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非小细胞肺癌生物标志物检测的“何时”“何地”与“如何”。

What, When, and How of Biomarker Testing in Non-Small Cell Lung Cancer.

机构信息

Presented by Gregory L. Riely, MD, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.

出版信息

J Natl Compr Canc Netw. 2017 May;15(5S):686-688. doi: 10.6004/jnccn.2017.0073.

Abstract

Biomarker testing is recommended for all patients diagnosed with non-small cell lung cancer. At a minimum, testing should include the mutations/fusions , and the protein programmed death ligand-1 (PD-L1), because FDA-approved therapies are available for these alterations. Other actionable molecular findings include rearrangements, mutations, and exon 14 alterations. If adequate testing was not performed at treatment initiation, molecular testing should be performed before administration of subsequent lines of therapy. In patients with -mutant lung cancer, when resistance develops, physicians should seek to identify the T790M mutation using plasma and tissue assays, because osimertinib therapy is available for this mutation.

摘要

生物标志物检测推荐用于所有诊断为非小细胞肺癌的患者。至少应包括基因突变/融合和程序性死亡配体 1(PD-L1)蛋白检测,因为已有 FDA 批准的治疗方法适用于这些改变。其他可治疗的分子发现包括重排、突变和外显子 14 改变。如果在治疗开始时未进行充分的检测,则应在进行后续治疗线之前进行分子检测。在具有 -突变的肺癌患者中,当耐药性出现时,医生应使用血浆和组织检测来寻找 T790M 突变,因为奥希替尼治疗适用于这种突变。

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