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REVIEW 4 major objections 4 minor 1 cited by

CADS: A Comprehensive Anatomical Dataset and Segmentation for Whole-Body Anatomy in Computed Tomography

T0 review · 4 major / 4 minor · reviewed 2026-08-06 · deepseek-v4-flash

Pith's one-line read The paper claims that comprehensive, standardized training data — 22,022 CT volumes labeled for 167 structures — rather than architectural innovation, is what advances whole-body CT segmentation, and supports this with a model that beats…

desk verdict Valuable dataset release, but the headline performance advantage over TotalSegmentator is not established because the evaluation is curated and partly development-involved. read the letter →

arxiv 2507.22953 v1 pith:2AJN54YD submitted 2025-07-29 eess.IV cs.CV

classification eess.IVcs.CV
keywords whole-bodyCTsegmentationpseudo-labelinganatomicaldatasetnnU-Netsemi-supervisedlearningorgan-at-riskdelineationdata-centricAIradiationoncology
verification ladder T0 review T1 audit T2 compute T3 formal

The pith

A machine-rendered reading of the paper's core claim, the machinery that carries it, and where it could break.

The reading

This paper argues that the bottleneck in whole-body CT segmentation is training data, not network architecture, and that a large, heterogeneous, consistently labeled collection can push a standard model past specialized and prior whole-body systems. To show this, the authors assemble the CADS-dataset: 22,022 CT volumes from more than 40 sources across 16 countries, with labels for 167 anatomical structures, roughly 18 times more scans and 60% more targets than the previous standard collection. Because only about one in five scans came with existing annotations, the rest were generated through an automated pseudo-labeling pipeline with shape-based quality control and structure-specific label selection. On the 119 structures shared with the TotalSegmentator baseline, the CADS-model trained with the same nnU-Net family reaches a mean Dice of 90.52% versus 88.09% for the baseline, and it adds 48 previously unsupported structures. Validation across 18 public datasets and an independent hospital cohort of 2,864 oncology patients, including expert contour review, supports the central claim that comprehensive data, rather than novel architectures, is what moves the field.

What carries the argument

The load-bearing mechanism is the annotation pipeline that converts a mostly unlabeled collection into a fully labeled one. Specialized region models trained on small seed sets (TotalSegmentator's 1,203 annotated volumes, Han-Seg's 42, VISCERAL, SAROS) generate whole-body pseudo-labels for the roughly 17,000 remaining scans; a shape prior built on neural implicit functions ranks every pseudo-label by its 90-percentile Hausdorff distance to a reconstruction, flagging anatomically implausible shapes for exclusion. Three complementary 'flavor' models — one trained on original ground truth, one on all pseudo-labels, one on shape-filtered pseudo-labels — are then compared per structure with statistical tests (ANOVA, Welch's ANOVA, or Kruskal-Wallis with post-hoc), and the best-performing flavor's label is selected for each of the 167 structures. A progressive merging order and targeted anatomical refinements, notably retrieval of the costovertebral joints of the ribs via a vessel-detection foundation model, complete the dataset. This pipeline is what makes the paper's scale argument possible: it turns data volume into training signal while attempting to control the noise that pseudo-labels introduce.

What would settle it

Have radiologists manually re-annotate a random sample of roughly 200 of the ~17,000 scans whose only labels came from the pseudo-labeling pipeline, covering the liver, one mid-thoracic vertebra, one rib, and buccal mucosa, and compare those manual contours against the CADS-dataset labels. If per-structure Dice on this sample is close to the model's reported performance rather than near expert-level agreement, the 'complete annotations' claim inherits the pseudo-label noise, and the model's margin over the baseline would need to be re-attributed.

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Extended reading notes

Core claim

The paper's central claim is that a data-centric strategy — systematic integration, standardization, and labeling of heterogeneous CT sources — is what lifts whole-body segmentation performance, and that established architectures are sufficient to reap the benefit. The CADS-model is trained on the assembled 22,022-volume dataset using the nnU-Net framework with region-specialized models and class-balancing oversampling for rare structures; no architectural novelty is introduced. On the 119 targets shared with TotalSegmentator, the CADS-model achieves a mean Dice of 90.52% (median 92.33%) against 88.09% (median 90.13%) for the baseline, with 71 structures improved and 44 of those improvements statistically significant. Across all 167 targets the model reports 85.87% mean Dice, with the shortfall concentrated in structures that were rarely annotated, very small (under 0.5 mL), or anatomically complex. The authors also report that training on the larger dataset improves boundary precision by an average of 3.94 mm HD95 across 18 test datasets, and that expert radiation-oncologist review deems the segmentations clinically usable for treatment planning.

Load-bearing premise

The entire annotation set rests on the assumption that models trained on small seed sets can assign accurate labels for all 167 structures across the roughly 17,000 scans that had no annotations, and that the shape-based filter that removes 'implausible' labels removes only errors, not genuine but unusual anatomy.

Editorial extensions

If this is right

  • A single CADS-model can segment 167 structures from head to knees, including 48 targets no prior whole-body model covered, so assembling separate per-organ models becomes unnecessary for this target set.
  • The documented errors in TotalSegmentator ground-truth labels (mislabeled ribs and vertebrae, organ misattributions, over-extended bladder labels) imply that models trained or evaluated on those labels inherit the errors, so existing benchmark numbers may need revisiting.
  • In the independent 2,864-patient hospital cohort, structures critical for radiation planning improve most (brainstem +43.8%, larynx +23.08%, parotid glands +19-21%), supporting direct use of the model in treatment-planning workflows.
  • The public release of the 22,022-volume dataset with 167 standardized structures gives other segmentation, landmark-detection, registration, and anatomy-guided reconstruction models a common training ground.

Reading between the lines

Editorial extensions of the paper, not claims the author makes directly.

  • The paper's variance-reduction argument implies that adding even more unlabeled scans through the same pseudo-labeling loop should continue to close performance gaps on rare and small structures; a direct test would be running the pipeline on a fresh pool of, say, 20,000 hospital CTs and measuring per-structure Dice rather than the mean.
  • Because the shape-outlier filter discards rather than corrects atypical shapes, the dataset likely under-represents pathological anatomy; if that is true, per-structure performance on rare deformities (e.g., the paper's own examples of resection or transitional vertebrae) would lag well behind the reported averages.
  • The corrected rib and vertebra labels are a natural by-product resource: releasing the curated re-annotations separately would let the community re-benchmark the many models built on the previous dataset.
  • The approach treats annotation conventions — brain mask scope, trachea as air column, rectum length — as the real ceiling, so standardizing those definitions across institutions is likely to matter more than further architecture changes.
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Editorial analysis

A structured set of objections, weighed in public.

Desk editor's note, referee report, and a circularity audit.

Referee Report

4 major / 4 minor

Summary. The paper introduces CADS, a data-centric framework for whole-body CT segmentation: a collection of 22,022 CT volumes from 40 sources annotated for 167 anatomical structures via iterative pseudo-labeling, shape-based quality control, and multi-flavor label selection, together with an nnU-Net-based CADS-model and a 3D Slicer plugin. The central quantitative claim is that the CADS-model outperforms the TotalSegmentator baseline on 119 mutual targets, with mean Dice 90.52% versus 88.09%, supported by evaluations across 18 public datasets and a 2,864-patient real-world oncology cohort.

Significance. If the claims hold, CADS would be a valuable community resource: the dataset is an order of magnitude larger than existing whole-body CT segmentation collections, the annotation coverage of 167 structures is substantially broader, and the data, models, and clinical plugin are publicly released. The paper is also commendably transparent about limitations, including the shape-filter exclusion of atypical cases and known imperfections in the final labels. The multi-source aggregation pipeline and the external hospital validation are serious engineering and evaluation efforts. However, the empirical support for the headline performance advantage is weakened by evaluation protocols that are partly development-involved and post-hoc curated; the dataset contribution is more robust than the specific performance comparison as currently presented.

major comments (4)
  1. [Online Methods §6.2; Results, 'Anatomical precision'] The headline comparison is computed after manually correcting 'obvious systematic errors such as mislabeled ribs and vertebrae' in the 65-image TotalSegmentator test set and excluding structures flagged as unreliable. Because §3.2 specifically engineers costovertebral joint retrieval and rib-label refinement, this curation can selectively favor CADS over the TotalSegmentator baseline. Please report results on the unmodified reference labels and on the automatically flagged subset, and make the curation protocol and exclusion list available.
  2. [Online Methods §2.4; Results, 'Cross-dataset versatility'] Flavor selection uses out-of-distribution validation from 'other labeled datasets in our collection,' explicitly including LiTS, VISCERAL, and BTCV-Abdomen, which are also among the 18 evaluation datasets. The primary cohort is described as 'heavily involved in the model development process.' This overlap means that the reported improvements on those sources are not independent of model selection. Please provide a version of the comparison restricted to sources never used in model development or flavor selection, or otherwise demonstrate that the selection procedure does not bias the reported gains.
  3. [Results, 'Anatomical precision'] The reported 95% confidence intervals for the two means overlap substantially: CADS 90.52% (88.12–92.41) versus TotalSegmentator 88.09% (85.18–90.48). As presented, the 2.4-point advantage is not statistically robust to test-set composition. Please report paired per-structure tests, effect sizes, and the number of structures with non-overlapping intervals, and clarify whether the confidence intervals are computed across structures or across scans.
  4. [Online Methods §2.1–2.3; Discussion, limitation (1)] The 167-structure 'complete annotations' rest on pseudo-labels generated by models seeded from small datasets (e.g., 42 Han-Seg volumes, 40 VISCERAL volumes, 1,203 TotalSegmentator volumes) and filtered by shape priors trained on ground truth from the same data sources. The paper acknowledges that the shape filter may exclude pathological or atypical anatomies. For the dataset claim, label correctness for rare structures such as buccal mucosa and arytenoid cartilage is not established beyond the seed sets. Please provide per-structure pseudo-label quality estimates, for example a stratified random human-review sample that includes rare structures and atypical cases, with agreement rates.
minor comments (4)
  1. [Table 1 and Figure 1 captions] There are minor typos: 'V erSe' in Table 1, 'Gluteus minius' in Figure 1 and Supplementary Figure A.2, and 'distnace' in Online Methods §2.2. These should be corrected.
  2. [Abstract and Figure 3 caption] The abstract's claim of '18 times more scans' is consistent with Table 1 (22,022 versus 1,203), but the Figure 3 caption contains a grammatical error ('This results demonstrates') that should be fixed.
  3. [Supplementary Table A.12] The structure-level comparison table is very dense and hard to read in print; consider providing it as a machine-readable CSV or splitting it into multiple smaller tables for the main text.
  4. [Results, 'From bench to bedside'] The expert review protocol is described as selecting three representative cases per structure around the median Dice score; please state how many total cases were reviewed and whether the reviewer was blinded to model identity.

Circularity Check

2 steps flagged · score 6.0 of 10

Head-to-head Dice advantage is partly constructed by flavor-selection and development-involved evaluation loops; independent hospital cohort keeps the core data-centric claim from being fully circular.

  1. fitted input called prediction [Online Methods §2.4 (Statistical ranking and selection of model flavors); Results 'Cross-dataset versatility: Dataset-level performance analysis']
    "OOD validation images come from other labeled datasets in our collection (e.g., for liver segmentation, while the model is trained on TotalSegmentator dataset (ID), its OOD validation leverages annotations from LiTS, VISCERAL, BTCV-Abdomen datasets, and etc.). We prioritize OOD performance metrics when available because they can better reflect model generalization. ... The highest-ranked flavor’s pseudo-label becomes the final label for that structure in the CADS-dataset."

    The same sources named as OOD validation (LiTS, VISCERAL, BTCV-Abdomen) are among the 18 test datasets used to report CADS-model Dice. Because the CADS-dataset label for each structure is set to the output of the flavor model that scored best on those OOD sources, the subsequently reported Dice on those sources is the label-selection objective, not an independent generalization result. The advantage over TotalSegmentator on those datasets is therefore partly forced by the construction of the training labels.

  2. other [Results, 'Cross-dataset versatility: Dataset-level performance analysis']
    "For a more nuanced evaluation, we stratify our analysis into two cohorts: (1) a primary cohort with complete ground truth annotations across all structures, which are heavily involved in the model development process and represent an optimal benchmark for accuracy assessment under ideal conditions"

    This primary cohort supplies the main mutual-target comparison (90.52% vs 88.09%, Figure 4a). Because the same data sources were used in model development (initial training seeds, shape-prior training, and OOD flavor selection), reporting the model's score on this cohort as evidence of generalization is circular: the 'test' performance is a development-set performance. The paper counters with a secondary cohort and an independent hospital cohort, so the circularity is partial.

full rationale

The paper's core contribution is a dataset and a model, and much of the derivation is an empirical engineering pipeline rather than a formal derivation. The principal circularity is in the evaluation loop: the CADS-dataset labels are assembled by choosing, per structure, the 'flavor' model with the highest Dice on OOD validation datasets drawn from the same collection, and those same datasets (LiTS, VISCERAL, BTCV-Abdomen, etc.) are then used among the 18 public test sources to report CADS-model Dice vs TotalSegmentator. This is a fitted-input-called-prediction pattern: the reported generalization score on those sources is partly the objective function used to construct the labels, not an independent prediction. A second loop is the paper's own admission that its primary evaluation cohort is 'heavily involved in the model development process,' and the headline 90.52 vs 88.09 comparison is run on this cohort; the manual correction of rib/vertebra labels in the TotalSegmentator test set (Section 6.2), after the CADS pipeline specifically engineered rib/vertebra refinements, further aligns the reference standard with CADS conventions. These loops do not make the whole paper circular: the independent 2,864-patient hospital cohort, the 48 structures with no baseline, and the released dataset/models provide externally checkable content. Self-citations to prior work on neural implicit shape priors and vesselFM are methodological and not used to rule out alternatives, so they do not add circularity. Overall: partial circularity concentrated in the headline mutual-target comparison, with independent checkpoints preventing a score above 6.

Assumptions & free parameters 6 free parameters · 5 assumptions · 0 invented entities

The central claim rests on the pseudo-label pipeline's ability to produce acceptable labels at scale. Hand-chosen thresholds and domain assumptions about cluster structure, shape-prior quality, registration-based labels, and expert curation are load-bearing. No new physical entities are introduced.

free parameters (6)
  • Pseudo-label exclusion threshold = 10% of lowest-scoring images per structure
    Shape-flavor model trains only on pseudo-labels above this quality rank; hand-chosen in Section 2.3 to balance quality and volume.
  • Brain coverage voxel threshold = 2,000 predicted brain voxels
    Used to filter head-related pseudo-label generation; chosen as approximately 10% of brain volume interquartile range in Section 3.1.
  • Head cropping bounding box = ±[100,100,133] voxels for brain, ±[100,100,200] for head-neck
    Postprocessing to remove hallucinations outside the head in Section 3.1; dimensions chosen by hand.
  • Costovertebral joint component size filter = 100 to 1,500 voxels
    Retains candidate joint components from vesselFM predictions in Section 3.2; threshold chosen empirically.
  • FN penalization thresholds = GT volume >90% of average means missed; GT volume <10% of average is excluded
    Defines when a missing organ is penalized in evaluation; directly affects reported Dice and HD95 values in Section 5.1.
  • NSD tolerance = 3 mm
    Set based on 1.5 mm voxel spacing in Section 5.1; used for Normalized Surface Dice computation.
assumptions (5)
  • domain assumption Cluster assumption for pseudo-labeling
    Section 2.1 states that data points of the same class form cohesive clusters in feature space; the benefit of pseudo-labeling depends on this assumption.
  • domain assumption Shape-prior quality ranking validity
    Section 2.2 assumes Hausdorff distance between a pseudo-label and its reconstruction from a shape prior trained on clean GT is a valid quality score for outlier detection.
  • domain assumption Registration-derived brain labels are accurate
    Section 2.1 uses non-rigid registration from Han-Seg CT to a SimNIBS MRI atlas to generate brain structure labels; the accuracy of these labels is assumed, not manually verified.
  • domain assumption Expert curation reliability
    Section 6.2 assumes in-house medical professionals' corrections and flags on TotalSegmentator ground truth produce a more truthful benchmark; no inter-observer agreement is reported.
  • domain assumption Variance reduction via aggregation
    Discussion invokes a central-limit-theorem-style argument that aggregating diverse pseudo-labels reduces variance errors; this heuristic is not empirically demonstrated.

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Cite this review

Pith. "Pith review of CADS: A Comprehensive Anatomical Dataset and Segmentation for Whole-Body Anatomy in Computed Tomography." pith.science (2026). https://pith.science/paper/2AJN54YD

@misc{pith2026250722953,
  author       = {Pith},
  title        = {Pith review of: CADS: A Comprehensive Anatomical Dataset and Segmentation for Whole-Body Anatomy in Computed Tomography},
  year         = {2026},
  howpublished = {\url{https://pith.science/paper/2AJN54YD}},
  note         = {Machine review of arXiv:2507.22953}
}
read the original abstract

Accurate delineation of anatomical structures in volumetric CT scans is crucial for diagnosis and treatment planning. While AI has advanced automated segmentation, current approaches typically target individual structures, creating a fragmented landscape of incompatible models with varying performance and disparate evaluation protocols. Foundational segmentation models address these limitations by providing a holistic anatomical view through a single model. Yet, robust clinical deployment demands comprehensive training data, which is lacking in existing whole-body approaches, both in terms of data heterogeneity and, more importantly, anatomical coverage. In this work, rather than pursuing incremental optimizations in model architecture, we present CADS, an open-source framework that prioritizes the systematic integration, standardization, and labeling of heterogeneous data sources for whole-body CT segmentation. At its core is a large-scale dataset of 22,022 CT volumes with complete annotations for 167 anatomical structures, representing a significant advancement in both scale and coverage, with 18 times more scans than existing collections and 60% more distinct anatomical targets. Building on this diverse dataset, we develop the CADS-model using established architectures for accessible and automated full-body CT segmentation. Through comprehensive evaluation across 18 public datasets and an independent real-world hospital cohort, we demonstrate advantages over SoTA approaches. Notably, thorough testing of the model's performance in segmentation tasks from radiation oncology validates its direct utility for clinical interventions. By making our large-scale dataset, our segmentation models, and our clinical software tool publicly available, we aim to advance robust AI solutions in radiology and make comprehensive anatomical analysis accessible to clinicians and researchers alike.

Figures

Figures reproduced from arXiv: 2507.22953 by the authors.

Figure 1
Figure 1. Overview of CADS framework’s anatomical coverage. Comprehensive visualization of 167 anatomical targets segmented by the CADS framework, spanning from head to knees. These clinically relevant structures are organized into nine anatomical groups: (1) major abdominal organs, primary tho￾racic organs (lungs), and major abdominal vasculature; (2) complete set of individual vertebrae from cervical to lumbar regions; (3) … view at source ↗
Figure 2
Figure 2. Overview of the multi-stage development process for whole-body CT segmentation CADS-model. The pipeline consists of four key stages: (1) initial region-specific model training and pseudo-label generation across 22,022 CT volumes, utilizing specialized models for nine anatomical regions covering all 167 target structures; (2) automated quality control employing neural implicit functions and shape priors to filter unr… view at source ↗
Figure 3
Figure 3. Structure-level performance analysis. Visualization of segmentation performance across 167 anatomical structures grouped by anatomical systems. The radar plot presents Dice scores (increasing radially from 0 at center to 1 at periphery) for the CADS-model compared against existing approaches, evaluated on diverse validation sets from 18 public datasets. Performance is shown for CADS-model (orange), TotalSegmentator … view at source ↗
Figures from the paper (2 more)
Figure 4
Figure 4. Figure 4: Clinical evaluation of CADS-model performance. Multi-faceted analysis of segmentation performance across different validation scenarios: (a) Comparison between CADS-model and baseline model TotalSegmentator on mutual anatomical targets, evaluated across primary (comple…
Figure 5
Figure 5. Figure 5: Qualitative assessment of CADS-model segmentation performance. Visual evaluation of segmentation results across three key aspects: (a) Comparison of skeletal structure segmentation between existing methods and CADS-model, demonstrating significant improvements aligned …

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Reference graph

Works this paper leans on

110 extracted references · 70 canonical work pages · cited by 1 Pith paper

  1. [1]

    Medical technologies - examinations by medical imaging techniques (CT, MRI and PET)

    Eurostat, “Medical technologies - examinations by medical imaging techniques (CT, MRI and PET).” https: //ec.europa.eu/eurostat/databrowser/view/hlth_co_exam/default/table?lang=en, 2024. Last updated: 2024-09-03

  2. [2]

    Deep learning empowered volume delineation of whole-body organs-at-risk for accelerated radiotherapy,

    F. Shi, W. Hu, J. Wu, M. Han, J. Wang, W. Zhang, Q. Zhou, J. Zhou, Y. Wei, Y. Shao, et al. , “Deep learning empowered volume delineation of whole-body organs-at-risk for accelerated radiotherapy,” Nature communications, vol. 13, no. 1, p. 6566, 2022

  3. [3]

    Multi- task weak supervision enables anatomically-resolved abnormality detection in whole-body FDG-PET/CT,

    S. Eyuboglu, G. Angus, B. N. Patel, A. Pareek, G. Davidzon, J. Long, J. Dunnmon, and M. P. Lungren, “Multi- task weak supervision enables anatomically-resolved abnormality detection in whole-body FDG-PET/CT,” Nature communications, vol. 12, no. 1, p. 1880, 2021

  4. [4]

    A decision support system for the identification of metastases of metastatic melanoma using whole-body FDG PET/CT images,

    T. P. Vagenas, T. L. Economopoulos, C. Sachpekidis, A. Dimitrakopoulou-Strauss, L. Pan, A. Provata, and G. K. Matsopoulos, “A decision support system for the identification of metastases of metastatic melanoma using whole-body FDG PET/CT images,” IEEE Journal of Biomedical and Health Informatics , vol. 27, no. 3, pp. 1397–1408, 2022

  5. [5]

    Automated abdominal segmentation of CT scans for body composition analysis using deep learning,

    A. D. Weston, P. Korfiatis, T. L. Kline, K. A. Philbrick, P. Kostandy, T. Sakinis, M. Sugimoto, N. Takahashi, and B. J. Erickson, “Automated abdominal segmentation of CT scans for body composition analysis using deep learning,” Radiology, vol. 290, no. 3, pp. 669–679, 2019

  6. [6]

    Multi-atlas-based segmentation with local decision fusion—application to cardiac and aortic segmentation in CT scans,

    I. Isgum, M. Staring, A. Rutten, M. Prokop, M. A. Viergever, and B. Van Ginneken, “Multi-atlas-based segmentation with local decision fusion—application to cardiac and aortic segmentation in CT scans,” IEEE transactions on medical imaging , vol. 28, no. 7, pp. 1000–1010, 2009

  7. [7]

    Novel and powerful 3d adaptive crisp active contour method applied in the segmentation of CT lung images,

    P. P. Rebou¸ cas Filho, P. C. Cortez, A. C. da Silva Barros, V. H. C. Albuquerque, and J. M. R. Tavares, “Novel and powerful 3d adaptive crisp active contour method applied in the segmentation of CT lung images,”Medical image analysis , vol. 35, pp. 503–516, 2017

  8. [8]

    Model-based segmentation of abdominal aortic aneurysms in CTA images,

    M. De Bruijne, B. Van Ginneken, W. J. Niessen, M. Loog, and M. A. Viergever, “Model-based segmentation of abdominal aortic aneurysms in CTA images,” in Medical imaging 2003: Image processing, vol. 5032, pp. 1560– 1571, SPIE, 2003

Show all 110 references
  1. [9]

    Automated abdominal multi-organ segmentation with subject-specific atlas generation,

    R. Wolz, C. Chu, K. Misawa, M. Fujiwara, K. Mori, and D. Rueckert, “Automated abdominal multi-organ segmentation with subject-specific atlas generation,” IEEE transactions on medical imaging , vol. 32, no. 9, pp. 1723–1730, 2013

  2. [10]

    Regression forests for efficient anatomy detection and localization in CT studies,

    A. Criminisi, J. Shotton, D. Robertson, and E. Konukoglu, “Regression forests for efficient anatomy detection and localization in CT studies,” in Medical Computer Vision. Recognition Techniques and Applications in Medical Imaging (B. Menze, G. Langs, Z. Tu, and A. Criminisi, e...

  3. [11]

    Entangled decision forests and their application for semantic segmentation of CT images,

    A. Montillo, J. Shotton, J. Winn, J. E. Iglesias, D. Metaxas, and A. Criminisi, “Entangled decision forests and their application for semantic segmentation of CT images,” in Information Processing in Medical Imaging: 22nd International Conference, IPMI 2011, Kloster Irsee, Ger...

  4. [12]

    Cloud-based evaluation of anatomical structure seg- mentation and landmark detection algorithms: Visceral anatomy benchmarks,

    O. Jimenez-del Toro, H. M¨ uller, M. Krenn, K. Gruenberg, A. A. Taha, M. Winterstein, I. Eggel, A. Foncubierta-Rodr ´ ıguez, O. Goksel, A. Jakab,et al. , “Cloud-based evaluation of anatomical structure seg- mentation and landmark detection algorithms: Visceral anatomy benchmar...

  5. [13]

    Segment anything in medical images,

    J. Ma, Y. He, F. Li, L. Han, C. You, and B. Wang, “Segment anything in medical images,” Nature Commu- nications, vol. 15, no. 1, p. 654, 2024

  6. [14]

    One-prompt to segment all medical images,

    J. Wu and M. Xu, “One-prompt to segment all medical images,” in Proceedings of the IEEE/CVF Conference on Computer Vision and Pattern Recognition , pp. 11302–11312, 2024

  7. [15]

    U-net: Convolutional networks for biomedical image segmentation,

    O. Ronneberger, P. Fischer, and T. Brox, “U-net: Convolutional networks for biomedical image segmentation,” in Medical image computing and computer-assisted intervention–MICCAI 2015: 18th international conference, Munich, Germany, October 5-9, 2015, proceedings, part III 18 , ...

  8. [16]

    V-net: Fully convolutional neural networks for volumetric medical image segmentation,

    F. Milletari, N. Navab, and S.-A. Ahmadi, “V-net: Fully convolutional neural networks for volumetric medical image segmentation,” in 2016 fourth international conference on 3D vision (3DV) , pp. 565–571, Ieee, 2016

  9. [17]

    Deeporgan: Multi- level deep convolutional networks for automated pancreas segmentation,

    H. R. Roth, L. Lu, A. Farag, H.-C. Shin, J. Liu, E. B. Turkbey, and R. M. Summers, “Deeporgan: Multi- level deep convolutional networks for automated pancreas segmentation,” in Medical Image Computing and Computer-Assisted Intervention–MICCAI 2015: 18th International Conferenc...

  10. [18]

    Scribbleprompt: fast and flexible interactive segmentation for any biomedical image,

    H. E. Wong, M. Rakic, J. Guttag, and A. V. Dalca, “Scribbleprompt: fast and flexible interactive segmentation for any biomedical image,” in European Conference on Computer Vision , pp. 207–229, Springer, 2024

  11. [20]

    Universeg: Universal medical image segmentation,

    V. I. Butoi, J. J. G. Ortiz, T. Ma, M. R. Sabuncu, J. Guttag, and A. V. Dalca, “Universeg: Universal medical image segmentation,” inProceedings of the IEEE/CVF International Conference on Computer Vision, pp. 21438–21451, 2023

  12. [21]

    Medical vision generalist: Unifying medical imaging tasks in context,

    S. Ren, X. Huang, X. Li, J. Xiao, J. Mei, Z. Wang, A. Yuille, and Y. Zhou, “Medical vision generalist: Unifying medical imaging tasks in context,” arXiv preprint arXiv:2406.05565 , 2024

  13. [22]

    nnu-net: a self-configuring method for deep learning-based biomedical image segmentation,

    F. Isensee, P. F. Jaeger, S. A. Kohl, J. Petersen, and K. H. Maier-Hein, “nnu-net: a self-configuring method for deep learning-based biomedical image segmentation,” Nature methods, vol. 18, no. 2, pp. 203–211, 2021. CADS 17

  14. [23]

    An image is worth 16x16 words: Transformers for image recognition at scale,

    A. Dosovitskiy, L. Beyer, A. Kolesnikov, D. Weissenborn, X. Zhai, T. Unterthiner, M. Dehghani, M. Minderer, G. Heigold, S. Gelly, et al. , “An image is worth 16x16 words: Transformers for image recognition at scale,” arXiv preprint arXiv:2010.11929 , 2020

  15. [24]

    The effectiveness of mae pre-pretraining for billion-scale pretraining,

    M. Singh, Q. Duval, K. V. Alwala, H. Fan, V. Aggarwal, A. Adcock, A. Joulin, P. Doll´ ar, C. Feichtenhofer, R. Girshick, et al. , “The effectiveness of mae pre-pretraining for billion-scale pretraining,” in Proceedings of the IEEE/CVF international conference on computer visio...

  16. [25]

    Imagenet: A large-scale hierarchical image database,

    J. Deng, W. Dong, R. Socher, L.-J. Li, K. Li, and L. Fei-Fei, “Imagenet: A large-scale hierarchical image database,” in 2009 IEEE conference on computer vision and pattern recognition , pp. 248–255, Ieee, 2009

  17. [26]

    Learning multiple layers of features from tiny images,

    A. Krizhevsky, G. Hinton, et al. , “Learning multiple layers of features from tiny images,” 2009

  18. [27]

    Totalsegmentator: robust segmentation of 104 anatomic structures in CT images,

    J. Wasserthal, H.-C. Breit, M. T. Meyer, M. Pradella, D. Hinck, A. W. Sauter, T. Heye, D. T. Boll, J. Cyriac, S. Yang, et al., “Totalsegmentator: robust segmentation of 104 anatomic structures in CT images,” Radiology: Artificial Intelligence, vol. 5, no. 5, 2023

  19. [28]

    Monai label: A framework for ai-assisted interactive labeling of 3d medical images,

    A. Diaz-Pinto, S. Alle, V. Nath, Y. Tang, A. Ihsani, M. Asad, F. P´ erez-Garc ´ ıa, P. Mehta, W. Li, M. Flores, et al. , “Monai label: A framework for ai-assisted interactive labeling of 3d medical images,” Medical Image Analysis, vol. 95, p. 103207, 2024

  20. [29]

    Swin smt: Global sequential modeling for enhancing 3d medi- cal image segmentation,

    S. P lotka, M. Chrabaszcz, and P. Biecek, “Swin smt: Global sequential modeling for enhancing 3d medi- cal image segmentation,” in International Conference on Medical Image Computing and Computer-Assisted Intervention, pp. 689–698, Springer, 2024

  21. [30]

    Continual segment: Towards a single, unified and non-forgetting continual segmentation model of 143 whole-body organs in CT scans,

    Z. Ji, D. Guo, P. Wang, K. Yan, L. Lu, M. Xu, Q. Wang, J. Ge, M. Gao, X. Ye, et al. , “Continual segment: Towards a single, unified and non-forgetting continual segmentation model of 143 whole-body organs in CT scans,” in Proceedings of the IEEE/CVF International Conference on...

  22. [31]

    Abdomenatlas: A large-scale, detailed-annotated, & multi-center dataset for efficient transfer learning and open algorithmic benchmarking,

    W. Li, C. Qu, X. Chen, P. R. Bassi, Y. Shi, Y. Lai, Q. Yu, H. Xue, Y. Chen, X. Lin, et al. , “Abdomenatlas: A large-scale, detailed-annotated, & multi-center dataset for efficient transfer learning and open algorithmic benchmarking,” Medical Image Analysis, vol. 97, p. 103285, 2024

  23. [32]

    Cosst: Multi-organ segmentation with partially labeled datasets using comprehensive supervisions and self-training,

    H. Liu, Z. Xu, R. Gao, H. Li, J. Wang, G. Chabin, I. Oguz, and S. Grbic, “Cosst: Multi-organ segmentation with partially labeled datasets using comprehensive supervisions and self-training,” IEEE Transactions on Medical Imaging, 2024

  24. [33]

    Fully automated, semantic segmentation of whole-body 18F-FDG PET/CT images based on data-centric artificial intelligence,

    L. K. S. Sundar, J. Yu, O. Muzik, O. C. Kulterer, B. Fueger, D. Kifjak, T. Nakuz, H. M. Shin, A. K. Sima, D. Kitzmantl, et al. , “Fully automated, semantic segmentation of whole-body 18F-FDG PET/CT images based on data-centric artificial intelligence,” Journal of Nuclear Medic...

  25. [34]

    Towards unifying anatomy segmentation: automated generation of a full-body CT dataset via knowledge aggregation and anatomical guidelines,

    A. Jaus, C. Seibold, K. Hermann, A. Walter, K. Giske, J. Haubold, J. Kleesiek, and R. Stiefelhagen, “Towards unifying anatomy segmentation: automated generation of a full-body CT dataset via knowledge aggregation and anatomical guidelines,” arXiv preprint arXiv:2307.13375 , 2023

  26. [35]

    The cancer imaging archive (tcia): maintaining and operating a public information repository,

    K. Clark, B. Vendt, K. Smith, J. Freymann, J. Kirby, P. Koppel, S. Moore, S. Phillips, D. Maffitt, M. Pringle, et al., “The cancer imaging archive (tcia): maintaining and operating a public information repository,”Journal of digital imaging , vol. 26, pp. 1045–1057, 2013

  27. [36]

    Grand challenge

    “Grand challenge.” https://grand-challenge.org. Accessed: September 10, 2025

  28. [37]

    MICCAI Challenges

    MICCAI Society, “MICCAI Challenges.” https://miccai.org/index.php/special-interest-groups/ challenges/miccai-registered-challenges/ . Accessed: September 10, 2025

  29. [38]

    3d slicer as an image computing platform for the quantitative imaging network,

    A. Fedorov, R. Beichel, J. Kalpathy-Cramer, J. Finet, J.-C. Fillion-Robin, S. Pujol, C. Bauer, D. Jennings, F. Fennessy, M. Sonka,et al., “3d slicer as an image computing platform for the quantitative imaging network,” Magnetic resonance imaging , vol. 30, no. 9, pp. 1323–1341, 2012

  30. [39]

    Forty years of snomed: a literature review,

    R. Cornet and N. de Keizer, “Forty years of snomed: a literature review,” BMC medical informatics and decision making, vol. 8, pp. 1–6, 2008

  31. [40]

    Data from the national lung screening trial (NLST)

    N. L. S. T. R. Team, “Data from the national lung screening trial (NLST).” The Cancer Imaging Archive

  32. [41]

    Developing generalist foundation models from a multimodal dataset for 3d computed tomography,

    I. E. Hamamci, S. Er, F. Almas, A. G. Simsek, S. N. Esirgun, I. Dogan, M. F. Dasdelen, O. F. Durugol, B. Wittmann, T. Amiranashvili, et al., “Developing generalist foundation models from a multimodal dataset for 3d computed tomography,” arXiv preprint arXiv:2403.17834 , 2024

  33. [42]

    Abdomenct-1k: Is abdominal organ segmentation a solved problem?,

    J. Ma, Y. Zhang, S. Gu, C. Zhu, C. Ge, Y. Zhang, X. An, C. Wang, Q. Wang, X. Liu, et al., “Abdomenct-1k: Is abdominal organ segmentation a solved problem?,” IEEE Transactions on Pattern Analysis and Machine Intelligence, vol. 44, no. 10, pp. 6695–6714, 2021

  34. [43]

    Han-seg: The head and neck organ-at-risk CT and MR segmentation dataset,

    G. Podobnik, P. Strojan, P. Peterlin, B. Ibragimov, and T. Vrtovec, “Han-seg: The head and neck organ-at-risk CT and MR segmentation dataset,” Medical physics, vol. 50, no. 3, pp. 1917–1927, 2023

  35. [44]

    Saros: A dataset for whole-body region and organ segmentation in CT imaging,

    S. Koitka, G. Baldini, L. Kroll, N. van Landeghem, O. B. Pollok, J. Haubold, O. Pelka, M. Kim, J. Kleesiek, F. Nensa, et al., “Saros: A dataset for whole-body region and organ segmentation in CT imaging,” Scientific Data, vol. 11, no. 1, p. 483, 2024

  36. [45]

    Learning shape reconstruction from sparse measurements with neural implicit functions,

    T. Amiranashvili, D. L¨ udke, H. B. Li, B. Menze, and S. Zachow, “Learning shape reconstruction from sparse measurements with neural implicit functions,” in International Conference on Medical Imaging with Deep Learning, pp. 22–34, PMLR, 2022

  37. [46]

    Learning continuous shape priors from sparse data with neural implicit functions,

    T. Amiranashvili, D. L¨ udke, H. B. Li, S. Zachow, and B. H. Menze, “Learning continuous shape priors from sparse data with neural implicit functions,” Medical Image Analysis, vol. 94, p. 103099, 2024

  38. [47]

    Organ at risk delineation for radiation therapy clinical trials: Global harmonization group consensus guidelines,

    R. Mir, S. M. Kelly, Y. Xiao, A. Moore, C. H. Clark, E. Clementel, C. Corning, M. Ebert, P. Hoskin, C. W. Hurkmans, et al., “Organ at risk delineation for radiation therapy clinical trials: Global harmonization group consensus guidelines,” Radiotherapy and Oncology, vol. 150, ...

  39. [48]

    Open health imaging foundation viewer: an extensible open-source framework for building web-based imaging applications to support cancer research,

    E. Ziegler, T. Urban, D. Brown, J. Petts, S. D. Pieper, R. Lewis, C. Hafey, and G. J. Harris, “Open health imaging foundation viewer: an extensible open-source framework for building web-based imaging applications to support cancer research,” JCO clinical cancer informatics , ...

  40. [49]

    Vision foundation models for computed tomography,

    S. Pai, I. Hadzic, D. Bontempi, K. Bressem, B. H. Kann, A. Fedorov, R. H. Mak, and H. J. Aerts, “Vision foundation models for computed tomography,” arXiv preprint arXiv:2501.09001 , 2025

  41. [50]

    Clip-driven universal model for organ segmentation and tumor detection,

    J. Liu, Y. Zhang, J.-N. Chen, J. Xiao, Y. Lu, B. A Landman, Y. Yuan, A. Yuille, Y. Tang, and Z. Zhou, “Clip-driven universal model for organ segmentation and tumor detection,” in Proceedings of the IEEE/CVF international conference on computer vision , pp. 21152–21164, 2023

  42. [51]

    Medlsam: Localize and segment anything model for 3d CT images,

    W. Lei, W. Xu, K. Li, X. Zhang, and S. Zhang, “Medlsam: Localize and segment anything model for 3d CT images,” Medical Image Analysis, vol. 99, p. 103370, 2025

  43. [52]

    Stu-net: Scalable and transferable medical image segmentation models empowered by large-scale supervised pre-training,

    Z. Huang, H. Wang, Z. Deng, J. Ye, Y. Su, H. Sun, J. He, Y. Gu, L. Gu, S. Zhang, et al. , “Stu-net: Scalable and transferable medical image segmentation models empowered by large-scale supervised pre-training,”arXiv preprint arXiv:2304.06716, 2023

  44. [53]

    On balancing bias and variance in unsupervised multi-source-free domain adaptation,

    M. Shen, Y. Bu, and G. W. Wornell, “On balancing bias and variance in unsupervised multi-source-free domain adaptation,” in International conference on machine learning , pp. 30976–30991, PMLR, 2023

  45. [54]

    Multi-class probabilistic bounds for majority vote classifiers with partially labeled data,

    V. Feofanov, E. Devijver, and M.-R. Amini, “Multi-class probabilistic bounds for majority vote classifiers with partially labeled data,” Journal of Machine Learning Research , vol. 25, no. 104, pp. 1–47, 2024

  46. [55]

    Bagging predictors,

    L. Breiman, “Bagging predictors,” Machine learning, vol. 24, no. 2, pp. 123–140, 1996

  47. [56]

    Hastie, R

    T. Hastie, R. Tibshirani, J. H. Friedman, and J. H. Friedman, The elements of statistical learning: data mining, inference, and prediction , vol. 2. Springer, 2009

  48. [57]

    The state of the art in kidney and kidney tumor segmentation in contrast-enhanced CT imaging: Results of the kits19 challenge,

    N. Heller, F. Isensee, K. H. Maier-Hein, X. Hou, C. Xie, F. Li, Y. Nan, G. Mu, Z. Lin, M. Han, et al. , “The state of the art in kidney and kidney tumor segmentation in contrast-enhanced CT imaging: Results of the kits19 challenge,” Medical image analysis , vol. 67, p. 101821, 2021

  49. [58]

    The liver tumor segmentation benchmark (lits),

    P. Bilic, P. Christ, H. B. Li, E. Vorontsov, A. Ben-Cohen, G. Kaissis, A. Szeskin, C. Jacobs, G. E. H. Mamani, G. Chartrand, et al. , “The liver tumor segmentation benchmark (lits),” Medical Image Analysis , vol. 84, p. 102680, 2023

  50. [59]

    Miccai multi-atlas labeling be- yond the cranial vault–workshop and challenge,

    B. Landman, Z. Xu, J. Igelsias, M. Styner, T. Langerak, and A. Klein, “Miccai multi-atlas labeling be- yond the cranial vault–workshop and challenge,” in Proc. MICCAI Multi-Atlas Labeling Beyond Cranial Vault—Workshop Challenge, vol. 5, p. 12, 2015

  51. [60]

    Chaos challenge-combined (CT-MR) healthy abdominal organ segmentation,

    A. E. Kavur, N. S. Gezer, M. Barı¸ s, S. Aslan, P.-H. Conze, V. Groza, D. D. Pham, S. Chatterjee, P. Ernst, S. ¨Ozkan, et al., “Chaos challenge-combined (CT-MR) healthy abdominal organ segmentation,”Medical Image Analysis, vol. 69, p. 101950, 2021

  52. [61]

    Verse: a vertebrae labelling and segmentation benchmark for multi-detector CT images,

    A. Sekuboyina, M. E. Husseini, A. Bayat, M. L¨ offler, H. Liebl, H. Li, G. Tetteh, J. Kukaˇ cka, C. Payer, D. ˇStern, et al. , “Verse: a vertebrae labelling and segmentation benchmark for multi-detector CT images,” Medical image analysis , vol. 73, p. 102166, 2021

  53. [62]

    Extraction of airways from CT (EXACT’09),

    P. Lo, B. Van Ginneken, J. M. Reinhardt, T. Yavarna, P. A. De Jong, B. Irving, C. Fetita, M. Ortner, R. Pinho, J. Sijbers, et al. , “Extraction of airways from CT (EXACT’09),” IEEE Transactions on Medical Imaging, vol. 31, no. 11, pp. 2093–2107, 2012

  54. [63]

    Computer aided detection for pulmonary embolism challenge (CAD-PE),

    G. Gonz´ alez, D. Jimenez-Carretero, S. Rodr ´ ıguez-L´ opez, C. Cano-Espinosa, M. Cazorla, T. Agarwal, V. Agar- wal, N. Tajbakhsh, M. B. Gotway, J. Liang, et al. , “Computer aided detection for pulmonary embolism challenge (CAD-PE),” arXiv preprint arXiv:2003.13440 , 2020

  55. [64]

    Deep-learning- assisted detection and segmentation of rib fractures from CT scans: Development and validation of fracnet,

    L. Jin, J. Yang, K. Kuang, B. Ni, Y. Gao, Y. Sun, P. Gao, W. Ma, M. Tan, H. Kang, et al. , “Deep-learning- assisted detection and segmentation of rib fractures from CT scans: Development and validation of fracnet,” EBioMedicine, vol. 62, 2020

  56. [65]

    Learn2reg: comprehensive multi-task medical image registration challenge, dataset and evaluation in the era of deep learning,

    A. Hering, L. Hansen, T. C. Mok, A. C. Chung, H. Siebert, S. H¨ ager, A. Lange, S. Kuckertz, S. Heldmann, W. Shao, et al. , “Learn2reg: comprehensive multi-task medical image registration challenge, dataset and evaluation in the era of deep learning,” IEEE Transactions on Medi...

  57. [66]

    Lndb challenge on automatic lung cancer patient management,

    J. Pedrosa, G. Aresta, C. Ferreira, G. Atwal, H. A. Phoulady, X. Chen, R. Chen, J. Li, L. Wang, A. Galdran, et al. , “Lndb challenge on automatic lung cancer patient management,” Medical image analysis , vol. 70, p. 102027, 2021

  58. [67]

    LObe and Lung Analysis 2011 (LOLA11)

    Eva van Rikxoort and Bram van Ginneken and Sjoerd Kerkstra, “LObe and Lung Analysis 2011 (LOLA11).” https://lola11.grand-challenge.org/, 2011

  59. [68]

    Comparison and evaluation of methods for liver segmentation from CT datasets,

    T. Heimann, B. Van Ginneken, M. A. Styner, Y. Arzhaeva, V. Aurich, C. Bauer, A. Beck, C. Becker, R. Beichel, G. Bekes, et al. , “Comparison and evaluation of methods for liver segmentation from CT datasets,” IEEE transactions on medical imaging , vol. 28, no. 8, pp. 1251–1265, 2009

  60. [69]

    Study of thoracic CT in COVID-19: the STOIC project,

    M.-P. Revel, S. Boussouar, C. de Margerie-Mellon, I. Saab, T. Lapotre, D. Mompoint, G. Chassagnon, A. Milon, M. Lederlin, S. Bennani, et al. , “Study of thoracic CT in COVID-19: the STOIC project,” Ra- diology, vol. 301, no. 1, pp. E361–E370, 2021

  61. [70]

    Evaluation of registration methods on thoracic CT: the EMPIRE10 challenge,

    K. Murphy, B. Van Ginneken, J. M. Reinhardt, S. Kabus, K. Ding, X. Deng, K. Cao, K. Du, G. E. Christensen, V. Garcia, et al. , “Evaluation of registration methods on thoracic CT: the EMPIRE10 challenge,” IEEE transactions on medical imaging , vol. 30, no. 11, pp. 1901–1920, 2011

  62. [71]

    Amos: A large-scale abdominal multi-organ benchmark for versatile medical image segmentation,

    Y. Ji, H. Bai, C. Ge, J. Yang, Y. Zhu, R. Zhang, Z. Li, L. Zhanng, W. Ma, X. Wan,et al., “Amos: A large-scale abdominal multi-organ benchmark for versatile medical image segmentation,” Advances in neural information processing systems, vol. 35, pp. 36722–36732, 2022

  63. [72]

    CT-ORG: A dataset of CT volumes with multiple organ segmentations

    B. Rister, K. Shivakumar, T. Nobashi, and D. L. Rubin, “CT-ORG: A dataset of CT volumes with multiple organ segmentations.” The Cancer Imaging Archive, 2019. CADS 19

  64. [73]

    Data from LIDC-IDRI

    S. G. A. III and et al., “Data from LIDC-IDRI.” The Cancer Imaging Archive, 2015

  65. [74]

    A new 2.5 D representation for lymph node detection in CT (CT lymph nodes)

    H. Roth and et al., “A new 2.5 D representation for lymph node detection in CT (CT lymph nodes).” The Cancer Imaging Archive, 2015

  66. [75]

    The clinical proteomic tumor analysis consortium clear cell renal cell carcinoma collection (CPTAC-CCRCC)

    N. C. I. C. P. T. A. C. (CPTAC), “The clinical proteomic tumor analysis consortium clear cell renal cell carcinoma collection (CPTAC-CCRCC).” The Cancer Imaging Archive, 2018

  67. [76]

    The clinical proteomic tumor analysis consortium lung adenocarcinoma collection (CPTAC-LUAD)

    N. C. I. C. P. T. A. C. (CPTAC), “The clinical proteomic tumor analysis consortium lung adenocarcinoma collection (CPTAC-LUAD).” The Cancer Imaging Archive, 2018

  68. [77]

    CT images in COVID-19

    P. An and et al., “CT images in COVID-19.” The Cancer Imaging Archive, 2020

  69. [78]

    Data for NSCLC radiogenomics collection

    S. Bakr and et al., “Data for NSCLC radiogenomics collection.” The Cancer Imaging Archive, 2017

  70. [79]

    Data from pancreas-CT

    H. Roth, A. Farag, E. B. Turkbey, L. Lu, J. Liu, and R. M. Summers, “Data from pancreas-CT.” The Cancer Imaging Archive, 2016

  71. [80]

    Breath-hold CT and cone-beam CT images with expert manual organ-at-risk segmen- tations from radiation treatments of locally advanced pancreatic cancer (Pancreatic-CT-CBCT-SEG)

    J. Hong and et al., “Breath-hold CT and cone-beam CT images with expert manual organ-at-risk segmen- tations from radiation treatments of locally advanced pancreatic cancer (Pancreatic-CT-CBCT-SEG).” The Cancer Imaging Archive, Oct. 2021

  72. [81]

    Coffee-break lung CT collection with scan images reconstructed at multiple imaging parameters

    B. Zhao, L. H. Schwartz, M. G. Kris, and G. J. Riely, “Coffee-break lung CT collection with scan images reconstructed at multiple imaging parameters.” The Cancer Imaging Archive, 2015

  73. [82]

    The cancer genome atlas kidney chromophobe collection (TCGA-KICH)

    M. W. Linehan, R. Gautam, C. A. Sadow, and S. Levine, “The cancer genome atlas kidney chromophobe collection (TCGA-KICH).” The Cancer Imaging Archive, 2016

  74. [83]

    The cancer genome atlas kidney renal clear cell carcinoma collection (TCGA-KIRC)

    O. Akin and et al., “The cancer genome atlas kidney renal clear cell carcinoma collection (TCGA-KIRC).” The Cancer Imaging Archive, 2016

  75. [84]

    The cancer genome atlas cervical kidney renal papillary cell carcinoma collection (TCGA-KIRP)

    M. Linehan and et al., “The cancer genome atlas cervical kidney renal papillary cell carcinoma collection (TCGA-KIRP).” The Cancer Imaging Archive, 2016

  76. [85]

    The cancer genome atlas liver hepatocellular carcinoma collection (TCGA-LIHC)

    B. J. Erickson and et al., “The cancer genome atlas liver hepatocellular carcinoma collection (TCGA-LIHC).” The Cancer Imaging Archive, 2016

  77. [86]

    Automated detection of the contrast phase in MDCT by an artificial neural network improves the accuracy of opportunistic bone mineral density measurements,

    S. R¨ uhling, F. Navarro, A. Sekuboyina, M. El Husseini, T. Baum, B. Menze, R. Braren, C. Zimmer, and J. S. Kirschke, “Automated detection of the contrast phase in MDCT by an artificial neural network improves the accuracy of opportunistic bone mineral density measurements,” E...

  78. [87]

    Automated thoracolumbar stump rib detection and analysis in a large ct cohort,

    H. M¨ oller, H. Sch¨ on, A. Dima, B. Keinert-Weth, R. Graf, M. Atad, J. Paetzold, F. Jungmann, R. Braren, F. Kofler, et al. , “Automated thoracolumbar stump rib detection and analysis in a large ct cohort,” arXiv preprint arXiv:2505.05004, 2025

  79. [89]

    Metrics reloaded: recommendations for image analysis validation,

    L. Maier-Hein, A. Reinke, P. Godau, M. D. Tizabi, F. Buettner, E. Christodoulou, B. Glocker, F. Isensee, J. Kleesiek, M. Kozubek, et al. , “Metrics reloaded: recommendations for image analysis validation,” Nature methods, vol. 21, no. 2, pp. 195–212, 2024

  80. [90]

    seg-metrics: a python package to compute segmentation metrics,

    J. Jia, M. Staring, and B. C. Stoel, “seg-metrics: a python package to compute segmentation metrics,” medRxiv, pp. 2024–02, 2024

  81. [91]

    Surface Distance Metrics

    Google DeepMind, “Surface Distance Metrics.” https://github.com/google-deepmind/surface-distance ,

  82. [92]

    Vista3d: Versatile imaging segmentation and annotation model for 3D computed tomography,

    Y. He, P. Guo, Y. Tang, A. Myronenko, V. Nath, Z. Xu, D. Yang, C. Zhao, B. Simon, M. Belue, et al. , “Vista3d: Versatile imaging segmentation and annotation model for 3D computed tomography,” arXiv preprint arXiv:2406.05285, 2024

  83. [93]

    Annotation- efficient deep learning for automatic medical image segmentation,

    S. Wang, C. Li, R. Wang, Z. Liu, M. Wang, H. Tan, Y. Wu, X. Liu, H. Sun, R. Yang, et al. , “Annotation- efficient deep learning for automatic medical image segmentation,” Nature communications, vol. 12, no. 1, p. 5915, 2021

  84. [94]

    Scaling vision transformers,

    X. Zhai, A. Kolesnikov, N. Houlsby, and L. Beyer, “Scaling vision transformers,” in Proceedings of the IEEE/CVF conference on computer vision and pattern recognition , pp. 12104–12113, 2022

  85. [95]

    Data-centric foundation models in computational healthcare: A survey,

    Y. Zhang, J. Gao, Z. Tan, L. Zhou, K. Ding, M. Zhou, S. Zhang, and D. Wang, “Data-centric foundation models in computational healthcare: A survey,” arXiv preprint arXiv:2401.02458 , 2024

  86. [96]

    Semi-supervised learning,

    C. Olivier, S. Bernhard, and Z. Alexander, “Semi-supervised learning,” IEEE Transactions on Neural Net- works, vol. 20, no. 3, pp. 542–542, 2006

  87. [97]

    Accurate and robust whole-head segmentation from magnetic resonance images for individualized head modeling,

    O. Puonti, K. Van Leemput, G. B. Saturnino, H. R. Siebner, K. H. Madsen, and A. Thielscher, “Accurate and robust whole-head segmentation from magnetic resonance images for individualized head modeling,” Neuroimage, vol. 219, p. 117044, 2020

  88. [98]

    Advanced normalization tools (ants),

    B. B. Avants, N. Tustison, G. Song, et al., “Advanced normalization tools (ants),” Insight j, vol. 2, no. 365, pp. 1–35, 2009

  89. [99]

    Weakly supervised vessel segmentation in x-ray angiograms by self-paced learning from noisy labels with suggestive annotation,

    J. Zhang, G. Wang, H. Xie, S. Zhang, N. Huang, S. Zhang, and L. Gu, “Weakly supervised vessel segmentation in x-ray angiograms by self-paced learning from noisy labels with suggestive annotation,” Neurocomputing, vol. 417, pp. 114–127, 2020

  90. [100]

    Semi-supervised semantic segmentation with error localization network,

    D. Kwon and S. Kwak, “Semi-supervised semantic segmentation with error localization network,” in Pro- ceedings of the IEEE/CVF Conference on Computer Vision and Pattern Recognition , pp. 9957–9967, 2022

  91. [101]

    Domain adaptation for medical image analysis: a survey,

    H. Guan and M. Liu, “Domain adaptation for medical image analysis: a survey,” IEEE Transactions on Biomedical Engineering, vol. 69, no. 3, pp. 1173–1185, 2021

  92. [102]

    Source-free domain adaptation for medical image seg- mentation via prototype-anchored feature alignment and contrastive learning,

    Q. Yu, N. Xi, J. Yuan, Z. Zhou, K. Dang, and X. Ding, “Source-free domain adaptation for medical image seg- mentation via prototype-anchored feature alignment and contrastive learning,” in International Conference on Medical Image Computing and Computer-Assisted Intervention ,...

  93. [103]

    S-cuda: self-cleansing unsupervised domain adaptation for medical image segmentation,

    L. Liu, Z. Zhang, S. Li, K. Ma, and Y. Zheng, “S-cuda: self-cleansing unsupervised domain adaptation for medical image segmentation,” Medical Image Analysis, vol. 74, p. 102214, 2021

  94. [104]

    Semi-supervised training using cooperative labeling of weakly annotated data for nodule detection in chest CT,

    M. Maynord, M. M. Farhangi, C. Ferm¨ uller, Y. Aloimonos, G. Levine, N. Petrick, B. Sahiner, and A. Pezeshk, “Semi-supervised training using cooperative labeling of weakly annotated data for nodule detection in chest CT,” Medical Physics, vol. 50, no. 7, pp. 4255–4268, 2023. CADS 29

  95. [105]

    Halos: Hallucination-free organ seg- mentation after organ resection surgery,

    A.-M. Rickmann, M. Xu, T. N. Wolf, O. Kovalenko, and C. Wachinger, “Halos: Hallucination-free organ seg- mentation after organ resection surgery,” in International Conference on Information Processing in Medical Imaging, pp. 667–678, Springer, 2023

  96. [106]

    Rethinking abdominal organ segmentation (raos) in the clin- ical scenario: A robustness evaluation benchmark with challenging cases,

    X. Luo, Z. Li, S. Zhang, W. Liao, and G. Wang, “Rethinking abdominal organ segmentation (raos) in the clin- ical scenario: A robustness evaluation benchmark with challenging cases,” arXiv preprint arXiv:2406.13674 , 2024

  97. [107]

    vesselfm: A foundation model for universal 3d blood vessel segmentation,

    B. Wittmann, Y. Wattenberg, T. Amiranashvili, S. Shit, and B. Menze, “vesselfm: A foundation model for universal 3d blood vessel segmentation,” arXiv preprint arXiv:2411.17386 , 2024

  98. [108]

    Analyzing overfitting under class imbalance in neural networks for image segmentation,

    Z. Li, K. Kamnitsas, and B. Glocker, “Analyzing overfitting under class imbalance in neural networks for image segmentation,” IEEE transactions on medical imaging , vol. 40, no. 3, pp. 1065–1077, 2020

  99. [109]

    Understanding imbalanced semantic segmentation through neural collapse,

    Z. Zhong, J. Cui, Y. Yang, X. Wu, X. Qi, X. Zhang, and J. Jia, “Understanding imbalanced semantic segmentation through neural collapse,” in Proceedings of the IEEE/CVF conference on computer vision and pattern recognition, pp. 19550–19560, 2023

  100. [110]

    Learning deep representation for imbalanced classification,

    C. Huang, Y. Li, C. C. Loy, and X. Tang, “Learning deep representation for imbalanced classification,” in Proceedings of the IEEE conference on computer vision and pattern recognition , pp. 5375–5384, 2016

  101. [111]

    nnu-net revisited: A call for rigorous validation in 3d medical image segmentation,

    F. Isensee, T. Wald, C. Ulrich, M. Baumgartner, S. Roy, K. Maier-Hein, and P. F. Jaeger, “nnu-net revisited: A call for rigorous validation in 3d medical image segmentation,” arXiv preprint arXiv:2404.09556 , 2024. 30 Xu et al. Supplementary Fig. A.6: CADS-model integration in...

  102. [2024]

    New Hospital Data - Head

    Accessed: September 10, 2025. 20 Xu et al. A Online Methods Ethics statement This study has received ethical approval from two independent institutional review boards. The Clin- ical Research Ethics Committee at Istanbul Medipol University (E-10840098-772.02-6841, 27/10/2023) ...

Pith tools

Reviewed August 6, 2026 · model on record in the stance chip above.