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Pathology-Guided Virtual Staining Metric for Evaluation and Training

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arxiv 2507.12624 v1 pith:VSOFKDNU submitted 2025-07-16 eess.IV cs.CVcs.SYeess.SY

Pathology-Guided Virtual Staining Metric for Evaluation and Training

classification eess.IV cs.CVcs.SYeess.SY
keywords stainingvirtualevaluationpapisimageperceptualexistingfeatures
verification ladder T0 review T1 audit T2 compute T3 formal T4 reserved
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Virtual staining has emerged as a powerful alternative to traditional histopathological staining techniques, enabling rapid, reagent-free image transformations. However, existing evaluation methods predominantly rely on full-reference image quality assessment (FR-IQA) metrics such as structural similarity, which are originally designed for natural images and often fail to capture pathology-relevant features. Expert pathology reviews have also been used, but they are inherently subjective and time-consuming. In this study, we introduce PaPIS (Pathology-Aware Perceptual Image Similarity), a novel FR-IQA metric specifically tailored for virtual staining evaluation. PaPIS leverages deep learning-based features trained on cell morphology segmentation and incorporates Retinex-inspired feature decomposition to better reflect histological perceptual quality. Comparative experiments demonstrate that PaPIS more accurately aligns with pathology-relevant visual cues and distinguishes subtle cellular structures that traditional and existing perceptual metrics tend to overlook. Furthermore, integrating PaPIS as a guiding loss function in a virtual staining model leads to improved histological fidelity. This work highlights the critical need for pathology-aware evaluation frameworks to advance the development and clinical readiness of virtual staining technologies.

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  1. HAPS: Rethinking Image Similarity for Virtual Staining

    cs.CV 2026-05 unverdicted novelty 7.0

    Proposes HAPS metric using frozen histopathology encoder with linear head, validated on expert-annotated H&E-IHC pairs and shown to improve virtual staining models by filtering low-similarity training data in the MIST...