Division of Pathology and Clinical Laboratory Division, National Cancer Center Hospital, Tokyo, Japan.
Division of Pathology and Clinical Laboratory Division, National Cancer Center Hospital, Tokyo, Japan; Division of Thoracic Surgery, National Cancer Center Hospital, Tokyo, Japan.
Lung Cancer. 2013 Sep;81(3):371-376. doi: 10.1016/j.lungcan.2013.06.012. Epub 2013 Jul 26.
The present study aimed to determine the ability of the revised International Association for the Study of Lung Cancer (IASLC)/American Thoracic Society (ATS)/European Respiratory Society (ERS) classification of lung adenocarcinoma to predict patient survivals and driver gene alterations.
A reclassification of 904 surgically resected adenocarcinomas was performed. The results were statistically analyzed to examine the correlation between the classification and overall survival (OS) using Cox regression analyses, and integrated discrimination improvement (IDI) analyses.
The 5-year OS rates for adenocarcinomas in situ (AIS) or minimally invasive adenocarcinoma (MIA) were 98%. Five-year OS rates of Lepidic-, acinar-, papillary-, micropapillary-, and solid-predominant adenocarcinomas was 93%, 67%, 74%, 62%, and 58%, respectively. The IDI estimates revealed that classification of ADC into the 7 subgroups had a higher estimated (0.0175) than did the combined histological grouping (AIS + MIA, lepidic + acinar + papillary, micropapillary + solid + others) (0.0111). Epidermal growth factor receptor mutations, KRAS gene mutations, and anaplastic lymphoma kinase gene alterations were statistically prevalent in papillary-predominant (P = 0.00001), invasive mucinous (P = 0.00001), and micropapillary- and acinar-predominant (P = 0.00001) adenocarcinomas, respectively.
The new classification reflects disease prognosis, and was also associated with driver gene alterations.
本研究旨在确定修订后的国际肺癌研究协会(IASLC)/美国胸科学会(ATS)/欧洲呼吸学会(ERS)肺腺癌分类法预测患者生存和驱动基因改变的能力。
对 904 例手术切除的腺癌进行了重新分类。使用 Cox 回归分析和综合判别改善(IDI)分析对结果进行了统计学分析,以检查分类与总生存期(OS)之间的相关性。
原位腺癌(AIS)或微浸润性腺癌(MIA)的 5 年 OS 率为 98%。Lepidic、acinar、papillary、micropapillary 和 solid 为主的腺癌的 5 年 OS 率分别为 93%、67%、74%、62%和 58%。IDI 估计表明,将 ADC 分为 7 个亚组的估计值(0.0175)高于组合组织学分组(AIS+MIA、lepidic+acinar+papillary、micropapillary+solid+其他)(0.0111)。表皮生长因子受体突变、KRAS 基因突变和间变性淋巴瘤激酶基因改变在以乳头状为主的腺癌(P=0.00001)、侵袭性黏液腺癌(P=0.00001)和以微乳头状和腺泡状为主的腺癌(P=0.00001)中均有统计学意义。
新分类反映了疾病的预后,并且与驱动基因改变有关。