Tumor Immune Response as a Biomarker for Metastasis-Free Survival of Breast Cancer and Immune Checkpoint Inhibition Therapy: A Retrospective Cohort Study.

IF 1.9 Q3 ONCOLOGY
Breast Cancer : Basic and Clinical Research Pub Date : 2025-08-24 eCollection Date: 2025-01-01 DOI:10.1177/11782234251363665
Chung-Wu Lin, Kai-Ming Chang, Wen-Hui Ku, Kuo-Jang Kao
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引用次数: 0

Abstract

Background: Breast cancers (BRCs) can be classified into 6 molecular subtypes based on gene expression profiles. Previous research suggests that tumor-infiltrating lymphocytes are associated with metastasis-free survival (MFS) in triple-negative and HER2-overexpressing BRC.

Objectives: Our study aims to investigate further how the immune response (IR) may impact MFS in different molecular subtypes of BRC.

Design: A single hospital-based retrospective cohort study.

Methods: A training series of 327 BRCs was used to identify 297 IR transcripts that were correlated with the T cell-associated CD3D transcript or the B cell-associated CD19 transcript. Using these IR transcripts, each of the 6 molecular subtypes was hierarchically clustered into high and low immune responders. An IR score based on the average of the 297 IR transcripts was determined for each BRC. Correlations between the IR score and 3 signatures for IR or response to immune checkpoint inhibition therapy (ICIT) were investigated. A series of 884 BRCs from public datasets was used for confirmation, and the other independent series of 988 BRCs was used for validation.

Results: For subtype I, high immune responders had a statistically significantly better MFS than low immune responders in all the training, confirmation, and validation series by Kaplan-Meier survival analysis (P = .0039, .049, .039, log-rank test). The same trend was observed for subtype II (P = .16, .052, .015) and subtype IV (P = .0078, .0002, .12). Our IR scores were linearly correlated with the Teschendorff, the T-effector and IFNg, and the T-cell inflamed signatures for IR or ICIT. The IR scores were also linearly correlated with the expression of 6 different immune checkpoint genes.

Conclusions: Tumor IR is a biomarker for MFS for BRCs of I, II, and IV subtypes. Our study supports the potential use of the IR score for identifying patients responsive to ICIT.

肿瘤免疫反应作为乳腺癌无转移生存和免疫检查点抑制治疗的生物标志物:一项回顾性队列研究。
背景:乳腺癌(BRCs)可根据基因表达谱分为6个分子亚型。先前的研究表明,在三阴性和her2过表达的BRC中,肿瘤浸润淋巴细胞与无转移生存(MFS)相关。目的:我们的研究旨在进一步探讨免疫反应(IR)如何影响BRC不同分子亚型的MFS。设计:单医院回顾性队列研究。方法:使用327个BRCs训练序列来鉴定297个与T细胞相关CD3D转录物或B细胞相关CD19转录物相关的IR转录物。利用这些IR转录本,将6种分子亚型中的每一种按等级聚集为高免疫应答者和低免疫应答者。基于297个IR转录本的平均值确定每个BRC的IR评分。研究IR评分与IR或免疫检查点抑制治疗(immune checkpoint inhibition therapy)应答的3个特征之间的相关性。来自公共数据集的884个brc序列用于确认,另外988个brc序列用于验证。结果:Kaplan-Meier生存分析显示,在所有训练、确认和验证系列中,对于I亚型,高免疫应答者的MFS均显著优于低免疫应答者(P =。0039年,。049年,。039, log-rank检验)。亚型II也有相同的趋势(P =。16日。052年,。015)和亚型IV (P =。0078年,。0002 .12点)。我们的IR得分与Teschendorff、t效应因子和IFNg以及t细胞的IR或its炎症特征呈线性相关。IR评分也与6种不同免疫检查点基因的表达呈线性相关。结论:肿瘤IR是I、II和IV亚型BRCs的MFS的生物标志物。我们的研究支持IR评分用于识别对其有反应的患者的潜在用途。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
5.10
自引率
3.40%
发文量
22
审稿时长
8 weeks
期刊介绍: Breast Cancer: Basic and Clinical Research is an international, open access, peer-reviewed, journal which considers manuscripts on all areas of breast cancer research and treatment. We welcome original research, short notes, case studies and review articles related to breast cancer-related research. Specific areas of interest include, but are not limited to, breast cancer sub types, pathobiology, metastasis, genetics and epigenetics, mammary gland biology, breast cancer models, prevention, detection, therapy and clinical interventions, and epidemiology and population genetics.
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