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Visual Language Pretrained Multiple Instance Zero-Shot Transfer for Histopathology Images

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arxiv 2306.07831 v1 pith:FS2F3QVD submitted 2023-06-13 cs.CV

classification cs.CV
keywords zero-shotpretrainedavailableencodershistopathologyimageimagesmi-zero
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Contrastive visual language pretraining has emerged as a powerful method for either training new language-aware image encoders or augmenting existing pretrained models with zero-shot visual recognition capabilities. However, existing works typically train on large datasets of image-text pairs and have been designed to perform downstream tasks involving only small to medium sized-images, neither of which are applicable to the emerging field of computational pathology where there are limited publicly available paired image-text datasets and each image can span up to 100,000 x 100,000 pixels. In this paper we present MI-Zero, a simple and intuitive framework for unleashing the zero-shot transfer capabilities of contrastively aligned image and text models on gigapixel histopathology whole slide images, enabling multiple downstream diagnostic tasks to be carried out by pretrained encoders without requiring any additional labels. MI-Zero reformulates zero-shot transfer under the framework of multiple instance learning to overcome the computational challenge of inference on extremely large images. We used over 550k pathology reports and other available in-domain text corpora to pre-train our text encoder. By effectively leveraging strong pre-trained encoders, our best model pretrained on over 33k histopathology image-caption pairs achieves an average median zero-shot accuracy of 70.2% across three different real-world cancer subtyping tasks. Our code is available at: https://github.com/mahmoodlab/MI-Zero.

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Cited by 1 Pith paper

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  1. F3-Net: Foundation Model for Full Abnormality Segmentation of Medical Images with Flexible Input Modality Requirement

    cs.CV 2025-07 reject novelty 3.0 of 10

    F3-Net combines multi-encoder nnU-Net with zero-filled missing modalities to segment glioma, metastasis, stroke, and white matter lesions, but the missing-modality claim is untested and comparisons are incomplete.

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