脑转移的深度学习预测转移性NSCLC中EGFR基因型和EGFR- tki治疗反应:一项多中心研究

IF 4.8 3区 工程技术 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Frontiers in Bioengineering and Biotechnology Pub Date : 2025-10-02 eCollection Date: 2025-01-01 DOI:10.3389/fbioe.2025.1637095
Shuailin You, Ying Fan, Zhiguang Yang, Chunna Yang, Yiyao Sun, Yahong Luo, Zekun Wang, Bo Sun, Wenyan Jiang
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引用次数: 0

摘要

背景:脑转移在晚期非小细胞肺癌(NSCLC)患者中很常见,尤其是那些携带EGFR突变的患者,准确预测EGFR突变状态和治疗反应对于指导靶向治疗至关重要。本研究旨在采用深度学习(DL)方法自动预测非小细胞肺癌合并脑转移瘤(BM)患者表皮生长因子受体(EGFR)基因型和对EGFR-酪氨酸激酶抑制剂(TKI)治疗的反应。方法:为了训练和验证DL模型,从2014年7月至2022年12月,从三个中心招募了388名患者(中心1 230名,中心2 80名,中心3 78名)。获得每位患者治疗前的对比增强t1加权(T1CE)和t2加权(T2W)脑MRI图像进行分析。我们开发了一种EGFR- tki系统(ETS),用于自动检测脑转移(BM)病变,区分EGFR突变状态并预测对EGFR- tki治疗的反应。通过受试者工作特征(ROC)曲线分析对模型进行了严格的评估,其中检查了曲线下面积(AUC)、敏感性和特异性等指标。结果:在预测EGFR突变状态方面,整合影像学特征和临床因素的ETS在内部验证、外部验证1和外部验证2队列上的auc分别为0.842、0.833和0.832。为了预测EGFR-TKI治疗的疗效,将MRI与临床因素合并建立的融合模型在内部验证、外部验证1和外部验证2队列上的auc分别为0.747、0.726和0.728。结论:ETS可能有潜力作为一种非侵入性工具来预测EGFR突变状态和对EGFR- tki治疗的反应,这有望作为一种非侵入性工具来帮助临床医生制定个性化治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Deep learning on brain metastasis for predicting EGFR genotype and EGFR-TKI therapy response in metastatic NSCLC: a multicenter study.

Deep learning on brain metastasis for predicting EGFR genotype and EGFR-TKI therapy response in metastatic NSCLC: a multicenter study.

Deep learning on brain metastasis for predicting EGFR genotype and EGFR-TKI therapy response in metastatic NSCLC: a multicenter study.

Deep learning on brain metastasis for predicting EGFR genotype and EGFR-TKI therapy response in metastatic NSCLC: a multicenter study.

Background: Brain metastases are common in patients with advanced non-small cell lung cancer (NSCLC), particularly those harboring EGFR mutations, and accurate prediction of EGFR mutation status and therapeutic response is crucial for guiding targeted therapy. This study aims to conduct a deep learning (DL) approach to automatically predict epidermal growth factor receptor (EGFR) genotype and response to EGFR-tyrosine kinase inhibitor (TKI) therapy in NSCLC patients with brain metastatic tumor (BM).

Methods: For training and validating the DL models, 388 patients were enrolled from three centers between Jul. 2014 and Dec.2022 (230 from center 1, 80 from center 2 and 78 from center 3). Contrast-enhanced T1-weighted (T1CE) and T2-weighted (T2W) brain MRI images before treatment for each patient were obtained for analyses. We developed an EGFR-TKI system (ETS) for automated detection of brain metastatic (BM) lesions and to differentiate EGFR mutation status and predict response to EGFR-TKI therapy. The models underwent rigorous evaluation through receiver operating characteristic (ROC) curve analyses, where metrics such as area under the curve (AUC), sensitivity, and specificity were examined.

Results: For prediction of EGFR mutation status, the ETS integrating radiological-based features and clinical factors achieved AUCs of 0.842, 0.833 and 0.832 on the internal validation, external validation 1 and external validation 2 cohort, respectively. For forecasting response to EGFR-TKI therapy, the fusion model created by amalgamating MRI with clinical factors generated AUCs of 0.747, 0.726 and 0.728 on the internal validation, external validation 1, and external validation 2 cohort, respectively.

Conclusion: The ETS may have the potential to work as a non-invasive tool for predicting EGFR mutation status and response to EGFR-TKI therapy, which holds promise as a non-invasive tool to assist clinicians in making decisions about personalized treatment strategies.

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来源期刊
Frontiers in Bioengineering and Biotechnology
Frontiers in Bioengineering and Biotechnology Chemical Engineering-Bioengineering
CiteScore
8.30
自引率
5.30%
发文量
2270
审稿时长
12 weeks
期刊介绍: The translation of new discoveries in medicine to clinical routine has never been easy. During the second half of the last century, thanks to the progress in chemistry, biochemistry and pharmacology, we have seen the development and the application of a large number of drugs and devices aimed at the treatment of symptoms, blocking unwanted pathways and, in the case of infectious diseases, fighting the micro-organisms responsible. However, we are facing, today, a dramatic change in the therapeutic approach to pathologies and diseases. Indeed, the challenge of the present and the next decade is to fully restore the physiological status of the diseased organism and to completely regenerate tissue and organs when they are so seriously affected that treatments cannot be limited to the repression of symptoms or to the repair of damage. This is being made possible thanks to the major developments made in basic cell and molecular biology, including stem cell science, growth factor delivery, gene isolation and transfection, the advances in bioengineering and nanotechnology, including development of new biomaterials, biofabrication technologies and use of bioreactors, and the big improvements in diagnostic tools and imaging of cells, tissues and organs. In today`s world, an enhancement of communication between multidisciplinary experts, together with the promotion of joint projects and close collaborations among scientists, engineers, industry people, regulatory agencies and physicians are absolute requirements for the success of any attempt to develop and clinically apply a new biological therapy or an innovative device involving the collective use of biomaterials, cells and/or bioactive molecules. “Frontiers in Bioengineering and Biotechnology” aspires to be a forum for all people involved in the process by bridging the gap too often existing between a discovery in the basic sciences and its clinical application.
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