Skip to content
DraconiticResearch
Search Sources API
203,203 studies31 sourcesUpdated 28 min ago
PreprintarXiv licencearXiv

Bayesian Uncertainty Quantification of Breast-Cancer Pathology AI Agreement under Reader- and Annotation-Condition-Dependent Reference Labels

Abstract

Human reference labels used to evaluate medical AI can vary across readers and annotation workflows. We quantified agreement of a fixed pathology AI system with a future qualified reader without treating inferred consensus as error-free biological truth. Linked Evaluation and Unbiased NuCLS multirater data were analyzed using a fixed external HoVer-Net decision vector. The selected frame contained 1,144 anchors, 52 fields of view, five slides/patients, and five primary readers. The target was fixed-AI agreement with a future reader, with descriptive contrast Δ=θE−θU. Analyses included raw agreement and iMRMC benchmarks, reader-only and shared-detectability Bayesian models, structural sensitivities, adversarial simulations, and predictive assessment. Among 5,188 reader-anchor pairs observed in both conditions, 19.62% changed AI-agreement state, while raw agreement was 0.5466 in Unbiased and 0.5473 in Evaluation. The reader-only model gave Δ=−0.0008 (95% CrI, −0.0033 to $0.0008$), and the shared-detectability model gave Δ≈0 (−0.0140 to $0.0127$). Across structural perturbations, absolute agreement ranged from 0.420 to 0.646 in Unbiased and 0.409 to 0.640 in Evaluation. Frozen adversarial simulations met the comparative-stability criterion (median R=0.295; 14/16 model-scenario cells had R<1). Held-out-AI prediction supported shared predictive information, but varied by slide composition. The Evaluation-minus-Unbiased contrast was comparatively stable, whereas absolute agreement was structurally sensitive. These findings do not establish equivalence, causal assistance effects, biological accuracy, or new-patient transportability. Evaluations using variable human references should report reader population, selected frame, observation mechanism, and structural sensitivity.

Related

  1. DeepU-PRS: nonlinear and uncertainty-aware SNP heritability modeling for annotation-informed polygenic risk scoring.
    Junhyeong Lee, Dokyoon Kim, Seunggeun Lee
    Briefings in bioinformaticsPeer-reviewedCC BY-NCFull textGenetics & genomicsEurope PMC
  2. Representation-aware conformal prediction for reliable uncertainty quantification in drug-target affinity
    Xinya Li, Yaxin Zhang, Ximin Zeng +3
    BioinformaticsPeer-reviewedCC BY 4.0Full textBioinformatics & computational biologyCrossrefPMC
  3. A Framework for SPICE MRSI Reconstruction Posterior Uncertainty Quantification
    T. Lyu, S. Jbabdi, S. M. Finney +1
    bioRxivPreprintCC BYFull textNeurosciencebioRxiv
  4. Uncertainty Quantification in Stochastic Dynamical Gene Regulatory Networks
    F. Pizarro Galleguillos, S. Bhonsale, J. VAN IMPE
    bioRxivPreprintCC BY-NC-NDFull textSystems & synthetic biologybioRxiv
  5. Uncertainty Quantification in Cardiac Model Personalisation from Ultrafast Ultrasound
    Camilla Ferrario, Maelys Venet, Olivier Villemain +1
    arXivPreprintarXiv licenceFull textBioinformatics & computational biologyBiological & medical physicsarXiv
BibTeX
@misc{olayinka2026bayesian,
  title = {{Bayesian Uncertainty Quantification of Breast-Cancer Pathology AI Agreement under Reader- and Annotation-Condition-Dependent Reference Labels}},
  author = {Hammed A. Olayinka},
  howpublished = {arXiv},
  year = {2026},
  month = oct,
  doi = {10.48550/arxiv.2610.14642},
  eprint = {2610.14642},
  archivePrefix = {arXiv},
  url = {https://arxiv.org/abs/2610.14642},
}
RIS
TY  - UNPB
TI  - Bayesian Uncertainty Quantification of Breast-Cancer Pathology AI Agreement under Reader- and Annotation-Condition-Dependent Reference Labels
AU  - Hammed A. Olayinka
PY  - 2026
DA  - 2026/10/10
PB  - arXiv
DO  - 10.48550/arxiv.2610.14642
UR  - https://arxiv.org/abs/2610.14642
AB  - Human reference labels used to evaluate medical AI can vary across readers and annotation workflows. We quantified agreement of a fixed pathology AI system with a future qualified reader without treating inferred consensus as error-free biological truth. Linked Evaluation and Unbiased NuCLS multirater data were analyzed using a fixed external HoVer-Net decision vector. The selected frame contained 1,144 anchors, 52 fields of view, five slides/patients, and five primary readers. The target was fixed-AI agreement with a future reader, with descriptive contrast Δ=θ_E−θ_U. Analyses included raw agreement and iMRMC benchmarks, reader-only and shared-detectability Bayesian models, structural sensitivities, adversarial simulations, and predictive assessment. Among 5,188 reader-anchor pairs observed in both conditions, 19.62% changed AI-agreement state, while raw agreement was 0.5466 in Unbiased and 0.5473 in Evaluation. The reader-only model gave Δ=−0.0008 (95% CrI, −0.0033 to $0.0008$), and the shared-detectability model gave Δ≈0 (−0.0140 to $0.0127$). Across structural perturbations, absolute agreement ranged from 0.420 to 0.646 in Unbiased and 0.409 to 0.640 in Evaluation. Frozen adversarial simulations met the comparative-stability criterion (median R=0.295; 14/16 model-scenario cells had R<1). Held-out-AI prediction supported shared predictive information, but varied by slide composition. The Evaluation-minus-Unbiased contrast was comparatively stable, whereas absolute agreement was structurally sensitive. These findings do not establish equivalence, causal assistance effects, biological accuracy, or new-patient transportability. Evaluations using variable human references should report reader population, selected frame, observation mechanism, and structural sensitivity.
ER  -