Measuring extent of ductal carcinoma in situ in breast excision specimens: a comparison of 4 methods
Measuring the extent of nonpalpable ductal carcinoma in situ (DCIS) in a breast specimen is challenging but important because it influences patient management. There is no standardized method for estimating the extent of DCIS, although serial sequential sampling with mammographic correlation is cons...
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Veröffentlicht in: | Archives of pathology & laboratory medicine (1976) 2009-01, Vol.133 (1), p.31-37 |
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description | Measuring the extent of nonpalpable ductal carcinoma in situ (DCIS) in a breast specimen is challenging but important because it influences patient management. There is no standardized method for estimating the extent of DCIS, although serial sequential sampling with mammographic correlation is considered an accurate method.
To estimate the extent of DCIS using various methods and to compare these estimations with the extent as determined by the serial sequential sampling method.
A total of 78 primary breast excisions with DCIS were retrospectively reviewed. All specimens had been sampled using the serial sequential sampling method, which involved mapping the location of each block on the sliced specimen radiograph and calculating the extent through 3-dimensional reconstruction. The other measures for estimating extent included (1) calculating size based on areas of calcification, (2) recording the number of blocks involved by DCIS and multiplying that number by 0.3 cm, and (3) measuring the largest extent of DCIS on a single slide.
All 3 alternative methods tended to underestimate the DCIS. Discrepancies became more pronounced as size increased. The percentage of cases estimated to within 1 cm of the serial sequential sampling method were 81%, 72%, and 50%, respectively, for the calcification, blocks, and single-slide methods; differences of more than 2 cm were seen in 9%, 8%, and 30% of cases, respectively.
The single-slide method performed poorly and should be used only when DCIS is limited to a single slide. Although the calcification and the blocks methods gave better estimates, both produced substantial underestimates and/or overestimates that could affect clinical decision making. |
doi_str_mv | 10.1043/1543-2165-133.1.31 |
format | Article |
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To estimate the extent of DCIS using various methods and to compare these estimations with the extent as determined by the serial sequential sampling method.
A total of 78 primary breast excisions with DCIS were retrospectively reviewed. All specimens had been sampled using the serial sequential sampling method, which involved mapping the location of each block on the sliced specimen radiograph and calculating the extent through 3-dimensional reconstruction. The other measures for estimating extent included (1) calculating size based on areas of calcification, (2) recording the number of blocks involved by DCIS and multiplying that number by 0.3 cm, and (3) measuring the largest extent of DCIS on a single slide.
All 3 alternative methods tended to underestimate the DCIS. Discrepancies became more pronounced as size increased. The percentage of cases estimated to within 1 cm of the serial sequential sampling method were 81%, 72%, and 50%, respectively, for the calcification, blocks, and single-slide methods; differences of more than 2 cm were seen in 9%, 8%, and 30% of cases, respectively.
The single-slide method performed poorly and should be used only when DCIS is limited to a single slide. Although the calcification and the blocks methods gave better estimates, both produced substantial underestimates and/or overestimates that could affect clinical decision making.</description><identifier>EISSN: 1543-2165</identifier><identifier>DOI: 10.1043/1543-2165-133.1.31</identifier><identifier>PMID: 19123733</identifier><language>eng</language><publisher>United States</publisher><subject>Breast Neoplasms - metabolism ; Breast Neoplasms - pathology ; Breast Neoplasms - surgery ; Calcinosis - diagnostic imaging ; Calcinosis - metabolism ; Calcinosis - pathology ; Carcinoma, Intraductal, Noninfiltrating - metabolism ; Carcinoma, Intraductal, Noninfiltrating - pathology ; Carcinoma, Intraductal, Noninfiltrating - surgery ; Female ; Humans ; Image Processing, Computer-Assisted - methods ; Imaging, Three-Dimensional - methods ; Mammography - methods ; Microtomy - methods ; Reproducibility of Results ; Retrospective Studies</subject><ispartof>Archives of pathology & laboratory medicine (1976), 2009-01, Vol.133 (1), p.31-37</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27915,27916</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19123733$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Grin, Andrea</creatorcontrib><creatorcontrib>Horne, Garnet</creatorcontrib><creatorcontrib>Ennis, Marguerite</creatorcontrib><creatorcontrib>O'Malley, Frances P</creatorcontrib><title>Measuring extent of ductal carcinoma in situ in breast excision specimens: a comparison of 4 methods</title><title>Archives of pathology & laboratory medicine (1976)</title><addtitle>Arch Pathol Lab Med</addtitle><description>Measuring the extent of nonpalpable ductal carcinoma in situ (DCIS) in a breast specimen is challenging but important because it influences patient management. There is no standardized method for estimating the extent of DCIS, although serial sequential sampling with mammographic correlation is considered an accurate method.
To estimate the extent of DCIS using various methods and to compare these estimations with the extent as determined by the serial sequential sampling method.
A total of 78 primary breast excisions with DCIS were retrospectively reviewed. All specimens had been sampled using the serial sequential sampling method, which involved mapping the location of each block on the sliced specimen radiograph and calculating the extent through 3-dimensional reconstruction. The other measures for estimating extent included (1) calculating size based on areas of calcification, (2) recording the number of blocks involved by DCIS and multiplying that number by 0.3 cm, and (3) measuring the largest extent of DCIS on a single slide.
All 3 alternative methods tended to underestimate the DCIS. Discrepancies became more pronounced as size increased. The percentage of cases estimated to within 1 cm of the serial sequential sampling method were 81%, 72%, and 50%, respectively, for the calcification, blocks, and single-slide methods; differences of more than 2 cm were seen in 9%, 8%, and 30% of cases, respectively.
The single-slide method performed poorly and should be used only when DCIS is limited to a single slide. Although the calcification and the blocks methods gave better estimates, both produced substantial underestimates and/or overestimates that could affect clinical decision making.</description><subject>Breast Neoplasms - metabolism</subject><subject>Breast Neoplasms - pathology</subject><subject>Breast Neoplasms - surgery</subject><subject>Calcinosis - diagnostic imaging</subject><subject>Calcinosis - metabolism</subject><subject>Calcinosis - pathology</subject><subject>Carcinoma, Intraductal, Noninfiltrating - metabolism</subject><subject>Carcinoma, Intraductal, Noninfiltrating - pathology</subject><subject>Carcinoma, Intraductal, Noninfiltrating - surgery</subject><subject>Female</subject><subject>Humans</subject><subject>Image Processing, Computer-Assisted - methods</subject><subject>Imaging, Three-Dimensional - methods</subject><subject>Mammography - methods</subject><subject>Microtomy - methods</subject><subject>Reproducibility of Results</subject><subject>Retrospective Studies</subject><issn>1543-2165</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kEtLxDAUhYMgzjj6B1xIVu469uamaepOBkeFETezL3lVI32ZtKD_3gyOrg58fPdwuIRcQb6GnOMtFBwzBqLIAHENa4QTsvyHC3Ie40ee5xVjcEYWUAHDEnFJ7ItTcQ6-f6Pua3L9RIeG2tlMqqVGBeP7oVPU9zT6aT6kDulgSrLx0Q-Jj874zvXxjipqhm5UwcfEUw2nnZveBxsvyGmj2uguj7ki--3DfvOU7V4fnzf3u2w8DNWyEtoYcKICaRteVrIExRFAa-RpuuGMl7JgCm3D0CnjZFFpNBI1WDC4Ije_tWMYPmcXp7rz0bi2Vb0b5lgLIXMupEji9VGcdedsPQbfqfBd_70FfwD_kWMf</recordid><startdate>200901</startdate><enddate>200901</enddate><creator>Grin, Andrea</creator><creator>Horne, Garnet</creator><creator>Ennis, Marguerite</creator><creator>O'Malley, Frances P</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>200901</creationdate><title>Measuring extent of ductal carcinoma in situ in breast excision specimens: a comparison of 4 methods</title><author>Grin, Andrea ; Horne, Garnet ; Ennis, Marguerite ; O'Malley, Frances P</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p543-b896bcc1e6918df479871a4311bb34092c4247852a3df23eace859b3c83b1d1c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Breast Neoplasms - metabolism</topic><topic>Breast Neoplasms - pathology</topic><topic>Breast Neoplasms - surgery</topic><topic>Calcinosis - diagnostic imaging</topic><topic>Calcinosis - metabolism</topic><topic>Calcinosis - pathology</topic><topic>Carcinoma, Intraductal, Noninfiltrating - metabolism</topic><topic>Carcinoma, Intraductal, Noninfiltrating - pathology</topic><topic>Carcinoma, Intraductal, Noninfiltrating - surgery</topic><topic>Female</topic><topic>Humans</topic><topic>Image Processing, Computer-Assisted - methods</topic><topic>Imaging, Three-Dimensional - methods</topic><topic>Mammography - methods</topic><topic>Microtomy - methods</topic><topic>Reproducibility of Results</topic><topic>Retrospective Studies</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Grin, Andrea</creatorcontrib><creatorcontrib>Horne, Garnet</creatorcontrib><creatorcontrib>Ennis, Marguerite</creatorcontrib><creatorcontrib>O'Malley, Frances P</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Archives of pathology & laboratory medicine (1976)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Grin, Andrea</au><au>Horne, Garnet</au><au>Ennis, Marguerite</au><au>O'Malley, Frances P</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Measuring extent of ductal carcinoma in situ in breast excision specimens: a comparison of 4 methods</atitle><jtitle>Archives of pathology & laboratory medicine (1976)</jtitle><addtitle>Arch Pathol Lab Med</addtitle><date>2009-01</date><risdate>2009</risdate><volume>133</volume><issue>1</issue><spage>31</spage><epage>37</epage><pages>31-37</pages><eissn>1543-2165</eissn><abstract>Measuring the extent of nonpalpable ductal carcinoma in situ (DCIS) in a breast specimen is challenging but important because it influences patient management. There is no standardized method for estimating the extent of DCIS, although serial sequential sampling with mammographic correlation is considered an accurate method.
To estimate the extent of DCIS using various methods and to compare these estimations with the extent as determined by the serial sequential sampling method.
A total of 78 primary breast excisions with DCIS were retrospectively reviewed. All specimens had been sampled using the serial sequential sampling method, which involved mapping the location of each block on the sliced specimen radiograph and calculating the extent through 3-dimensional reconstruction. The other measures for estimating extent included (1) calculating size based on areas of calcification, (2) recording the number of blocks involved by DCIS and multiplying that number by 0.3 cm, and (3) measuring the largest extent of DCIS on a single slide.
All 3 alternative methods tended to underestimate the DCIS. Discrepancies became more pronounced as size increased. The percentage of cases estimated to within 1 cm of the serial sequential sampling method were 81%, 72%, and 50%, respectively, for the calcification, blocks, and single-slide methods; differences of more than 2 cm were seen in 9%, 8%, and 30% of cases, respectively.
The single-slide method performed poorly and should be used only when DCIS is limited to a single slide. Although the calcification and the blocks methods gave better estimates, both produced substantial underestimates and/or overestimates that could affect clinical decision making.</abstract><cop>United States</cop><pmid>19123733</pmid><doi>10.1043/1543-2165-133.1.31</doi><tpages>7</tpages></addata></record> |
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source | MEDLINE; Allen Press Journals; EZB-FREE-00999 freely available EZB journals |
subjects | Breast Neoplasms - metabolism Breast Neoplasms - pathology Breast Neoplasms - surgery Calcinosis - diagnostic imaging Calcinosis - metabolism Calcinosis - pathology Carcinoma, Intraductal, Noninfiltrating - metabolism Carcinoma, Intraductal, Noninfiltrating - pathology Carcinoma, Intraductal, Noninfiltrating - surgery Female Humans Image Processing, Computer-Assisted - methods Imaging, Three-Dimensional - methods Mammography - methods Microtomy - methods Reproducibility of Results Retrospective Studies |
title | Measuring extent of ductal carcinoma in situ in breast excision specimens: a comparison of 4 methods |
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