非小细胞肺癌分子和临床背景下三级淋巴样结构的空间分布。

IF 4.9 2区 医学 Q2 CELL BIOLOGY
Cellular Oncology Pub Date : 2025-06-01 Epub Date: 2025-03-03 DOI:10.1007/s13402-025-01052-x
Hedvig Elfving, Hui Yu, Kaleab Kassete Fessehatsion, Hans Brunnström, Johan Botling, Miklos Gulyas, Max Backman, Amanda Lindberg, Carina Strell, Patrick Micke
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引用次数: 0

摘要

三级淋巴样结构(TLS)是类似次级淋巴样器官的淋巴细胞聚集体,在肿瘤免疫中起关键作用。TLS的模糊形态学定义使得确定其对患者生存和免疫治疗反应的临床影响具有挑战性。目的:本研究旨在表征肺癌患者苏木精-伊红组织切片中的TLS,评估其发生与局部免疫环境、突变背景和患者预后的关系。方法:两位病理学家对680例非小细胞肺癌患者切除标本的一整块组织切片进行评估。在肿瘤区域或周围对TLS进行空间量化,并根据生发中心(成熟TLS)的存在进一步分类。这些指标与免疫细胞计数、基因组和转录组学数据相结合,并与临床参数相关。结果:在536例可评估的病例中,TLS存在于86%,主要在肿瘤周围,每例中位数为8个TLS。成熟的TLS占24%。TLS的存在与浆细胞(CD138+)和淋巴细胞(CD3+、CD8+、FOXP3+)浸润增加呈正相关。肿瘤突变负荷越大,外周TLS数量越多。TLS的总数量与患者生存率的提高独立相关,而与TLS的成熟状态无关。这种预后相关性适用于外周TLS,但不适用于肿瘤TLS。结论:TLS在非小细胞肺癌中是常见的,其与特定免疫表型的相关性提示其在局部免疫反应中具有生物学相关性。该评分系统对常规苏木精-伊红切片的预后意义有可能增强非小细胞肺癌患者的诊断算法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Spatial distribution of tertiary lymphoid structures in the molecular and clinical context of non-small cell lung cancer.

Introduction: Tertiary lymphoid structures (TLS) are lymphocyte aggregates resembling secondary lymphoid organs and are pivotal in cancer immunity. The ambiguous morphological definition of TLS makes it challenging to ascertain their clinical impact on patient survival and response to immunotherapy.

Objectives: This study aimed to characterize TLS in hematoxylin-eosin tissue sections from lung cancer patients, assessing their occurrence in relation to the local immune environment, mutational background, and patient outcome.

Methods: Two pathologists evaluated one whole tissue section from resection specimens of 680 NSCLC patients. TLS were spatially quantified within the tumor area or periphery and further categorized based on the presence of germinal centers (mature TLS). Metrics were integrated with immune cell counts, genomic and transcriptomic data, and correlated with clinical parameters.

Results: TLS were present in 86% of 536 evaluable cases, predominantly in the tumor periphery, with a median of eight TLS per case. Mature TLS were found in 24% of cases. TLS presence correlated positively with increased plasma cell (CD138+) and lymphocytic cell (CD3+, CD8+, FOXP3+) infiltration. Tumors with higher tumor mutational burden exhibited higher numbers of peripheral TLS. The overall TLS quantity was independently associated with improved patient survival, irrespective of TLS maturation status. This prognostic association held true for peripheral TLS but not for tumor TLS.

Conclusion: TLS in NSCLC is common and their correlation with a specific immune phenotype suggests biological relevance in the local immune reaction. The prognostic significance of this scoring system on routine hematoxylin-eosin sections has the potential to augment diagnostic algorithms for NSCLC patients.

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来源期刊
Cellular Oncology
Cellular Oncology ONCOLOGY-CELL BIOLOGY
CiteScore
10.30
自引率
1.50%
发文量
86
审稿时长
12 months
期刊介绍: The Official Journal of the International Society for Cellular Oncology Focuses on translational research Addresses the conversion of cell biology to clinical applications Cellular Oncology publishes scientific contributions from various biomedical and clinical disciplines involved in basic and translational cancer research on the cell and tissue level, technical and bioinformatics developments in this area, and clinical applications. This includes a variety of fields like genome technology, micro-arrays and other high-throughput techniques, genomic instability, SNP, DNA methylation, signaling pathways, DNA organization, (sub)microscopic imaging, proteomics, bioinformatics, functional effects of genomics, drug design and development, molecular diagnostics and targeted cancer therapies, genotype-phenotype interactions. A major goal is to translate the latest developments in these fields from the research laboratory into routine patient management. To this end Cellular Oncology forms a platform of scientific information exchange between molecular biologists and geneticists, technical developers, pathologists, (medical) oncologists and other clinicians involved in the management of cancer patients. In vitro studies are preferentially supported by validations in tumor tissue with clinicopathological associations.
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