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<art>
   <ui>1477-7819-5-132</ui>
   <ji>1477-7819</ji>
   <fm>
      <dochead>Case report</dochead>
      <bibl>
         <title>
            <p>Optimization of sentinel lymph node biopsy in breast cancer using an operative gamma camera</p>
         </title>
         <aug>
            <au id="A1" ca="yes">
               <snm>Mathelin</snm>
               <fnm>Carole</fnm>
               <insr iid="I1"/>
               <email>carole.mathelin@chru-strasbourg.fr</email>
            </au>
            <au id="A2">
               <snm>Salvador</snm>
               <fnm>Samuel</fnm>
               <insr iid="I2"/>
               <email>dark_bass@hotmail.com</email>
            </au>
            <au id="A3">
               <snm>Croce</snm>
               <fnm>Sabrina</fnm>
               <insr iid="I3"/>
               <email>sabrina.croce@chru-strasbourg.fr</email>
            </au>
            <au id="A4">
               <snm>Andriamisandratsoa</snm>
               <fnm>Norosoa</fnm>
               <insr iid="I4"/>
               <email>norosoa.andrianatoandro@chru-strasbourg.fr</email>
            </au>
            <au id="A5">
               <snm>Huss</snm>
               <fnm>Daniel</fnm>
               <insr iid="I2"/>
               <email>daniel.huss@IReS.in2p3.fr</email>
            </au>
            <au id="A6">
               <snm>Guyonnet</snm>
               <fnm>Jean-Louis</fnm>
               <insr iid="I2"/>
               <email>jean-louis.guyonnet@IReS.in2p3.fr</email>
            </au>
         </aug>
         <insg>
            <ins id="I1">
               <p>Service de Gyn&#233;cologie-Obst&#233;trique, H&#244;pital Civil, 1 place de l'H&#244;pital. F-67091 Strasbourg Cedex, France</p>
            </ins>
            <ins id="I2">
               <p>Institut Pluridisciplinaire Hubert Curien. UMR 7178 &#8211; CNRS/IN2P3 et ULP. BP 28 &#8211; 23 rue du Loess. F-67037 Strasbourg Cedex 02, France</p>
            </ins>
            <ins id="I3">
               <p>D&#233;partement d'anatomie-pathologique. H&#244;pital de Hautepierre, Avenue Moli&#232;re. F-67200 Strasbourg Cedex, France</p>
            </ins>
            <ins id="I4">
               <p>Service de M&#233;decine Nucl&#233;aire. H&#244;pital Civil, 1 place de l'H&#244;pital. F-67091 Strasbourg Cedex, France</p>
            </ins>
         </insg>
         <source>World Journal of Surgical Oncology</source>
         <issn>1477-7819</issn>
         <pubdate>2007</pubdate>
         <volume>5</volume>
         <issue>1</issue>
         <fpage>132</fpage>
         <url>http://www.wjso.com/content/5/1/132</url>
         <xrefbib>
            <pubidlist>
               <pubid idtype="pmpid">18021418</pubid>
               <pubid idtype="doi">10.1186/1477-7819-5-132</pubid>
            </pubidlist>
         </xrefbib>
      </bibl>
      <history>
         <rec>
            <date>
               <day>25</day>
               <month>8</month>
               <year>2007</year>
            </date>
         </rec>
         <acc>
            <date>
               <day>17</day>
               <month>11</month>
               <year>2007</year>
            </date>
         </acc>
         <pub>
            <date>
               <day>17</day>
               <month>11</month>
               <year>2007</year>
            </date>
         </pub>
      </history>
      <cpyrt>
         <year>2007</year>
         <collab>Mathelin et al; licensee BioMed Central Ltd.</collab>
         <note>This is an Open Access article distributed under the terms of the Creative Commons Attribution License (<url>http://creativecommons.org/licenses/by/2.0</url>), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</note>
      </cpyrt>
      <abs>
         <sec>
            <st>
               <p>Abstract</p>
            </st>
            <sec>
               <st>
                  <p>Background</p>
               </st>
               <p>Sentinel lymph node (SLN) procedure is now a widely accepted method of LN staging in selected invasive breast cancers (unifocal, size &#8804; 2 cm, clinically N0, without previous treatment). Complete axillary clearance is no longer needed if the SLN is negative. However, the oncological safety of this procedure remains to be addressed in randomized clinical trials. One main pitfall is the failure to visualize SLN, resulting in incorrect tumor staging, leading to suboptimal treatment or axillary recurrence. Operative gamma cameras have therefore been developed to optimize the SLN visualization and the quality control of surgery.</p>
            </sec>
            <sec>
               <st>
                  <p>Case presentation</p>
               </st>
               <p>A 44-year-old female patient with a 14-mm infiltrative ductal carcinoma underwent the SLN procedure. An operative gamma camera was used during and after the surgery. The conventional lymphoscintigraphy showed only one SLN, which was also detected by the operative gamma camera, then removed and measured (9.6 kBq). It was analyzed by frozen sections, showing no cancer cells. During this analysis, the exploration of the axillary area with the operative gamma camera enabled the identification of a second SLN with low activity (0.5 kBq) that conventional lymphoscintigraphy, surgical probe and blue staining had failed to visualize. Histological examination revealed a macrometastasis. Axillary clearance was then performed, followed by a postoperative image proving that no SLN remained. Therefore, the use of the operative gamma camera prevented an under-estimation of staging which would have resulted in a suboptimal treatment for this patient.</p>
            </sec>
            <sec>
               <st>
                  <p>Conclusion</p>
               </st>
               <p>This case report illustrates that an efficient operative gamma camera may be able to decrease the risk of false negative rate of the SLN procedure, and could be an additional tool to control the quality of the surgery.</p>
            </sec>
            <sec>
               <st>
                  <p>Trial Registration</p>
               </st>
               <p>ClinicalTrials.gov Identifier: NCT00357487</p>
            </sec>
         </sec>
      </abs>
   </fm>
   <meta>
      <classifications>
         <classification type="bmc" subtype="user_supplied_xml" id="endnote"/>
      </classifications>
   </meta>
   <bdy>
      <sec>
         <st>
            <p>Background</p>
         </st>
         <p>As lymph node (LN) metastasis is one of the most important prognostic factors for survival, the assessment of regional LN is essential in the staging of breast cancer, ascertaining a prognosis, and determining of optimal adjuvant treatments. The sentinel node (SLN) procedure consists of recognizing and removing the first LN that filter lymphatic fluid from the tumor. It is now a widely accepted method of LN staging in selected invasive breast cancer (unifocal, size &#8804; 2 cm, clinically N0, without previous treatment). The complete axillary clearance is no longer needed if the SLN is normal <abbrgrp><abbr bid="B1">1</abbr></abbrgrp>. However, its oncological safety remains to be addressed in randomized clinical trials <abbrgrp><abbr bid="B2">2</abbr></abbrgrp>. One main pitfall is the failure to visualize SLN, resulting in incorrect tumor staging, leading to suboptimal treatment or axillary recurrence. Several factors including advanced age, high body mass index, massive metastasis invasion <abbrgrp><abbr bid="B3">3</abbr></abbrgrp> or tumor location other than upper outer quadrant <abbrgrp><abbr bid="B4">4</abbr></abbrgrp> may contribute to SLN non-visualization.</p>
         <p>Operative gamma cameras (OGC) have therefore been developed to optimize the SLN visualization and the quality control of surgery <abbrgrp><abbr bid="B5">5</abbr><abbr bid="B6">6</abbr><abbr bid="B7">7</abbr><abbr bid="B8">8</abbr><abbr bid="B9">9</abbr><abbr bid="B10">10</abbr></abbrgrp>. In our ongoing clinical trial <abbrgrp><abbr bid="B11">11</abbr></abbrgrp>, an OGC, named CarolIReS, with a current field of view (FOV) of 50 &#215; 50 mm<sup>2 </sup>is being used <abbrgrp><abbr bid="B12">12</abbr></abbrgrp>. It is made of a lead parallel collimator, a thin Gd<sub>2</sub>SiO<sub>5</sub>:Ce scintillating crystal and a multianode photomultiplier (10 mm spatial resolution and 2.2 cps.kBq<sup>-1 </sup>sensitivity for the <sup>99m</sup>Tc). We present the first case in which OGC, used at the end of the surgery, enabled the detection of a residual metastatic SLN.</p>
      </sec>
      <sec>
         <st>
            <p>Case presentation</p>
         </st>
         <p>A 44-year-old female patient with a 14 mm infiltrative ductal carcinoma, Scarf-Bloom-Richardson grade 2 (diagnosed by core biopsy) was enrolled in the clinical study <abbrgrp><abbr bid="B11">11</abbr></abbrgrp> after informed consent had been obtained. She was free of chemotherapy, loco-regional radiotherapy, prevalent axillary LN and her body mass index was normal (21 kg/m<sup>2</sup>). The tumor was located in the upper outer quadrant of the left breast. The SLN procedure was initiated the day prior to the surgery using 4 subareolar injections of rhenium sulfur colloidal and technetium (<sup>99m</sup>Tc) (0.4 ml, 22 MBq (595 &#956;Ci), Cis bio international<sup>&#174;</sup>, France). Scintigraphic images (anterior, lateral and oblique views), obtained 3 hours after rhenium sulfur injections with a conventional gamma camera (H&#233;lix<sup>&#174;</sup>, Elscint, Ha&#239;fa), showed one SLN (figure <figr fid="F1">1</figr>). Immediately before surgery, when the patient was in operative position, four images (2 minutes data acquisition each) were obtained with the OGC to map the full axillary area (figure <figr fid="F2">2</figr> represents a picture of the OGC). The precise localization of this SLN and an estimation of its depth were determined from the data by using the width of the image cumulative profiles (figure <figr fid="F3">3</figr>).</p>
         <fig id="F1">
            <title>
               <p>Figure 1</p>
            </title>
            <caption>
               <p>The anterior view of the conventional lymphoscintigraphy shows one SLN indicated by the yellow arrow</p>
            </caption>
            <text>
               <p>The anterior view of the conventional lymphoscintigraphy shows one SLN indicated by the yellow arrow. The purple arrow indicates the injection site.</p>
            </text>
            <graphic file="1477-7819-5-132-1"/>
         </fig>
         <fig id="F2">
            <title>
               <p>Figure 2</p>
            </title>
            <caption>
               <p>Picture of the CarolIReS gamma camera built at the IPHC, Strasbourg, France</p>
            </caption>
            <text>
               <p>Picture of the CarolIReS gamma camera built at the IPHC, Strasbourg, France.</p>
            </text>
            <graphic file="1477-7819-5-132-2"/>
         </fig>
         <fig id="F3">
            <title>
               <p>Figure 3</p>
            </title>
            <caption>
               <p>Preoperative image of the axillary area obtained with the CarolIReS gamma camera</p>
            </caption>
            <text>
               <p>Preoperative image of the axillary area obtained with the CarolIReS gamma camera. The x and y cumulative profiles (red stars) are used to determine the planar coordinates and the anatomical depth of the first SLN.</p>
            </text>
            <graphic file="1477-7819-5-132-3"/>
         </fig>
         <p>The surgery began with 4 subareolar injections of Methylene Blue (Lab Aguettant<sup>&#174;</sup>, Lyon, France), and the search for the SLN was carried out using the CarolIReS intra-operative probe <abbrgrp><abbr bid="B13">13</abbr></abbrgrp>, which detected only one SLN. This SLN was blue stained and its measured activity was 9.6 kBq (0.26 &#956;Ci). It was subsequently submitted for frozen section analysis, which showed the absence of cancer cells. During this analysis, the axillary area was thoroughly palpated by the surgeon and no nodes showing signs of extensive tumor involvement were identified. A second exploration of this area was then performed using the OGC enabling the identification of a second SLN located at a distance from the first one of less than the spatial resolution of the OGC (figure <figr fid="F4">4</figr>). This SLN was not stained and had a low activity of 0.5 kBq (0.01 &#956;Ci) concentrated in its hilum.</p>
         <fig id="F4">
            <title>
               <p>Figure 4</p>
            </title>
            <caption>
               <p>Peroperative image of the axillary area obtained with the CarolIReS gamma camera</p>
            </caption>
            <text>
               <p>Peroperative image of the axillary area obtained with the CarolIReS gamma camera. The x and y cumulative profiles (red stars) are used to determine the planar coordinates and the anatomical depth of the second SLN.</p>
            </text>
            <graphic file="1477-7819-5-132-4"/>
         </fig>
         <p>The histological examination revealed an 8-mm macrometastasis occupying the whole structure of this SLN without residual sinusoidal macrophages (figure <figr fid="F5">5</figr>). Axillary clearance was then performed and each of the 11 LN removed was negative. Axillary surgery was followed by lumpectomy. A postoperative OGC image proved that no SLN remained (figure <figr fid="F6">6</figr>) and was considered a quality control document.</p>
         <fig id="F5">
            <title>
               <p>Figure 5</p>
            </title>
            <caption>
               <p>Ductal breast carcinoma metastasis destroying nodal architecture (Hematoxilin and Eosin &#215;20)</p>
            </caption>
            <text>
               <p>Ductal breast carcinoma metastasis destroying nodal architecture (Hematoxilin and Eosin &#215;20). Inset: metastatic cells (Hematoxilin and Eosin &#215;200) in the second SLN.</p>
            </text>
            <graphic file="1477-7819-5-132-5"/>
         </fig>
         <fig id="F6">
            <title>
               <p>Figure 6</p>
            </title>
            <caption>
               <p>Postoperative image of the axillary area obtained with the CarolIReS gamma camera</p>
            </caption>
            <text>
               <p>Postoperative image of the axillary area obtained with the CarolIReS gamma camera.</p>
            </text>
            <graphic file="1477-7819-5-132-6"/>
         </fig>
      </sec>
      <sec>
         <st>
            <p>Discussion</p>
         </st>
         <p>This is the first published case in which an OGC enabled the detection of a non-stained metastatic SLN, which was neither diagnosed by conventional lymphoscintigraphy, nor by operative probe, nor by palpation of the axillary area performed by an experienced surgeon. This can be partially explained by the very low activity of this SLN (0.5 kBq). It corresponds to 0.02&#8240; of the injected dose, which is inferior to our mean measured value of 0.5&#8240;. Metastatic SLN sometimes have very low activity, because they contain numerous cancer cells and few macrophages, the latter being the cells that retain radiocollo&#239;des <abbrgrp><abbr bid="B14">14</abbr></abbrgrp>. In our experience, the activity of metastatic SLN is less than 10 kBq in more than half of the cases. So the detection efficiency of OGC must be good, and that of the one we used in this reported case was 2.2 cps.kBq<sup>-1</sup>. Future clinical trials will have to determine whether or not there is an inferior threshold for the activity of the SLN which should be removed.</p>
         <p>In addition, ongoing trials using OGC will have to evaluate if the latter lead to unnecessary SLN removal and increase morbidity or if they decrease the false negative rate (FNR). However, it has been demonstrated that the identification of multiple SLN, when present, reduced the FNR. For example, Goyal <it>et al</it>. <abbrgrp><abbr bid="B15">15</abbr></abbrgrp> studied a series of 803 patients with breast cancer who underwent successful SLN procedure followed by an axillary clearance. In patients who had one SLN harvested, the FNR was 10%, compared with 1% in patients who had 3 or more SLN removed. Factors associated with finding multiple SLN (62.4% of patients) were age less than 50 years, low body mass index, tumor in the outer half of the breast, SLN visualization on lymphoscintigraphy and an interval of 12 hours or less between radioisotope injection and SLN procedure. For 99.6% of node-positive tumors, metastases were detected within the first 4 SLN removed and the authors suggested that the removal of more than 4 SLN was unnecessary <abbrgrp><abbr bid="B15">15</abbr></abbrgrp>. Ongoing clinical trials will have to discuss precisely the usefulness of OGC according to the number of SLN found with conventional procedures (less than or equal to 4 or greater than 4).</p>
      </sec>
      <sec>
         <st>
            <p>Conclusion</p>
         </st>
         <p>This case report illustrates that an efficient OGC may be able to decrease the risk of FNR of the SLN procedure, and could be an additional tool to control the quality of the surgery. But a precise evaluation of OGC should be based upon data from a large number of patients. Our ongoing clinical trial <abbrgrp><abbr bid="B11">11</abbr></abbrgrp> will be soon published and a new clinical trial, including 100 breast cancer patients, will begin at the end of 2007 to evaluate the usefulness of the new CarolIRes OGC (FOV : 100 &#215; 100 mm<sup>2</sup>) in the SLN procedure.</p>
      </sec>
      <sec>
         <st>
            <p>Abbreviations</p>
         </st>
         <p>FNR: false negative rate</p>
         <p>FOV: field of view</p>
         <p>OGC: operative gamma camera</p>
         <p>SLN: sentinel lymph node</p>
      </sec>
      <sec>
         <st>
            <p>Competing interests</p>
         </st>
         <p>The author(s) declare that they have no competing interests.</p>
      </sec>
      <sec>
         <st>
            <p>Authors' contributions</p>
         </st>
         <p><b>CM </b>carried out the clinical trial, performed the surgical treatment and drafted the manuscript. <b>SC </b>performed the pathological analysis and helped to draft the manuscript. <b>NA </b>performed the lymphoscintigraphy and was medical investigator of the clinical trial. <b>JLG</b>, <b>SS </b>and <b>DH </b>were scientific investigators of the clinical trial, helped to draft the manuscript and performed the statistical analysis of the clinical trial. All authors read and approved the final manuscript.</p>
      </sec>
   </bdy>
   <bm>
      <ack>
         <sec>
            <st>
               <p>Acknowledgements</p>
            </st>
            <p>We thank Jean-Pierre Bellocq, Jean-Philippe Brettes, Marie-Pierre Chenard, Doris Frankhauser, Philippe Li&#233;geois, Jean-Louis Mehl and Roland Schaeffer for their collaboration and David Brasse and Karl Neuberger for their helpful discussions. This work was supported by funds from the Centre National de la Recherche Scientifique, the H&#244;pitaux Universitaires de Strasbourg, the University Louis Pasteur and the R&#233;gion Alsace. We are indebted to the Ligue Nationale Fran&#231;aise contre le Cancer and the Comit&#233;s du Haut-Rhin et du Bas-Rhin for their constant and considerable financial support.</p>
            <p>Written consent was obtained from the patient for publication of study.</p>
         </sec>
      </ack>
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