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 imaging genomics in targeted diagnosis and treatment of non-small cell lung cancer

  • 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)占80%~85%,随着对基因组学的深入研究,现已证实NSCLC的发生发展主要是由携带致癌基因的体细胞的突变驱动。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,其与临床参数及人工智能方法的进一步结合可提高预测准确率。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、疗效评估的重要方法。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 80%−85%. With the deepening of genomics research, it has been confirmed that the occurrence and development of NSCLC are mainly driven by somatic cell mutations in oncogenes. Compared with chemotherapy, targeted treatment of NSCLC can effectively prolong the progression-free survival and overall survival time of patients with targeted oncogene mutation. 18F-fluorodeoxyglucose (FDG) PET/CT imaging genomics for predicting the mutation status of epidermal growth factor receptor (EGFR), Kirsten rat sarcoma viral oncogene homolog, anaplastic lymphoma kinase, Kelch-like ECH-associated protein 1, nuclear factor erythroid 2-related factor 2, and for evaluating the prognosis of EGFR-tyrosine kinase inhibitor related targeted treatment in patients with NSCLC, have become research hotspots. Further combination with clinical parameters and artificial intelligence methods can improve the 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. The authors reviewed the research progress of 18F-FDG PET/CT radiogenomics in targeted diagnosis and treatment of NSCLC in recent years.

     

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