[Clinical Advanced in Early-stage ALK-positive Non-small Cell Lung Cancer Patients]

Zhongguo Fei Ai Za Zhi. 2017 Feb 20;20(2):124-129. doi: 10.3779/j.issn.1009-3419.2017.02.07.
[Article in Chinese]

Abstract

Lung cancer is the leading cause of cancer death in China. Non-small cell lung cancer (NSCLC) accounts for 85% of lung cancer cases, with the majority of the cases diagnosed at the advanced stage. Molecular targeted therapy is becoming the focus attention for advanced NSCLC. Echinoderm microtubule-associated protein-like 4 gene and the anaplastic lymphoma kinase gene (EML4-ALK) is among the most common molecular targets of NSCLC; its specific small-molecule tyrosine kinase inhibitors (TKIs) are approved for use in advanced NSCLC cases of ALK-positive. However, the influence of EML4-ALK fusion gene on the outcome of early-stage NSCLC cases and the necessity of application of TKIs for early-stage ALK-positive NSCLC patients are still uncertain. In this paper, we summarized the progression of testing methods for ALK-positive NSCLC patients as well as clinicopathological implication, outcome, and necessity of application of TKIs for early-stage ALK-positive NSCLC patients.

肺癌是我国癌症死亡最主要的原因。其中非小细胞肺癌(non-small cell lung cancer, NSCLC)占肺癌患者的85%,且大部分患者初诊时即为晚期。针对晚期NSCLC患者,分子靶向治疗成为人们关注的热点。棘皮动物微管相关蛋白-间变淋巴瘤激酶(echinoderm microtubule-associated protein-like 4 gene and the anaplastic lymphoma kinase gene, EML4-ALK)是NSCLC最常见的分子靶点之一,其特异性的小分子酪氨酸激酶抑制剂(tyrosine kinase inhibitors, TKIs)已被批准应用于ALK阳性晚期NSCLC患者的治疗。然而,ALK融合基因对早期NSCLC患者预后的影响,以及ALK阳性的早期NSCLC患者应用TKIs的必要性等问题尚不明确。本文主要围绕ALK阳性NSCLC患者的检测进展,早期ALK阳性NSCLC患者的临床病理特征、预后、ALK-TKIs应用必要性等情况做一简要综述。.

Publication types

  • Review

MeSH terms

  • Anaplastic Lymphoma Kinase
  • Carcinoma, Non-Small-Cell Lung / diagnosis
  • Carcinoma, Non-Small-Cell Lung / enzymology*
  • Carcinoma, Non-Small-Cell Lung / genetics
  • Carcinoma, Non-Small-Cell Lung / pathology*
  • Gene Fusion
  • Humans
  • Lung Neoplasms / diagnosis
  • Lung Neoplasms / enzymology*
  • Lung Neoplasms / genetics
  • Lung Neoplasms / pathology*
  • Neoplasm Staging
  • Prognosis
  • Receptor Protein-Tyrosine Kinases / genetics
  • Receptor Protein-Tyrosine Kinases / metabolism*

Substances

  • ALK protein, human
  • Anaplastic Lymphoma Kinase
  • Receptor Protein-Tyrosine Kinases

Grants and funding

本文受国家自然科学基金面上项目(No.81372467)资助