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Histopathological classification of lung cancer: relevance of cytokeratin and TTF-1 immunophenotyping

Johansson, Leif LU (2004) In Annals of Diagnostic Pathology 8(5). p.259-267
Abstract
istopathologic classification of lung carcinoma is important, as a prognostic factor and in the evaluation of treatment modalities. Although the World Health Organization classification of lung cancer is based on routine microscopy, immunohistochemistry is an important additional aspect in modern pathologic practice. This study examines whether the main histologic types of lung carcinomas are more reliably diagnosed with immunohistochemical technique using antibodies for the lung tissue-specific antigen thyroid transcription factor-1 (TTF-1) and a panel of cytokeratin (CK) antibodies. Forty-five cases of lung cancer (12 squamous cell carcinoma, 13 small cell carcinoma, 11 adenocarcinoma, 9 large cell carcinoma [LCC]/pleomorphic carcinoma)... (More)
istopathologic classification of lung carcinoma is important, as a prognostic factor and in the evaluation of treatment modalities. Although the World Health Organization classification of lung cancer is based on routine microscopy, immunohistochemistry is an important additional aspect in modern pathologic practice. This study examines whether the main histologic types of lung carcinomas are more reliably diagnosed with immunohistochemical technique using antibodies for the lung tissue-specific antigen thyroid transcription factor-1 (TTF-1) and a panel of cytokeratin (CK) antibodies. Forty-five cases of lung cancer (12 squamous cell carcinoma, 13 small cell carcinoma, 11 adenocarcinoma, 9 large cell carcinoma [LCC]/pleomorphic carcinoma) were stained with antibodies to CK CAM5.2, CK5, CK7, CK20, and TTF-1. All 45 cases were positive with CAM5.2, 16 of 45 cases with CK5, 34 of 45 cases with CK7, 4 of 45 cases with CK20, and 29 of 45 with TTF-1. Squamous cell carcinoma (epidermoid carcinoma) had the immunophenotype CK5+/TTF-1−, and at least 20% were also positive with CK7. Most nonepidermoid tumors had the “lung-specific” phenotype CK5−/TTF-1+; all small cell carcinomas had the phenotype CK5−/CK8+/TTF-1+, all adenocarcinomas CK5−/CK7+/TTF-1+ and (more than 50%) of LCC CK5−/CK7+/TTF-1+. Thus, more than 50% of LCCs were of the same phenotype as adenocarcinomas. The immunophenotypes of the main histologic types of lung carcinoma are stable and highly reproducible. However, because of considerable overlapping, immunophenotyping should not be used alone for histopathologic classification of lung cancer, but only as an adjunct to light microscopy. It is also suggested that CK5+ lung carcinomas with basaloid features should be regarded as variants of squamous cell carcinoma and not as LCC. (Less)
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author
organization
publishing date
type
Contribution to journal
publication status
published
subject
in
Annals of Diagnostic Pathology
volume
8
issue
5
pages
259 - 267
publisher
Elsevier
external identifiers
  • scopus:5644291814
ISSN
1532-8198
DOI
10.1016/j.anndiagpath.2004.07.001
language
English
LU publication?
yes
additional info
The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Pathology, (Lund) (013030000)
id
b7dce8df-dc31-44b5-899b-76c3c862792c (old id 1130188)
date added to LUP
2016-04-01 11:56:09
date last changed
2022-01-26 20:27:11
@article{b7dce8df-dc31-44b5-899b-76c3c862792c,
  abstract     = {{istopathologic classification of lung carcinoma is important, as a prognostic factor and in the evaluation of treatment modalities. Although the World Health Organization classification of lung cancer is based on routine microscopy, immunohistochemistry is an important additional aspect in modern pathologic practice. This study examines whether the main histologic types of lung carcinomas are more reliably diagnosed with immunohistochemical technique using antibodies for the lung tissue-specific antigen thyroid transcription factor-1 (TTF-1) and a panel of cytokeratin (CK) antibodies. Forty-five cases of lung cancer (12 squamous cell carcinoma, 13 small cell carcinoma, 11 adenocarcinoma, 9 large cell carcinoma [LCC]/pleomorphic carcinoma) were stained with antibodies to CK CAM5.2, CK5, CK7, CK20, and TTF-1. All 45 cases were positive with CAM5.2, 16 of 45 cases with CK5, 34 of 45 cases with CK7, 4 of 45 cases with CK20, and 29 of 45 with TTF-1. Squamous cell carcinoma (epidermoid carcinoma) had the immunophenotype CK5+/TTF-1−, and at least 20% were also positive with CK7. Most nonepidermoid tumors had the “lung-specific” phenotype CK5−/TTF-1+; all small cell carcinomas had the phenotype CK5−/CK8+/TTF-1+, all adenocarcinomas CK5−/CK7+/TTF-1+ and (more than 50%) of LCC CK5−/CK7+/TTF-1+. Thus, more than 50% of LCCs were of the same phenotype as adenocarcinomas. The immunophenotypes of the main histologic types of lung carcinoma are stable and highly reproducible. However, because of considerable overlapping, immunophenotyping should not be used alone for histopathologic classification of lung cancer, but only as an adjunct to light microscopy. It is also suggested that CK5+ lung carcinomas with basaloid features should be regarded as variants of squamous cell carcinoma and not as LCC.}},
  author       = {{Johansson, Leif}},
  issn         = {{1532-8198}},
  language     = {{eng}},
  number       = {{5}},
  pages        = {{259--267}},
  publisher    = {{Elsevier}},
  series       = {{Annals of Diagnostic Pathology}},
  title        = {{Histopathological classification of lung cancer: relevance of cytokeratin and TTF-1 immunophenotyping}},
  url          = {{http://dx.doi.org/10.1016/j.anndiagpath.2004.07.001}},
  doi          = {{10.1016/j.anndiagpath.2004.07.001}},
  volume       = {{8}},
  year         = {{2004}},
}