Detection of malignant epithelial cells in effusions using flow cytometric immunophenotyping: An analysis of 92 cases

We compared the efficiency of immunophenotyping using flow cytometry (FCM) and a combination of morphologic and immunocytochemical studies for detecting malignant cells in 92 effusions. Cytologic results were as follows: carcinoma cells, 43 specimens; benign, 42 specimens; suggestive of nonepithelia...

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Veröffentlicht in:American journal of clinical pathology 2002-07, Vol.118 (1), p.85-92
Hauptverfasser: DAVIDSON, Ben, HIEP PHUC DONG, BERNER, Aasmund, CHRISTENSEN, Jette, NIELSEN, Siren, JOHANSEN, Preben, BRYNE, Magne, ASSCHENFELDT, Pia, RISBERG, Bjørn
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container_title American journal of clinical pathology
container_volume 118
creator DAVIDSON, Ben
HIEP PHUC DONG
BERNER, Aasmund
CHRISTENSEN, Jette
NIELSEN, Siren
JOHANSEN, Preben
BRYNE, Magne
ASSCHENFELDT, Pia
RISBERG, Bjørn
description We compared the efficiency of immunophenotyping using flow cytometry (FCM) and a combination of morphologic and immunocytochemical studies for detecting malignant cells in 92 effusions. Cytologic results were as follows: carcinoma cells, 43 specimens; benign, 42 specimens; suggestive of nonepithelial malignancy, 7 specimens. After immunocytochemical analysis, 5 benign specimens were reclassified as malignant and 4 malignant epithelial specimens as benign. With FCM, cells positive for Ber-EP4, B 72.3, AH6, and HB-TN were detected in 28 to 36 (64%-82%) of 44 carcinomas but only 2 to 12 (5%-29%) of 41 benign specimens. Significant association was seen for coexpression. Ber-EP4 and AH6 were the most sensitive; Ber-EP4 was the most specific. The presence of cells positive for 3 of 4 markers strongly suggested malignancy (34/44 carcinoma specimens [77%]; 3/41 reactive specimens [7%]). The presence of cells positive for all 4 markers was diagnostic of malignancy (17/44 malignant specimens [39%]; 0/41 reactive effusions [0%]). FCM and immunocytochemical resultsfor Ber-EP4 expression showed excellent association. FCM is a powerful tool for diagnosing difficult effusions and can quantify coexpression of various markers in fresh specimens. By using established cellular markers coupled with biological markers, FCM also has great promise for experimental purposes.
doi_str_mv 10.1309/M877-QABM-D9GB-FJAX
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Cytologic results were as follows: carcinoma cells, 43 specimens; benign, 42 specimens; suggestive of nonepithelial malignancy, 7 specimens. After immunocytochemical analysis, 5 benign specimens were reclassified as malignant and 4 malignant epithelial specimens as benign. With FCM, cells positive for Ber-EP4, B 72.3, AH6, and HB-TN were detected in 28 to 36 (64%-82%) of 44 carcinomas but only 2 to 12 (5%-29%) of 41 benign specimens. Significant association was seen for coexpression. Ber-EP4 and AH6 were the most sensitive; Ber-EP4 was the most specific. The presence of cells positive for 3 of 4 markers strongly suggested malignancy (34/44 carcinoma specimens [77%]; 3/41 reactive specimens [7%]). The presence of cells positive for all 4 markers was diagnostic of malignancy (17/44 malignant specimens [39%]; 0/41 reactive effusions [0%]). FCM and immunocytochemical resultsfor Ber-EP4 expression showed excellent association. 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Cytologic results were as follows: carcinoma cells, 43 specimens; benign, 42 specimens; suggestive of nonepithelial malignancy, 7 specimens. After immunocytochemical analysis, 5 benign specimens were reclassified as malignant and 4 malignant epithelial specimens as benign. With FCM, cells positive for Ber-EP4, B 72.3, AH6, and HB-TN were detected in 28 to 36 (64%-82%) of 44 carcinomas but only 2 to 12 (5%-29%) of 41 benign specimens. Significant association was seen for coexpression. Ber-EP4 and AH6 were the most sensitive; Ber-EP4 was the most specific. The presence of cells positive for 3 of 4 markers strongly suggested malignancy (34/44 carcinoma specimens [77%]; 3/41 reactive specimens [7%]). The presence of cells positive for all 4 markers was diagnostic of malignancy (17/44 malignant specimens [39%]; 0/41 reactive effusions [0%]). FCM and immunocytochemical resultsfor Ber-EP4 expression showed excellent association. FCM is a powerful tool for diagnosing difficult effusions and can quantify coexpression of various markers in fresh specimens. By using established cellular markers coupled with biological markers, FCM also has great promise for experimental purposes.</description><subject>Antibodies, Monoclonal</subject><subject>Antibodies, Neoplasm - analysis</subject><subject>Antigens, Surface - analysis</subject><subject>Ascitic Fluid - chemistry</subject><subject>Ascitic Fluid - pathology</subject><subject>Biological and medical sciences</subject><subject>Biomarkers, Tumor - analysis</subject><subject>Carcinoma - chemistry</subject><subject>Carcinoma - pathology</subject><subject>Epithelium - metabolism</subject><subject>Epithelium - pathology</subject><subject>Female</subject><subject>Flow Cytometry - methods</subject><subject>Fluorescent Antibody Technique, Indirect</subject><subject>Humans</subject><subject>Immunophenotyping - methods</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Miscellaneous. Technology</subject><subject>Neoplasms - chemistry</subject><subject>Neoplasms - pathology</subject><subject>Pathology. Cytology. Biochemistry. Spectrometry. 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Technology</topic><topic>Neoplasms - chemistry</topic><topic>Neoplasms - pathology</topic><topic>Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques</topic><topic>Pleural Effusion, Malignant - chemistry</topic><topic>Pleural Effusion, Malignant - pathology</topic><topic>Reproducibility of Results</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>DAVIDSON, Ben</creatorcontrib><creatorcontrib>HIEP PHUC DONG</creatorcontrib><creatorcontrib>BERNER, Aasmund</creatorcontrib><creatorcontrib>CHRISTENSEN, Jette</creatorcontrib><creatorcontrib>NIELSEN, Siren</creatorcontrib><creatorcontrib>JOHANSEN, Preben</creatorcontrib><creatorcontrib>BRYNE, Magne</creatorcontrib><creatorcontrib>ASSCHENFELDT, Pia</creatorcontrib><creatorcontrib>RISBERG, Bjørn</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of clinical pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>DAVIDSON, Ben</au><au>HIEP PHUC DONG</au><au>BERNER, Aasmund</au><au>CHRISTENSEN, Jette</au><au>NIELSEN, Siren</au><au>JOHANSEN, Preben</au><au>BRYNE, Magne</au><au>ASSCHENFELDT, Pia</au><au>RISBERG, Bjørn</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Detection of malignant epithelial cells in effusions using flow cytometric immunophenotyping: An analysis of 92 cases</atitle><jtitle>American journal of clinical pathology</jtitle><addtitle>Am J Clin Pathol</addtitle><date>2002-07-01</date><risdate>2002</risdate><volume>118</volume><issue>1</issue><spage>85</spage><epage>92</epage><pages>85-92</pages><issn>0002-9173</issn><eissn>1943-7722</eissn><coden>AJCPAI</coden><abstract>We compared the efficiency of immunophenotyping using flow cytometry (FCM) and a combination of morphologic and immunocytochemical studies for detecting malignant cells in 92 effusions. Cytologic results were as follows: carcinoma cells, 43 specimens; benign, 42 specimens; suggestive of nonepithelial malignancy, 7 specimens. After immunocytochemical analysis, 5 benign specimens were reclassified as malignant and 4 malignant epithelial specimens as benign. With FCM, cells positive for Ber-EP4, B 72.3, AH6, and HB-TN were detected in 28 to 36 (64%-82%) of 44 carcinomas but only 2 to 12 (5%-29%) of 41 benign specimens. Significant association was seen for coexpression. Ber-EP4 and AH6 were the most sensitive; Ber-EP4 was the most specific. The presence of cells positive for 3 of 4 markers strongly suggested malignancy (34/44 carcinoma specimens [77%]; 3/41 reactive specimens [7%]). The presence of cells positive for all 4 markers was diagnostic of malignancy (17/44 malignant specimens [39%]; 0/41 reactive effusions [0%]). FCM and immunocytochemical resultsfor Ber-EP4 expression showed excellent association. FCM is a powerful tool for diagnosing difficult effusions and can quantify coexpression of various markers in fresh specimens. By using established cellular markers coupled with biological markers, FCM also has great promise for experimental purposes.</abstract><cop>Chicago, IL</cop><pub>American Society of Clinical Pathologists</pub><pmid>12109861</pmid><doi>10.1309/M877-QABM-D9GB-FJAX</doi><tpages>8</tpages></addata></record>
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subjects Antibodies, Monoclonal
Antibodies, Neoplasm - analysis
Antigens, Surface - analysis
Ascitic Fluid - chemistry
Ascitic Fluid - pathology
Biological and medical sciences
Biomarkers, Tumor - analysis
Carcinoma - chemistry
Carcinoma - pathology
Epithelium - metabolism
Epithelium - pathology
Female
Flow Cytometry - methods
Fluorescent Antibody Technique, Indirect
Humans
Immunophenotyping - methods
Investigative techniques, diagnostic techniques (general aspects)
Male
Medical sciences
Miscellaneous. Technology
Neoplasms - chemistry
Neoplasms - pathology
Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques
Pleural Effusion, Malignant - chemistry
Pleural Effusion, Malignant - pathology
Reproducibility of Results
title Detection of malignant epithelial cells in effusions using flow cytometric immunophenotyping: An analysis of 92 cases
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