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Spatial Blindness in Whole-Slide Multiple Instance Learning

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Whole-slide MIL models are often called context-aware once graphs, Transform ers, or state-space modules are placed above patch embeddings. We show that this label can be deceptive. On pathology tasks where tissue architecture is part of the diagnostic signal, several strong MIL baselines retain nearly unchanged slide level AUC after patch coordinates are permuted. Their predictions are accurate, but largely compositional. We refer to this failure mode as spatial blindness. Our explanation is optimization-based: dense appearance statistics are learned early under slide-level supervision, leaving weak gradients for sparse spatial relations. ResTopoMIL addresses the issue by first fitting a permutation-invariant prototype histogram and then freezing it while a lightweight graph branch learns the residual under a coordinate-shuffling constraint. The architecture is simple by design; the intervention is in how the spatial branch is trained. Across 9 public WSI bench marks, ResTopoMIL improves classification and survival prediction with 1.15M parameters, restores sensitivity to coordinate perturbation, and gives stronger lo calization evidence on CAMELYON-16.

Xiangyu Li, Ran Su• 2026

Related benchmarks

TaskDatasetResultRank
Survival PredictionTCGA-LUAD
C-index0.6457
195
Survival PredictionTCGA-UCEC
C-index0.7058
179
Survival PredictionTCGA-STAD
C-index0.6807
89
Survival PredictionKIRC TCGA
C-Index0.7313
84
Cancer ClassificationTCGA-BRCA
Accuracy95.68
83
Survival PredictionTCGA-KIRP
C-index0.8182
63
WSI ClassificationPanda
Accuracy75.46
32
WSI ClassificationTCGA-NSCLC
Accuracy91.57
28
ClassificationPANDA (test)
Accuracy73.5
19
Tumor localizationCAMELYON-16
Dice0.624
14
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