Clinicopathological Features of Lung Adenocarcinoma With KRAS Mutations

被引:49
|
作者
Kakegawa, Seiichi [1 ]
Shimizu, Kimihiro [1 ]
Sugano, Masayuki [1 ]
Miyamae, Yohei [1 ]
Kaira, Kyoichi [2 ]
Araki, Takuya [3 ]
Nakano, Tetsuhiro [1 ]
Kamiyoshihara, Mitsuhiro [1 ]
Kawashima, Osamu [1 ]
Takeyoshi, Izumi [1 ]
机构
[1] Gunma Univ, Grad Sch Med, Dept Thorac & Visceral Organ Surg, Gunma 3718511, Japan
[2] Gunma Univ, Grad Sch Med, Dept Med & Mol Sci, Gunma 3718511, Japan
[3] Gunma Univ, Grad Sch Med, Dept Clin Pharmacol, Gunma 3718511, Japan
关键词
lung cancer; adenocarcinoma; KRAS mutation; mucinous bronchioloalveolar carcinoma; smoking history; GROWTH-FACTOR RECEPTOR; K-RAS GENE; SMART-AMPLIFICATION PROCESS; PROGNOSTIC-SIGNIFICANCE; NEVER SMOKERS; CANCER; GEFITINIB; EGFR; CARCINOMA; ONCOGENE;
D O I
10.1002/cncr.26010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND: KRAS and epidermal growth factor receptor (EGFR) mutations are thought to play an important role in the carcinogenesis of lung adenocarcinoma. However, clinicopathological findings of KRAS mutated adenocarcinoma cases have not yet been fully clarified. The authors analyzed the relationship between the KRAS mutation and corresponding clinicopathological findings, focusing on nonmucinous and mucinous bronchioloalveolar elements. METHODS: EGFR and KRAS mutations were detected in DNA samples extracted from 182 surgically resected tissues of lung adenocarcinomas by the Smart Amplification Process. The relations between gene mutation status and clinicopathological features were analyzed. All adenocarcinoma cases were divided into bronchioloalveolar carcinoma (BAC), adenocarcinoma with bronchioloalveolar features, and adenocarcinoma without BAC components (non-BAC). BAC/adenocarcinoma with bronchioloalveolar features tumors were further assessed for the presence of mucinous features. RESULTS: EGFR and KRAS mutations were found in 76 and 30 cases, respectively. In the KRAS mutant group, BAC/adenocarcinoma with bronchioloalveolar features was found in 22 cases, which included 10 nonmucinous and 12 mucinous tumors. Of 19 cases with mucinous BAC/adenocarcinoma with bronchioloalveolar features, KRAS mutations were detected in 12, but no EGFR mutation was detected. In the KRAS mutant group, BAC/adenocarcinoma with bronchioloalveolar features had significantly earlier pathological stages and more favorable prognoses than did non-BAC. Mucinous BAC/adenocarcinoma with bronchioloalveolar features showed less smoking history than did nonmucinous BAC/adenocarcinoma with bronchioloalveolar features and non-BAC. Furthermore, transversion type KRAS mutations were more common in non-BAC. CONCLUSIONS: KRAS mutated adenocarcinomas can be divided into BAC/adenocarcinoma with bronchioloalveolar features and non-BAC types. Non-BAC adenocarcinoma is related to smoking history and has a poor prognosis. BAC/adenocarcinoma with bronchioloalveolar features adenocarcinoma, however, has a more favorable prognosis, and mucinous BAC/adenocarcinoma with bronchioloalveolar features has little relationship to smoking history. Cancer 2011;117:4257-66. (C) 2011 American Cancer Society.
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收藏
页码:4257 / 4266
页数:10
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