Nomogram based on computed tomography radiomics features and clinicopathological factors to predict the prognosis of patients with non-small cell lung cancer receiving immune checkpoint inhibitor rechallenge.

IF 4 2区 医学 Q2 ONCOLOGY
Translational lung cancer research Pub Date : 2025-03-31 Epub Date: 2025-03-25 DOI:10.21037/tlcr-24-876
Junfeng Zhao, Ying Li, Ruyue Li, Xiujing Yao, Xue Dong, Lin Su, Yintao Li
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引用次数: 0

Abstract

Background: Whether patients with advanced non-small cell lung cancer (NSCLC) who experience progressive disease (PD) after the initial immunotherapy treatment benefit from subsequent immunotherapy remains unclear. In this study, we aimed to identify predictive factors and develop a nomogram to predict successful immunotherapy rechallenge for such patients with NSCLC to guide clinical treatment and improve prognosis.

Methods: Between January 2019 and December 2022, 352 patients with advanced NSCLC who received immunotherapy rechallenge after experiencing PD were divided into the training (n=246) and validation (n=106) cohorts. Clinicopathological factors and radiomics features were included in the univariate and multivariate analyses, with significant predictive factors being used to develop the nomogram.

Results: Univariate and multivariate analyses showed that time from the initial immunotherapy to PD occurrence (duration), clinical N stage, liver metastasis, treatment after PD following the first immunotherapy (post-PD treatment), and radiomics features were independent predictive factors for progression-free survival (PFS). In addition, age, duration, clinical N stage, post-PD treatment, and radiomics were independent predictive factors for overall survival (OS). Accordingly, these predictive factors were used to develop a nomogram. The area under the curves (AUCs) of the nomogram for predicting 6-, 12-, and 18-month PFS and 12-, 18-, and 24-month OS were 0.731, 0.809, 0.878, 0.742, 0.782, and 0.868, respectively, in the training cohorts, whereas the corresponding values in the validation cohort were 0.672, 0.774, 0.826, 0.833, 0.705, and 0.762. This indicated good discrimination.

Conclusions: We developed and validated a predictive nomogram based on clinicopathological factors and radiomics features for the prognosis of patients with advanced NSCLC who received immunotherapy rechallenge following PD after the first immunotherapy. The nomogram showed strong predictive utility and can be a suitable tool for such patients with advanced NSCLC.

基于计算机断层放射组学特征和临床病理因素的Nomogram预测接受免疫检查点抑制剂再挑战的非小细胞肺癌患者的预后。
背景:晚期非小细胞肺癌(NSCLC)患者在初始免疫治疗后出现进展性疾病(PD),是否能从后续免疫治疗中获益尚不清楚。在本研究中,我们旨在确定预测因素并开发一种nomogram来预测这类非小细胞肺癌患者成功的免疫治疗再挑战,以指导临床治疗和改善预后。方法:2019年1月至2022年12月,352例晚期非小细胞肺癌患者在经历PD后接受免疫治疗再挑战,分为训练组(n=246)和验证组(n=106)。临床病理因素和放射组学特征被包括在单因素和多因素分析中,重要的预测因素被用来制定nomogram。结果:单因素和多因素分析显示,从首次免疫治疗到PD发生的时间(持续时间)、临床N分期、肝转移、首次免疫治疗后PD的治疗(PD后治疗)和放射组学特征是无进展生存(PFS)的独立预测因素。此外,年龄、病程、临床N分期、pd后治疗和放射组学是总生存期(OS)的独立预测因素。因此,这些预测因素被用来开发一个nomogram。训练组预测6、12、18个月PFS和12、18、24个月OS的曲线下面积(auc)分别为0.731、0.809、0.878、0.742、0.782、0.868,而验证组预测的曲线下面积(auc)分别为0.672、0.774、0.826、0.833、0.705、0.762。这表明有良好的辨别能力。结论:我们开发并验证了一种基于临床病理因素和放射组学特征的预测图,用于晚期非小细胞肺癌患者在首次免疫治疗后PD后再次接受免疫治疗的预后。nomogram显示了很强的预测效用,可以作为这类晚期NSCLC患者的合适工具。
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
7.20
自引率
2.50%
发文量
137
期刊介绍: Translational Lung Cancer Research(TLCR, Transl Lung Cancer Res, Print ISSN 2218-6751; Online ISSN 2226-4477) is an international, peer-reviewed, open-access journal, which was founded in March 2012. TLCR is indexed by PubMed/PubMed Central and the Chemical Abstracts Service (CAS) Databases. It is published quarterly the first year, and published bimonthly since February 2013. It provides practical up-to-date information on prevention, early detection, diagnosis, and treatment of lung cancer. Specific areas of its interest include, but not limited to, multimodality therapy, markers, imaging, tumor biology, pathology, chemoprevention, and technical advances related to lung cancer.
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