<?xml version='1.0'?>
<!DOCTYPE art SYSTEM 'http://www.biomedcentral.com/xml/article.dtd'>
<art>
   <ui>bcr470</ui>
   <ji>BCJ</ji>
   <fm>
      <dochead>Meeting abstract</dochead>
      <bibl>
         <title>
            <p>UK National Health Service Breast Screening Programme (NHSBSP) multicentre image guided biopsy trial: an update</p>
         </title>
         <aug>
            <au id="A1">
               <cnm>The UK Mammotome Trial Group</cnm>
            </au>
            <au id="A2">
               <snm>Teh</snm>
               <fnm>W</fnm>
               <insr iid="I1"/>
            </au>
            <au id="A3">
               <snm>Michell</snm>
               <fnm>MJ</fnm>
               <insr iid="I1"/>
            </au>
            <au id="A4">
               <snm>Wilson</snm>
               <fnm>ARM</fnm>
               <insr iid="I1"/>
            </au>
            <au id="A5">
               <snm>Britton</snm>
               <fnm>P</fnm>
               <insr iid="I1"/>
            </au>
            <au id="A6">
               <snm>Shah</snm>
               <fnm>B</fnm>
               <insr iid="I1"/>
            </au>
         </aug>
         <insg>
            <ins id="I1">
               <p>Edgware, King's, Nottingham and Cambridge Breast Screening Units, Edgware, London, Nottingham and Cambridge, UK</p>
            </ins>
         </insg>
         <source>Breast Cancer Res</source>
         <supplement>
            <title>
               <p>Symposium Mammographicum 2002</p>
            </title>
            <note>Meeting abstracts</note>
         </supplement>
         <conference>
            <title>
               <p>Symposium Mammographicum 2002</p>
            </title>
            <location>York, UK</location>
            <date-range>17&#8211;19 July 2002</date-range>
         </conference>
         <issn>1465-5411</issn>
         <pubdate>2002</pubdate>
         <volume>4</volume>
         <issue>Suppl 1</issue>
         <fpage>15</fpage>
         <xrefbib>
            <pubid idtype="doi">10.1186/bcr470</pubid>
         </xrefbib>
      </bibl>
      <history>
         <pub>
            <date>
               <day>16</day>
               <month>7</month>
               <year>2002</year>
            </date>
         </pub>
      </history>
      <cpyrt>
         <year>2002</year>
         <collab>BioMed Central</collab>
      </cpyrt>
   </fm>
   <meta>
      <classifications>
         <classification type="BMC" subtype="old_arx_id">bcr-4-s1-15</classification>
      </classifications>
   </meta>
   <bdy>
      <sec>
         <st>
            <p/>
         </st>
         <p>This is an update on randomised control trials (RCTs) evaluating the efficacy of 11-gauge mammotome (Ma) to 14-gauge core biopsy (CB). A total of 614 women with impalpable clustered microcalcifications and/or distortions were prospectively recruited in a multicentre (Edgware, King's, Nottingham and Cambridge) RCT. Specimen radiographs were obtained for all biopsies performed for microcalcifications. Complete data for 585 women were analysed. Two hundred and ninety-three CB and 292 Ma had been performed on 554 microcalcifications, two distortions with microcalcifications and 29 distortions. There are 191 cancers (32%) consisting of 54 invasive and 137 <it>in situ</it> carcinoma. Comparing CB and Ma, the absolute sensitivity for ductal carcinoma <it>in situ</it> (DCIS) was 79.2% and 80%, respectively, with a complete sensitivity of 89.6% and 96.6%, respectively (<it>P</it> = 0.1). The absolute sensitivity for invasive disease is 33.3% and 58.3%, respectively (<it>P</it> = 0.06). Mammotomy is significantly less likely to under-stage malignant disease when a B3 result is obtained compared to CB (17.5% <it>versus</it> 64%, respectively). The analysis suggests that the greatest benefit of mammotomy is in clustered microcalcification with an indeterminate appearance and in minimising the under-diagnosis of associated malignant disease.</p>
      </sec>
   </bdy>
</art>
