The utility of the proposed IASLC/ATS/ERS lung adenocarcinoma subtypes for disease prognosis and correlation of driver gene alterations

被引:223
作者
Tsuta, Koji [1 ,2 ]
Kawago, Mitsumasa [1 ,2 ,3 ]
Inoue, Eisuke [4 ]
Yoshida, Akihiko [1 ,2 ]
Takahashi, Fumiaki [4 ]
Sakurai, Hiroyuki [3 ]
Watanabe, Shun-ichi [3 ]
Takeuchi, Masahiro [4 ]
Furuta, Koh [1 ,2 ]
Asamura, Hisao [3 ]
Tsuda, Hitoshi [1 ,2 ]
机构
[1] Natl Canc Ctr, Div Pathol, Tokyo 1040045, Japan
[2] Natl Canc Ctr, Clin Lab Div, Tokyo 1040045, Japan
[3] Natl Canc Ctr, Div Thorac Surg, Tokyo 1040045, Japan
[4] Kitasato Univ, Sch Pharm, Dept Clin Med Biostat, Tokyo, Japan
关键词
IASLC classification; Adenocarcinoma of the lung; ALK; EGFR; KRAS;
D O I
10.1016/j.lungcan.2013.06.012
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: 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. Patients and Methods: 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. Results: 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. Conclusions: The new classification reflects disease prognosis, and was also associated with driver gene alterations. (C) 2013 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:371 / 376
页数:6
相关论文
共 43 条
[1]  
[Anonymous], 2009, International Association for the Study of Lung Cancer staging handbook in throracic oncology
[2]  
Borezuk AC, 2009, AM J SURG PATHOL, V33, P462, DOI 10.1097/PAS.0b013e318190157c
[3]  
Bosl GJ, 1977, CANC PRINCIPLES PRAC, P1397
[4]  
Brechot JM, 1996, CANCER-AM CANCER SOC, V78, P2111, DOI 10.1002/(SICI)1097-0142(19961115)78:10<2111::AID-CNCR11>3.3.CO
[5]  
2-N
[6]   Performance of reclassification statistics in comparing risk prediction models [J].
Cook, Nancy R. ;
Paynter, Nina P. .
BIOMETRICAL JOURNAL, 2011, 53 (02) :237-258
[7]   BRONCHOALVEOLAR CARCINOMA - FACTORS AFFECTING SURVIVAL [J].
DALY, RC ;
TRASTEK, VF ;
PAIROLERO, PC ;
MURTAUGH, PA ;
HUANG, MS ;
ALLEN, MS ;
COLBY, TV .
ANNALS OF THORACIC SURGERY, 1991, 51 (03) :368-377
[8]   Mucinous differentiation correlates with absence of EGFR mutation and presence of KRAS mutation in lung adenocarcinomas with bronchioloalveolar features [J].
Finberg, Karin E. ;
Sequist, Lecia V. ;
Joshi, Victoria A. ;
Muzikansky, Alona ;
Miller, Julie M. ;
Han, Moonjoo ;
Beheshti, Javad ;
Chirieac, Lucian R. ;
Mark, Eugene J. ;
Iafrate, A. John .
JOURNAL OF MOLECULAR DIAGNOSTICS, 2007, 9 (03) :320-326
[9]   Clinicopathology of stromal invasion in lung adenocarcinoma [J].
Fujita, Atsushi ;
Kameda, Yoichi ;
Goya, Tomoyuki .
PATHOLOGY INTERNATIONAL, 2009, 59 (01) :1-6
[10]   Lymphatic Vessel Invasion is a Significant Prognostic Indicator in Stage IA Lung Adenocarcinoma [J].
Funai, Kazuhito ;
Sugimura, Haruhiko ;
Morita, Toyohiko ;
Shundo, Yasumasa ;
Shimizu, Kei ;
Shiiya, Norihiko .
ANNALS OF SURGICAL ONCOLOGY, 2011, 18 (10) :2968-2972