Institut für Pathologie, Charité Universitätsmedizin, Charitéplatz 1, 10117 Berlin, Germany.
Institut für Pathologie, Universitätsklinikum Heidelberg, Im Neuenheimer Feld 224, 69120 Heidelberg, Germany.
Lung Cancer. 2017 Jan;103:1-5. doi: 10.1016/j.lungcan.2016.11.008. Epub 2016 Nov 14.
The EML4-ALK pathway plays an important role in a significant subset of non-small cell lung cancer patients. Treatment options such as ALK tyrosine kinase inhibitors lead to improved progression free survival and overall survival. These therapeutic options are chosen on the basis of the identification of the underlying genetic signature of the EML-ALK translocation. Efficient and easily accessible testing tools are required to identify eligible patients in a timely fashion. While FISH techniques are commonly used to detect this translocation, the broad implementation of this type of ALK testing into routine diagnostics is not optimal due to technical, structural and financial reasons. Immunohistochemical techniques to screen for EML4-ALK translocations may therefore play an important role in the near future. This consensus paper provides recommendations for the test algorithm and quality of the respective test approaches, which are discussed in the light of the current literature.
EML4-ALK 通路在很大一部分非小细胞肺癌患者中起着重要作用。ALK 酪氨酸激酶抑制剂等治疗选择可改善无进展生存期和总生存期。这些治疗选择是基于确定 EML-ALK 易位的潜在遗传特征的基础上做出的。需要有效的且易于获得的检测工具,以便及时识别合格的患者。虽然荧光原位杂交 (FISH) 技术常用于检测这种易位,但由于技术、结构和财务原因,将这种类型的 ALK 检测广泛应用于常规诊断并不理想。免疫组织化学技术筛选 EML4-ALK 易位可能因此在不久的将来发挥重要作用。本共识文件提供了测试算法和各自测试方法的质量建议,这些建议是根据当前文献讨论的。