← 返回

预测黑色素瘤对免疫检查点抑制剂的反应:数字病理学、空间分析和机器学习中的新兴方法

英文原题:Predicting Response to Immune Checkpoint Inhibitors in Melanoma: Emerging Approaches in Digital Pathology, Spatial Profiling and Machine Learning.

查看英文原题

Predicting Response to Immune Checkpoint Inhibitors in Melanoma: Emerging Approaches in Digital Pathology, Spatial Profiling and Machine Learning.

PubMed 2026/06/10(内容时间) Int J Mol Sci Q1 · IF 5.6(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

中文摘要

过去十年中,将免疫检查点抑制剂(ICIs)引入黑色素瘤治疗已显著降低了死亡率。然而,并非所有患者都能观察到治疗获益,且治疗可能伴随严重不良事件。

因此,识别最可能从免疫治疗中获益的患者仍然至关重要。目前使用的生物标志物,如程序性死亡配体1(PD-L1)表达和TIL(肿瘤浸润淋巴细胞)(TILs)的人工评估,其预测价值有限。本叙述性综述对采用数字病理学工具、多重和空间技术(包括多重免疫荧光、成像质谱流式细胞术和数字空间分析)以及机器学习算法预测黑色素瘤患者对ICIs反应的研究进行了批判性评价。现有证据表明,最高的预测价值可能通过将免疫浸润的定量评估与其空间分布、功能状态及肿瘤微环境内相互作用信息相结合的方法来实现。与“免疫炎症型”、“免疫排斥型”和“免疫荒漠型”表型相关的特征、三级淋巴结构的存在以及局部免疫生态位的组织可能具有特别重要的意义。

此外,本综述强调了当前数据解读中的关键局限性,包括缺乏方法学标准化、数据异质性以及验证不足。还讨论了将这些方法应用于常规临床实践所必需的未来研究方向。

展开英文摘要原文

The introduction of immune checkpoint inhibitors (ICIs) into the treatment of melanoma has significantly reduced mortality over the past decade.

However, therapeutic benefit is not observed in all patients, and treatment may be associated with severe adverse events.

Therefore, identifying patients who are most likely to benefit from immunotherapy remains of critical importance. Currently used biomarkers, such as programmed death-ligand 1 (PD-L1) expression and manual assessment of tumour-infiltrating lymphocytes (TILs), have limited predictive value. This narrative review provides a critical appraisal of studies employing digital pathology tools, multiplex and spatial techniques (including multiplex immunofluorescence, imaging mass cytometry, and digital spatial profiling), as well as machine learning algorithms for predicting response to ICIs in patients with melanoma.

Available evidence suggests that the highest predictive value may be achieved by approaches integrating quantitative assessment of immune infiltration with information on its spatial distribution, functional state, and interactions within the tumour microenvironment. Particular relevance may be attributed to features associated with the "immune-inflamed", "immune-excluded", and "immune-desert" phenotypes, the presence of tertiary lymphoid structures, and the organisation of local immune niches.

In addition, this review highlights key limitations in the interpretation of current data, including lack of methodological standardisation, data heterogeneity, and insufficient validation. Directions for future research necessary for the implementation of these approaches into routine clinical practice are also discussed.

论文信息

作者
Banaszek J、Bąk D、Barańska K、Czajka A、Ciesielska D、Kleinrok J、Pająk W、Korolczuk A
第一作者单位
Chair and Department of Clinical Pathomorphology, Medical University of Lublin, Jaczewskiego 8b, 20-090 Lublin, Poland.Poland
通讯作者单位
Faculty of Chemistry, University of Warsaw, Ludwika Pasteura 1, 02-093 Warsaw, Poland.Poland
文献类型
综述
期刊
International journal of molecular sciences2026 Jun 10
原文标识
PubMed 42352966 · DOI 10.3390/ijms27125244