Improvement of the cytological diagnostic accuracy of follicular thyroid lesions by the use of the Ki-67 proliferative index in addition to cytokeratin-19 and HBME-1 immunomarkers: a study of 61 cases of liquid-based FNA cytology with histological controls

Objectives To evaluate HBME‐1, cytokeratin‐19 (CK‐19) and Ki‐67 immunomarkers in order to increase the diagnostic accuracy of preoperative thyroid fine needle aspiration (FNA) cytology. Methods Immunocytochemistry against HBME‐1, CK‐19 and Ki‐67 was performed on 123 thyroid FNAs processed by liquid‐...

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Veröffentlicht in:Cytopathology (Oxford) 2014-06, Vol.25 (3), p.160-169
Hauptverfasser: Lacoste-Collin, L., d'Aure, D., Bérard, E., Rouquette, I., Delisle, M. B., Courtade-Saïdi, M.
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container_issue 3
container_start_page 160
container_title Cytopathology (Oxford)
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creator Lacoste-Collin, L.
d'Aure, D.
Bérard, E.
Rouquette, I.
Delisle, M. B.
Courtade-Saïdi, M.
description Objectives To evaluate HBME‐1, cytokeratin‐19 (CK‐19) and Ki‐67 immunomarkers in order to increase the diagnostic accuracy of preoperative thyroid fine needle aspiration (FNA) cytology. Methods Immunocytochemistry against HBME‐1, CK‐19 and Ki‐67 was performed on 123 thyroid FNAs processed by liquid‐based cytology (LBC). Statistical analysis was carried out on 61 cases with histological control and sufficient material for one or more of the three markers. The Bethesda System was used for cytological diagnosis. Results Taking into account all the cytological categories, with a cut‐off of 30% of positive cells, HBME‐1 (n = 47) and CK‐19 (n = 53) showed a sensitivity for malignancy of 66.7% (95% confidence interval, 53.2–80.1) and 90.5% (82.6–98.4) and a specificity of 90.6% (82.3–99) and 75% (63.3–86.7), respectively. For Ki‐67 (n = 54) with a cut‐off of 1% of positive cells, the sensitivity was 85.0% (75.5–94.5) and the specificity 70.6% (58.4–82.7). In the follicular neoplasm/suspicious for follicular neoplasm (FN/SFN) category (n = 37), which was the focus of the study, papillary thyroid carcinomas (PTCs) were less numerous (four cases, three of which were the follicular variant), the positivity of the three immunomarkers combined showed an overall accuracy of 91% (21/23). The mean percentage of Ki‐67‐positive cells was increased in malignant lesions, with the exception of follicular variant PTCs: 16% ± 15.6% in two follicular carcinomas, 4.8% ± 3.2% in 13 classical PTCs, 1% ± 1.2% in five follicular variant PTCs and 0.5% ± 1.9% in 34 non‐malignant lesions. Conclusions Immunocytochemistry using HBME‐1, CK‐19 and the Ki‐67 proliferative index increased the diagnostic accuracy of FNA in the FN/SFN category of the Bethesda System, which may help to distinguish lesions in this category with a low or high risk of malignancy. Thus, clinical management would be improved.
doi_str_mv 10.1111/cyt.12128
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B. ; Courtade-Saïdi, M.</creator><creatorcontrib>Lacoste-Collin, L. ; d'Aure, D. ; Bérard, E. ; Rouquette, I. ; Delisle, M. B. ; Courtade-Saïdi, M.</creatorcontrib><description>Objectives To evaluate HBME‐1, cytokeratin‐19 (CK‐19) and Ki‐67 immunomarkers in order to increase the diagnostic accuracy of preoperative thyroid fine needle aspiration (FNA) cytology. Methods Immunocytochemistry against HBME‐1, CK‐19 and Ki‐67 was performed on 123 thyroid FNAs processed by liquid‐based cytology (LBC). Statistical analysis was carried out on 61 cases with histological control and sufficient material for one or more of the three markers. The Bethesda System was used for cytological diagnosis. Results Taking into account all the cytological categories, with a cut‐off of 30% of positive cells, HBME‐1 (n = 47) and CK‐19 (n = 53) showed a sensitivity for malignancy of 66.7% (95% confidence interval, 53.2–80.1) and 90.5% (82.6–98.4) and a specificity of 90.6% (82.3–99) and 75% (63.3–86.7), respectively. For Ki‐67 (n = 54) with a cut‐off of 1% of positive cells, the sensitivity was 85.0% (75.5–94.5) and the specificity 70.6% (58.4–82.7). In the follicular neoplasm/suspicious for follicular neoplasm (FN/SFN) category (n = 37), which was the focus of the study, papillary thyroid carcinomas (PTCs) were less numerous (four cases, three of which were the follicular variant), the positivity of the three immunomarkers combined showed an overall accuracy of 91% (21/23). The mean percentage of Ki‐67‐positive cells was increased in malignant lesions, with the exception of follicular variant PTCs: 16% ± 15.6% in two follicular carcinomas, 4.8% ± 3.2% in 13 classical PTCs, 1% ± 1.2% in five follicular variant PTCs and 0.5% ± 1.9% in 34 non‐malignant lesions. Conclusions Immunocytochemistry using HBME‐1, CK‐19 and the Ki‐67 proliferative index increased the diagnostic accuracy of FNA in the FN/SFN category of the Bethesda System, which may help to distinguish lesions in this category with a low or high risk of malignancy. Thus, clinical management would be improved.</description><identifier>ISSN: 0956-5507</identifier><identifier>EISSN: 1365-2303</identifier><identifier>DOI: 10.1111/cyt.12128</identifier><identifier>PMID: 24460983</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Adenocarcinoma, Follicular - diagnosis ; Adenocarcinoma, Follicular - genetics ; Adenocarcinoma, Follicular - pathology ; Biomarkers, Tumor - biosynthesis ; Biomarkers, Tumor - isolation &amp; purification ; Biopsy, Fine-Needle ; Carcinoma - diagnosis ; Carcinoma - genetics ; Carcinoma - pathology ; Carcinoma, Papillary ; Cell Proliferation - genetics ; Cytodiagnosis ; cytokeratin-19 ; fine needle aspiration ; fine needle aspiration, FNA cytology ; FNA cytology ; follicular neoplasms ; HBME-1 ; Humans ; Keratin-19 - biosynthesis ; Keratin-19 - isolation &amp; purification ; Ki-67 ; Ki-67 Antigen - biosynthesis ; Ki-67 Antigen - isolation &amp; purification ; risk of malignancy ; thyroid ; Thyroid Cancer, Papillary ; Thyroid Neoplasms - diagnosis ; Thyroid Neoplasms - genetics ; Thyroid Neoplasms - pathology ; Thyroid Nodule - pathology</subject><ispartof>Cytopathology (Oxford), 2014-06, Vol.25 (3), p.160-169</ispartof><rights>2014 John Wiley &amp; Sons Ltd</rights><rights>2014 John Wiley &amp; Sons Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fcyt.12128$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fcyt.12128$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24460983$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lacoste-Collin, L.</creatorcontrib><creatorcontrib>d'Aure, D.</creatorcontrib><creatorcontrib>Bérard, E.</creatorcontrib><creatorcontrib>Rouquette, I.</creatorcontrib><creatorcontrib>Delisle, M. B.</creatorcontrib><creatorcontrib>Courtade-Saïdi, M.</creatorcontrib><title>Improvement of the cytological diagnostic accuracy of follicular thyroid lesions by the use of the Ki-67 proliferative index in addition to cytokeratin-19 and HBME-1 immunomarkers: a study of 61 cases of liquid-based FNA cytology with histological controls</title><title>Cytopathology (Oxford)</title><addtitle>Cytopathology</addtitle><description>Objectives To evaluate HBME‐1, cytokeratin‐19 (CK‐19) and Ki‐67 immunomarkers in order to increase the diagnostic accuracy of preoperative thyroid fine needle aspiration (FNA) cytology. Methods Immunocytochemistry against HBME‐1, CK‐19 and Ki‐67 was performed on 123 thyroid FNAs processed by liquid‐based cytology (LBC). Statistical analysis was carried out on 61 cases with histological control and sufficient material for one or more of the three markers. The Bethesda System was used for cytological diagnosis. Results Taking into account all the cytological categories, with a cut‐off of 30% of positive cells, HBME‐1 (n = 47) and CK‐19 (n = 53) showed a sensitivity for malignancy of 66.7% (95% confidence interval, 53.2–80.1) and 90.5% (82.6–98.4) and a specificity of 90.6% (82.3–99) and 75% (63.3–86.7), respectively. For Ki‐67 (n = 54) with a cut‐off of 1% of positive cells, the sensitivity was 85.0% (75.5–94.5) and the specificity 70.6% (58.4–82.7). In the follicular neoplasm/suspicious for follicular neoplasm (FN/SFN) category (n = 37), which was the focus of the study, papillary thyroid carcinomas (PTCs) were less numerous (four cases, three of which were the follicular variant), the positivity of the three immunomarkers combined showed an overall accuracy of 91% (21/23). The mean percentage of Ki‐67‐positive cells was increased in malignant lesions, with the exception of follicular variant PTCs: 16% ± 15.6% in two follicular carcinomas, 4.8% ± 3.2% in 13 classical PTCs, 1% ± 1.2% in five follicular variant PTCs and 0.5% ± 1.9% in 34 non‐malignant lesions. Conclusions Immunocytochemistry using HBME‐1, CK‐19 and the Ki‐67 proliferative index increased the diagnostic accuracy of FNA in the FN/SFN category of the Bethesda System, which may help to distinguish lesions in this category with a low or high risk of malignancy. Thus, clinical management would be improved.</description><subject>Adenocarcinoma, Follicular - diagnosis</subject><subject>Adenocarcinoma, Follicular - genetics</subject><subject>Adenocarcinoma, Follicular - pathology</subject><subject>Biomarkers, Tumor - biosynthesis</subject><subject>Biomarkers, Tumor - isolation &amp; purification</subject><subject>Biopsy, Fine-Needle</subject><subject>Carcinoma - diagnosis</subject><subject>Carcinoma - genetics</subject><subject>Carcinoma - pathology</subject><subject>Carcinoma, Papillary</subject><subject>Cell Proliferation - genetics</subject><subject>Cytodiagnosis</subject><subject>cytokeratin-19</subject><subject>fine needle aspiration</subject><subject>fine needle aspiration, FNA cytology</subject><subject>FNA cytology</subject><subject>follicular neoplasms</subject><subject>HBME-1</subject><subject>Humans</subject><subject>Keratin-19 - biosynthesis</subject><subject>Keratin-19 - isolation &amp; purification</subject><subject>Ki-67</subject><subject>Ki-67 Antigen - biosynthesis</subject><subject>Ki-67 Antigen - isolation &amp; purification</subject><subject>risk of malignancy</subject><subject>thyroid</subject><subject>Thyroid Cancer, Papillary</subject><subject>Thyroid Neoplasms - diagnosis</subject><subject>Thyroid Neoplasms - genetics</subject><subject>Thyroid Neoplasms - pathology</subject><subject>Thyroid Nodule - pathology</subject><issn>0956-5507</issn><issn>1365-2303</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFUk1zFCEQRUvLrNGDf8Di6GUSPubTW7KVbFLGeFnLjwvFQJNFmSEZmCTz72Vns5EDNNXvve7XgNAHSo5oWsdqikeUUVa_RAvKyyJjnPBXaEGaosyKglQH6G0IfwihrGH8DTpgeV6SpuaLF-iyux38PXTQR-wNjhvASc47f2OVdFhbedP7EK3CUqlxkGrawox3zqrRySExpsFbjR0E6_uA22kWGQPs9b7YrKxwKuOsgUFGew_Y9hoe046l1jYmIo5-Lvx3RvQZbbDsNb44_XqWUWy7bux9J4eUDp-xxCGOeu6kpFjJAGEbO3s3Wp216a7x-fXJ3smEH2zc4I0N_40p38fUUXiHXhvpArx_Og_R9_Oz9fIiu_q2ulyeXGWW1U2daVPSqgKgTWMaUgKrlAbDlCGM6VZLqbjhuZSs1qrljEnOWqOqvIBGad4afog-7XTTHO5GCFF0NihwTvbgxyBowcqKc8ryBP34BB3bDrS4HWxyPon9qyXA8Q7wYB1Mz3lKxPY7iORazN9BLH-t5yAxsh0jjQAenxlpniJVrQrx43olfv_MV4SuK3HK_wG1GLv-</recordid><startdate>201406</startdate><enddate>201406</enddate><creator>Lacoste-Collin, L.</creator><creator>d'Aure, D.</creator><creator>Bérard, E.</creator><creator>Rouquette, I.</creator><creator>Delisle, M. B.</creator><creator>Courtade-Saïdi, M.</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>201406</creationdate><title>Improvement of the cytological diagnostic accuracy of follicular thyroid lesions by the use of the Ki-67 proliferative index in addition to cytokeratin-19 and HBME-1 immunomarkers: a study of 61 cases of liquid-based FNA cytology with histological controls</title><author>Lacoste-Collin, L. ; d'Aure, D. ; Bérard, E. ; Rouquette, I. ; Delisle, M. B. ; Courtade-Saïdi, M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i2898-df6177ee199f906e27cdef2cf022dbdaac3f34aa28dcb322a32bfc745e9cd3bf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adenocarcinoma, Follicular - diagnosis</topic><topic>Adenocarcinoma, Follicular - genetics</topic><topic>Adenocarcinoma, Follicular - pathology</topic><topic>Biomarkers, Tumor - biosynthesis</topic><topic>Biomarkers, Tumor - isolation &amp; purification</topic><topic>Biopsy, Fine-Needle</topic><topic>Carcinoma - diagnosis</topic><topic>Carcinoma - genetics</topic><topic>Carcinoma - pathology</topic><topic>Carcinoma, Papillary</topic><topic>Cell Proliferation - genetics</topic><topic>Cytodiagnosis</topic><topic>cytokeratin-19</topic><topic>fine needle aspiration</topic><topic>fine needle aspiration, FNA cytology</topic><topic>FNA cytology</topic><topic>follicular neoplasms</topic><topic>HBME-1</topic><topic>Humans</topic><topic>Keratin-19 - biosynthesis</topic><topic>Keratin-19 - isolation &amp; purification</topic><topic>Ki-67</topic><topic>Ki-67 Antigen - biosynthesis</topic><topic>Ki-67 Antigen - isolation &amp; purification</topic><topic>risk of malignancy</topic><topic>thyroid</topic><topic>Thyroid Cancer, Papillary</topic><topic>Thyroid Neoplasms - diagnosis</topic><topic>Thyroid Neoplasms - genetics</topic><topic>Thyroid Neoplasms - pathology</topic><topic>Thyroid Nodule - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lacoste-Collin, L.</creatorcontrib><creatorcontrib>d'Aure, D.</creatorcontrib><creatorcontrib>Bérard, E.</creatorcontrib><creatorcontrib>Rouquette, I.</creatorcontrib><creatorcontrib>Delisle, M. B.</creatorcontrib><creatorcontrib>Courtade-Saïdi, M.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Cytopathology (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lacoste-Collin, L.</au><au>d'Aure, D.</au><au>Bérard, E.</au><au>Rouquette, I.</au><au>Delisle, M. B.</au><au>Courtade-Saïdi, M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Improvement of the cytological diagnostic accuracy of follicular thyroid lesions by the use of the Ki-67 proliferative index in addition to cytokeratin-19 and HBME-1 immunomarkers: a study of 61 cases of liquid-based FNA cytology with histological controls</atitle><jtitle>Cytopathology (Oxford)</jtitle><addtitle>Cytopathology</addtitle><date>2014-06</date><risdate>2014</risdate><volume>25</volume><issue>3</issue><spage>160</spage><epage>169</epage><pages>160-169</pages><issn>0956-5507</issn><eissn>1365-2303</eissn><abstract>Objectives To evaluate HBME‐1, cytokeratin‐19 (CK‐19) and Ki‐67 immunomarkers in order to increase the diagnostic accuracy of preoperative thyroid fine needle aspiration (FNA) cytology. Methods Immunocytochemistry against HBME‐1, CK‐19 and Ki‐67 was performed on 123 thyroid FNAs processed by liquid‐based cytology (LBC). Statistical analysis was carried out on 61 cases with histological control and sufficient material for one or more of the three markers. The Bethesda System was used for cytological diagnosis. Results Taking into account all the cytological categories, with a cut‐off of 30% of positive cells, HBME‐1 (n = 47) and CK‐19 (n = 53) showed a sensitivity for malignancy of 66.7% (95% confidence interval, 53.2–80.1) and 90.5% (82.6–98.4) and a specificity of 90.6% (82.3–99) and 75% (63.3–86.7), respectively. For Ki‐67 (n = 54) with a cut‐off of 1% of positive cells, the sensitivity was 85.0% (75.5–94.5) and the specificity 70.6% (58.4–82.7). In the follicular neoplasm/suspicious for follicular neoplasm (FN/SFN) category (n = 37), which was the focus of the study, papillary thyroid carcinomas (PTCs) were less numerous (four cases, three of which were the follicular variant), the positivity of the three immunomarkers combined showed an overall accuracy of 91% (21/23). The mean percentage of Ki‐67‐positive cells was increased in malignant lesions, with the exception of follicular variant PTCs: 16% ± 15.6% in two follicular carcinomas, 4.8% ± 3.2% in 13 classical PTCs, 1% ± 1.2% in five follicular variant PTCs and 0.5% ± 1.9% in 34 non‐malignant lesions. Conclusions Immunocytochemistry using HBME‐1, CK‐19 and the Ki‐67 proliferative index increased the diagnostic accuracy of FNA in the FN/SFN category of the Bethesda System, which may help to distinguish lesions in this category with a low or high risk of malignancy. Thus, clinical management would be improved.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>24460983</pmid><doi>10.1111/cyt.12128</doi><tpages>10</tpages></addata></record>
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subjects Adenocarcinoma, Follicular - diagnosis
Adenocarcinoma, Follicular - genetics
Adenocarcinoma, Follicular - pathology
Biomarkers, Tumor - biosynthesis
Biomarkers, Tumor - isolation & purification
Biopsy, Fine-Needle
Carcinoma - diagnosis
Carcinoma - genetics
Carcinoma - pathology
Carcinoma, Papillary
Cell Proliferation - genetics
Cytodiagnosis
cytokeratin-19
fine needle aspiration
fine needle aspiration, FNA cytology
FNA cytology
follicular neoplasms
HBME-1
Humans
Keratin-19 - biosynthesis
Keratin-19 - isolation & purification
Ki-67
Ki-67 Antigen - biosynthesis
Ki-67 Antigen - isolation & purification
risk of malignancy
thyroid
Thyroid Cancer, Papillary
Thyroid Neoplasms - diagnosis
Thyroid Neoplasms - genetics
Thyroid Neoplasms - pathology
Thyroid Nodule - pathology
title Improvement of the cytological diagnostic accuracy of follicular thyroid lesions by the use of the Ki-67 proliferative index in addition to cytokeratin-19 and HBME-1 immunomarkers: a study of 61 cases of liquid-based FNA cytology with histological controls
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