Radiology Department, Zhongnan Hospital of Wuhan University, Wuhan University, Wuhan, China.
Pathology Department, Zhongnan Hospital of Wuhan University, Wuhan University, Wuhan, China.
Int J Clin Oncol. 2018 Apr;23(2):249-257. doi: 10.1007/s10147-017-1197-8. Epub 2017 Oct 7.
To analyse the differences in computed tomography (CT) features between patients with lung adenocarcinoma who have epidermal growth factor receptor (EGFR) mutations and those who have wild-type EGFR.
Patients with lung adenocarcinoma (n = 156) were enrolled from October 2013 to March 2016, including 56 patients with wild-type EGFR and 100 patients with EGFR mutations. Two independent radiologists evaluated patient characteristics and imaging features. Chi-squared test, Fisher's exact test or ANOVA was applied to discriminate clinical and CT characteristics between the genotypes. A prediction tool for EGFR mutation was devised from principal component analysis.
The proportion of females and non-smokers in the exon 19 deletion and exon 21 missense groups was higher than in the wild-type group (P < 0.01). Severe emphysema was higher in the wild-type group than in the exon 19 deletion group (P < 0.01). The maximum diameter in the mediastinal window (MaxD) in the wild-type group was longer than in the exon 19 deletion and exon 21 missense groups. The minimum diameter in the mediastinal window (MinD) in the wild-type group was also longer than in the exon 21 missense group, with a significant difference (P < 0.05). The tumor shadow disappearance rate (TDR) in the exon 19 deletion group was higher than in the wild-type group. Ground glass opacity (GGO) appeared to be more common in the exon 19 deletion group (P = 0.010). The prediction score for exon 19 deletion mutation was: 0.305 × gender + 0.254 × smoking history + 0.198 × MaxD + TDR × 0.254 + 0.280 × GGO + 0.095 × emphysema. The sensitivity and specificity for predicting exon 19 deletion were 59.09 and 76.79%, respectively. The prediction score for the exon 21 missense mutation was: 0.354 × gender + 0.291 × smoking history + 0.410 × MaxD + 0.408 × MinD. The sensitivity and specificity for predicting exon 21 missense mutation were 72.34 and 78.57%, respectively.
As well as gender, smoking history and GGO, adenocarcinomas with EGFR mutation were significantly associated with emphysema, TDR, and the diameter in the mediastinal window. As exon 19 deletion and 21 missense mutations might be predicted by those features, the scoring system might be valuable for clinical diagnosis.
分析表皮生长因子受体(EGFR)突变型和野生型肺腺癌患者 CT 特征的差异。
2013 年 10 月至 2016 年 3 月期间共纳入 156 例肺腺癌患者,包括 56 例 EGFR 野生型患者和 100 例 EGFR 突变型患者。两位独立的放射科医生评估了患者的特征和影像学特征。应用卡方检验、Fisher 确切概率法或方差分析来区分基因型之间的临床和 CT 特征。利用主成分分析建立了 EGFR 突变的预测工具。
与野生型组相比,外显子 19 缺失组和外显子 21 错义组中女性和不吸烟者的比例更高(P<0.01)。重度肺气肿在外显子 19 缺失组中较野生型组更为常见(P<0.01)。纵隔窗最大直径(MaxD)在野生型组中较外显子 19 缺失组和外显子 21 错义组更长。纵隔窗最小直径(MinD)在野生型组中也较外显子 21 错义组更长,差异有统计学意义(P<0.05)。外显子 19 缺失组的肿瘤阴影消失率(TDR)较高。在外显子 19 缺失组中,磨玻璃密度影(GGO)更为常见(P=0.010)。外显子 19 缺失突变的预测评分是:0.305×性别+0.254×吸烟史+0.198×MaxD+TDR×0.254+GGO×0.280+肺气肿×0.095。外显子 19 缺失的预测敏感性和特异性分别为 59.09%和 76.79%。外显子 21 错义突变的预测评分是:0.354×性别+0.291×吸烟史+0.410×MaxD+0.408×MinD。外显子 21 错义突变的预测敏感性和特异性分别为 72.34%和 78.57%。
除性别、吸烟史和 GGO 外,EGFR 突变型腺癌与肺气肿、TDR 和纵隔窗直径显著相关。由于外显子 19 缺失和 21 错义突变可能通过这些特征进行预测,评分系统可能对临床诊断有价值。