利用晚期非小细胞肺癌患者的临床和放射组学特征进行基于人工智能的个性化生存预测

IF 3.4 2区 医学 Q2 ONCOLOGY
Junji Koyama, Masahiro Morise, Taiki Furukawa, Shintaro Oyama, Reiko Matsuzawa, Ichidai Tanaka, Keiko Wakahara, Hideo Yokota, Tomoki Kimura, Yoshimune Shiratori, Yasuhiro Kondoh, Naozumi Hashimoto, Makoto Ishii
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引用次数: 0

摘要

背景:针对晚期非小细胞肺癌(NSCLC)已开发出多种一线治疗方案,每个亚组由预测性生物标志物决定,特别是驱动癌基因和程序性细胞死亡配体-1(PD-L1)状态。然而,个体患者最佳治疗选择的方法尚未确立。本研究旨在根据治疗选择建立基于人工智能(AI)的个性化生存预测模型:方法:利用患者特征、抗癌治疗史和原发肿瘤的放射组学特征,基于随机生存森林(RSF)算法建立预测模型。用外部测试数据验证了预测的准确性,并与考克斯比例危险(CPH)模型进行了比较:共招募了 459 名晚期 NSCLC 患者(训练,299 人;测试,160 人)。该算法识别出以下特征是与生存相关的重要因素:年龄、性别、表现状态、布林克曼指数、慢性阻塞性肺病合并症、组织学、分期、驱动癌基因状态、肿瘤PD-L1表达、服用的抗癌药物、血液检测的六项指标(钠、乳酸脱氢酶等),以及与肿瘤质地、体积和形状相关的三项放射组学特征。在测试数据中,RSF 模型的 C 指数为 0.841,高于 CPH 模型(0.775,P 结论):所提出的基于人工智能的算法能准确预测每位晚期 NSCLC 患者的生存率。基于人工智能的方法将为个性化医疗做出贡献:试验设计是根据赫尔辛基宣言进行的回顾性注册研究,并获得了名古屋大学医学研究生院机构审查委员会的批准(批准号:2020 - 0287)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Artificial intelligence-based personalized survival prediction using clinical and radiomics features in patients with advanced non-small cell lung cancer.

Background: Multiple first-line treatment options have been developed for advanced non-small cell lung cancer (NSCLC) in each subgroup determined by predictive biomarkers, specifically driver oncogene and programmed cell death ligand-1 (PD-L1) status. However, the methodology for optimal treatment selection in individual patients is not established. This study aimed to develop artificial intelligence (AI)-based personalized survival prediction model according to treatment selection.

Methods: The prediction model was built based on random survival forest (RSF) algorithm using patient characteristics, anticancer treatment histories, and radiomics features of the primary tumor. The predictive accuracy was validated with external test data and compared with that of cox proportional hazard (CPH) model.

Results: A total of 459 patients (training, n = 299; test, n = 160) with advanced NSCLC were enrolled. The algorithm identified following features as significant factors associated with survival: age, sex, performance status, Brinkman index, comorbidity of chronic obstructive pulmonary disease, histology, stage, driver oncogene status, tumor PD-L1 expression, administered anticancer agent, six markers of blood test (sodium, lactate dehydrogenase, etc.), and three radiomics features associated with tumor texture, volume, and shape. The C-index of RSF model for test data was 0.841, which was higher than that of CPH model (0.775, P < 0.001). Furthermore, the RSF model enabled to identify poor survivor treated with pembrolizumab because of tumor PD-L1 high expression and those treated with driver oncogene targeted therapy according to driver oncogene status.

Conclusions: The proposed AI-based algorithm accurately predicted the survival of each patient with advanced NSCLC. The AI-based methodology will contribute to personalized medicine.

Trial registration: The trial design was retrospectively registered study performed in accordance with the Declaration of Helsinki and approved by the Institutional Review Board of Nagoya University Graduate School of Medicine (approval: 2020 - 0287).

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来源期刊
BMC Cancer
BMC Cancer 医学-肿瘤学
CiteScore
6.00
自引率
2.60%
发文量
1204
审稿时长
6.8 months
期刊介绍: BMC Cancer is an open access, peer-reviewed journal that considers articles on all aspects of cancer research, including the pathophysiology, prevention, diagnosis and treatment of cancers. The journal welcomes submissions concerning molecular and cellular biology, genetics, epidemiology, and clinical trials.
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