Screening of Anaplastic Lymphoma Kinase Rearrangement by Immunohistochemistry in Non-small Cell Lung Cancer Correlation with Fluorescence In Situ Hybridization

被引:235
作者
Paik, Jin Ho [1 ]
Choe, Gheeyoung [1 ]
Kim, Hyojin [1 ]
Choe, Ji-Young [1 ]
Lee, Hyun Ju [1 ]
Lee, Choon-Taek [2 ]
Lee, Jong Seok [2 ]
Jheon, Sanghoon [3 ]
Chung, Jin-Haeng [1 ]
机构
[1] Seoul Natl Univ, Bundang Hosp, Dept Pathol, Coll Med, Songnam 463707, Gyeunggi Do, South Korea
[2] Seoul Natl Univ, Bundang Hosp, Dept Internal Med, Coll Med, Songnam 463707, Gyeunggi Do, South Korea
[3] Seoul Natl Univ, Bundang Hosp, Dept Thorac Surg, Coll Med, Songnam 463707, Gyeunggi Do, South Korea
关键词
EML4-ALK; Non-small cell lung cancer; Immunohistochemistry; Fluorescence in situ hybridization; GROWTH-FACTOR-RECEPTOR; EML4-ALK FUSION GENE; ADENOCARCINOMA; MUTATIONS; FEATURES; RARE;
D O I
10.1097/JTO.0b013e31820b82e8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The use of a standard immunohistochemistry (IHC) assay to detect the anaplastic lymphoma kinase (ALK) protein in lung cancer is challenging. There are no universally accepted, evidence-based guidelines on identifying patients with ALK-rearranged lung cancer using IHC. Methods: We retrospectively reviewed 465 resected specimens of non-small cell lung cancer using a tissue microarray as a test set. ALK protein expression using IHC with 5A4 monoclonal antibody (Novocastra) and ALK gene rearrangement using fluorescence in situ hybridization (FISH) with dual-color break-apart probes (Abbott molecular) were examined. Immunoreactivity was scored as 0, 1, 2, or 3, and the results were compared with the FISH results. A diagnostic algorithm was derived from the correlation of the IHC and FISH results and applied to an additional 187 adenocarcinoma samples used as a validation set. Results: In the test set, ALK protein expression was detected in 40 patients (40/465, 8.6%), consisting of IHC scores of 1 (n = 14), 2 (n = 10), and 3 (n = 16), whereas 19 patients (19/453, 4.2%) were FISH-positive. All the FISH-positive patients were assigned IHC scores of 2 or 3. All the patients with ALK IHC scores of 3 were FISH-positive, those with scores of 0 or 1 were FISH-negative, and those with scores of 2 were FISH variable. In the validation set, ALK protein expression was detected in 14 patients (scores of 1, n = 2; scores of 2, n = 6; and scores of 3, n = 6), of which nine patients (9/187, 4.8%) were FISH-positive. All the patients with IHC scores of 0 or 1 were FISH-negative, and those with scores of 3 were FISH-positive. Among the patients with IHC scores of 2, three (3/6, 50%) were FISH-positive. Conclusions: The sensitivity and specificity of IHC was 100% and 95.8%, respectively. These data supported an IHC scoring algorithm in which ALK IHC scores of 0, 1, or 3 were highly compatible with FISH results, and IHC scores of 2 were variable. Based on these findings, the IHC assay using the 5A4 antibody reliably detected non-small cell lung cancer with ALK rearrangement and may be useful as a screening method to identify these tumors.
引用
收藏
页码:466 / 472
页数:7
相关论文
共 21 条
[1]  
[Anonymous], J CLIN ONCOL
[2]   Anaplastic lymphoma kinase immunoreactivity correlates with ALK gene rearrangement and transcriptional up-regulation in non-small cell lung carcinomas [J].
Boland, Jennifer M. ;
Erdogan, Sibel ;
Vasmatzis, George ;
Yang, Ping ;
Tillmans, Lori S. ;
Johnson, Michele R. Erickson ;
Wang, Xiaoke ;
Peterson, Lisa M. ;
Halling, Kevin C. ;
Oliveira, Andre M. ;
Aubry, Marie Christine ;
Yi, Eunhee S. .
HUMAN PATHOLOGY, 2009, 40 (08) :1152-1158
[3]  
Camidge DR, 2010, J THORAC ONCOL, V5, pS233
[4]   Epidermal Growth Factor Receptor Mutation and Pathologic-Radiologic Correlation Between Multiple Lung Nodules with Ground-Glass Opacity Differentiates Multicentric Origin from Intrapulmonary Spread [J].
Chung, Jin-Haeng ;
Choe, Gheeyoung ;
Jheon, Sanghoon ;
Sung, Sook-Whan ;
Kim, Tae Jung ;
Lee, Kyung Won ;
Lee, Jae Ho ;
Lee, Choon-Taek .
JOURNAL OF THORACIC ONCOLOGY, 2009, 4 (12) :1490-1495
[5]   Assessment of the HER2 status in breast cancer by fluorescence in situ hybridization:: a technical review with interpretive guidelines [J].
Hicks, DG ;
Tubbs, RR .
HUMAN PATHOLOGY, 2005, 36 (03) :250-261
[6]   EML4-ALK lung cancers are characterized by rare other mutations, a TTF-1 cell lineage, an acinar histology, and young onset [J].
Inamura, Kentaro ;
Takeuchi, Kengo ;
Togashi, Yuki ;
Hatano, Satoko ;
Ninomiya, Hironori ;
Motoi, Noriko ;
Mun, Ming-yon ;
Sakao, Yukinori ;
Okumura, Sakae ;
Nakagawa, Ken ;
Soda, Manabu ;
Choi, Young Lim ;
Mano, Hiroyuki ;
Ishikawa, Yuichi .
MODERN PATHOLOGY, 2009, 22 (04) :508-515
[7]   Annual report to the nation on the status of cancer, 1975-2001, with a special feature regarding survival [J].
Jemal, A ;
Clegg, LX ;
Ward, E ;
Ries, LAG ;
Wu, XC ;
Jamison, PM ;
Wingo, PA ;
Howe, HL ;
Anderson, RN ;
Edwards, BK .
CANCER, 2004, 101 (01) :3-27
[8]   Patterns of cancer incidence, mortality, and prevalence across five continents: Defining priorities to reduce cancer disparities in different geographic regions of the world [J].
Kamangar, Farin ;
Dores, Graca M. ;
Anderson, William F. .
JOURNAL OF CLINICAL ONCOLOGY, 2006, 24 (14) :2137-2150
[9]   Protein overexpression and gene amplification of epidermal growth factor receptor in nonsmall cell lung carcinomas: Comparison of four commercially available antibodies by immunohistochemistry and fluorescence in situ hybridization study [J].
Lee, Hyun Ju ;
Xu, Xianhua ;
Choe, Gheeyoung ;
Chung, Doo Hyun ;
Seo, Jeong-Wook ;
Lee, Jae Ho ;
Lee, Choon-Taek ;
Jheon, Sanghoon ;
Sung, Sook-Whan ;
Chung, Jin-Haeng .
LUNG CANCER, 2010, 68 (03) :375-382
[10]   EML4-ALK Rearrangement in Non-Small Cell Lung Cancer and Non-Tumor Lung Tissues [J].
Martelli, Maria Paola ;
Sozzi, Gabriella ;
Hernandez, Luis ;
Pettirossi, Valentina ;
Navarro, Alba ;
Conte, Davide ;
Gasparini, Patrizia ;
Perrone, Federica ;
Modena, Piergiorgio ;
Pastorino, Ugo ;
Carbone, Antonino ;
Fabbri, Alessandra ;
Sidoni, Angelo ;
Nakamura, Shigeo ;
Gambacorta, Marcello ;
Luis Fernandez, Pedro ;
Ramirez, Jose ;
Chan, John K. C. ;
Grigioni, Walter Franco ;
Campo, Elias ;
Pileri, Stefano A. ;
Falini, Brunangelo .
AMERICAN JOURNAL OF PATHOLOGY, 2009, 174 (02) :661-670