Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, China.
J Clin Oncol. 2010 Oct 20;28(30):4616-20. doi: 10.1200/JCO.2010.29.6038. Epub 2010 Sep 20.
To determine the proportion of lung adenocarcinomas from East Asian never-smokers who harbor known oncogenic driver mutations.
In this surgical series, 52 resected lung adenocarcinomas from never-smokers (< 100 cigarettes in a lifetime) at a single institution (Fudan University, Shanghai, China) were analyzed concurrently for mutations in EGFR, KRAS, NRAS, HRAS, HER2, BRAF, ALK, PIK3CA, TP53 and LKB1.
Forty-one tumors harbored EGFR mutations, three harbored EML4-ALK fusions, two harbored HER2 insertions, and one harbored a KRAS mutation. All mutations were mutually exclusive. Thus, 90% (47 of 52; 95% CI, 0.7896 to 0.9625) of lung adenocarcinomas from never-smokers were found to harbor well-known oncogenic mutations in just four genes. No BRAF, NRAS, HRAS, or LKB1 mutations were detected, while 15 had TP53 mutations. Four tumors contained PIK3CA mutations, always together with EGFR mutations.
To our knowledge, this study represents the first comprehensive and concurrent analysis of major recurrent oncogenic mutations found in a large cohort of lung adenocarcinomas from East Asian never-smokers. Since drugs are now available that target mutant EGFR, HER2, and ALK, respectively, this result indicates that prospective mutation testing in these patients should successfully assign a targeted therapy in the majority of cases.
确定东亚从不吸烟的肺腺癌患者中携带已知致癌驱动突变的比例。
在这项单中心(中国上海复旦大学)的外科系列研究中,对 52 例从不吸烟(一生中吸烟量<100 支)的肺腺癌患者的肿瘤标本同时进行 EGFR、KRAS、NRAS、HRAS、HER2、BRAF、ALK、PIK3CA、TP53 和 LKB1 基因突变分析。
41 例肿瘤存在 EGFR 突变,3 例存在 EML4-ALK 融合,2 例存在 HER2 插入,1 例存在 KRAS 突变。所有突变均相互排斥。因此,90%(47/52;95%CI,0.7896 至 0.9625)的从不吸烟肺腺癌患者存在已知的致癌基因突变,而这些突变仅存在于四个基因中。未检测到 BRAF、NRAS、HRAS 或 LKB1 突变,而 15 例存在 TP53 突变。有 4 例肿瘤存在 PIK3CA 突变,且总是与 EGFR 突变同时存在。
据我们所知,这项研究代表了对东亚从不吸烟的肺腺癌患者中大量肿瘤中发现的主要复发性致癌突变进行的首次全面、同时分析。由于现在有针对突变型 EGFR、HER2 和 ALK 的药物,因此这一结果表明,在这些患者中进行前瞻性突变检测应该能够成功为大多数患者分配靶向治疗。