← 研踪 PaperTrailarXiv:2610.32493 · v2
K-CLUE: A Segmentation-to-Clustering Framework for Ki67 Cell Typing
首次提交 2026-10-23 19:08
版本更新 2026-10-27 19:26
雷达观测 2026-10-29 00:35
摘要
Ki67 is a key marker of tumor proliferation in breast cancer, but its quantification from immunohistochemistry images normally depends on supervised classifiers trained per dataset. We examine the role of frozen pretrained visual representations in annotation-free Ki67 cell typing. To this end, we use K-CLUE, a framework that segments individual nuclei, represents each nucleus with a pretrained encoder, reduces the resulting embeddings with principal component analysis, and separates Ki67-positive from Ki67-negative nuclei using k-means clustering, without task-specific training or manual annotations. Clustering the raw components is highly sensitive to the choice of encoder: across seven encoders, the Ki67-positive F1-score on matched MIST nuclei varies by 44 points, although Ki67 status remains linearly decodable from every representation, with supervised probe AUCs above 0.98. Analysis of the embedding spaces shows that clustering succeeds when DAB-related variation occupies the leading directions of variance. Whitening the retained principal components removes this dependence, reducing the spread across encoders to 1.00 F1-score point. Handcrafted color representations are also competitive, confirming that Ki67 status is strongly reflected in chromatic information, but they require an explicit choice of color space. In end-to-end evaluation, K-CLUE reaches F1-scores of 85.00% and 81.91% for Ki67-positive and Ki67-negative nuclei on MIST, and 79.59% and 81.16% on BCData, outperforming DeepLIIF and IHCScoreGAN on both datasets. These results show that pretrained representations can support annotation-free Ki67 typing when their variance structure is accounted for.
作者备注：Accepted at the BD-MedVis Workshop, BMVC 2026
观测到的版本
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v2 · 2026-10-27 19:26 · 最新观测版本
K-CLUE: A Segmentation-to-Clustering Framework for Ki67 Cell Typing
Ki67 is a key marker of tumor proliferation in breast cancer, but its quantification from immunohistochemistry images normally depends on supervised classifiers trained per dataset. We examine the role of frozen pretrained visual representations in annotation-free Ki67 cell typing. To this end, we use K-CLUE, a framework that segments individual nuclei, represents each nucleus with a pretrained encoder, reduces the resulting embeddings with principal component analysis, and separates Ki67-positive from Ki67-negative nuclei using k-means clustering, without task-specific training or manual annotations. Clustering the raw components is highly sensitive to the choice of encoder: across seven encoders, the Ki67-positive F1-score on matched MIST nuclei varies by 44 points, although Ki67 status remains linearly decodable from every representation, with supervised probe AUCs above 0.98. Analysis of the embedding spaces shows that clustering succeeds when DAB-related variation occupies the leading directions of variance. Whitening the retained principal components removes this dependence, reducing the spread across encoders to 1.00 F1-score point. Handcrafted color representations are also competitive, confirming that Ki67 status is strongly reflected in chromatic information, but they require an explicit choice of color space. In end-to-end evaluation, K-CLUE reaches F1-scores of 85.00% and 81.91% for Ki67-positive and Ki67-negative nuclei on MIST, and 79.59% and 81.16% on BCData, outperforming DeepLIIF and IHCScoreGAN on both datasets. These results show that pretrained representations can support annotation-free Ki67 typing when their variance structure is accounted for.
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