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人工智能在组织病理学分析中预测皮肤黑色素瘤免疫治疗反应

英文原题:Artificial Intelligence in Histopathological Analysis for Predicting Immunotherapy Response in Cutaneous Melanoma.

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Artificial Intelligence in Histopathological Analysis for Predicting Immunotherapy Response in Cutaneous Melanoma.

PubMed 2025/11/04(内容时间) Int J Mol Sci Q1 · IF 5.6(JCR 2025)

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中文摘要

人工智能(AI)已成为组织病理学中的变革性工具,为提升皮肤黑色素瘤的预后准确性并指导免疫治疗提供了新的机遇。TIL(肿瘤浸润淋巴细胞)(TILs)的预后意义已得到充分确立,但其人工评估仍具有主观性、劳动强度大,且通常局限于选定的组织区域。近期基于AI的方法实现了对全切片图像中TIL密度和空间免疫谱的自动化、可重复定量,提供了对肿瘤免疫微环境更全面的视角。在黑色素瘤中,这些方法已展现出预测免疫检查点阻断反应的潜力,其中空间分辨的TIL谱分析正成为一种尤为强大的预后和预测生物标志物。本综述总结了AI驱动的皮肤黑色素瘤组织病理学分析的最新进展,重点关注自动化TIL定量和空间免疫谱分析,并强调这些创新如何完善预后评估并改善对免疫治疗结局的预测。

展开英文摘要原文

Artificial intelligence (AI) has emerged as a transformative tool in histopathology, offering new opportunities to enhance prognostic accuracy and guide immunotherapy in cutaneous melanoma. The prognostic significance of tumor-infiltrating lymphocytes (TILs) is well established, yet their manual assessment remains subjective, labor-intensive, and often confined to selected tissue regions. Recent AI-based approaches enabled automated and reproducible quantification of TIL density and spatial immune profiling across whole-slide images, providing a more comprehensive view of the tumor immune microenvironment.

In melanoma, these methods have demonstrated the potential to predict response to immune checkpoint blockade, with spatially resolved TIL profiling emerging as a particularly powerful prognostic and predictive biomarker. This review summarizes recent advances in AI-driven histopathologic analysis of cutaneous melanoma, focusing on automated TIL quantification and spatial immune profiling, and highlights how these innovations refine prognostic evaluation and improve the prediction of immunotherapy outcomes.

论文信息

作者
Yoo S、Lee JH
单位
Department of Dermatology, Seoul St. Mary's Hospital, College of Medicine, The Catholic University of Korea, Seoul 06591, Republic of Korea.South Korea
文献类型
综述
期刊
International journal of molecular sciences2025 Nov 4
原文标识
PubMed 41226765 · DOI 10.3390/ijms262110729