Assessing the reproducibility, stability, and biological interpretability of multimodal computed tomography image features for prognosis in advanced non-small cell lung cancer

iRadiology Pub Date : 2024-02-05 DOI:10.1002/ird3.56
Jiajun Wang, Gang Dai, Xiufang Ren, Ruichuan Shi, Ruibang Luo, Jianhua Liu, Kexue Deng, Jiangdian Song
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Abstract

Background

Despite the existence of proposed prognostic features on computed tomography (CT) for patients with advanced-stage non-small cell lung cancer (NSCLC), including radiologists' handcrafted (RaH) features, radiomics features, and deep learning features, comprehensive studies that examine their reproducibility, stability, and biological interpretability remain limited.

Methods

The Image Biomarker Standardization Initiative-reported tolerance, Kappa, interclass correlation coefficient, and coefficient of variance were employed to identify reproducible features among RaH, radiomics, and deep learning features derived from NSCLC phantoms. The reproducible features were then input into six artificial intelligence algorithms to develop prognostic models for targeted therapy and immunotherapy using real-world patients with advanced-stage NSCLC to assess their capability and stability. Pathway enrichment was also conducted to explore the underlying biological pathways associated with these reproducible features.

Results

Reproducible features in advanced NSCLC included RaH features (9/9, 100%), radiomics features (572/1835, 31.17%), and deep learning features (3442/4096, 84.03%). Among the six artificial intelligence-based prognostic methods, the RaH features exhibited least variability. We also observed that the optimal CT-based prognostic approach differed depending on treatment regimens for advanced NSCLC. In analysis using the Cancer Genome Atlas Program lung adenocarcinoma dataset, the identified reproducible prognostic features, specifically tumor size-derived radiomics and RaH features, showed significant associations with five key signaling pathways involved in NSCLC survival outcomes (false-discovery rate p < 0.05).

Conclusions

By elucidating the reproducibility, stability, and biological associations of prognostic CT features, our study provides valuable evidence for future NSCLC studies and modeling approaches.

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评估用于晚期非小细胞肺癌预后判断的多模态计算机断层扫描图像特征的再现性、稳定性和生物学可解释性
尽管针对晚期非小细胞肺癌(NSCLC)患者的计算机断层扫描(CT)已提出了预后特征,包括放射医师手工制作的特征(RaH)、放射组学特征和深度学习特征,但对其可重复性、稳定性和生物学可解释性的全面研究仍然有限。我们采用了图像生物标记标准化倡议报告的容差、Kappa、类间相关系数和方差系数来识别从NSCLC模型中提取的RaH、放射组学和深度学习特征中的可再现特征。然后将这些可重复性特征输入六种人工智能算法,利用真实世界中的晚期NSCLC患者建立靶向治疗和免疫治疗的预后模型,以评估其能力和稳定性。晚期NSCLC的可重复特征包括RaH特征(9/9,100%)、放射组学特征(572/1835,31.17%)和深度学习特征(3442/4096,84.03%)。在六种基于人工智能的预后方法中,RaH 特征的变异性最小。我们还观察到,基于 CT 的最佳预后方法因晚期 NSCLC 治疗方案而异。在使用癌症基因组图谱计划肺腺癌数据集进行的分析中,所发现的可重现预后特征,特别是肿瘤大小衍生放射组学和RaH特征,显示出与NSCLC生存结果所涉及的五种关键信号通路有显著关联(假发现率P<0.05)。
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