Medical image segmentation continues to advance rapidly, yet rigorous comparison between methods remains challenging due to a lack of standardized and customizable tooling. In this work, we present the current state of the Medical Imaging Segmentation Toolkit (MIST), with a particular focus on its flexible and modular postprocessing framework designed for the BraTS 2025 pre- and post-treatment glioma segmentation challenge. Since its debut in the 2024 BraTS adult glioma post-treatment segmentation challenge, MIST's postprocessing module has been significantly extended to support a wide range of transforms, including removal or replacement of small objects, extraction of the largest connected components, and morphological operations such as hole filling and closing. These transforms can be composed into user-defined strategies, enabling fine-grained control over the final segmentation output. We evaluate three such strategies - ranging from simple small-object removal to more complex, class-specific pipelines - and rank their performance using the BraTS ranking protocol. Our results highlight how MIST facilitates rapid experimentation and targeted refinement, ultimately producing high-quality segmentations for the BraTS 2025 challenge. MIST remains open source and extensible, supporting reproducible and scalable research in medical image segmentation.

Data scarcity is a major challenge in medical imaging, particularly for deep learning models. While data pooling (combining datasets from multiple sources) and data addition (adding more data from a new dataset) have been shown to enhance model performance, they are not without complications. Specifically, increasing the size of the training dataset through pooling or addition can induce distributional shifts, negatively affecting downstream model performance, a phenomenon known as the "Data Addition Dilemma". While the traditional i.i.d. assumption may not hold in multi-source contexts, assuming exchangeability across datasets provides a more practical framework for data pooling. In this work, we investigate medical image segmentation under these conditions, drawing insights from causal frameworks to propose a method for controlling foreground-background feature discrepancies across all layers of deep networks. This approach improves feature representations, which are crucial in data-addition scenarios. Our method achieves state-of-the-art segmentation performance on histopathology and ultrasound images across five datasets, including a novel ultrasound dataset that we have curated and contributed. Qualitative results demonstrate more refined and accurate segmentation maps compared to prominent baselines across three model architectures. The code will be available on Github.

Scoring systems are widely adopted in medical applications for their inherent simplicity and transparency, particularly for classification tasks involving tabular data. In this work, we introduce RegScore, a novel, sparse, and interpretable scoring system specifically designed for regression tasks. Unlike conventional scoring systems constrained to integer-valued coefficients, RegScore leverages beam search and k-sparse ridge regression to relax these restrictions, thus enhancing predictive performance. We extend RegScore to bimodal deep learning by integrating tabular data with medical images. We utilize the classification token from the TIP (Tabular Image Pretraining) transformer to generate Personalized Linear Regression parameters and a Personalized RegScore, enabling individualized scoring. We demonstrate the effectiveness of RegScore by estimating mean Pulmonary Artery Pressure using tabular data and further refine these estimates by incorporating cardiac MRI images. Experimental results show that RegScore and its personalized bimodal extensions achieve performance comparable to, or better than, state-of-the-art black-box models. Our method provides a transparent and interpretable approach for regression tasks in clinical settings, promoting more informed and trustworthy decision-making. We provide our code at https://github.com/SanoScience/RegScore.

Mammography is the most commonly used imaging modality for breast cancer screening, driving an increasing demand for deep-learning techniques to support large-scale analysis. However, the development of accurate and robust methods is often limited by insufficient data availability and a lack of diversity in lesion characteristics. While generative models offer a promising solution for data synthesis, current approaches often fail to adequately emphasize lesion-specific features and their relationships with surrounding tissues. In this paper, we propose Gated Conditional Diffusion Model (GCDM), a novel framework designed to jointly synthesize holistic mammogram images and localized lesions. GCDM is built upon a latent denoising diffusion framework, where the noised latent image is concatenated with a soft mask embedding that represents breast, lesion, and their transitional regions, ensuring anatomical coherence between them during the denoising process. To further emphasize lesion-specific features, GCDM incorporates a gated conditioning branch that guides the denoising process by dynamically selecting and fusing the most relevant radiomic and geometric properties of lesions, effectively capturing their interplay. Experimental results demonstrate that GCDM achieves precise control over small lesion areas while enhancing the realism and diversity of synthesized mammograms. These advancements position GCDM as a promising tool for clinical applications in mammogram synthesis. Our code is available at https://github.com/lixinHUST/Gated-Conditional-Diffusion-Model/

Purpose: Accurate tumor segmentation is vital for adaptive radiation therapy (ART) but remains time-consuming and user-dependent. Segment Anything Model 2 (SAM2) shows promise for prompt-based segmentation but struggles with tumor accuracy. We propose prior knowledge-based augmentation strategies to enhance SAM2 for ART. Methods: Two strategies were introduced to improve SAM2: (1) using prior MR images and annotations as contextual inputs, and (2) improving prompt robustness via random bounding box expansion and mask erosion/dilation. The resulting model, SAM2-Aug, was fine-tuned and tested on the One-Seq-Liver dataset (115 MRIs from 31 liver cancer patients), and evaluated without retraining on Mix-Seq-Abdomen (88 MRIs, 28 patients) and Mix-Seq-Brain (86 MRIs, 37 patients). Results: SAM2-Aug outperformed convolutional, transformer-based, and prompt-driven models across all datasets, achieving Dice scores of 0.86(liver), 0.89(abdomen), and 0.90(brain). It demonstrated strong generalization across tumor types and imaging sequences, with improved performance in boundary-sensitive metrics. Conclusions: Incorporating prior images and enhancing prompt diversity significantly boosts segmentation accuracy and generalizability. SAM2-Aug offers a robust, efficient solution for tumor segmentation in ART. Code and models will be released at https://github.com/apple1986/SAM2-Aug.

Pancreatic cancer carries a poor prognosis and relies on endoscopic ultrasound (EUS) for targeted biopsy and radiotherapy. However, the speckle noise, low contrast, and unintuitive appearance of EUS make segmentation of pancreatic tumors with fully supervised deep learning (DL) models both error-prone and dependent on large, expert-curated annotation datasets. To address these challenges, we present TextSAM-EUS, a novel, lightweight, text-driven adaptation of the Segment Anything Model (SAM) that requires no manual geometric prompts at inference. Our approach leverages text prompt learning (context optimization) through the BiomedCLIP text encoder in conjunction with a LoRA-based adaptation of SAM's architecture to enable automatic pancreatic tumor segmentation in EUS, tuning only 0.86% of the total parameters. On the public Endoscopic Ultrasound Database of the Pancreas, TextSAM-EUS with automatic prompts attains 82.69% Dice and 85.28% normalized surface distance (NSD), and with manual geometric prompts reaches 83.10% Dice and 85.70% NSD, outperforming both existing state-of-the-art (SOTA) supervised DL models and foundation models (e.g., SAM and its variants). As the first attempt to incorporate prompt learning in SAM-based medical image segmentation, TextSAM-EUS offers a practical option for efficient and robust automatic EUS segmentation. Our code will be publicly available upon acceptance.

Pancreatic cancer carries a poor prognosis and relies on endoscopic ultrasound (EUS) for targeted biopsy and radiotherapy. However, the speckle noise, low contrast, and unintuitive appearance of EUS make segmentation of pancreatic tumors with fully supervised deep learning (DL) models both error-prone and dependent on large, expert-curated annotation datasets. To address these challenges, we present TextSAM-EUS, a novel, lightweight, text-driven adaptation of the Segment Anything Model (SAM) that requires no manual geometric prompts at inference. Our approach leverages text prompt learning (context optimization) through the BiomedCLIP text encoder in conjunction with a LoRA-based adaptation of SAM's architecture to enable automatic pancreatic tumor segmentation in EUS, tuning only 0.86% of the total parameters. On the public Endoscopic Ultrasound Database of the Pancreas, TextSAM-EUS with automatic prompts attains 82.69% Dice and 85.28% normalized surface distance (NSD), and with manual geometric prompts reaches 83.10% Dice and 85.70% NSD, outperforming both existing state-of-the-art (SOTA) supervised DL models and foundation models (e.g., SAM and its variants). As the first attempt to incorporate prompt learning in SAM-based medical image segmentation, TextSAM-EUS offers a practical option for efficient and robust automatic EUS segmentation. Code is available at https://github.com/HealthX-Lab/TextSAM-EUS .

Medical image segmentation is a complex and challenging task, which aims to accurately segment various structures or abnormal regions in medical images. However, obtaining accurate segmentation results is difficult because of the great uncertainty in the shape, location, and scale of the target region. To address these challenges, we propose a higher-order spatial interaction framework with dual cross global efficient attention (DGEAHorNet), which employs a neural network architecture based on recursive gate convolution to adequately extract multi-scale contextual information from images. Specifically, a Dual Cross-Attentions (DCA) is added to the skip connection that can effectively blend multi-stage encoder features and narrow the semantic gap. In the bottleneck stage, global channel spatial attention module (GCSAM) is used to extract image global information. To obtain better feature representation, we feed the output from the GCSAM into the multi-branch dense layer (SENetV2) for excitation. Furthermore, we adopt Depthwise Over-parameterized Convolutional Layer (DO-Conv) in order to replace the common convolutional layer in the input and output part of our network, then add Efficient Attention (EA) to diminish computational complexity and enhance our model's performance. For evaluating the effectiveness of our proposed DGEAHorNet, we conduct comprehensive experiments on four publicly-available datasets, and achieving 0.9320, 0.9337, 0.9312 and 0.7799 in Dice similarity coefficient on ISIC2018, ISIC2017, CVC-ClinicDB and HRF respectively. Our results show that DGEAHorNet has better performance compared with advanced methods. The code is publicly available at https://github.com/penghaixin/mymodel .

The Diffusion Probabilistic Model (DPM) has demonstrated remarkable performance across a variety of generative tasks. The inherent randomness in diffusion models helps address issues such as blurring at the edges of medical images and labels, positioning Diffusion Probabilistic Models (DPMs) as a promising approach for lesion segmentation. However, we find that the current training and inference strategies of diffusion models result in an uneven distribution of attention across different timesteps, leading to longer training times and suboptimal solutions. To this end, we propose UniSegDiff, a novel diffusion model framework designed to address lesion segmentation in a unified manner across multiple modalities and organs. This framework introduces a staged training and inference approach, dynamically adjusting the prediction targets at different stages, forcing the model to maintain high attention across all timesteps, and achieves unified lesion segmentation through pre-training the feature extraction network for segmentation. We evaluate performance on six different organs across various imaging modalities. Comprehensive experimental results demonstrate that UniSegDiff significantly outperforms previous state-of-the-art (SOTA) approaches. The code is available at https://github.com/HUYILONG-Z/UniSegDiff.

Many deep learning methods have been proposed for brain tumor segmentation from multi-modal Magnetic Resonance Imaging (MRI) scans that are important for accurate diagnosis and treatment planning. However, supervised learning needs a large amount of labeled data to perform well, where the time-consuming and expensive annotation process or small size of training set will limit the model's performance. To deal with these problems, self-supervised pre-training is an appealing solution due to its feature learning ability from a set of unlabeled images that is transferable to downstream datasets with a small size. However, existing methods often overlook the utilization of multi-modal information and multi-scale features. Therefore, we propose a novel Self-Supervised Learning (SSL) framework that fully leverages multi-modal MRI scans to extract modality-invariant features for brain tumor segmentation. First, we employ a Siamese Block-wise Modality Masking (SiaBloMM) strategy that creates more diverse model inputs for image restoration to simultaneously learn contextual and modality-invariant features. Meanwhile, we proposed Overlapping Random Modality Sampling (ORMS) to sample voxel pairs with multi-scale features for self-distillation, enhancing voxel-wise representation which is important for segmentation tasks. Experiments on the BraTS 2024 adult glioma segmentation dataset showed that with a small amount of labeled data for fine-tuning, our method improved the average Dice by 3.80 percentage points. In addition, when transferred to three other small downstream datasets with brain tumors from different patient groups, our method also improved the dice by 3.47 percentage points on average, and outperformed several existing SSL methods. The code is availiable at https://github.com/HiLab-git/Vox-MMSD.