Immunostaining with EGFR mutation-specific antibodies: a reliable screening method for lung adenocarcinomas harboring EGFR mutation in biopsy and resection samples

被引:25
作者
Fan, Xiangshan [1 ]
Liu, Biao [1 ]
Xu, Haodong [2 ]
Yu, Bo [1 ]
Shi, Shanshan [1 ]
Zhang, Jin [1 ]
Wang, Xuan [1 ]
Wang, Jiandong [1 ]
Lu, Zhenfeng [1 ]
Ma, Henghui [1 ]
Zhou, Xiaojun [1 ]
机构
[1] Nanjing Univ, Nanjing Jinling Hosp, Coll Med, Dept Pathol,Clin Sch, Nanjing 210008, Jiangsu, Peoples R China
[2] Univ Rochester, Med Ctr, Dept Pathol & Lab Med, Rochester, NY 14642 USA
基金
中国国家自然科学基金;
关键词
Lung adenocarcinoma; Biopsy; Resection; EGFR Mutation; Immunohistochemistry; Mutation-specific monoclonal antibody; EPIDERMAL-GROWTH-FACTOR; FACTOR-RECEPTOR GENE; IMMUNOHISTOCHEMICAL DETECTION; ADENOSQUAMOUS CARCINOMA; CANCER; GEFITINIB; ERLOTINIB; THERAPY;
D O I
10.1016/j.humpath.2012.12.002
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Mutation analysis of epidermal growth factor receptor (EGFR) is essential in determining the therapeutic strategy for lung adenocarcinoma. Immunohistochemical (IHC) staining with EGFR mutation-specific antibodies of del E746-A750 in exon 19 and L858R in exon 21 has been evaluated in resection specimens in a few studies but rarely in biopsy samples. A total of 169 cases (78 biopsies and 91 resected specimens) of lung adenocarcinoma with EGFR mutation status predefined by direct DNA sequencing were histologically examined, and IHC was performed using EGFR mutation-specific antibodies of del E746-A750 and L858R. The cases with positive results by IHC but negative results by direct DNA sequencing were examined by amplified refractory mutation system. Our results showed that the frequency of EGFR mutations for both E746-A750 deletion and L858R mutation was 38.5% (65/169) by DNA sequencing or amplified refractory mutation system and 34.3% (58/169) by IHC in lung adenocarcinomas. Based on molecular test results, the overall sensitivity, specificity, positive predictive value, and negative predictive value of IHC using these 2 antibodies in all (biopsy/resection) cases were 87.7% (80%/94.3%), 99.0% (97.9%/100%), 98.3% (96%/100%), and 92.8% (88.7%/96.6%), respectively. Lung adenocarcinomas with a predominant acinar, papillary, lepidic, or solid growth pattern more often harbor EGFR mutation of del E746-A750 or L858R. In conclusion, the immunostaining with EGFR del E746-A750 and L858R mutation antibodies is a reliable screening method with high specificity and sensitivity for identifying the EGFR mutation in both resected and biopsied lung adenocarcinomas. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:1499 / 1507
页数:9
相关论文
共 22 条
[1]   Assessment of EGFR Mutation Status in Lung Adenocarcinoma by Immunohistochemistry Using Antibodies Specific to the Two Major Forms of Mutant EGFR [J].
Brevet, Marie ;
Arcila, Maria ;
Ladanyi, Marc .
JOURNAL OF MOLECULAR DIAGNOSTICS, 2010, 12 (02) :169-176
[2]   A rapid and sensitive enzymatic method for epidermal growth factor receptor mutation screening [J].
Jänne, PA ;
Borras, AM ;
Kuang, YN ;
Rogers, AM ;
Joshi, VA ;
Liyanage, H ;
Lindeman, N ;
Lee, JC ;
Halmos, B ;
Maher, EA ;
Distel, RJ ;
Meyerson, M ;
Johnson, BE .
CLINICAL CANCER RESEARCH, 2006, 12 (03) :751-758
[3]   Identical epidermal growth factor receptor mutations in adenocarcinomatous and squamous cell carcinomatous components of adenosquamous carcinoma of the lung [J].
Kang, Shin Myung ;
Kang, Hyun Ju ;
Shin, Ju Hye ;
Kim, Hoguen ;
Shin, Dong Hwan ;
Kim, Se Kyu ;
Kim, Joo-Hang ;
Chung, Kyung Young ;
Kim, Sung Kyu ;
Chang, Joon .
CANCER, 2007, 109 (03) :581-587
[4]   Novel Epidermal Growth Factor Receptor Mutation-Specific Antibodies for Non-small Cell Lung Cancer Immunohistochemistry as a Possible Screening Method for Epidermal Growth Factor Receptor Mutations [J].
Kato, Yasufumi ;
Peled, Nir ;
Wynes, Murry W. ;
Yoshida, Koichi ;
Pardo, Marta ;
Mascaux, Celine ;
Ohira, Tatsuo ;
Tsuboi, Masahiro ;
Matsubayashi, Jun ;
Nagao, Toshitaka ;
Ikeda, Norihiko ;
Hirsch, Fred R. .
JOURNAL OF THORACIC ONCOLOGY, 2010, 5 (10) :1551-1558
[5]   Identification of non-small-cell lung cancer with activating EGFR mutations in malignant effusion and cerebrospinal fluid: Rapid and sensitive detection of exon 19 deletion E746-A750 and exon 21 L858R mutation by immunocytochemistry [J].
Kawahara, Akihiko ;
Azuma, Koichi ;
Sumi, Akiko ;
Taira, Tomoki ;
Nakashima, Kazutaka ;
Aikawa, Emiko ;
Abe, Hideyuki ;
Yamaguchi, Tomohiko ;
Takamori, Shinzo ;
Akiba, Jun ;
Kage, Masayoshi .
LUNG CANCER, 2011, 74 (01) :35-40
[6]   Molecular Diagnosis of Activating EGFR Mutations in Non-Small Cell Lung Cancer Using Mutation-Specific Antibodies for Immunohistochemical Analysis [J].
Kawahara, Akihiko ;
Yamamoto, Chizuko ;
Nakashima, Kazutaka ;
Azuma, Koichi ;
Hattori, Satoshi ;
Kashihara, Masaki ;
Aizawa, Hisamichi ;
Basaki, Yuji ;
Kuwano, Michihiko ;
Kage, Masayoshi ;
Mitsudomi, Tetsuya ;
Ono, Mayumi .
CLINICAL CANCER RESEARCH, 2010, 16 (12) :3163-3170
[7]   Immunohistochemical Detection of EGFR Mutation Using Mutation-Specific Antibodies in Lung Cancer [J].
Kitamura, Atsuko ;
Hosoda, Waki ;
Sasaki, Eiichi ;
Mitsudomi, Tetsuya ;
Yatabe, Yasushi .
CLINICAL CANCER RESEARCH, 2010, 16 (13) :3349-3355
[8]   Mutations of the epidermal growth factor receptor gene in lung cancer:: Biological and clinical implications [J].
Kosaka, T ;
Yatabe, Y ;
Endoh, H ;
Kuwano, H ;
Takahashi, T ;
Mitsudomi, T .
CANCER RESEARCH, 2004, 64 (24) :8919-8923
[9]   The usefulness of mutation-specific antibodies in detecting epidermal growth factor receptor mutations and in predicting response to tyrosine kinase inhibitor therapy in lung adenocarcinoma [J].
Kozu, Yoshiki ;
Tsuta, Koji ;
Kohno, Takashi ;
Sekine, Ikuo ;
Yoshida, Akihiko ;
Watanabe, Shunichi ;
Tamura, Tomohide ;
Yokota, Jun ;
Suzuki, Kenji ;
Asamura, Hisao ;
Furuta, Koh ;
Tsuda, Hitoshi .
LUNG CANCER, 2011, 73 (01) :45-50
[10]   Activating mutations in the epidermal growth factor receptor underlying responsiveness of non-small-cell lung cancer to gefitinib [J].
Lynch, TJ ;
Bell, DW ;
Sordella, R ;
Gurubhagavatula, S ;
Okimoto, RA ;
Brannigan, BW ;
Harris, PL ;
Haserlat, SM ;
Supko, JG ;
Haluska, FG ;
Louis, DN ;
Christiani, DC ;
Settleman, J ;
Haber, DA .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (21) :2129-2139