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Slot-Mixup with Subsampling: A Simple Regularization for WSI Classification

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arxiv 2311.17466 v1 pith:X2T2K4GV submitted 2023-11-29 cs.CV cs.AIcs.LG

classification cs.CVcs.AIcs.LG
keywords augmentationpatchessubsamplingattentionclassificationlabelsmethodsmixup
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Whole slide image (WSI) classification requires repetitive zoom-in and out for pathologists, as only small portions of the slide may be relevant to detecting cancer. Due to the lack of patch-level labels, multiple instance learning (MIL) is a common practice for training a WSI classifier. One of the challenges in MIL for WSIs is the weak supervision coming only from the slide-level labels, often resulting in severe overfitting. In response, researchers have considered adopting patch-level augmentation or applying mixup augmentation, but their applicability remains unverified. Our approach augments the training dataset by sampling a subset of patches in the WSI without significantly altering the underlying semantics of the original slides. Additionally, we introduce an efficient model (Slot-MIL) that organizes patches into a fixed number of slots, the abstract representation of patches, using an attention mechanism. We empirically demonstrate that the subsampling augmentation helps to make more informative slots by restricting the over-concentration of attention and to improve interpretability. Finally, we illustrate that combining our attention-based aggregation model with subsampling and mixup, which has shown limited compatibility in existing MIL methods, can enhance both generalization and calibration. Our proposed methods achieve the state-of-the-art performance across various benchmark datasets including class imbalance and distribution shifts.

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Cited by 1 Pith paper

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  1. Pathology Foundation Models are Scanner Sensitive: Benchmark and Mitigation with Contrastive ScanGen Loss

    q-bio.QM 2025-07 conditional novelty 5.0 of 10

    Pathology foundation models produce scanner-dependent predictions, and the ScanGen contrastive loss reduces this scanner bias during fine-tuning for EGFR mutation prediction from whole slide images.

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