<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">ABCR</journal-id><journal-title-group><journal-title>Advances in Breast Cancer Research</journal-title></journal-title-group><issn pub-type="epub">2168-1589</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/abcr.2014.34019</article-id><article-id pub-id-type="publisher-id">ABCR-51130</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Non-Axillary Sentinel Node in Breast Cancer. Are we Staging Correctly? A Multicenter Study
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>avier</surname><given-names>Encinas Méndez</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Joan</surname><given-names>Francesc Julián Ibáñez</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Manel</surname><given-names>Cremades Pérez</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Jordi</surname><given-names>Navinés</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Josep</surname><given-names>Verge Schulte-Eversum</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Manel</surname><given-names>Fraile López-Amor</given-names></name><xref ref-type="aff" rid="aff2"><sup>2</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Manel</surname><given-names>Armengol Carrasco</given-names></name><xref ref-type="aff" rid="aff3"><sup>3</sup></xref></contrib></contrib-group><aff id="aff2"><addr-line>Hospital Germans Trias i Pujol, Badalona, Spain</addr-line></aff><aff id="aff1"><addr-line>Consorci Sanitari Garraf. H. Sant Camil, Sant Pere de Ribes, Spain</addr-line></aff><aff id="aff3"><addr-line>H. U. Vall d’ Hebron, Barcelona, Spain</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>Mcremades@outlook.com(MCP)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>22</day><month>10</month><year>2014</year></pub-date><volume>03</volume><issue>04</issue><fpage>124</fpage><lpage>130</lpage><history><date date-type="received"><day>22</day>	<month>August</month>	<year>2014</year></date><date date-type="rev-recd"><day>20</day>	<month>September</month>	<year>2014</year>	</date><date date-type="accepted"><day>14</day>	<month>October</month>	<year>2014</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Purpose: The study of the sentinel lymph node is the best technique to stage, have a prognosis and decide the adequate treatment in breast cancer. The usual technique implies studding the axillary lymph node. Our work tries to identify affected nodes in other regions apart from the axilla and its possible impact in staging and treatment. Methods: The sentinel lymph node technique was performed on 1660 patients included in an observational and multicentric study designed to observe the presence of metastatic cells in axillary and non-axillary lymph nodes. Results: In 19% of the patients the sentinel lymph node was detected in non-axillary regions. In these cases metastatic cells were more frequent which could suppose a change in the stage and/or treatment. As protective factor against non-axillary nodes involvement we found the localization of the cancer in external quadrants while youth and injecting the tracer inside the tumor were found to be risk factors. Conclusions: Detecting and studding non-axillary lymph nodes in breast cancer leads to a more precise staging of the disease which could imply a change in the optimal treatment.
 
</p></abstract><kwd-group><kwd>Breast Neoplasms</kwd><kwd> Sentinel Lymph Node Biopsy</kwd><kwd> Neoplasm Staging</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>Sentinel lymph node (SLN) assessment is the gold standard method to achieve a correct breast cancer staging [<xref ref-type="bibr" rid="scirp.51130-ref1">1</xref>]</p><p>and, subsequently, decide its optimal treatment. Moreover, it is known to be one of the main prognostic factors in this disease [<xref ref-type="bibr" rid="scirp.51130-ref2">2</xref>] .</p><p>It is remarkable that its use has usually been focused on the axillary lymph nodes, undervaluing hypothetic positive nodes in other areas and its possible consequences [<xref ref-type="bibr" rid="scirp.51130-ref3">3</xref>] .</p><p>Nevertheless, traditional interpretation of SLN biopsy (SLNB) results is recently being questioned. As almost 70% of positive axillary SLN patients do not have metastasis performing an axillary lymph node dissection (ALND) seems to be overtreatment [<xref ref-type="bibr" rid="scirp.51130-ref4">4</xref>] . Selected patients with specific tumor characteristic, even with a positive axillary SLN, may benefit from a conservative attitude, thus eliminating complications of axillary surgery with no adverse effect on survival [<xref ref-type="bibr" rid="scirp.51130-ref5">5</xref>] [<xref ref-type="bibr" rid="scirp.51130-ref6">6</xref>] .</p><p>Currently not many trials have been done to confirm this hypothesis so more research in this field is needed.</p><p>However, despite the decisions taken after this possible new interpretation, the SLN technique remains the main staging test in breast cancer.</p><p>That is why it is relevant to identify and examine sentinel lymph nodes located in other areas than the axilla to reach a more precise staging [<xref ref-type="bibr" rid="scirp.51130-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.51130-ref8">8</xref>] of the disease, changing its treatment if necessary.</p></sec><sec id="s2"><title>2. Material and Methods</title><p>A prospective, multicenter cohort study was undertaken in 9 different hospitals in Catalonia (Spain) from January 2000 to February 2008.</p><p>All patients diagnosed of breast cancer who underwent a sentinel lymph node assessment and accomplished the selection criteria (<xref ref-type="table" rid="table1">Table 1</xref>, <xref ref-type="table" rid="table2">Table 2</xref>) were enrolled.</p><p>The sample size was calculated using the ENE program and fixed to 1660 patients. As reference we took an estimated prevalence of 20% of positive non-axillary nodes (CI 95% and accuracy +/−2%).</p><p>We focused our study on nodal identification, whether axillary or non-axillary.</p><p>As secondary variables, and related to the breast cancer, we assessed the patients age, preoperative diagnostic, radiological diagnostic, margin status, palpable nodes, presence of micrometastasis, single or multiple nodal involvement, location, histological type, vascular or lymphatic infiltration, tumor size, positive hormone receptors and/or Erb2 and type of treatment.</p><p>Related to the SLN biopsy we studied the injection method, the number of nodes identified in the lymphoscintigraphy, the number of nodes identified in the dissection and the number of nodal metastasis.</p><p>To carry out the study all the institutions followed the same protocol.</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Inclusion criteria</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Inclusion Criteria</th></tr></thead><tr><td align="center" valign="middle" >Infiltrative carcinomas, less than 3 cm wide, with clinically negative axillary nodes</td></tr><tr><td align="center" valign="middle" >Multifocal tumor in the same breast quadrant</td></tr><tr><td align="center" valign="middle" >Large intraductal in situ carcinoma (&gt;3 cm, high grade and/or comedo)</td></tr><tr><td align="center" valign="middle" >Male patients with breast cancer and the same characteristics</td></tr></tbody></table></table-wrap><table-wrap id="table2" ><label><xref ref-type="table" rid="table2">Table 2</xref></label><caption><title> Exclusion criteria</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Exclusion Criteria</th></tr></thead><tr><td align="center" valign="middle" >Patients with no nodal involvement after SLNB</td></tr><tr><td align="center" valign="middle" >Pregnancy</td></tr><tr><td align="center" valign="middle" >Multicentric tumors</td></tr><tr><td align="center" valign="middle" >Patients with advanced disease who require preoperative chemotherapy or those who present metastatic axillary nodes after FNA</td></tr><tr><td align="center" valign="middle" >Inflammatory breast carcinoma</td></tr><tr><td align="center" valign="middle" >Previous axillary radiotherapy</td></tr><tr><td align="center" valign="middle" >Previous axillary surgery</td></tr></tbody></table></table-wrap><p>The day before surgery patients were visited and, after and axillary sonography to rule out suspicious unpalpable lymph nodes, 0.3 ml of tracer (99 m-Tc labeled human albumin) was injected either inside of the tumor, peritumorally, subdermally or subareorarly. No colorant was used.</p><p>In case of positive sonography fine needle aspiration (FNA) cytology was performed.</p><p>Sentinel nodes (SNs) were initially identified with lymphoscintigraphy to ease surgical location and dissection. Surgery took place the day after the lymphoscintigraphic study and a hand-held γ-probe was used to identify SNs following the 10% rule.</p><p>Cytology was carried out perioperatively when axillary SNs were located, proceeding to perform an axillary lymph node dissection (ALND) if positive. On the other hand, when internal mammary SNs were located its study was completed postoperatively as results would not modify the surgical procedure.</p><p>Next, all SNs were studied with immunohistochemical analysis to detect unseen metastasis in the cytology.</p><p>In case of positive results our therapeutic approach varied depending on the size and location:</p><p>&#183; More than 2 mm: We performed a complete ALND;</p><p>&#183; Between 0.2 and 2 mm (micrometastasis): Patients joined a clinical trial where ALND and routine controls were compared [<xref ref-type="bibr" rid="scirp.51130-ref9">9</xref>] ;</p><p>&#183; Less than 0.2 mm: Were considered as isolated tumor cells (ITC) so no ALND was carried out;</p><p>&#183; If located in the internal mammary radiotherapy was indicated.</p><p>Once all data was collected we carried out descriptive, bivariate and multivariate analysis with the statistical softwares SPSS and G-Stat with a P value &lt; 0.05.</p></sec><sec id="s3"><title>3. Results</title><p>A middle age woman, with a single palpable tumor located in the upper outer quadrants was the most common presentation. Infiltrative ductal carcinoma with hormone receptor expression represented the typical histology. The most frequent nodal location was axillary followed by simultaneous axillary and non-axillary drainage.</p><p>Lymph node metastasis varied depending on its location. Thus, patients with drainage to axillary and non- axillary nodes, without involvement of internal mammary ones, were the group of patients who presented a higher rate of metastasis. Afterwards, we found those who had involvement of non-axillary nodes with exception of internal mammary ones, followed by those who presented simultaneous axillary and internal mammary nodes. It is not until the fourth group that we found patients with only axillary drainage and, finally, patients with only involvement of internal mammary nodes.</p><p>Patients, tumor and drainage characteristics are presented in <xref ref-type="table" rid="table3">Table 3</xref>.</p></sec><sec id="s4"><title>4. Bivariate Statistical Analysis</title><p>Patients that presented non-axillary drainage were statistically younger, with an average age of 52 yo, in comparison with those who had axillary drainage (p &lt; 0.001) (<xref ref-type="table" rid="table4">Table 4</xref>). Similarly, younger patients presented a greater proportion of non-axillary drainage.</p><p>Regarding the injection technique, intratumoral and peritumoral injection also showed a greater tendency towards non-axillary nodes [<xref ref-type="bibr" rid="scirp.51130-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.51130-ref11">11</xref>] than subdermal or subareolar injection (p = 0.009) (<xref ref-type="table" rid="table5">Table 5</xref>).</p><p>It’s also remarkable that the number of sentinel nodes detected was statistically larger when non-axillary drainage was present (p &lt; 0.001) and the incidence of metastatic nodes was higher too in this scenario (p &lt; 0.001).</p><p>Tumor location, as described in the literature, is clearly related to lymph drainage. Accordingly, in our study, tumors in outer quadrants tended to have a lymphatic drain towards axillary nodes (53% vs 39%; p &lt; 0.001) while those in inner quadrants presented opposite results (47% vs 61%; p &lt; 0.001).</p><p>Patients with non-axillary nodes affected had more aggressive tumors. Mastectomies were more frequent in these cases than tumorectomies (18 vs 13%; p = 0.014) and vascular and lymphatic infiltration were more prevalent (33% vs 18%) although the difference was not statistically significant (p = 0.064).</p><p>There were no apparent differences in tumor size, presence of free margins after surgery, micrometastasis, hormone receptors, HER 2 expression, histologic type and grade of cancer.</p></sec><sec id="s5"><title>5. Multivariate Statistical Analysis</title><p>A logistic regression was carried out to identify important dependent variables related with axillary and non- axillary lymph draining.</p><p>As dependent variables we included the tumor location, the number of nodes dissected, the number of metastatic nodes, the age and the tracer injection method. The model was statistically significant with p &lt; 0.001.</p><p>Results showed that being less than 50 yo (OR = 2.21) and intratumoral and peritumoral tracer injection (OR = 1.52) were risk factors to present non-axillary lymph nodes involvement (<xref ref-type="table" rid="table6">Table 6</xref>).</p><table-wrap id="table3" ><label><xref ref-type="table" rid="table3">Table 3</xref></label><caption><title> Patient, tumor and drainage characteristics</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Number of Patients</th><th align="center" valign="middle" >1660 Women</th></tr></thead><tr><td align="center" valign="middle" >Mean Age</td><td align="center" valign="middle" >57 years old</td></tr><tr><td align="center" valign="middle" >Major Incidence Range</td><td align="center" valign="middle" >50 to 63 years old</td></tr><tr><td align="center" valign="middle" >Palpable Tumor</td><td align="center" valign="middle" >53% of cases</td></tr><tr><td align="center" valign="middle" >Single Tumor</td><td align="center" valign="middle" >89% of cases</td></tr><tr><td align="center" valign="middle"  rowspan="8"  >Location</td><td align="center" valign="middle" >34.96% upper outer quadrant</td></tr><tr><td align="center" valign="middle" >16.20% upper quadrant union</td></tr><tr><td align="center" valign="middle" >11.44% upper inner quadrant</td></tr><tr><td align="center" valign="middle" >10.38% outer quadrant union</td></tr><tr><td align="center" valign="middle" >9.19% inner quadrant union</td></tr><tr><td align="center" valign="middle" >8.38% areolar</td></tr><tr><td align="center" valign="middle" >5.13% lower outer quadrant</td></tr><tr><td align="center" valign="middle" >4.32% lower inner quadrant</td></tr><tr><td align="center" valign="middle"  rowspan="5"  >Histology</td><td align="center" valign="middle" >70.4% infiltrative ducal carcinoma</td></tr><tr><td align="center" valign="middle" >11.87% intraductal in situ carcinoma</td></tr><tr><td align="center" valign="middle" >5.86% infiltrative intraductal carcinoma</td></tr><tr><td align="center" valign="middle" >5.73% lobulillar carcinoma</td></tr><tr><td align="center" valign="middle" >8.14% others</td></tr><tr><td align="center" valign="middle" >Size</td><td align="center" valign="middle" >1.82 cm (SD 0.98; range 0.2 - 8.1 cm)</td></tr><tr><td align="center" valign="middle" >Vascular or Linfatic Infiltration</td><td align="center" valign="middle" >28% of cases</td></tr><tr><td align="center" valign="middle" >Positive Hormone Receptors</td><td align="center" valign="middle" >83% of cases</td></tr><tr><td align="center" valign="middle" >Positive Erb2</td><td align="center" valign="middle" >30% of cases</td></tr><tr><td align="center" valign="middle"  rowspan="4"  >Tracer Injection</td><td align="center" valign="middle" >59.81% intratumoral</td></tr><tr><td align="center" valign="middle" >31.57% intratumoral + subdermal</td></tr><tr><td align="center" valign="middle" >6.44% peritumoral</td></tr><tr><td align="center" valign="middle" >2.19% subareolar</td></tr><tr><td align="center" valign="middle" >Number of Nodes Biopsied</td><td align="center" valign="middle" >1.44 (SD 0.69)</td></tr><tr><td align="center" valign="middle" >Number of Metastatic Sentinel Nodes</td><td align="center" valign="middle" >0.3 (SD 0.56)</td></tr><tr><td align="center" valign="middle"  rowspan="3"  >Nodal Location</td><td align="center" valign="middle" >1.364 axillary (82.2%)</td></tr><tr><td align="center" valign="middle" >267 axillary and non-axillary (16.1%)</td></tr><tr><td align="center" valign="middle" >29 extra-axillary (1.7%)</td></tr><tr><td align="center" valign="middle"  rowspan="2"  >Surgical Treatment</td><td align="center" valign="middle" >86.45% tumorectomy</td></tr><tr><td align="center" valign="middle" >13.55% mastectomy</td></tr><tr><td align="center" valign="middle" >Axillary Lymph Node Dissection</td><td align="center" valign="middle" >24% of cases</td></tr><tr><td align="center" valign="middle" >Metastatic Nodes</td><td align="center" valign="middle" >0.87 (SD 2.15; range 0 - 21)</td></tr></tbody></table></table-wrap><table-wrap id="table4" ><label><xref ref-type="table" rid="table4">Table 4</xref></label><caption><title> Quantitative variables comparing axillary vs non-axillary drainage</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >Non-Axillary (mean)</th><th align="center" valign="middle" >Axillary (mean)</th><th align="center" valign="middle" >p-Value</th></tr></thead><tr><td align="center" valign="middle" >Age</td><td align="center" valign="middle" >52</td><td align="center" valign="middle" >58</td><td align="center" valign="middle" >&lt;0.001</td></tr><tr><td align="center" valign="middle" >Nodes Identified</td><td align="center" valign="middle" >2.05</td><td align="center" valign="middle" >1.29</td><td align="center" valign="middle" >&lt;0.001</td></tr><tr><td align="center" valign="middle" >Mestatatic Nodes</td><td align="center" valign="middle" >0.46</td><td align="center" valign="middle" >0.26</td><td align="center" valign="middle" >&lt;0.001</td></tr><tr><td align="center" valign="middle" >Tumoral Size (cm)</td><td align="center" valign="middle" >1.87</td><td align="center" valign="middle" >1.81</td><td align="center" valign="middle" >0.299</td></tr></tbody></table></table-wrap><table-wrap id="table5" ><label><xref ref-type="table" rid="table5">Table 5</xref></label><caption><title> Qualitative variables comparing axillary vs non-axillary drainage</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >Non-Axillary N (%)</th><th align="center" valign="middle" >Axillary N (%)</th><th align="center" valign="middle" >p-Value</th></tr></thead><tr><td align="center" valign="middle" >Age</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >&lt;0.001</td></tr><tr><td align="center" valign="middle" >&lt;50 yo</td><td align="center" valign="middle" >155 (49.4)</td><td align="center" valign="middle" >379 (28.6)</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >&gt;50 yo</td><td align="center" valign="middle" >159 (50.6)</td><td align="center" valign="middle" >945 (71.4)</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Injection Method</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >0.009</td></tr><tr><td align="center" valign="middle" >Intratumoral</td><td align="center" valign="middle" >204 (65.2)</td><td align="center" valign="middle" >781 (58.5)</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Peritumoral</td><td align="center" valign="middle" >24 (7.7)</td><td align="center" valign="middle" >82 (6.1)</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Subdermal</td><td align="center" valign="middle" >84 (26.8)</td><td align="center" valign="middle" >436 (31.6)</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Subareolar</td><td align="center" valign="middle" >1 (0.3)</td><td align="center" valign="middle" >35 (2.6)</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Treatment</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >0.014</td></tr><tr><td align="center" valign="middle" >Tumorectomy</td><td align="center" valign="middle" >261 (82.1)</td><td align="center" valign="middle" >1162 (87.5)</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Mastectomy</td><td align="center" valign="middle" >57 (17.9)</td><td align="center" valign="middle" >166 (12.5)</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Tumor Location</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >&lt;0.001</td></tr><tr><td align="center" valign="middle" >Outer Quadrants</td><td align="center" valign="middle" >122 (39.2)</td><td align="center" valign="middle" >685 (53.2)</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Inner Quadrants</td><td align="center" valign="middle" >189 (60.8)</td><td align="center" valign="middle" >603 (46.8)</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Vascular/Lymphatic Infiltration</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Yes</td><td align="center" valign="middle" >54 (33.5)</td><td align="center" valign="middle" >375 (26.3)</td><td align="center" valign="middle" >0.064</td></tr><tr><td align="center" valign="middle" >No</td><td align="center" valign="middle" >107 (66.5)</td><td align="center" valign="middle" >522 (73.7)</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Number of Nodes</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >1 or more</td><td align="center" valign="middle" >101 (31.8)</td><td align="center" valign="middle" >328 (24.4)</td><td align="center" valign="middle" >0.007</td></tr><tr><td align="center" valign="middle" >0</td><td align="center" valign="middle" >217 (68.2)</td><td align="center" valign="middle" >1014 (75.6)</td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Free Margins</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >0.501</td></tr><tr><td align="center" valign="middle" >Cytology</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >0.169</td></tr><tr><td align="center" valign="middle" >Micrometastasis</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >0.843</td></tr><tr><td align="center" valign="middle" >Single/Multiple</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >0.346</td></tr><tr><td align="center" valign="middle" >Histology</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >0.130</td></tr><tr><td align="center" valign="middle" >Hormone Receptors</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >0.222</td></tr><tr><td align="center" valign="middle" >Erb2</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td><td align="center" valign="middle" >0.184</td></tr></tbody></table></table-wrap><table-wrap id="table6" ><label><xref ref-type="table" rid="table6">Table 6</xref></label><caption><title> Multivariate analysis</title></caption><table><tbody><thead><tr><th align="center" valign="middle" ></th><th align="center" valign="middle" >p-Value</th><th align="center" valign="middle" >OR</th><th align="center" valign="middle" >CI 95%</th></tr></thead><tr><td align="center" valign="middle" >Age</td><td align="center" valign="middle" >&lt;0.001</td><td align="center" valign="middle" >2.21</td><td align="center" valign="middle" >1.64 - 2.98</td></tr><tr><td align="center" valign="middle" >Number of nodes</td><td align="center" valign="middle" >&lt;0.001</td><td align="center" valign="middle" >0.22</td><td align="center" valign="middle" >0.18 - 0.28</td></tr><tr><td align="center" valign="middle" >Metastasic nodes</td><td align="center" valign="middle" >0.579</td><td align="center" valign="middle" ></td><td align="center" valign="middle" ></td></tr><tr><td align="center" valign="middle" >Location</td><td align="center" valign="middle" >&lt;0.001</td><td align="center" valign="middle" >0.49</td><td align="center" valign="middle" >0.36 - 0.67</td></tr><tr><td align="center" valign="middle" >Injection method</td><td align="center" valign="middle" >&lt;0.001</td><td align="center" valign="middle" >1.52</td><td align="center" valign="middle" >1.10 - 2.10</td></tr></tbody></table></table-wrap><p>On the contrary, outer quadrants location of the tumor seemed to be a protective factor (OR = 0.49).</p><p>The number of nodes detected remained higher when non-axillary drainage was detected but the number of metastatic nodes was not statistically different when analyzed simultaneously with the number of nodes detected (p = 0.579).</p></sec><sec id="s6"><title>6. Discussion</title><p>Breast cancer is a very prevalent illness and implies important clinical and aesthetic consequences, mainly in women. Nevertheless, thanks to the evolution of diagnostics and treatments, almost 80% of patients get cured.</p><p>But not only rates of cure must be taken into account. To avoid consequences of surgical treatment the SLNB technique was developed, saving lots of unnecessary axillary dissections.</p><p>Nowadays this question is more up-to-date than ever given that, even with a positive axillary SLN, the necessity of performing an ALND is being questioned in the literature [<xref ref-type="bibr" rid="scirp.51130-ref4">4</xref>] -[<xref ref-type="bibr" rid="scirp.51130-ref6">6</xref>] [<xref ref-type="bibr" rid="scirp.51130-ref12">12</xref>] . Essentially, this implies that to improve our treatments and adapt them to each patient needs, an accurate staging must previously be carried out.</p><p>Consequently, although axillary draining is the most common and its implications have been well studied, non-axillary drainage is often underestimated. Current research shows draining towards internal mammary nodes in a range between 2.4% and 23.3% [<xref ref-type="bibr" rid="scirp.51130-ref7">7</xref>] [<xref ref-type="bibr" rid="scirp.51130-ref13">13</xref>] [<xref ref-type="bibr" rid="scirp.51130-ref14">14</xref>] . Obviously, this proportion gets higher when Rotter, in- tramammary or intercostal nodes are also included. This fact may lead to suppose that an incorrect staging is sometimes performed, meaning that a suboptimal treatment could be given.</p><p>It is important to highlight that almost 20% of breast neoplasm present lymphatic draining to non-axillary nodes, the vast majority with concomitant draining to axillary ones, being more frequently metastatic.</p><p>The presence of metastatic nodes in non-axillary regions would imply a change in the illness stage in case of negative axillary ones. Moreover, those patients presenting both axillary and non-axillary metastatic nodes would remain in the same illness stage but optimal treatment would require addition of radiotherapy, at least in internal mammary nodal chain [<xref ref-type="bibr" rid="scirp.51130-ref14">14</xref>] .</p><p>Another interesting consequence is that, traditionally, it has been proposed that the presence of nodal metastasis could imply a lymphatic block that could lead to alternative drainage pathways. This may be the reason why there seems to be more metastatic nodes when simultaneous drainage to axillary and non-axillary regions is present [<xref ref-type="bibr" rid="scirp.51130-ref10">10</xref>] . However, more studies need to be done to confirm this hypothesis.</p><p>If that was the case, the attitude in patients with positive preoperative axillary nodes should be reconsidered as, currently, the SLNB is dismissed and an ALND is directly performed. Consequently, we fail to know if there is simultaneous draining towards non-axillary nodes which would be an indication of postoperative radiotherapy.</p><p>Unfortunately, given the usual difficulty to reach non-axillary nodes, its dissection is hardly ever performed.</p><p>In conclusion, we consider that doing a biopsy of non-axillary nodes is an important factor to carry out an accurate staging of the disease, and therefore, decide the optimal treatment in each patient [<xref ref-type="bibr" rid="scirp.51130-ref8">8</xref>] . Moreover, traditional staging should also be reconsidered given that atypical nodal location is not considered.</p></sec><sec id="s7"><title>NOTES</title></sec></body><back><ref-list><title>References</title><ref id="scirp.51130-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Moncayo, V.M., Aarsvold, J.N., Grant, S.F., Bartley, S.C. and Alazraki, N.P. (2013) Status of Sentinel Lymph Node for Breast Cancer. Seminars in Nuclear Medicine, 43, 281-293. http://dx.doi.org/10.1053/j.semnuclmed.2013.02.004</mixed-citation></ref><ref id="scirp.51130-ref2"><label>2</label><mixed-citation publication-type="other" xlink:type="simple">García Fernández, A., Chabrera, C., García Font, M., Fraile, M., Lain, J.M., Barco, I., González, C., Gónzalez, S., Rene, A., Veloso, E., Cassadó, J., Pessarrodona, A. and Giménez, N. (2013) Positive versus Negative Sentinel Nodes in Early Breast Cancer Patients: Axillary or Loco-Regional Relapse and Survival. A Study Spanning 2000-2012. Breast, 22, 902-907. http://dx.doi.org/10.1016/j.breast.2013.04.015</mixed-citation></ref><ref id="scirp.51130-ref3"><label>3</label><mixed-citation publication-type="other" xlink:type="simple">Kim, H., Shin, M.J., Kim, S.J., Kim, I.J. and Park, I. (2014) The Relation of Visualization of Internal Mammary Lymph Nodes on Lymphoscintigraphy to Axillary Lymph Node Metastases in Breast Cancer. Lymphatic Research and Biology, 21.</mixed-citation></ref><ref id="scirp.51130-ref4"><label>4</label><mixed-citation publication-type="other" xlink:type="simple">Grabau, D., Dihge, L., Ferno, M., Ingvar, C. and Rydén, L. (2013) Completion Axillary Dissection Can Safely Be Omitted in Screen Detected Breast Cancer Patients with Micrometastases. A Decade’s Experience from a Single Institution. European Journal of Surgical Oncology (EJSO), 39, 601-607. http://dx.doi.org/10.1016/j.ejso.2013.03.012</mixed-citation></ref><ref id="scirp.51130-ref5"><label>5</label><mixed-citation publication-type="other" xlink:type="simple">Krishnan, MS, Recht, A., Bellon, J.R. and Punglia, R.S. (2013) Trade-Offs Associated with Axillary Lymph Node Dissection with Breast Irradiation versus Breast Irradiation Alone in patients with a Positive Sentinel Node in Relation to the Risk of Non-Sentinel Node Involvement: Implications of ACOSOG Z0011. Breast Cancer Research and Treatment, 138, 205-213.</mixed-citation></ref><ref id="scirp.51130-ref6"><label>6</label><mixed-citation publication-type="other" xlink:type="simple">Suyoi, A., Bains, S.K., Kothari, A., Douek, M., Agbaje, O., Hamed, H., Fentiman, I., Pinder, S. and Purushotham, A.D. (2014) When Is a Completion Axillary Lymph Node Dissection Necessary in the Presence of a Positive Sentinel Lymph Node? European Journal of Cancer, 50, 690-697. http://dx.doi.org/10.1016/j.ejca.2013.11.024</mixed-citation></ref><ref id="scirp.51130-ref7"><label>7</label><mixed-citation publication-type="other" xlink:type="simple">Gnerlich, J.L., Barreto-Andrade, J.C., Czechura, T., John, J.R., Turk, M.A., Kennedy, T.J. and Winchester, D.J. (2014) Accurate Staging with Internal Mammary Chain Sentinel Node Biopsy for Breast Cancer. Annals of Surgical Oncology, 21, 368-374. http://dx.doi.org/10.1245/s10434-013-3263-4</mixed-citation></ref><ref id="scirp.51130-ref8"><label>8</label><mixed-citation publication-type="other" xlink:type="simple">Caudle, A.S., Yi, M., Hoffman, K.E., Mittendorf, E.A., Babiera, G.V., Hwang, R.F., Meric-Bernstam, F., Sahin, A.A. and Hunt, K.K. (2014) Impact of Identification of Internal Mammary Sentinel Lymph Node Metastasis in Breast Cancer Patients. Annals of Surgical Oncology, 21, 60-65. http://dx.doi.org/10.1245/s10434-013-3276-z</mixed-citation></ref><ref id="scirp.51130-ref9"><label>9</label><mixed-citation publication-type="other" xlink:type="simple">Solá, M., Alberro, J.A., Fraile, M., Santesteban, P., Ramos, M., Fabregas, R., Moral, A., Ballester, B. and Vidal, S. (2013) Complete Axillary Lymph Node Dissection versus Clinical Follow-Up in Breast Cancer Patients with Sentinel Node Micrometastasis: Final Results from the Multicenter Clinical Trial AATRM 048/13/2000. Annals of Surgical Oncology, 20, 120-127. http://dx.doi.org/10.1245/s10434-012-2569-y</mixed-citation></ref><ref id="scirp.51130-ref10"><label>10</label><mixed-citation publication-type="other" xlink:type="simple">Garcia-Manero, M., Olartecoechea, B. and Royo, P. (2010) Different Injection Sites of Radionuclide for Sentinel Lymph Node Detection in Breast Cancer: Single Institution Experience. European Journal of Obstetrics &amp; Gynecology and Reproductive Biology, 153, 185-187. http://dx.doi.org/10.1016/j.ejogrb.2010.06.024</mixed-citation></ref><ref id="scirp.51130-ref11"><label>11</label><mixed-citation publication-type="other" xlink:type="simple">Noushi, F., Spillane, A.J., Uren, R.F., Cooper, R., Allwright, S., Snook, K.L., Gillet, D., Pearce, A.M. and Gebski, V. (2013) High Discordance Rates between Sub-Areolar and Peri-Tumoural Breast Lymphoscintigraphy. European Journal of Surgical Oncology (EJSO), 39, 1053-1060. http://dx.doi.org/10.1016/j.ejso.2013.06.006</mixed-citation></ref><ref id="scirp.51130-ref12"><label>12</label><mixed-citation publication-type="other" xlink:type="simple">Gatzemeier, W. and Mann, G.B. (2013) Which Sentinel Lymph-Node (SLN) Positive Breast Cancer Patient Needs an Axillary Lymph-Node Dissection (ALND)—ACOSOG Z0011 Results and beyond. Breast, 22, 211-216.</mixed-citation></ref><ref id="scirp.51130-ref13"><label>13</label><mixed-citation publication-type="other" xlink:type="simple">Van der Ploeg, I.M., Tanis, P.J., Valdés Olmos, R.A., Kroon, B.B., Rutgers, E.J. and Nieweg, O.E. (2008) Breast Cancer Patients with Extra-Axillary Sentinel Nodes Only May Be Spared Axillary Lymph Node Dissection. Annals of Surgical Oncology, 15, 3239-3243. http://dx.doi.org/10.1245/s10434-008-0120-y</mixed-citation></ref><ref id="scirp.51130-ref14"><label>14</label><mixed-citation publication-type="other" xlink:type="simple">Cong, B.B., Qiu, P.F. and Wang, Y.S. (2014) Internal Mammary Sentinel Lymph Node Biopsy: Minimally Invasive Staging and Tailored Internal Mammary Radiotherapy. Annals of Surgical Oncology, 21, 2119-2121.  
http://dx.doi.org/10.1245/s10434-014-3650-5</mixed-citation></ref></ref-list></back></article>