. Additional fundus and optical coherence tomography experts learn from paired data while the original image and text embedding paths remain frozen. With a ViT-Large backbone, the proposed technique achieves the best or tied-best result in 24 of 25 benchmark settings across nine modalities: 10 of 11 zero-shot classification benchmarks, all 10 linear probes, and all four retrieval benchmarks. Mean balanced accuracy is 0.674 for zero-shot classification and 0.856 for linear probing, and mean bidirectional retrieval recall is 20.70%. A separate three-seed sequential experiment with matched adaptation data yields fundus and OCT retrieval gains of 14.95 and 9.31 percentage points, with no measured loss on preceding fundus or pathology tasks. The preservation argument requires unchanged existing computation paths and inference conditions, and feature-identity checks verify retention on evaluated inputs. The proposed technique provides a modular approach to learning and expanding medical vision-language representations.
https://arxiv.org/abs/2610.29881
Translating structured biomedical information into accurate, patient-friendly narratives remains a challenging biomedical data-to-text (D2T) task. While small language models (SLMs) are attractive for healthcare applications because of their lower computational cost, easier deployment, and improved data governance, the impact of post-training alignment on biomedical D2T generation has not been systematically studied. In this work, we compare four alignment methods: supervised fine-tuning (SFT), direct preference optimization (DPO), odds ratio preference optimization (ORPO), and group relative policy optimization (GRPO), using Qwen-2.5 models for medication leaflet generation. We further introduce FDALeaflets, a dataset derived from OpenFDA drug labels, to evaluate cross-regulatory generalization in a zero-shot setting. Selected aligned SLMs outperform GPT-5 on several reference-based metrics, whereas GPT-5 achieves better hallucination and adequacy scores on FDALeaflets under LLM-as-judge evaluation. Among RL-free alignment methods, ORPO achieves the best in-domain semantic performance, reaching a semantic textual similarity (STS) score of 0.9752. GRPO achieves the highest FDALeaflets STS (0.9407), exceeding GPT-5 (0.9295). These findings show that post-training alignment is a key factor in improving both semantic fidelity and generalization for biomedical D2T generation, while clinical safety and patient readability require human verification.
https://arxiv.org/abs/2607.13430
Literature-searching language agents are becoming a standard component of scientific assistants for the life sciences, yet there is little controlled evidence on which parts of their harness matter. We run a controlled ablation on biomedical claim verification (SciFact) with the live PubMed API as the only tool. Holding the backbone and output format fixed, we compare four harnesses: closed-book answering, single-shot retrieval using the claim as the query, a ReAct-style agent that writes its own PubMed queries, and an oracle given the gold abstracts, each with two efficient frontier backbones. Naive single-shot retrieval finds the gold paper for only 6% of claims and turns overconfident errors into abstentions without improving accuracy. Letting the model formulate its own queries triples gold recall and yields the best verdicts (62% accuracy vs. 49-59% for the other realistic harnesses), although these differences are not significant at our sample size and agents use fewer than half of their search budget. With gold abstracts, the same models reach 79-86% accuracy, a significant 17-24 point gap showing that retrieval, not reasoning, is the main bottleneck. Finally, a citation audit shows that closed-book models cite PubMed IDs that almost always exist (327/335) but are almost never relevant: a cross-family LLM judge rates only 3 of 327 existing citations as relevant to the claim, versus 67% for citations produced by the search agent. Existence checks are therefore insufficient safeguards for scientific agents. We release code, prompts, and all cached tool calls at this https URL.
https://arxiv.org/abs/2610.29812
Edge medical segmentation must reconcile small model size, high accuracy, and fast inference. TernScope addresses this tradeoff through model--hardware co-design, learning a compact segmentation network whose low-bit operators also simplify hardware execution. Split-channel large-kernel blocks preserve spatial context with limited computation, while branch fusion removes redundant inference paths. Ternary Progressive Quantization-aware Training (TPQ) then adapts the fused network from deep to shallow layers, through the decoder, and finally to the input and prediction layers. All 25 convolutions use ternary weights and 8-bit activations, enabling packed storage and multiplier-free computation. The resulting model uses 0.2483 M parameters and 0.0949 GMACs while retaining competitive segmentation accuracy on in-domain and external datasets. Under the same 45 nm technology, TernScope reduces compute-array area by 88.46% compared with the original Gemmini, a systolic-array accelerator with 8-bit $\times$ 8-bit multipliers. These results demonstrate a path from accurate lightweight medical segmentation to compact low-bit hardware.
https://arxiv.org/abs/2610.29617
Automatic phenotype information extraction plays an important role in rare disease diagnosis, genotype-phenotype analysis, and precision medicine. However, accurately identifying phenotype concepts and determining their associations with specific patients remain challenging, particularly in full-text biomedical articles involving multiple patients and complex clinical descriptions. This paper presents an overview of CHIP 2026 Shared Task 1, which aims to promote the development of methods for patient-specific phenotype concept recognition from full-text biomedical literature. The task consists of two subtasks: full-text phenotype concept recognition and patient-specific phenotype association. For this evaluation, we used 200 annotated full-text biomedical articles from the PatientPheX dataset, containing 506 patients, 15,193 phenotype mentions, and 5,656 patient-phenotype associations. A total of 455 teams registered for the competition, with 189 and 103 valid submissions received on the Phase A and Phase B leaderboards, respectively. The best-performing system achieved an overall score of 0.7389 on the final test set, outperforming the baseline by 8.37 percentage points. The top-performing teams explored diverse approaches combining biomedical language models, large language models (LLMs), and ensemble strategies. The evaluation results highlight both the potential of these approaches and the remaining challenges in patient attribution and phenotype normalization from full-text biomedical literature. The post-evaluation phase remains open at this https URL.
https://arxiv.org/abs/2610.29606
Vision-language models (VLMs) achieve remarkable performance on 2D medical images, such as X-rays or pathology images, while 3D VLMs that directly process CT/MRI volumes lag behind due to limited 3D training data and the predominance of 2D foundation architectures. To leverage powerful 2D VLMs for analyzing medical volumes, which contain hundreds of slices, it is therefore necessary to focus only on those few slices, which are diagnostically relevant. To enable such a prioritization, we propose XGLASS, a method that transfers medical expertise from 2D X-rays to 3D CT for task-aware slice prioritization. XGLASS uses disease-conditioned importance maps derived from language-aligned radiologist gaze on X-rays and spatially aligns them with coronal CT projections, bringing gaze priors and CT content into a shared 2D representation. The fused gaze-prior/CT projection is then used to predict a disease-specific ordering of axial slices, prioritizing diagnostically relevant slices. XGLASS significantly improves budgeted retrieval over 2D and 3D-native baselines, achieving a top-10 hit rate up to 75.9% for the best-performing disease. In practice, this means that after inspecting only the top 10 slices (4.17% of a 240-slice scan), XGLASS identifies a diagnostically relevant slice in more than 75% of cases. For downstream slice-wise finding classification, an XGLASS-selected 30-slice candidate set reduces model calls by 87.5% while improving F1 by 11.3 percentage points over all-slice inference, 4.2 points over the strongest 2D selector, and remains competitive with 3D-native selectors while requiring up to 130.8 times less time and 10.9 times less GPU memory per finding, supporting its use as a lightweight preselector for volumetric CT analysis. The code and pretrained checkpoint are available on this https URL.
https://arxiv.org/abs/2610.26255
A generated chest radiograph can be useful as declared augmentation, but the same image becomes unsupported evidence when submitted as the record of a real examination. We study this problem by separating three questions: whether an image passes an automated quality check, whether an origin classifier flags it as generated, and whether a trusted record supports the claimed acquisition. In our experiments, Qwen selects up to 20 images from pools of 1,000 existing Cheff-identified or SynthCheX candidates. A receiver evaluates quality with MedGemma and predicted origin with a classifier on frozen DINOv3 features. Quality-based selection raises quality passes from 12 to 19 of 20 for Cheff-identified images and from 8 to 17 for SynthCheX. We find no evidence that selection improves passage through both checks: no selected Cheff-identified image passes both, while uniform, quality, and quality-constrained surrogate selection produce 2, 1, and 2 SynthCheX passes. On unprocessed test images, the origin classifier flags 4,677 of 5,000 SynthCheX images, but it also misclassify 110 of 2,297 NIH (real) images and 568 of 957 genuine images from another collection as fake. Our results further show that JPEG compression reduces SynthCheX-versus-NIH AUROC from 0.987 to 0.841. Even without processing, 152 SynthCheX images pass both pixel checks. These checks can filter submissions, but they cannot verify an acquisition claim. We strongly advocate that source and intended use must be recorded and checked separately for admission of chest radiographs in medical datasets.
https://arxiv.org/abs/2610.29152
Merging different models into a single model is highly desirable for multi-task deployment, particularly in regulated domains like healthcare. In such settings, models are often locally fine-tuned due to strict data privacy policies, necessitating that aggregation operates exclusively on the fine-tuned weights. Existing methods apply a uniform merge across all tasks, ignoring the geometric relationships among their learned subspaces. When task updates occupy misaligned subspaces, projecting them onto a shared low-rank basis discards task-relevant directions, a failure mode named \emph{subspace interference}. Through this study, we show that the per-task projection error of a merged model is governed by the principal-angle alignment between each task and the shared subspace, so that grouping geometrically compatible tasks provably reduces this error within each group. Motivated by this observation, we propose \textbf{Group-wise Rank-Aware Model Merging (GRAM)}, which uses the principal-angle geometry of task vectors to decide which tasks should be merged together and then performs a standard SVD-based merge within each coalition; the pipeline requires only the fine-tuned weights at merge time. With only one additional model ($\nK{=}2$), GRAM significantly mitigates subspace interference and consistently outperforms prior merging methods across language understanding (GLUE with Flan-T5), 8-task CLIP vision, and medical instruction tuning (Qwen2-7B-Instruct with four English/Chinese medical LoRAs).
https://arxiv.org/abs/2610.29110
Task-oriented dialogue summarization aims to automatically extract key information to generate domain summaries to improve service efficiency and quality. Task-oriented dialogue is inherently logical and surrounds specific topic. How to effectively capture the dialogue topic and the most salient information becomes one of the major challenges of this task. In this paper, we propose a task-oriented dialogue summarization model utilizing a multi-level encoder with global topic (MLEGT). This model discovers temporal and spatial dependencies through a multi-level encoder, while simultaneously obtaining a simple yet effective global topic in the process of graph construction. It not only captures the crucial details but also breaks the long-range limit and discover the intrinsic structure across the dialogue. Then, a global topic guided pointer mechanism is added into the summrizer to capture ignored but important information, which is helpful to improve the accuracy of the summary. A comprehensive study of two public datasets, including a real-world large-scale Chinese police interrogation dataset and a medical reporting service dataset proves the superiority of our method on several strong baselines.
https://arxiv.org/abs/2610.29097
Abdominal organ segmentation is essential in modern medical applications. While existing deep learning approaches demonstrate promising performance, their heavy reliance on large-scale image data raises concerns over generalization capability and privacy risks. This motivates the development of generalizable segmentation training paradigms based on domain-randomized image synthesis, facilitating generalization across unseen real image domains. However, existing paradigms either suffer from limited segmentation performance when applied to abdominal organs, or require dataset-specific finetuning. To address these limitations, we propose ReSeg, a novel two-stage retraining-free framework for domain-agnostic zero-shot abdominal organ segmentation. At the first stage, our organ-agnostic synthetic data-driven pretraining approach exploits semantically and visually diverse synthetic images generated by a dedicated data engine to optimize a Generalizable Semantic Representation Network (GSRNet). The network is thereby capable of learning semantic features robust against variations in anatomical structure, imaging contrast, resolution and spatial context, which provide universal representation capabilities that serve as a foundation for segmentation learning. Subsequently, in the second stage, we continue to train an Organ-specific Encoder-decoder Segmentation Network (OESNet), whose encoder is initialized with the pretrained weights. This training process is facilitated by another dedicated data engine, which generates diversified visual images while strictly retaining the inherent spatial layout of abdominal organs. Comprehensive evaluation on seven abdominal organ segmentation datasets across three different modalities including CT, MRI, and PET demonstrates that ReSeg consistently outperforms existing state-of-the-art (SOTA) methods while eliminating the need for real training images.
https://arxiv.org/abs/2610.29090
True whole-body medical imaging captures a patient from head to toe and provides comprehensive anatomical and/or functional information. This coverage enables reconstruction of the external body surface, yielding patient body models. However, scanner geometry (e.g., bore diameter), patient characteristics, and positioning can leave body regions missing (e.g., lateral arms/torso, hands, forearms, elbows), producing incomplete patient body models. Such incompleteness limits downstream medical analyses, including derivation of body-habitus metrics (BHMs), such as body volume and surface area, for injected radiotracer activity regimens, cardiometabolic risk assessment, and computational anatomical modeling for medical imaging simulation and radiation dosimetry. We present the Medical Body model Optimization-based Estimator (MedBOE), an automated, training-free framework for estimating complete patient body models from whole-body images with missing body regions. Our innovation is to leverage the Skinned Multi-Person Linear (SMPL) template, a parametric body mesh representing a broad range of body shapes and poses, in medical imaging. MedBOE aligns the SMPL template to the incomplete patient body models via attribute-guided optimization and estimates missing body regions through geometrically and volumetrically constrained deformation. We evaluated MedBOE using two public datasets: AutoPET (91 whole-body PET-CT images) and Human Implicit Tissues (HIT; 40 whole-body segmentations from MRI images). MedBOE achieved the best overall volumetric and geometric performance among evaluated methods. BHMs derived from MedBOE were within 2% error, suggesting low percentage errors for downstream analyses. MedBOE offers an automated, training-free method for estimating complete patient body models from whole-body images with missing body regions.
https://arxiv.org/abs/2610.28985
In vision and scientific domains involving spatial data, a key question is whether node feature values vary independently across space or form coherent spatial structures. Classical spatial autocorrelation statistics such as Moran's $I$ and Geary's $C$ quantify this phenomenon but operate on a single scalar variable with fixed neighbourhood weights, limiting their use for high-dimensional graph-like data. We introduce SAIL (Spatial Autocorrelation Index Learner), a differentiable framework that generalises spatial autocorrelation into a learnable operator by jointly learning feature projections defining candidate scalar fields and inter-node neighbourhood affinities. SAIL produces interpretable local and global spatial coherence descriptors, enabling supervised prediction and unsupervised discovery of spatial autocorrelation modes and hotspots. We show that SAIL exactly recovers classical spatial statistics under appropriate parametrisations and, for tasks driven by latent spatial autocorrelation, can approximate the Bayes-optimal predictor with an inductive bias matched to such tasks. Experiments on synthetic data and large-scale biomedical graphs demonstrate statistical correctness and discovery of spatial coherence with applications across vision, geospatial analysis, and biomedicine. The code repository is available at: this https URL.
https://arxiv.org/abs/2610.28806
Deep learning models have become essential tools in medical imaging, yet training them end-to-end for diverse tasks remains challenging due to limited labeled data and computational constraints. To address this, we introduce Brain2Vec, a foundation model pre-trained on 74,425 T1-weighted Magnetic Resonance Imaging (MRI) scans pooled from multiple studies. Brain2Vec can serve both as a weight initialization backbone for fine-tuning downstream tasks and as a standalone feature extractor. We evaluated Brain2Vec in three tasks: downstream predictive performance, convergence speed, and embedding quality. Using Brain2Vec's pretrained weights as initialization and fine-tuning on labeled data for a brain age prediction task, results demonstrate improved final accuracy and faster convergence compared to random initialization. Additionally, its frozen embeddings outperform anatomically defined volumetric features on four of five downstream classification tasks and perform competitively with a state-of-the-art foundation model pre-trained on substantially more data. Lastly, we show that Brain2Vec encodes information primarily from a spatially localized and neuroanatomically meaningful set of brain regions, and that manipulating a subset of latent features produces monotonic, region-specific effects on the reconstructed anatomy. Brain2Vec code and trained models are available as an open-source package on this https URL. Users can apply Brain2Vec locally by installing the package, or directly through the NiChart cloud platform this https URL, where Brain2Vec features can be derived without requiring local installation or specialized infrastructure.
https://arxiv.org/abs/2610.28411
Deep learning has become the default tool for medical image analysis, driven by the open-source movement. However, achieving the best performance on a given task remains difficult, with architecture selection and hyperparameter optimization (HPO) still considered "more of an art than a science". Automated machine learning (AutoML) automates parts of model training, yet helps little in medical imaging: general-purpose approaches lack medical architectures and preprocessing, and medical-focused ones demand engineering expertise and remain confined to narrow tasks such as 3D segmentation. We introduce MedicalMLOmni, a multi-agent AutoML framework that automates model training for diverse single- and multi-modal medical tasks through a natural language interface. Specifically, MedicalMLOmni performs evidence-based planning by retrieving published results to guide model selection and configuration, and employs parallel HPO where multiple agents explore adjustment strategies concurrently. MedicalMLOmni achieves the best score on 19 of 20 benchmarks; PMC-VQA is the exception, where a vision-language model with broader pre-training leads. Backbone-matched controls attribute the gains to the framework, not the backbone. By removing coding requirements, MedicalMLOmni lowers the barrier for domain experts with rich datasets but limited engineering expertise.
https://arxiv.org/abs/2610.28410
Realistic few-shot adaptation of medical vision-language models (VLMs) can leave low-prevalence classes without any labeled support. The training-free SS- Text+ solver remains operational in this setting, but its zero-support prototypes receive no visual adaptation and fall back to a purely textual class prototype. We in- troduce Gated Knowledge-Guided Prototype Transfer (GProtoT), a pre-repulsion module that transfers supported-class visual residuals to missing classes using VLM similarity and an ontology-based clinical distance. A validation-free evidence gate scales transfer based on semantic relevance and residual agreement, thereby limiting unsupported extrapolation. In 50 paired realistic one-shot trials on MESSIDOR with FLAIR features, severe and proliferative diabetic retinopathy were absent from every support set. Relative to SS-Text+, gated ProtoT improved missing-class recall by 5.23 points, average class accuracy by 1.37 points, and the missing/supported recall harmonic mean by 1.83 points. It reduced negative- transfer frequency from 46-48% for ungated transfer to 2%, while at the cost of reductions of 1.20 percentage points in supported-class recall and 0.45 percentage points in top-1 accuracy. These results indicate that evidence-based gating provides a safety mechanism for the knowledge source. GProtoT is based on SS- Text+ and requires no gradients, validation data, or additional model inference, of- fering a low-compute path toward accountable adaptation under incomplete clini- cal supervision. Code is available: this https URL
https://arxiv.org/abs/2610.28350
VGL-stGen is a multimodal large language model adapted from a pretrained medical vision-language model using paired lung H&E and spatial transcriptomics with single-cell references. Training integrates image-expression and expression-cell-type pairs, and gene-conditioned pseudo-labels transfer transcriptomic cell-type supervision to histology images. One deployed checkpoint supports thirteen evaluated tasks spanning tissue and cell-type classification, gene prediction and conditional expression completion from combinations of histology, cell identity and observed gene expression. Task-specific decoding produces categorical labels, gene lists and structured expression levels. For conditional completion, fixing queried gene identities and predicting their levels autoregressively improves structured prediction. Controlled adaptation shows that restricting supervision to requested expression-level tokens can further improve image-conditioned completion. Image-permutation experiments indicate that correctly paired histology adds information beyond observed expression. External classification relies partly on computational references with shared annotation lineage, and some H&E sources were exposed during cancer training or model development. Within these conditions, VGL-stGen demonstrates how a medical vision-language backbone can learn from spatial transcriptomics and histology to connect tissue morphology and molecular states through shared generative modeling.
https://arxiv.org/abs/2610.28266
Adapting Vision Foundation Models (VFMs) to medical imaging via LoRA has become standard practice, yet model selection is guided almost entirely by downstream task metrics, treating backbones with similar performance as interchangeable. We investigate whether equal performance implies equal internal representational shift. We analyse four ViT-B/16 backbones, DINOv3, SigLIP2, MerMED-FM, and BiomedCLIP, pre-trained with different objectives (self-distillation vs. contrastive vision-language) and on different data domains (natural vs. medical images). We adapt each to brain tumour segmentation and evaluate on six datasets covering both segmentation and Alzheimer's disease classification. Using attention divergence, weight-change analysis, and activation patching, we find that the four models converge to similar segmentation performance (mean Dice 78-81%) through markedly different internal dynamics, yet diverge in cross-task transfer: segmentation adaptation improves Alzheimer's disease classification for DINOv3 but degrades it for the other three backbones. We reveal a dissociation between modification magnitude and causal importance: the most heavily modified layers are not the causally relevant ones, with early-to-mid layers identified as sufficient for segmentation recovery. Restricting LoRA to these layers matches or approaches full-layer segmentation while reducing classification degradation in the three affected backbones, providing a mechanistically grounded strategy that is more parameter-efficient and more robust than standard full-layer adaptation.
https://arxiv.org/abs/2610.28255
Large Language Models (LLMs) depend fundamentally on the diversity, depth, and factual rigor of their pre-training corpora. However, contemporary foundational pre-training datasets (such as The Pile, S2ORC, and Dolma) exhibit a severe structural omission: African scientific, medical, legal, and agricultural scholarship constitutes less than 0.5% of global pre-training tokens. Consequently, state-of-the-art models suffer from systematic failure modes when reasoning about tropical epidemiology, localized smallholder agro-ecologies, regional economic governance, and indigenous linguistic structures. To resolve this representation deficit and advance African intellectual sovereignty in artificial intelligence, we introduce Africa-Papers, the largest curated multi-domain Pan-African academic pre-training corpus to date. Comprising over 844,807 full-text papers spanning 10.15 billion tokens across 879 Parquet shards, Africa-Papers unifies four primary scientific streams: (1) continental peer-reviewed journals indexed in DOAJ across 31 African nations, (2) the CGIAR CGSpace agricultural repository, (3) African-authored and African-focused STEM/AI preprints on arXiv, and (4) open-access international publications by scholars affiliated with African institutions indexed via OpenAlex. The entire corpus is processed into layout-aware, clean Markdown preserving section hierarchies, mathematical equations, and tabular data, accompanied by exact BPE token counts and a standardized 8-domain taxonomy. We release Africa-Papers openly on the Hugging Face Hub under the AfriSpeech organization to accelerate continual pre-training and domain evaluation for foundation models globally.
https://arxiv.org/abs/2610.28173
Smartphone clinical images provide a low-cost data source for computer-aided skin lesion classification in resource-constrained settings, but images alone cannot fully capture patients' medical histories and lesion symptoms. To address the lack of structured organization among heterogeneous clinical variables, the ambiguity between observed and imputed values, and the risk that clinical information may interfere with visual evidence, we propose GAMF-Net, a grouped availability-aware multimodal fusion network. Ten clinical variables are divided into three semantic groups---demographics, history-related risk, and lesion presentation---and each group jointly encodes field values and field-level availability masks. The image branch produces the base classification logits, while each clinical group generates image-conditioned class-level residual evidence. Only available groups participate in availability-normalized equal-weight fusion; when all clinical information is unavailable, the model reduces exactly to the image-only pathway. We evaluate the method on PAD-UFES-20 under a patient-disjoint five-fold protocol with separate training, validation, and test partitions. GAMF-Net achieves an Accuracy of $74.17\pm2.85\%$, a balanced accuracy (BACC) of $70.11\pm2.11\%$, a Macro-F1 of $68.85\pm0.85\%$, and a Macro-AUROC of $93.42\pm1.20\%$, outperforming all image-only and multimodal baselines reimplemented under a unified protocol. Compared with the strongest baseline, MetaBlock, the corresponding improvements are 2.37, 2.59, 4.14, and 1.02 percentage points, respectively. Ablation results show that clinical information substantially improves class-balanced performance, constrained equal-weight fusion is more effective than dynamic fusion, and the lesion-presentation group provides the most informative clinical complement.
https://arxiv.org/abs/2610.28129