LeCor: Learning to Be Corrected by Meta-Learned Test-Time Training for Interactive 3D Lung-Tumour Segmentation
Read the original on arXiv Computer Vision →The Flow has not summarised this story yet — read it at arXiv Computer Vision.
The Flow has not summarised this story yet — read it at arXiv Computer Vision.
The paper introduces the first adaptation of the MedSAM2 foundation model for interactive 3D segmentation of interstitial lung disease (ILD) on thoracic CT scans. It evaluates three fine‑tuning strategies and four prompt types—bounding‑boxes, points, lassos, and scribbles—finding that full model fine‑tuning yields the best performance, improving Dice scores by 4.7 percentage points over the baseline. A proof‑of‑concept workflow is presented where MedSAM2 is first initialized with an automatic prior and then refined by radiologist prompts, with all resources released on GitHub.
Purpose: To compare 2D, 2.5D, and 3D residual networks for pulmonary nodule malignancy-risk classification and evaluate momentum-contrast pretraining, mild augmentation, and exclusion of indeterminate...
The paper presents a pragmatic segmentation pipeline for brain metastases in the BraTS 2026 Task 1, using a 5‑fold nnU-Net ResEnc‑L ensemble trained for 1,000 epochs on 1,296 four‑modality cases. A rule‑based post‑processing cascade tuned for the lesion‑wise Dice similarity coefficient (LW‑DSC) improves performance, achieving LW‑DSC scores of 0.733, 0.751, 0.713, and 0.549 on enhancing tumour, tumour core, whole tumour, and resection cavity, respectively. The authors audit each post‑processing stage with a five‑fold out‑of‑fold analysis, confirm two stages as robust, and provide a mechanistic analysis of LW‑DSC, along with thirteen negative results that challenge common intuitions.
The paper presents a segmentation pipeline for brain metastases in both pre‑ and post‑treatment cases using a 5‑fold nnU‑Net ResEnc‑L ensemble trained on 1,296 four‑modality cases. A rule‑based post‑processing cascade improves the lesion‑wise Dice similarity coefficient (LW‑DSC) for enhancing tumour, tumour core, whole tumour, and resection cavity sub‑regions, achieving LW‑DSC scores of 0.733, 0.751, 0.713, and 0.549 respectively on the official validation leaderboard. The authors conduct a five‑fold out‑of‑fold analysis to validate the robustness of each post‑processing stage, provide a mechanistic explanation of LW‑DSC behaviour, and report thirteen negative results that challenge common intuitions, with all code released under Apache‑2.0.
The study compares 2D, 2.5D, and 3D residual networks for classifying pulmonary nodule malignancy risk using a retrospective LIDC‑IDRI cohort of 2,654 nodules. Models were trained with random initialization, momentum‑contrast pretraining, and mild data augmentation, and evaluated on patient‑disjoint splits. Augmented 2.5D models achieved the highest test Macro‑F1 (0.6537) and accuracy (0.6869), while 2D and 3D models performed lower, and pretraining generally reduced performance.
The paper reports the submissions of team nucli to the HECKTOR 2026 challenge, which evaluates machine learning methods for head‑and‑neck cancer imaging. The team used self‑supervised pre‑trained encoders, training a 2D DINOv2 encoder on PET scans and combining a DynUNet with a SwinUNETR for segmentation, achieving a mean Dice of 0.5409. For TN staging, they fused geometric features from segmentation masks with PET‑DINOv2‑MIPs deep features via logistic regression, obtaining balanced accuracies of 0.3962 (T‑stage) and 0.6432 (N‑stage). For recurrence‑free survival prognosis, they fine‑tuned the PET‑DINOv2‑MIPs ViT‑S encoder with an MLP head under a CoxPH loss, achieving a Harrell's C‑index of 0.6577 and a weighted challenge score of 0.5802.