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Pyrosequencing cut-off value identifying BRAFV600E mutation in fine needle aspiration samples of thyroid nodules
Summary Context Recently, tremendous efforts have been made towards the development of sensitive techniques to detect the BRAFV600E mutation in fine needle aspiration biopsy (FNAB) samples. However, newly developed quantitative and semi‐quantitative methods, such as dual‐priming oligonucleotide (DP...
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Published in: | Clinical endocrinology (Oxford) 2011-10, Vol.75 (4), p.555-560 |
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creator | Yeo, Min-Kyung Liang, Zhe Long Oh, Taejeong Moon, Youngho An, Sungwhan Kim, Min Kyeong Kim, Koon Soon Shong, Minho Kim, Jin-Man Jo, Young Suk |
description | Summary
Context Recently, tremendous efforts have been made towards the development of sensitive techniques to detect the BRAFV600E mutation in fine needle aspiration biopsy (FNAB) samples. However, newly developed quantitative and semi‐quantitative methods, such as dual‐priming oligonucleotide (DPO)‐based multiplex polymerase chain reaction (PCR), have the potential to generate false‐positive (FP) results.
Objectives To eliminate the possibility of FP results, we generated a receiver operating characteristic (ROC) curve to investigate the diagnostic accuracy of pyrosequencing using quantitative data.
Design Cytological diagnoses of 983 thyroid nodules were made according to the Bethesda System 2007. The BRAFV600E mutation was analysed by pyrosequencing, and statistical analyses were performed.
Results Of the 983 nodules, 902 were adopted to evaluate the diagnostic value of pyrosequencing. The number of pathologically confirmed malignancies was 192, of which 182 were papillary thyroid cancer (PTC). By generating an ROC curve, we defined the optimal cut‐off value of the mutant allele peak as 5·95% (area under the curve, 0·849; sensitivity, 0·55; 1‐specificity, 0). When we applied this selective cut‐off value, the number of PTCs positive for BRAFV600E was 99 (54·4% of the total number of PTCs). With cytology alone, the diagnostic sensitivity and specificity of detecting malignancy were 71·2% and 100%, respectively. Pyrosequencing improved the diagnostic sensitivity from 71·2% to 78·5% (McNemar’s test, P 0·05).
Conclusions Pyrosequencing is an effective method for detecting the BRAFV600E mutation in FNAB samples. By allowing the optimal cut‐off value to be determined, pyrosequencing improves the diagnostic sensitivity while eliminating the possibility of FP results. |
doi_str_mv | 10.1111/j.1365-2265.2011.04115.x |
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Context Recently, tremendous efforts have been made towards the development of sensitive techniques to detect the BRAFV600E mutation in fine needle aspiration biopsy (FNAB) samples. However, newly developed quantitative and semi‐quantitative methods, such as dual‐priming oligonucleotide (DPO)‐based multiplex polymerase chain reaction (PCR), have the potential to generate false‐positive (FP) results.
Objectives To eliminate the possibility of FP results, we generated a receiver operating characteristic (ROC) curve to investigate the diagnostic accuracy of pyrosequencing using quantitative data.
Design Cytological diagnoses of 983 thyroid nodules were made according to the Bethesda System 2007. The BRAFV600E mutation was analysed by pyrosequencing, and statistical analyses were performed.
Results Of the 983 nodules, 902 were adopted to evaluate the diagnostic value of pyrosequencing. The number of pathologically confirmed malignancies was 192, of which 182 were papillary thyroid cancer (PTC). By generating an ROC curve, we defined the optimal cut‐off value of the mutant allele peak as 5·95% (area under the curve, 0·849; sensitivity, 0·55; 1‐specificity, 0). When we applied this selective cut‐off value, the number of PTCs positive for BRAFV600E was 99 (54·4% of the total number of PTCs). With cytology alone, the diagnostic sensitivity and specificity of detecting malignancy were 71·2% and 100%, respectively. Pyrosequencing improved the diagnostic sensitivity from 71·2% to 78·5% (McNemar’s test, P < 0·001), without any change in the diagnostic specificity. When ‘suspicious for malignancy’ was considered a positive cytological outcome, pyrosequencing increased the diagnostic sensitivity of cytology from 95·8% to 96·9%; however, this improvement did not show statistical significance (McNemar’s test, P > 0·05).
Conclusions Pyrosequencing is an effective method for detecting the BRAFV600E mutation in FNAB samples. By allowing the optimal cut‐off value to be determined, pyrosequencing improves the diagnostic sensitivity while eliminating the possibility of FP results.</description><identifier>ISSN: 0300-0664</identifier><identifier>EISSN: 1365-2265</identifier><identifier>DOI: 10.1111/j.1365-2265.2011.04115.x</identifier><identifier>PMID: 21609347</identifier><identifier>CODEN: CLECAP</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Adult ; Biological and medical sciences ; Biopsy, Fine-Needle ; DNA Mutational Analysis ; Endocrinopathies ; Female ; Fundamental and applied biological sciences. Psychology ; Humans ; Male ; Medical sciences ; Middle Aged ; Mutation ; Non tumoral diseases. Target tissue resistance. Benign neoplasms ; Proto-Oncogene Proteins B-raf - genetics ; Thyroid Nodule - genetics ; Thyroid. Thyroid axis (diseases) ; Vertebrates: endocrinology</subject><ispartof>Clinical endocrinology (Oxford), 2011-10, Vol.75 (4), p.555-560</ispartof><rights>2011 Blackwell Publishing Ltd</rights><rights>2015 INIST-CNRS</rights><rights>2011 Blackwell Publishing Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24496756$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21609347$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yeo, Min-Kyung</creatorcontrib><creatorcontrib>Liang, Zhe Long</creatorcontrib><creatorcontrib>Oh, Taejeong</creatorcontrib><creatorcontrib>Moon, Youngho</creatorcontrib><creatorcontrib>An, Sungwhan</creatorcontrib><creatorcontrib>Kim, Min Kyeong</creatorcontrib><creatorcontrib>Kim, Koon Soon</creatorcontrib><creatorcontrib>Shong, Minho</creatorcontrib><creatorcontrib>Kim, Jin-Man</creatorcontrib><creatorcontrib>Jo, Young Suk</creatorcontrib><title>Pyrosequencing cut-off value identifying BRAFV600E mutation in fine needle aspiration samples of thyroid nodules</title><title>Clinical endocrinology (Oxford)</title><addtitle>Clin Endocrinol (Oxf)</addtitle><description>Summary
Context Recently, tremendous efforts have been made towards the development of sensitive techniques to detect the BRAFV600E mutation in fine needle aspiration biopsy (FNAB) samples. However, newly developed quantitative and semi‐quantitative methods, such as dual‐priming oligonucleotide (DPO)‐based multiplex polymerase chain reaction (PCR), have the potential to generate false‐positive (FP) results.
Objectives To eliminate the possibility of FP results, we generated a receiver operating characteristic (ROC) curve to investigate the diagnostic accuracy of pyrosequencing using quantitative data.
Design Cytological diagnoses of 983 thyroid nodules were made according to the Bethesda System 2007. The BRAFV600E mutation was analysed by pyrosequencing, and statistical analyses were performed.
Results Of the 983 nodules, 902 were adopted to evaluate the diagnostic value of pyrosequencing. The number of pathologically confirmed malignancies was 192, of which 182 were papillary thyroid cancer (PTC). By generating an ROC curve, we defined the optimal cut‐off value of the mutant allele peak as 5·95% (area under the curve, 0·849; sensitivity, 0·55; 1‐specificity, 0). When we applied this selective cut‐off value, the number of PTCs positive for BRAFV600E was 99 (54·4% of the total number of PTCs). With cytology alone, the diagnostic sensitivity and specificity of detecting malignancy were 71·2% and 100%, respectively. Pyrosequencing improved the diagnostic sensitivity from 71·2% to 78·5% (McNemar’s test, P < 0·001), without any change in the diagnostic specificity. When ‘suspicious for malignancy’ was considered a positive cytological outcome, pyrosequencing increased the diagnostic sensitivity of cytology from 95·8% to 96·9%; however, this improvement did not show statistical significance (McNemar’s test, P > 0·05).
Conclusions Pyrosequencing is an effective method for detecting the BRAFV600E mutation in FNAB samples. By allowing the optimal cut‐off value to be determined, pyrosequencing improves the diagnostic sensitivity while eliminating the possibility of FP results.</description><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Biopsy, Fine-Needle</subject><subject>DNA Mutational Analysis</subject><subject>Endocrinopathies</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Mutation</subject><subject>Non tumoral diseases. Target tissue resistance. Benign neoplasms</subject><subject>Proto-Oncogene Proteins B-raf - genetics</subject><subject>Thyroid Nodule - genetics</subject><subject>Thyroid. Thyroid axis (diseases)</subject><subject>Vertebrates: endocrinology</subject><issn>0300-0664</issn><issn>1365-2265</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNpdkVuP0zAQhSMEYsvCX0CWEOIpYRzHjv3Aw7a0C6JaEOIi8WI58QRcciNOdtt_j0NLkfCLLZ_vzNhzoohQSGhYL3cJZYLHaSp4kgKlCWSU8mR_L1qchfvRAhhADEJkF9Ej73cAwCXkD6OLlApQLMsXUf_hMHQef03Ylq79TsppjLuqIremnpA4i-3oqsOsLD9ebb4IgDVpptGMrmuJa0nlWiQtoq2RGN-74ah40_Q1etJVZPwROjhL2s5O4epx9KAytccnp_0y-rxZf1q9ibfvr9-urraxS4HzOLclk2gLBpUoUobKSkAhM5srhUZRWqiUQyWZAiwqLpEi5soYBdQaZDm7jF4c6_ZDF37nR904X2Jdmxa7yWspJWNCMhnIZ_-Ru24a2vA4TXnGZWgGNFBPT9RUNGh1P7jGDAf9d5QBeH4CjC9NXQ0mTNT_47JMiZyLwL06cneuxsNZp6DnaPVOzwnqOUE9R6v_RKv3erW-mU_BHx_9zo-4P_vN8FOLnOVcf7251stvy9fq3YbpLfsNjX2lrQ</recordid><startdate>201110</startdate><enddate>201110</enddate><creator>Yeo, Min-Kyung</creator><creator>Liang, Zhe Long</creator><creator>Oh, Taejeong</creator><creator>Moon, Youngho</creator><creator>An, Sungwhan</creator><creator>Kim, Min Kyeong</creator><creator>Kim, Koon Soon</creator><creator>Shong, Minho</creator><creator>Kim, Jin-Man</creator><creator>Jo, Young Suk</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7QP</scope><scope>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope></search><sort><creationdate>201110</creationdate><title>Pyrosequencing cut-off value identifying BRAFV600E mutation in fine needle aspiration samples of thyroid nodules</title><author>Yeo, Min-Kyung ; Liang, Zhe Long ; Oh, Taejeong ; Moon, Youngho ; An, Sungwhan ; Kim, Min Kyeong ; Kim, Koon Soon ; Shong, Minho ; Kim, Jin-Man ; Jo, Young Suk</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i2055-7dc38edb30f6b23e9d80e684d799ea911b9250f8390ebf58e1ee79aa901dae373</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Biopsy, Fine-Needle</topic><topic>DNA Mutational Analysis</topic><topic>Endocrinopathies</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Mutation</topic><topic>Non tumoral diseases. Target tissue resistance. Benign neoplasms</topic><topic>Proto-Oncogene Proteins B-raf - genetics</topic><topic>Thyroid Nodule - genetics</topic><topic>Thyroid. Thyroid axis (diseases)</topic><topic>Vertebrates: endocrinology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yeo, Min-Kyung</creatorcontrib><creatorcontrib>Liang, Zhe Long</creatorcontrib><creatorcontrib>Oh, Taejeong</creatorcontrib><creatorcontrib>Moon, Youngho</creatorcontrib><creatorcontrib>An, Sungwhan</creatorcontrib><creatorcontrib>Kim, Min Kyeong</creatorcontrib><creatorcontrib>Kim, Koon Soon</creatorcontrib><creatorcontrib>Shong, Minho</creatorcontrib><creatorcontrib>Kim, Jin-Man</creatorcontrib><creatorcontrib>Jo, Young Suk</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical endocrinology (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yeo, Min-Kyung</au><au>Liang, Zhe Long</au><au>Oh, Taejeong</au><au>Moon, Youngho</au><au>An, Sungwhan</au><au>Kim, Min Kyeong</au><au>Kim, Koon Soon</au><au>Shong, Minho</au><au>Kim, Jin-Man</au><au>Jo, Young Suk</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pyrosequencing cut-off value identifying BRAFV600E mutation in fine needle aspiration samples of thyroid nodules</atitle><jtitle>Clinical endocrinology (Oxford)</jtitle><addtitle>Clin Endocrinol (Oxf)</addtitle><date>2011-10</date><risdate>2011</risdate><volume>75</volume><issue>4</issue><spage>555</spage><epage>560</epage><pages>555-560</pages><issn>0300-0664</issn><eissn>1365-2265</eissn><coden>CLECAP</coden><abstract>Summary
Context Recently, tremendous efforts have been made towards the development of sensitive techniques to detect the BRAFV600E mutation in fine needle aspiration biopsy (FNAB) samples. However, newly developed quantitative and semi‐quantitative methods, such as dual‐priming oligonucleotide (DPO)‐based multiplex polymerase chain reaction (PCR), have the potential to generate false‐positive (FP) results.
Objectives To eliminate the possibility of FP results, we generated a receiver operating characteristic (ROC) curve to investigate the diagnostic accuracy of pyrosequencing using quantitative data.
Design Cytological diagnoses of 983 thyroid nodules were made according to the Bethesda System 2007. The BRAFV600E mutation was analysed by pyrosequencing, and statistical analyses were performed.
Results Of the 983 nodules, 902 were adopted to evaluate the diagnostic value of pyrosequencing. The number of pathologically confirmed malignancies was 192, of which 182 were papillary thyroid cancer (PTC). By generating an ROC curve, we defined the optimal cut‐off value of the mutant allele peak as 5·95% (area under the curve, 0·849; sensitivity, 0·55; 1‐specificity, 0). When we applied this selective cut‐off value, the number of PTCs positive for BRAFV600E was 99 (54·4% of the total number of PTCs). With cytology alone, the diagnostic sensitivity and specificity of detecting malignancy were 71·2% and 100%, respectively. Pyrosequencing improved the diagnostic sensitivity from 71·2% to 78·5% (McNemar’s test, P < 0·001), without any change in the diagnostic specificity. When ‘suspicious for malignancy’ was considered a positive cytological outcome, pyrosequencing increased the diagnostic sensitivity of cytology from 95·8% to 96·9%; however, this improvement did not show statistical significance (McNemar’s test, P > 0·05).
Conclusions Pyrosequencing is an effective method for detecting the BRAFV600E mutation in FNAB samples. By allowing the optimal cut‐off value to be determined, pyrosequencing improves the diagnostic sensitivity while eliminating the possibility of FP results.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>21609347</pmid><doi>10.1111/j.1365-2265.2011.04115.x</doi><tpages>6</tpages></addata></record> |
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subjects | Adult Biological and medical sciences Biopsy, Fine-Needle DNA Mutational Analysis Endocrinopathies Female Fundamental and applied biological sciences. Psychology Humans Male Medical sciences Middle Aged Mutation Non tumoral diseases. Target tissue resistance. Benign neoplasms Proto-Oncogene Proteins B-raf - genetics Thyroid Nodule - genetics Thyroid. Thyroid axis (diseases) Vertebrates: endocrinology |
title | Pyrosequencing cut-off value identifying BRAFV600E mutation in fine needle aspiration samples of thyroid nodules |
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