Miao Yingying, Zhu Suhua, Li Huijuan, Zou Jiawei, Zhu Qingqing, Lv Tangfeng, Song Yong
Department of Respiratory Medicine, Jinling Hospital, Medical School of Nanjing University, Nanjing 210002, China.
Nanjing University Institute of Respiratory Medicine, Nanjing 210002, China.
J Thorac Dis. 2017 Oct;9(10):3927-3937. doi: 10.21037/jtd.2017.08.134.
Gene analysis could not be performed in all patients, especially in advanced non-small cell lung cancer (NSCLC). We aimed to find some clinical futures and CT or FDG-PET characteristics, which could be combined to help distinguish anaplastic lymphoma kinase () rearrangement form epidermal growth factor receptor () mutations in treatment naïve advanced lung adenocarcinoma of Chinese patients.
We retrospectively reviewed clinical and radiological characteristics of 145 patients with treatment naïve advanced lung adenocarcinoma. The one-way ANOVA, the Mann-Whitney test, chi-square test and logistic regression were used for comparison between patients with rearrangement and those with mutation.
Among 145 patients with advanced lung adenocarcinoma, only six patients had both rearrangement and mutation, the sample size was too small to analysis. Univariate analysis revealed that patients with rearrangement were younger (P=0.001) and with lower serum carcinoembryonic antigen (CEA) level (P=0.008) than those with mutation. More of tumors with rearrangement were well defined (P=0.023) and have bubble lucency (P=0.026) compared with those with mutation (P=0.026). Lymphadenopathy was seen more frequently in patients with rearrangement (P=0.167). Twenty-six patients received FDG-PET/CT, among this population, lesion standardized uptake values (SUV) >6.95 and lymph nodes SUV >6.25 were more often seen in rearrangement group (P=0.011, both). In multivariate analysis, patients younger than 50 years (RR =9.878, 95% CI: 2.318-42.090, P=0.002), with lower CEA level than 4.95 µg/L (RR =8.166, 95% CI: 1.085-31.983, P=0.003) and without brain metastasis (RR =7.304, 95% CI: 1.099-48.558, P=0.040) were more likely to be rearrangement than mutation. Tumor diameter less than 36 mm were prone to be mutation (RR =0.078, 95% CI: 0.017-0.356, P=0.001).
Treatment naïve advanced lung adenocarcinomas with rearrangement were more likely to have younger age, lower serum CEA level, larger tumor volume, well defined tumor border, and non-brain metastasis than those with mutation. Bubble lucency and higher FDG uptake of lesion and lymph nodes may help distinguish rearrangement from mutation in the absence of genetic analysis.
并非所有患者都能进行基因分析,尤其是晚期非小细胞肺癌(NSCLC)患者。我们旨在寻找一些临床特征以及CT或FDG-PET特征,将它们结合起来以帮助区分中国初治晚期肺腺癌患者中间变性淋巴瘤激酶(ALK)重排与表皮生长因子受体(EGFR)突变。
我们回顾性分析了145例初治晚期肺腺癌患者的临床和影像学特征。采用单因素方差分析、曼-惠特尼检验、卡方检验和逻辑回归对ALK重排患者和EGFR突变患者进行比较。
在145例晚期肺腺癌患者中,仅有6例患者同时存在ALK重排和EGFR突变,样本量过小无法进行分析。单因素分析显示,ALK重排患者比EGFR突变患者更年轻(P = 0.001),血清癌胚抗原(CEA)水平更低(P = 0.008)。与EGFR突变的肿瘤相比,ALK重排的肿瘤边界更清晰(P = 0.023)且有气泡样透亮区(P = 0.026)。ALK重排患者的淋巴结病更为常见(P = 0.167)。26例患者接受了FDG-PET/CT检查,在这组人群中,ALK重排组的病灶标准化摄取值(SUV)>6.95以及淋巴结SUV>6.25更为常见(均为P = 0.011)。多因素分析显示,年龄小于50岁(RR = 9.878,95%CI:2.318 - 42.090,P = 0.002)、CEA水平低于4.95μg/L(RR = 8.166,95%CI:1.085 - 31.983,P = 0.003)且无脑转移(RR = 7.304,95%CI:1.099 - 48.558,P = 0.040)的患者ALK重排比EGFR突变更常见。肿瘤直径小于36mm的患者更易发生EGFR突变(RR = 0.078,95%CI:0.017 - 0.356,P = 0.001)。
与EGFR突变的初治晚期肺腺癌相比,ALK重排的患者更可能年龄较轻、血清CEA水平较低、肿瘤体积较大、肿瘤边界清晰且无脑转移。在缺乏基因分析的情况下,气泡样透亮区以及病灶和淋巴结较高的FDG摄取可能有助于区分ALK重排与EGFR突变。