与肿瘤免疫异质性相关的放射组学特征可预测局部复发鼻咽癌患者的生存率

Da-Feng Lin, Hai-Lin Li, Ting Liu, Xiao-Fei Lv, Chuan-Miao Xie, Xiao-Min Ou, Jian Guan, Ye Zhang, Wen-Bin Yan, Mei-Lin He, Meng-Yuan Mao, Xun Zhao, Lian-Zhen Zhong, Wen-Hui Chen, Qiu-Yan Chen, Hai-Qiang Mai, Rou-Jun Peng, Jie Tian, Lin-Quan Tang, Di Dong
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引用次数: 0

摘要

背景 局部复发性鼻咽癌(lrNPC)传统临床指标的预后价值有限,因为它们无法反映肿瘤内的异质性。我们的目的是开发一种放射组学特征,以揭示肿瘤免疫异质性并预测 lrNPC 的生存期。方法 这项多中心回顾性研究纳入了 921 例 lrNPC 患者。在一个训练队列中开发了基于治疗前磁共振成像特征的机器学习特征和提名图,用于预测总生存期(OS),并在两个独立队列中进行了验证。为进行比较,还构建了临床提名图和综合提名图。通过一致性指数(C-index)和接收者操作特征曲线分析评估了提名图的性能。据此,患者被划分为不同的风险组别。通过 RNA 测序(RNA-seq)分析探讨了特征的生物学特征和免疫浸润。结果 机器学习特征和提名图显示出与临床提名图相当的预后能力,在训练组、内部组和外部验证组中的C指数分别为0.729、0.718和0.731。该特征与临床变量的整合大大提高了预测性能。所提出的特征能有效区分OS率明显不同的风险组别。亚组分析表明,建议对低风险患者进行局部挽救治疗。探索性RNA-seq分析显示,不同风险组的干扰素反应和淋巴细胞浸润存在差异。结论 基于MRI的放射学特征能更准确地预测OS。所提出的与肿瘤免疫异质性相关的特征可作为一种有价值的工具,帮助对lrNPC患者进行预后分层并指导个体化治疗。
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Radiomic signatures associated with tumor immune heterogeneity predict survival in locally recurrent nasopharyngeal carcinoma
Background The prognostic value of traditional clinical indicators for locally recurrent nasopharyngeal carcinoma (lrNPC) is limited due to their inability to reflect intratumor heterogeneity. We aimed to develop a radiomic signature to reveal tumor immune heterogeneity and predict survival in lrNPC. Methods This multicenter, retrospective study included 921 patients with lrNPC. A machine learning signature and nomogram based on pretreatment MRI features were developed for predicting overall survival (OS) in a training cohort and validated in two independent cohorts. A clinical nomogram and an integrated nomogram were constructed for comparison. Nomogram performance was evaluated by concordance index (C-index) and receiver operating characteristic curve analysis. Accordingly, patients were classified into risk groups. The biological characteristics and immune infiltration of the signature were explored by RNA sequencing (RNA-seq) analysis. Results The machine learning signature and nomogram demonstrated comparable prognostic ability to a clinical nomogram, achieving C-indexes of 0.729, 0.718, and 0.731 in the training, internal, and external validation cohorts, respectively. Integration of the signature and clinical variables significantly improved the predictive performance. The proposed signature effectively distinguished patients between risk groups with significantly distinct OS rates. Subgroup analysis indicated the recommendation of local salvage treatments for low-risk patients. Exploratory RNA-seq analysis revealed differences in interferon response and lymphocyte infiltration between risk groups. Conclusions An MRI-based radiomic signature predicted OS more accurately. The proposed signature associated with tumor immune heterogeneity may serve as a valuable tool to facilitate prognostic stratification and guide individualized management for lrNPC patients.
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