Prompt-Free Lightweight SAM Adaptation for Histopathology Nuclei Segmentation with Strong Cross-Dataset Generalization

arXiv cs.CV / 3/24/2026

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Key Points

  • The paper addresses histopathology nuclei segmentation, focusing on the practical issues of computational cost and weak cross-dataset generalization in existing methods.
  • It proposes a prompt-free, lightweight adaptation of SAM that uses multi-level encoder features and residual decoding to better handle dense nuclei and heterogeneous appearances.
  • The approach fine-tunes only LoRA modules while keeping the main SAM encoder frozen, reducing training to just 4.1M trainable parameters for improved efficiency.
  • Experiments on TNBC, MoNuSeg, and PanNuke report state-of-the-art results along with strong cross-dataset generalization, suggesting improved deployment viability for histopathology workflows.

Abstract

Histopathology nuclei segmentation is crucial for quantitative tissue analysis and cancer diagnosis. Although existing segmentation methods have achieved strong performance, they are often computationally heavy and show limited generalization across datasets, which constrains their practical deployment. Recent SAM-based approaches have shown great potential in general and medical imaging, but typically rely on prompt guidance or complex decoders, making them less suitable for histopathology images with dense nuclei and heterogeneous appearances. We propose a prompt-free and lightweight SAM adaptation that leverages multi-level encoder features and residual decoding for accurate and efficient nuclei segmentation. The framework fine-tunes only LoRA modules within the frozen SAM encoder, requiring just 4.1M trainable parameters. Experiments on three benchmark datasets TNBC, MoNuSeg, and PanNuke demonstrate state-of-the-art performance and strong cross-dataset generalization, highlighting the effectiveness and practicality of the proposed framework for histopathology applications.