Spatial patterns and MRI-based radiomic prediction of high peritumoral tertiary lymphoid structure density in hepatocellular carcinoma: a multicenter study.

IF 10.3 1区 医学 Q1 IMMUNOLOGY
Shichao Long, Mengsi Li, Juan Chen, Linhui Zhong, Aerzuguli Abudulimu, Lan Zhou, Wenguang Liu, Deng Pan, Ganmian Dai, Kai Fu, Xiong Chen, Yigang Pei, Wenzheng Li
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引用次数: 0

Abstract

Background: Tertiary lymphoid structures (TLS) within the tumor microenvironment have been associated with cancer prognosis and therapeutic response. However, the immunological pattern of a high peritumoral TLS (pTLS) density and its clinical potential in hepatocellular carcinoma (HCC) remain poor. This study aimed to elucidate biological differences related to pTLS density and develop a radiomic classifier for predicting pTLS density in HCC, offering new insights for clinical diagnosis and treatment.

Methods: Spatial transcriptomics (n=4) and RNA sequencing data (n=952) were used to identify critical regulators of pTLS density and evaluate their prognostic significance in HCC. Baseline MRI images from 660 patients with HCC who had undergone surgery treatment between October 2015 and January 2023 were retrospectively recruited for model development and validation. This included training (n=307) and temporal validation (n=76) cohorts from Xiangya Hospital, and external validation cohorts from three independent hospitals (n=277). Radiomic features were extracted from intratumoral and peritumoral regions of interest and analyzed using machine learning algorithms to develop a predictive classifier. The classifier's performance was evaluated using the area under the curve (AUC), with prognostic and predictive value assessed across four independent cohorts and in a dual-center outcome cohort of 41 patients who received immunotherapy.

Results: Patients with HCC and a high pTLS density experienced prolonged median overall survival (p<0.05) and favorable immunotherapy response (p=0.03). Moreover, immune infiltration by mature B cells was observed in the high pTLS density region. Spatial pseudotime analysis and immunohistochemistry staining revealed that expansion of pTLS in HCC was associated with elevated CXCL9 and CXCL10 co-expression. We developed an optimal radiomic-based classifier with excellent discrimination for predicting pTLS density, achieving an AUC of 0.91 (95% CI 0.87, 0.94) in the external validation cohort. This classifier also exhibited promising stratification ability in terms of overall survival (p<0.01), relapse-free survival (p<0.05), and immunotherapy response (p<0.05).

Conclusion: We identified key regulators of pTLS density in patients with HCC and proposed a non-invasive radiomic classifier capable of assisting in stratification for prognosis and treatment.

肝细胞癌瘤周三级淋巴结构高密度的空间模式和基于核磁共振成像的放射学预测:一项多中心研究。
背景:肿瘤微环境中的三级淋巴结构(TLS)与癌症预后和治疗反应有关。然而,瘤周三级淋巴结构(pTLS)密度高的免疫学模式及其在肝细胞癌(HCC)中的临床潜力仍不乐观。本研究旨在阐明与pTLS密度相关的生物学差异,并开发一种用于预测HCC中pTLS密度的放射组学分类器,为临床诊断和治疗提供新的见解:方法:利用空间转录组学(n=4)和RNA测序数据(n=952)确定pTLS密度的关键调节因子,并评估其在HCC中的预后意义。回顾性收集了2015年10月至2023年1月期间接受手术治疗的660名HCC患者的基线MRI图像,用于模型开发和验证。其中包括来自湘雅医院的训练队列(n=307)和时间验证队列(n=76),以及来自三家独立医院的外部验证队列(n=277)。从瘤内和瘤周感兴趣区提取放射学特征,并使用机器学习算法进行分析,以开发预测分类器。分类器的性能使用曲线下面积(AUC)进行评估,预后和预测价值在四个独立队列和一个由41名接受免疫疗法的患者组成的双中心结果队列中进行评估:结果:pTLS密度高的HCC患者的中位总生存期(pConclusion)延长:我们确定了 HCC 患者 pTLS 密度的关键调节因素,并提出了一种非侵入性放射学分类方法,该方法能够帮助对预后和治疗进行分层。
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来源期刊
Journal for Immunotherapy of Cancer
Journal for Immunotherapy of Cancer Biochemistry, Genetics and Molecular Biology-Molecular Medicine
CiteScore
17.70
自引率
4.60%
发文量
522
审稿时长
18 weeks
期刊介绍: The Journal for ImmunoTherapy of Cancer (JITC) is a peer-reviewed publication that promotes scientific exchange and deepens knowledge in the constantly evolving fields of tumor immunology and cancer immunotherapy. With an open access format, JITC encourages widespread access to its findings. The journal covers a wide range of topics, spanning from basic science to translational and clinical research. Key areas of interest include tumor-host interactions, the intricate tumor microenvironment, animal models, the identification of predictive and prognostic immune biomarkers, groundbreaking pharmaceutical and cellular therapies, innovative vaccines, combination immune-based treatments, and the study of immune-related toxicity.
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