18F-FDG PET/CT影像基因组学在非小细胞肺癌靶向诊疗中的研究进展

Research progress of 18F-FDG PET/CT radiogenomics in targeted diagnosis and treatment of NSCLC

  • 摘要: 肺癌是世界上最常见的恶性肿瘤,其中非小细胞肺癌(NSCLC)约占肺部恶性肿瘤的80%~85%,随着基因组学研究的深入,现已证实NSCLC的发生发展主要是由致癌基因的体细胞突变驱动。与化疗相比,NSCLC靶向治疗可有效延长靶向癌基因突变患者的无进展生存期和总生存期。18F-FDG PET/CT影像基因组学对NSCLC患者的表皮生长因子受体(EGFR)、Kirsten大鼠肉瘤病毒癌基因同源物、间变性淋巴瘤激酶、Kelch样环氧氯丙烷相关蛋白1、核转录因子E2相关因子2的突变状态及EGFR-酪氨酸激酶抑制剂相关靶向治疗预后的预测评估已成为研究热点,进一步结合临床参数及人工智能方法可提高其预测准确率。18F-FDG PET/CT影像基因组学有望成为从基因水平进行无创诊断、评估疗效的重要方法。笔者就近年来18F-FDG PET/CT影像基因组学在NSCLC靶向诊疗中的研究进展进行综述。

     

    Abstract: Lung cancer is the most common malignant tumor in the world, of which non-small cell lung cancer (NSCLC) accounts for about 80%~85% of lung malignancies. With the deepening of cancer genomics research, it has been confirmed that the occurrence and development of NSCLC are mainly driven by somatic mutations in oncogenes. Compared with chemotherapy, targeted therapy of NSCLC can effectively prolong the progression-free survival and overall survival time of patients with targeted oncogene mutation. 18F-FDG PET/CT radiogenomics has become a research hotspot to predict epidermal growth factor receptor (EGFR), kirsten rat sarcoma viral oncogene homolog, anaplastic lymphoma kinase, kelch-like ECH-associated protein1, homo sapiens nuclear factor erythroid 2-like 2 mutation and evaluate the prognosis of EGFR- tyrosine kinase inhibitor related targeted therapy in patients with NSCLC. Further combination of clinical parameters and artificial intelligence methods can improve its prediction accuracy. 18F-FDG PET/CT radiogenomics may be an important method for non-invasive diagnosis and evaluation of curative effect at the gene level. This article reviews the research progress of 18F-FDG PET/CT radiogenomics in targeted diagnosis and treatment of NSCLC in recent years.

     

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