<?xml version="1.0" encoding="ISO-8859-1"?><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
<front>
<journal-meta>
<journal-id>1646-5830</journal-id>
<journal-title><![CDATA[Acta Obstétrica e Ginecológica Portuguesa]]></journal-title>
<abbrev-journal-title><![CDATA[Acta Obstet Ginecol Port]]></abbrev-journal-title>
<issn>1646-5830</issn>
<publisher>
<publisher-name><![CDATA[Euromédice, Edições Médicas Lda.]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S1646-58302016000300007</article-id>
<title-group>
<article-title xml:lang="pt"><![CDATA[Esvaziamento axilar: um procedimento em desuso?]]></article-title>
<article-title xml:lang="en"><![CDATA[Axillary lymph node dissection: still a necessary procedure?]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Valadares]]></surname>
<given-names><![CDATA[Sara Lince]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
<xref ref-type="aff" rid="A03"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Oliveira]]></surname>
<given-names><![CDATA[Sónia]]></given-names>
</name>
<xref ref-type="aff" rid="A04"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Pires]]></surname>
<given-names><![CDATA[Francisca]]></given-names>
</name>
<xref ref-type="aff" rid="A05"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Sereno]]></surname>
<given-names><![CDATA[Pedro]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Mira]]></surname>
<given-names><![CDATA[Ricardo]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
<xref ref-type="aff" rid="A02"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Centro Hospitalar Lisboa Central Maternidade Dr. Alfredo da Costa Unidade de Patologia Mamária]]></institution>
<addr-line><![CDATA[Lisboa ]]></addr-line>
</aff>
<aff id="A02">
<institution><![CDATA[,Universidade NOVA de Lisboa Faculdade Ciências Médicas ]]></institution>
<addr-line><![CDATA[Lisboa ]]></addr-line>
</aff>
<aff id="A03">
<institution><![CDATA[,Hospital da Luz  ]]></institution>
<addr-line><![CDATA[ ]]></addr-line>
</aff>
<aff id="A04">
<institution><![CDATA[,Centro Hospitalar Lisboa Central Hospital Sto António dos Capuchos ]]></institution>
<addr-line><![CDATA[Lisboa ]]></addr-line>
</aff>
<aff id="A05">
<institution><![CDATA[,Instituto Português de Oncologia de Lisboa, Francisco Gentil  ]]></institution>
<addr-line><![CDATA[Lisboa ]]></addr-line>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>09</month>
<year>2016</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>09</month>
<year>2016</year>
</pub-date>
<volume>10</volume>
<numero>3</numero>
<fpage>230</fpage>
<lpage>239</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_arttext&amp;pid=S1646-58302016000300007&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_abstract&amp;pid=S1646-58302016000300007&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://scielo.pt/scielo.php?script=sci_pdf&amp;pid=S1646-58302016000300007&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="en"><p><![CDATA[Sentinel lymph node biopsy (SLNB) is the gold standard procedure for breast cancer staging and axillary lymph node dissection (AD) is recommended when metastasis are found. Two recent practice-changing studies altered this paradigm. They brought into discussion old unanswered questions, such as the impact of AD on morbidity, survival and choice of adjuvant therapy as well as new questions, like the role of radiotherapy and the omission of AD after positive SLNB. The authors reviewed the literature focusing on these issues and concluded that AD after positive SLNB can be omitted in selected cases.]]></p></abstract>
<kwd-group>
<kwd lng="en"><![CDATA[Breast neoplasm]]></kwd>
<kwd lng="en"><![CDATA[Lymph node excision]]></kwd>
<kwd lng="en"><![CDATA[Sentinel node]]></kwd>
<kwd lng="en"><![CDATA[Axilla]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[ <p align="right"><font size="2"><b>ARTIGO DE REVIS&#195;O/</B>REVIEW ARTICLE</font></p>     <p><font size="4"><b>Esvaziamento axilar: um procedimento em desuso?</b></font></p>     <p><font size="3"><b>Axillary lymph node dissection: still a necessary procedure?</b></font></p>     <p><b>Sara Lince Valadares*, S&#243;nia Oliveira**, Francisca Pires***, Pedro Sereno****, Ricardo Mira***** </b></p>     <p>Unidade de Patologia Mam&#225;ria da Maternidade Dr. Alfredo da Costa / Centro Hospitalar Lisboa Central</p>     <p>Faculdade Ci&#234;ncias M&#233;dicas da Universidade NOVA de Lisboa</p>     <p>*Assistente Hospitalar de Ginecologia e Obstetr&#237;cia da Maternidade Dr. Alfredo Costa/Centro Hospitalar Lisboa Central e Hospital da Luz</p>     <p>**Assistente Hospitalar de Oncologia M&#233;dica, Hospital Sto Ant&#243;nio dos Capuchos/Centro Hospitalar Lisboa Central</p>     <p>***Assistente Hospitalar de Radioterapia, Instituto Portugu&#234;s de Oncologia de Lisboa, Francisco Gentil, Lisboa</p>     <p>****Assistente Hospitalar de Ginecologia e Obstetr&#237;cia da Maternidade Dr. Alfredo Costa/Centro Hospitalar Lisboa Central</p>     ]]></body>
<body><![CDATA[<p>*****Diretor do Servi&#231;o de Ginecologia e Obstetr&#237;cia do Centro Hospitalar Lisboa Central; Professor Auxiliar Convidado da Faculdade de Ci&#234;ncias M&#233;dicas da Universidade Nova de Lisboa</p>     <p><a href="#c0">Endere&ccedil;o para correspond&ecirc;ncia</a> | <a href="#c0">Direcci&oacute;n para correspondencia</a> | <a href="#c0">Correspondence</a><a name="topc0"></a></p> <hr/>     <p>&nbsp;</p>     <p><b>ABSTRACT</b></p>     <p>Sentinel lymph node biopsy (SLNB) is the gold standard procedure for breast cancer staging and axillary lymph node dissection (AD) is recommended when metastasis are found. Two recent practice-changing studies altered this paradigm. They brought into discussion old unanswered questions, such as the impact of AD on morbidity, survival and choice of adjuvant therapy as well as new questions, like the role of radiotherapy and the omission of AD after positive SLNB. The authors reviewed the literature focusing on these issues and concluded that AD after positive SLNB can be omitted in selected cases.</p>     <p><b>Keywords: </b>Breast neoplasm; Lymph node excision; Sentinel node; Axilla.</p> <hr/>     <p>&nbsp;</p>     <p><b>Introdu&#231;&#227;o</b></p>     <p>Halsted, no in&#237;cio do s&#233;culo XX, prop&#244;s a mastectomia radical como tratamento <i>goldstandard</i> no cancro da mama<sup>1</sup>. Desde ent&#227;o, em virtude da morbilidade associada a este procedimento e em resultado dos progressos entretanto verificados no conhecimento da biologia do tumor, aquela realidade tem vindo a mudar. Assim, na d&#233;cada de 80 vem a confirmar-se, em ensaios cl&#237;nicos<sup>2-4</sup> que o tratamento conservador da mama &#233; seguro, pelo que esta possibilidade passa a ser oferecida &#224; maioria das mulheres com cancro precocemente detetado.</p>     <p>Uma nova barreira &#233; ultrapassada com a introdu&#231;&#227;o e uso generalizado da bi&#243;psia de g&#226;nglio sentinela (BGS) no estadiamento da axila<sup>5,6</sup>. Se o estado da axila &#233; um dos principais fatores de progn&#243;stico no cancro da mama<sup>7,8</sup>, j&#225; o impacto do esvaziamento axilar (EA) no curso da doen&#231;a &#233; mais controverso, tendo vindo a ser posto em causa por in&#250;meros estudos. </p>     ]]></body>
<body><![CDATA[<p>Os autores rev&#234;m a evid&#234;ncia existente na avalia&#231;&#227;o e tratamento da axila com particular enfoque em dois estudos recentes e potencialmente modificadores da conduta cl&#237;nica, ACOSOGZ0011<sup>9</sup> e AMAROS<sup>10</sup>, procurando responder, nesta perspetiva, &#224;s seguintes perguntas: Qual a morbilidade associada ao esvaziamento axilar? Qual a import&#226;ncia do esvaziamento axilar para a sobreviv&#234;ncia? Ap&#243;s biopsia de g&#226;nglio sentinela podemos suprimir o EA na presen&#231;a de micromet&#225;stases? Ap&#243;s biopsia de g&#226;nglio sentinela podemos suprimir o EA na presen&#231;a de macromet&#225;stases? Qual o papel da radioterapia (RT) da axila? Qual a import&#226;ncia do EA na escolha de terap&#234;utica adjuvante? </p>     <p><b>Qual a morbilidade associada ao esvaziamento axilar?</b></p>     <p>A taxa de complica&#231;&#245;es associada ao EA situa-se entre 15 a 20% e compreende dor cr&#243;nica, parestesias, disfun&#231;&#227;o articular do ombro e linfedema<sup>11,12</sup>. No estudo AMAROS, o linfedema foi reportado em 23% das doentes submetidas a EA e noutros m&#250;ltiplos estudos, nos quais foi feita randomiza&#231;&#227;o para EA vs RT axila ou isen&#231;&#227;o de interven&#231;&#227;o sobre a axila, os resultados levaram, de forma consensual, &#224; conclus&#227;o que o EA est&#225; associado a uma maior morbilidade<sup>13,14</sup>. </p>     <p>Aos mesmos resultados e conclus&#245;es chegou o ensaio ACOSOGZ0011 desenhado com o objetivo secund&#225;rio de avaliar a morbilidade do EA. Comparou entre realiza&#231;&#227;o de EA ou n&#227;o em doentes submetidas a tumorectomia com BGS positiva. No grupo com EA foi referida uma maior taxa de infe&#231;&#227;o, seroma e parestesia. A presen&#231;a de linfedema tamb&#233;m foi significativamente superior neste grupo (13% vs 2% ao fim de 1 ano). Globalmente a taxa de complica&#231;&#245;es cir&#250;rgicas foi de 70% no grupo com EA e 25% no grupo com BGS (p&lt;,001)<sup>14</sup>.</p>     <p>Assim, a morbilidade do EA, a maioria das vezes permanente, est&#225; bem documentada, sendo ainda de salientar, nos casos em que o EA &#233; feito num segundo tempo operat&#243;rio, as complica&#231;&#245;es e custos associados a uma nova interven&#231;&#227;o.</p>     <p><b>Qual a import&#226;ncia do esvaziamento axilar para a sobreviv&#234;ncia?</b></p>     <p>O n&#250;mero de g&#226;nglios axilares metast&#225;ticos &#233; um excelente fator preditivo de sobreviv&#234;ncia livre de doen&#231;a (SLD) sabendo-se que o seu n&#250;mero aumenta em propor&#231;&#227;o com o tamanho do componente invasivo do tumor<sup>7,8,15</sup>, mas o impacto do EA no curso da doen&#231;a, abordado em in&#250;meros estudos, &#233; controverso. </p>     <p>Nos primeiros estudos foram analisadas s&#233;ries de doentes aos quais o EA n&#227;o foi efetuado sem aparente preju&#237;zo na respetiva sobreviv&#234;ncia. Uma s&#233;rie de 327 doentes, clinicamente nos estadios I e II, tratadas com cirurgia conservadora mais RT, obteve uma sobreviv&#234;ncia global (SG), a 10 anos, de 71% com 3% de recidiva axilar<sup>16</sup>. </p>     <p>Silverstein publica dados referentes &#224; taxa de envolvimento axilar de acordo com o tamanho tumoral e conclui que, para tumores inferiores a 5 mm, com uma taxa de g&#226;nglios axilares positivos de 3%, seria seguro omitir o EA<sup>15</sup>. </p>     <p>Greco em 2000 publica os resultados do acompanhamento durante 5 anos de 401 doentes submetidas a cirurgia mam&#225;ria sem EA, com estadiamento cl&#237;nico T1-2 N0, e que fizeram tamoxifeno como &#250;nica terap&#234;utica adjuvante. A taxa de recidiva axilar foi de 2% e 1,7% para as doentes com tumores T1a e T1b e mais alta para as mulheres com tumores T1c e T2, respetivamente 10% e 18%. A taxa de met&#225;stases &#224; dist&#226;ncia foi inferior a 6% nos primeiros dois grupos e apresentou valores de 15% para os tumores T1c e 34% para os T2. Sendo estas taxas mais baixas que as historicamente esperadas, os autores concluem que para tumores T1a e T1b, provavelmente o EA traz poucos beneficios<sup>17</sup>. </p>     ]]></body>
<body><![CDATA[<p>Posteriormente foram surgindo resultados de estudos randomizados, destacando-se dois referentes a mulheres com mais de 60 anos. O <i>International Breast Cancer Study Group</i> publicou em 2006 um estudo randomizado de 473 mulheres com mais de 60 anos, axila clinicamente negativa e com indica&#231;&#227;o para terap&#234;utica adjuvante com tamoxifeno em dois grupos: cirurgia mais EA ou sem EA. Aos 6,6 anos de seguimento n&#227;o houve diferen&#231;a na SLD (67% <i>vs</i> 66%) ou na SG (75% <i>vs</i> 73%) entre ambos os grupos. Face ao observado, os autores concluem que suprimir o EA nestas doentes n&#227;o condicionaria negativamente o controlo da doen&#231;a<sup>18</sup>. A conclus&#227;o semelhante, a 5 anos de seguimento, chegou um ensaio de 219 mulheres com idade entre 60 e 80 anos, com tumores clinicamente T1N0, submetidas a cirurgia conservadora mais RT local e tamoxifeno, randomizadas em EA vs nenhuma cirurgia axilar<sup>19</sup>. </p>     <p>Ao inv&#233;s, em mulheres com axila positiva foi encontrado benef&#237;cio no EA. Um estudo randomizado com 658 mulheres com axila positiva e um tamanho tumoral at&#233; 3 cm comparou tumorectomia com e sem EA. Todas as mulheres foram submetidas a RT. Houve uma melhoria da sobreviv&#234;ncia e menor recidiva no grupo com EA, ap&#243;s 5 anos de seguimento<sup>20</sup>. Nestes casos os autores defendem a realiza&#231;&#227;o de EA no contexto de axila positiva, mas admitem que estes resultados possam ser explicados pela(s) terap&#234;utica(s) adjuvante(s) institu&#237;da(s) e n&#227;o pelo efeito do EA.</p>     <p>Tamb&#233;m para entender o papel das met&#225;stases axilares ocultas, Veronesi selecionou aleatoriamente 435 doentes com mais de 45 anos, tumores menores que 1,2 cm e axila clinicamente negativa, num primeiro grupo com cirurgia conservadora mais RT da mama e num segundo grupo com cirurgia conservadora mais RT da mama e da axila. Ap&#243;s 5 anos de seguimento a recidiva axilar foi baixa, 3 casos (1,5%) no primeiro grupo e 1 caso (0,5%) no segundo. A sobreviv&#234;ncia aos 5 anos foi semelhante em ambos os grupos, com valores na ordem dos 96%. O autor conclui que parte das met&#225;stases axilares ocultas nunca chegam a manifestar-se clinicamente e que em tumores pequenos com axila clinicamente negativa poder&#225; ser omitido o EA<sup>21</sup>.</p>     <p>Finalmente, um ensaio indispens&#225;vel para compreender esta problem&#225;tica &#233; o trabalho de Fisher<sup>7,22</sup>. Em 1971 inicia a randomiza&#231;&#227;o de 1.079 mulheres com axila clinicamente negativa comparando mastectomia radical (MR), mastectomia simples (MS) mais irradia&#231;&#227;o local e mastectomia simples com EA posterior quando houvesse recidiva regional. 70% destas mulheres tinham idade superior a 60 anos e o tamanho m&#233;dio do tumor era de 3,3 cm. N&#227;o foram reportadas diferen&#231;as na SLD sist&#233;mica e SG aos 10 e 25 anos de seguimento (a SG foi de 19%, 13% e 19% aos 25 anos respetivamente nos grupos com MR, MS+RT e MS). A incid&#234;ncia de recidiva regional foi menor no grupo submetido a RT. Aos 25 anos de seguimento somente 20% das mulheres com axila negativa estavam vivas e livres de doen&#231;a. Independentemente do estado da axila a maioria dos eventos prim&#225;rios foram recidivas &#224; dist&#226;ncia e morte n&#227;o relacionada com cancro, concretamente este &#250;ltimo ocorreu em cerca de 1/3 dos casos. Um resultado interessante deste estudo &#233; a constata&#231;&#227;o que a recidiva axilar, quando ocorre, tende a ser um evento precoce (das 365 mulheres submetidas a MS, 68 tiveram recidiva ganglionar nos primeiros 5 anos e 7 mulheres ap&#243;s 5 anos). Outro dado importante a reter &#233; que em 40% das mulheres submetidas a MR houve confirma&#231;&#227;o histol&#243;gica de met&#225;stases ganglionares, assim sendo, seria de esperar a mesma taxa de doen&#231;a axilar nas mulheres submetidas s&#243; a MS. Uma vez que a SG foi semelhante nestes dois grupos, pode deduzir-se que a doen&#231;a ganglionar oculta influencia a taxa de recidiva axilar mas n&#227;o a SG e a doen&#231;a &#224; dist&#226;ncia.</p>     <p>Na generalidade os estudos acima referidos, apontam para a seguran&#231;a em omitir o EA em subgrupos de doentes com axila clinicamente negativa, nomeadamente mulheres mais velhas, tumores pequenos, com recetores de estrog&#233;nio (RE) positivos e com programa&#231;&#227;o de algum tipo de irradia&#231;&#227;o axilar.</p>     <p>Outro ensaio pertinente publicado pelo j&#225; citado Veronesi, consistiu na randomiza&#231;&#227;o de 737 doentes, ap&#243;s mastectomia mais cirurgia axilar, de ex&#233;rese ou n&#227;o dos g&#226;nglios da cadeia da mam&#225;ria interna. O estudo n&#227;o encontra diferen&#231;as na sobreviv&#234;ncia entre os dois grupos, ainda que no primeiro o envolvimento patol&#243;gico dos g&#226;nglios da mam&#225;ria interna tenha sido confirmado em 21% dos casos<sup>23</sup>.</p>     <p>Podemos concluir que o EA permite uma excelente avalia&#231;&#227;o do progn&#243;stico, tendo um papel importante no controlo regional da doen&#231;a. O seu impacto na sobreviv&#234;ncia livre de doen&#231;a &#224; dist&#226;ncia &#233; mais controverso ou, por outras palavras, o EA indica a probabilidade de doen&#231;a sist&#233;mica mas n&#227;o a impede propriamente de acontecer.</p>     <p><b>Ap&#243;s biopsia de g&#226;nglio sentinela podemos suprimir o esvaziamento axilar na presen&#231;a de micromet&#225;stases?</b></p>     <p>No in&#237;cio dos anos 90 foram publicados os primeiros relatos do mapeamento linf&#225;tico e biopsia de g&#226;nglio sentinela (BGS). Esta t&#233;cnica apesar de assumir uma taxa de falsos negativos cerca de 7%, embora sem repercuss&#227;o na sobreviv&#234;ncia e uma taxa de recidiva axilar de 1%<sup>5,6,24</sup>, obteve uma r&#225;pida aceita&#231;&#227;o pela comunidade cient&#237;fica tornando-se <i>goldstandard</i> na aferi&#231;&#227;o da axila e poupando a muitas mulheres os efeitos adversos do EA.</p>     <p>A BGS requer uma an&#225;lise mais pormenorizada do g&#226;nglio, obrigando a quantificar e classificar os diferentes dep&#243;sitos de invas&#227;o ganglionar encontrados em c&#233;lulas tumorais isoladas (dep&#243;sitos tumorais &#8804; 0,2mm), micromet&#225;stases (dep&#243;sitos entre 0,2 a 2 mm) ou macromet&#225;stases (dep&#243;sitos &gt;2 mm). O estudo MIRROR demonstrou que esta classifica&#231;&#227;o tem implica&#231;&#245;es progn&#243;sticas a ter em conta na institui&#231;&#227;o de terap&#234;utica adjuvante. Este estudo comparou doentes com BGS negativa que n&#227;o efetuaram terap&#234;utica adjuvante com doentes submetidos a BGS com CTI ou micromet&#225;stases. Neste &#250;ltimo grupo estavam inclu&#237;dos doentes que n&#227;o fizeram nenhum tipo de terap&#234;utica adjuvante e doentes que apesar das <i>guidelines </i>ent&#227;o vigentes n&#227;o recomendarem terap&#234;utica adjuvante, esta havia sido administrada (tumores inferiores a 1cm ou maiores at&#233; 3 cm mas grau I ou II). O estudo mostrou um agravamento no progn&#243;stico aos 5 anos na presen&#231;a de CTI ou micromet&#225;stases e um aumento na SLD destas doentes quando sujeitas a terap&#234;utica adjuvante, refor&#231;ando a import&#226;ncia de uma maior liberaliza&#231;&#227;o na indica&#231;&#227;o de tratamento adjuvante neste grupo<sup>25</sup>.</p>     ]]></body>
<body><![CDATA[<p>Recentemente o grupo do Instituto Europeu de Oncologia (IEO) apresentou a sua s&#233;rie retrospetiva de 5.262 doentes com BGS negativa tratados entre 1996 e 2006<sup>24</sup>. Nesta s&#233;rie, 91% das doentes foram submetidas a cirurgia conservadora, e destas, 67% receberam RT externa (dois campos tangenciais) e 26% receberam RT intraoperat&#243;ria com electr&#245;es, sendo 80% dos tumores de tamanho inferior a 2 cm. Os resultados mostraram uma taxa de SG de 91% a 10 anos. Em 91 doentes (1,7%) ocorreu recidiva axilar e nestas, a sobreviv&#234;ncia aos 10 anos ap&#243;s o aparecimento de doen&#231;a axilar, foi de 72%. De real&#231;ar o papel protetor da RT, uma vez que o risco de recidiva axilar foi superior nas doentes submetidas a mastectomia que n&#227;o fizeram RT. H&#225; que atentar na import&#226;ncia deste estudo que refor&#231;a a seguran&#231;a desta t&#233;cnica com seguimentos a 10 anos.</p>     <p>Em Portugal, um estudo com sele&#231;&#227;o aleat&#243;ria de 125 doentes para a realiza&#231;&#227;o de BGS ou BGS seguida de EA tamb&#233;m mostrou resultados semelhantes em ambos os grupos relativamente &#224; SG, SLD e recorr&#234;ncia regional, com um acompanhamento de longa dura&#231;&#227;o<sup>26</sup>.</p>     <p>Atualmente, &#224; exce&#231;&#227;o do carcinoma inflamat&#243;rio, s&#227;o praticamente inexistentes as contra-indica&#231;&#245;es absolutas para a realiza&#231;&#227;o de BGS em axila clinicamente negativa e, apesar de alguns receios nos tumores multic&#234;ntricos ou extensos, normalmente submetidos a mastectomia, &#233; consensual n&#227;o fazer EA ap&#243;s BGS negativa.</p>     <p>Diversos estudos apoiam tamb&#233;m a omiss&#227;o do EA no caso de micromet&#225;stases ou CTI no g&#226;nglio sentinela.</p>     <p>Uma meta-an&#225;lise publicada em 2004 incluindo estudos com BGS com baixo volume de doen&#231;a axilar ou CTI mostrou uma taxa de envolvimento axilar, ap&#243;s EA, de 10 a 15%<sup>27</sup>.</p>     <p>&#160;O ensaio cl&#237;nico multic&#234;ntrico IBCSG B23 reportou a avalia&#231;&#227;o de pacientes com micrometast&#225;stases no g&#226;nglio sentinela. Como esperado, estas doentes integravam um grupo de baixo risco: 67% apresentavam tumores T1, 74% doen&#231;a grau I ou II, 89% dos tumores expressavam RE e em 67% as micromet&#225;stases encontradas eram &lt;1 mm. Quanto &#224; terap&#234;utica realizada, 75% tinham feito cirurgia conservadora e 25% mastectomia, 89% tinham sido submetidas a radioterapia adjuvante<sup>13</sup>. Neste estudo a SG e a SLD aos 5 anos de seguimento foi semelhante nos dois grupos (com e sem EA). Os resultados deste estudo fornecem, atualmente, o maior justificativo para dispensar o EA na presen&#231;a de micromet&#225;stases.</p>     <p><b>Ap&#243;s biopsia de g&#226;nglio sentinela com macromet&#225;stases podemos suprimir o esvaziamento axilar?</b></p>     <p>A partir da generaliza&#231;&#227;o da BGS as controv&#233;rsias relacionadas com o tratamento cir&#250;rgico da axila abrandaram. Apesar disso, e com base na evid&#234;ncia apresentada anteriormente, alguns cl&#237;nicos e mulheres t&#234;m optado pela omiss&#227;o do EA em casos de BGS positiva. Em 2010 foram publicados os dados da &#171;Surveillance, Epidemiology, and End Results Database&#187; que identificou 26.986 doentes com doen&#231;a axilar, tratadas nos EUA entre 1998 e 2004, das quais 4.425 (16,4%) haviam sido submetidas a BGS sem EA. Estas doentes, tendencialmente, apresentavam idade mais avan&#231;ada, tumores de menor grau e maior propor&#231;&#227;o de casos hormonodependentes. Aos 50 meses de seguimento n&#227;o foi encontrada diferen&#231;a na SG entre estas doentes e as submetidas a EA ap&#243;s BGS positiva<sup>28</sup>.</p>     <p>Bilimoria publicou a an&#225;lise de 97.314 mulheres da &#171;National Cancer Data Base&#187; com axila clinicamente negativa e BGS positiva. Entre 1998 e 2000 foram identificadas 20.075 mulheres com macromet&#225;stases e 2.203 com micromet&#225;stases. Mais uma vez a omiss&#227;o de EA esteve associado a idades mais velhas, tumores mais pequenos e maior comorbilidade. A an&#225;lise multivariada n&#227;o mostrou diferen&#231;as significativas na recidiva axilar (entre 1 e 1,2% em todos os grupos) nem na sobreviv&#234;ncia global entre o grupo apenas submetido a BGS e o grupo com EA, embora se tenha verificado uma tend&#234;ncia para maior sobreviv&#234;ncia nas mulheres com macromet&#225;stases sujeitas a EA. Esta an&#225;lise permite concluir que a omiss&#227;o de EA &#233; segura nas doentes com micromet&#225;stases e, em casos espec&#237;ficos, naquelas que apresentam macromet&#225;stases<sup>29</sup>. </p>     <p>Outra tentativa de selecionar os casos a omitir o EA ap&#243;s BGS positiva tem sido a utiliza&#231;&#227;o de nomogramas que recorrem a vari&#225;veis do tumor e caracter&#237;sticas do g&#226;nglio sentinela para predi&#231;&#227;o de outros g&#226;nglios n&#227;o sentinela metast&#225;ticos. Entre os nomogramas mais utilizados destaca se o desenvolvido no &#171;Memorial Sloan-Kettering Cancer Center&#187; e o de &#171;Stanford&#187;. Estas ferramentas estat&#237;sticas ajudam na decis&#227;o cl&#237;nica, embora n&#227;o existam estudos randomizados que avaliem o impacto do seu uso na recidiva ou sobreviv&#234;ncia<sup>30,31</sup>. </p>     ]]></body>
<body><![CDATA[<p>&#160;Neste contexto &#233; publicado em 2011 o ensaio ACOSOG Z0011<sup>9</sup> que pretende avaliar a omiss&#227;o do EA ap&#243;s BGS positiva. O suporte cient&#237;fico para a realiza&#231;&#227;o deste estudo provem de evid&#234;ncias acumuladas, designadamente em primeiro lugar a constata&#231;&#227;o de que a probabilidade de o GS ser o &#250;nico g&#226;nglio positivo &#233; de cerca de 60 a 70% no caso de macromet&#225;stase e de 90% no caso de micromet&#225;stases ou CTI<sup>28</sup>, em segundo, a identifica&#231;&#227;o de s&#233;ries de doentes onde o EA foi omitido apresentando taxas de recidiva baixas e, finalmente, que a recidiva axilar ap&#243;s BGS negativa era mais baixa do que a taxa de falsos negativos da t&#233;cnica<sup>28,29</sup> fazendo supor que h&#225; doen&#231;a axilar que nunca evolui ou &#233; tratada pela terap&#234;utica sist&#233;mica e RT. Este ensaio incluiu doentes com tumores at&#233; 5 cm, axila clinicamente negativa, submetidas a tumorectomia mais RT da mama com incid&#234;ncias tangenciais e BGS com doen&#231;a metast&#225;tica at&#233; 2 g&#226;nglios positivos. Foram exclu&#237;das mulheres com CTI, mais de dois g&#226;nglios positivos ou com doen&#231;a axilar extraganglionar. Foram ainda exclu&#237;das, mulheres submetidas a mastectomia, a tumorectomia mais braquiterapia ou mais RT sem incid&#234;ncias tangenciais, sem RT ou submetidas a tratamento neoadjuvante. Ap&#243;s BGS positiva foram randomizadas 445 doentes submetidas a EA e 446 a quem n&#227;o foi efetuado EA. O n&#250;mero m&#233;dio de g&#226;nglios removidos foi de 17 no primeiro grupo e 2 no grupo s&#243; com BGS, como esperado. No grupo de doentes submetidas a EA, foram isolados g&#226;nglios positivos adicionais em 27% dos casos. A maioria das mulheres realizou RT, 89% no grupo com EA e 90% no grupo com BGS. </p>     <p>N&#227;o foi encontrada diferen&#231;a significativa aos 6,3 anos de seguimento medio na SG, SLD e recorr&#234;ncia regional. A SG aos 5 anos foi de 91,8% no bra&#231;o que efetuou EA e de 92,5% no bra&#231;o de BGS, tendo ocorrido 94 mortes (52 com EA e 42 com BGS). A SLD foi de 82% e 84%, respetivamente em ambos os grupos (p=,14). A taxa de recidiva regional aos 5 anos foi de 3,1% com EA e 1,6% com BGS (p=,11). Do mesmo modo, na an&#225;lise do subgrupo de tumores com RE negativos (n=127) n&#227;o foram objetivadas diferen&#231;as nem na SG nem na SLD.</p>     <p>No ensaio de Fisher a SG em todos os bra&#231;os aos 5 anos foi de 60%, com uma estimativa de doen&#231;a axilar em 40% dos doentes (baseada na percentagem de doentes com axila positiva no grupo que fez EA). No estudo ACOSOGZ0011 a SG foi de 90% e uma taxa de recidiva axilar de somente 0,9%, apesar de todas as doentes terem axila positiva. Os autores explicam estes bons resultados pelos avan&#231;os no diagn&#243;stico e a maior precis&#227;o das terap&#234;uticas adjuvantes, e alertam que estes avan&#231;os devem ser tidos em conta na escolha de terap&#234;utica cir&#250;rgica. Concluem ainda que, sendo a recidiva axilar usualmente um acontecimento precoce<sup>18,19,5</sup>, verificando-se raramente ap&#243;s os 5 anos, &#233; pouco prov&#225;vel que haja diferen&#231;as nos resultados com um acompanhamento mais prolongado. </p>     <p>Um dos aspetos controversos deste estudo foi apontado por Jagsi. Este autor investigou os protocolos de RT utilizados. Apenas teve acesso aos dados de 228 doentes dos quais 185 (81%) receberam RT com incid&#234;ncias tangenciais. Verificou que 18,9% receberam RT axilar com 3 campos (22 casos no EA e 21 no grupo com BGS) e alguns doentes n&#227;o fizeram RT. Apesar de n&#227;o se terem apurado diferen&#231;as entre os dois bra&#231;os do ensaio, concluiu que dever&#225; ser realizada uma norma de conduta para padroniza&#231;&#227;o do tratamento de RT a aplicar nestes doentes<sup>32</sup>.</p>     <p>O ensaio ACOSOGZ0011<sup>9</sup> tem limita&#231;&#245;es. Do ponto de vista metodol&#243;gico n&#227;o foi atingido nem o n&#250;mero de doentes nem o n&#250;mero de eventos inicialmente previstos de acordo com o desenho inicial (1.900 doentes previstos mas apenas 891 foram inclu&#237;dos; 500 mortes previstas mas apenas 94 reportadas). Tendo recrutado menos de metade da amostra inicialmente calculada, a pot&#234;ncia estat&#237;stica para detetar n&#227;o inferioridade &#233; question&#225;vel. Al&#233;m disso, a maioria da popula&#231;&#227;o inclu&#237;da apresentava mais de 50 anos de idade (64%), doen&#231;a hormodependente (77%), tumor at&#233; 2cm (68%) e apenas um g&#226;nglio sentinela positivo (60%). N&#227;o existem dados quanto &#224; express&#227;o de <i>Human Epidermal growth factor Receptor 2</i> (HER2). Ainda assim os autores concluem que &#224; luz dos conhecimentos atuais e com as terap&#234;uticas adjuvantes dispon&#237;veis n&#227;o &#233; l&#237;cito deixar que mulheres que cumpram os crit&#233;rios de inclus&#227;o e exclus&#227;o do estudo sejam sujeitas &#224; morbilidade de um EA sem vantagens significativas na sua sobreviv&#234;ncia, controlo regional da doen&#231;a e na decis&#227;o de terap&#234;utica adjuvante. Mas depreende-se que ser&#225; segura a omiss&#227;o de EA nos doentes maioritariamente representados no estudo, ou seja, com mais de 50 anos com pT1, RE positivos e um g&#226;nglio sentinela positivo.</p>     <p><b>Qual o papel da radioterapia da axila? </b></p>     <p>Existem in&#250;meros estudos que mostram o efeito do controlo regional da RT.</p>     <p>Como mencionado anteriormente a serie retrospetiva de 5.262 doentes do IEO com BGS negativa tratados entre 1996 e 2006<sup>24</sup> mostrou um risco de recidiva axilar maior nas doentes submetidas a mastectomia que n&#227;o fizeram RT.</p>     <p>A RT adjuvante ap&#243;s cirurgia conservadora reduz o risco de recidiva ipsilateral num fator de 3 e reduz o risco de qualquer tipo recidiva resultando numa melhoria significativa da SG<sup>33</sup>. A RT ap&#243;s mastectomia com doen&#231;a ganglionar reduz mais de 3 vezes a recorr&#234;ncia regional e melhora a SG em 6%<sup>34</sup>.</p>     <p>Antes da introdu&#231;&#227;o da BGS a RT foi apresentada como alternativa ao EA em doentes com axila negativa, tendo-se verificado um bom controlo da doen&#231;a regional e menos efeitos secund&#225;rios com a RT<sup>35,36</sup>.</p>     ]]></body>
<body><![CDATA[<p>&#201; neste contexto que em 2001 foi iniciado o ensaio AMAROS<sup>10</sup> tendo como objetivo a avalia&#231;&#227;o de RT axilar enquanto tratamento igualmente valorado em rela&#231;&#227;o ao EA, tendo a taxa de recorr&#234;ncia regional ipsilateral como resultado esperado. 4.806 doentes com tumores T1-2 e axila clinicamente negativa , foram divididos em dois grupos, previamente &#224; realiza&#231;&#227;o de BGS: um para EA e outro para RT posterior. Destes, tiveram BGS positiva 744 no grupo EA e 681 no grupo para RT axilar. A RT axilar devia incluir os tr&#234;s n&#237;veis da axila e segmento medial da fossa supraclavicular com a dose de 50 Gy em 25 fra&#231;&#245;es. O tratamento cir&#250;rgico foi tumorectomia ou mastectomia conforme o clinicamente indicado. O EA foi definido como a ex&#233;rese de pelo menos 10 g&#226;nglios incluindo n&#237;vel I e II. </p>     <p>A taxa de recorr&#234;ncia axilar aos 5 anos foi de 0,54% ap&#243;s realiza&#231;&#227;o de EA e 1,02% ap&#243;s RT axilar. N&#227;o foram reportadas diferen&#231;as com significado estat&#237;stico nem na SG nem na SLD aos 5 anos: SG foi 93,3% com EA e 92,5% com RT axilar, a SLD foi de 86,9% no subgrupo que realizou EA e 82,7% no subgrupo submetido a RT axilar. A an&#225;lise de subgrupos tamb&#233;m n&#227;o mostrou diferen&#231;as significativas na SLD.</p>     <p>Foi encontrado menos linfedema no grupo da RT e n&#227;o houve diferen&#231;as significativas no que respeita a mobilidade do ombro (numericamente superior no grupo da RT). Aos 5 anos, foi reportado linfedema em 23% dos doentes submetidos a EA e 11% nos doentes submetidos a RT, esta diferen&#231;a n&#227;o teve repercuss&#227;o na qualidade de vida. De real&#231;ar a taxa de 58% de linfedema encontrado em 27 doentes sujeitas a EA e RT (p&lt;,001). </p>     <p>O estudo AMAROS, no entanto, deve ser lido com reservas tendo em conta que a avalia&#231;&#227;o prevista de n&#227;o inferioridade n&#227;o obteve pot&#234;ncia estat&#237;stica, provavelmente pelo n&#250;mero baixo de eventos. </p>     <p>No entanto, os resultados do estudo AMAROS corroboram a import&#226;ncia quer da RT quer do EA no controlo regional mesmo em doentes com BGS positiva. A RT axilar, administrada de acordo com o protocolo do estudo, pode ser considerada no subgrupo de doentes inclu&#237;das (pT1-pT2, cN0 com BGS positiva), por&#233;m a sua utiliza&#231;&#227;o generalizada &#233; question&#225;vel.</p>     <p>Finalmente, se por um lado o estudo AMAROS tentou provar que a omiss&#227;o de EA &#233; uma forma de poupar os doentes a efeitos adversos, levanta por outro lado, a quest&#227;o de sobre-tratamento com RT: actualmente, em doentes com pT1-pT2, cN0 com BGS positiva n&#227;o &#233; consensual irradiar de forma terap&#234;utica considerando como volume alvo de tratamento os tr&#234;s n&#237;veis da axila e segmento medial da fossa supraclavicular.</p>     <p>Na pr&#225;tica cl&#237;nica di&#225;ria defrontamo-nos com uma quest&#227;o fundamental: em face de doente com pT1-pT2, cN0 com BGS positiva em que a decis&#227;o, tomada em reuni&#227;o multidisciplinar, tenha sido a omiss&#227;o de EA, que tratamento de RT realizar? </p>     <p><b>Qual a import&#226;ncia do esvaziamento axilar na escolha de terap&#234;utica adjuvante?</b></p>     <p>&#160;Classicamente os fatores de progn&#243;stico mais importantes no cancro da mama inicial s&#227;o a express&#227;o RE/RP/HER2, marcadores de prolifera&#231;&#227;o, n&#250;mero de g&#226;nglios envolvidos, histologia tumoral, tamanho tumoral, grau tumoral e presen&#231;a ou aus&#234;ncia de envolvimento linfovascular (ESMO <i>guidelines</i> 2014). Em 2000, a equipa de Perou utilizando uma t&#233;cnica de DNA <i>microarrays</i> descreveu quatro subtipos moleculares, <i>basal-like</i>, <i>HER2-enriched</i>,<i>normal-like</i> e <i>luminal</i><sup>37</sup>. Este trabalho, entre outros, vem confirmar que o cancro da mama n&#227;o pode ser interpretado como uma &#250;nica doen&#231;a.</p>     <p>Os subtipos tumorais t&#234;m vindo a ganhar cada vez maior import&#226;ncia na atividade cl&#237;nica. Os consensos de &#171;St Gallen&#187; de 2013 vieram refor&#231;ar o papel dos subtipos intr&#237;nsecos do cancro da mama, corroborando a utiliza&#231;&#227;o de caracter&#237;sticas moleculares e sugerindo a utiliza&#231;&#227;o de biomarcadores segundo t&#233;cnicas de imunohistoqu&#237;mica para a sua classifica&#231;&#227;o (como seja a express&#227;o de RE, RP e HER2 e a determina&#231;&#227;o do Ki67). A Sociedade Europeia de Oncologia M&#233;dica (ESMO) nas suas mais recentes <i>guidelines</i>, espelhando os consensos de St Gallen, enfatiza o papel dos subtipos intr&#237;nsecos como fator preponderante na decis&#227;o de terap&#234;utica adjuvante. No entanto, o estadiamento da doen&#231;a permanece importante para a decis&#227;o de tratamento adjuvante. </p>     ]]></body>
<body><![CDATA[<p>O estudo AMAROS, no seu desenho inicial, programou uma an&#225;lise interina com o objetivo de avaliar o papel do EA na decis&#227;o de tratamento sist&#233;mico adjuvante. Neste estudo, os autores testaram uma hip&#243;tese: a administra&#231;&#227;o de tratamento adjuvante sist&#233;mico seria semelhante em ambos os bra&#231;os. Foram inclu&#237;dos, 566 doentes com BGS positiva submetidos a EA (n=300) ou RT axilar (n=266) de acordo com a randomiza&#231;&#227;o. Segundo os autores, n&#227;o foram observadas diferen&#231;as na percentagem de doentes submetidas a quimioterapia, que se traduziu por 58% de doentes no bra&#231;o de EA e 61% no bra&#231;o de RT. Tamb&#233;m n&#227;o foram reportadas diferen&#231;as quanto &#224; utiliza&#231;&#227;o de terap&#234;utica end&#243;crina entre os dois grupos, 78% de doentes no bra&#231;o de EA e 76% no bra&#231;o de RT. A an&#225;lise multivariada mostrou que as vari&#225;veis que influenciaram significativamente a escolha de quimioterapia adjuvante foram a idade, o grau tumoral, multifocalidade e o tamanho das met&#225;stases ganglionares. Os autores concluem que o conhecimento do estadiamento patol&#243;gico da axila n&#227;o foi determinante na escolha da terap&#234;utica adjuvante na popula&#231;&#227;o estudada<sup>38</sup>. &#201; importante referir que os dados relativos ao <i>status</i> hormonal s&#227;o dados indiretos extrapolados da utiliza&#231;&#227;o de terap&#234;utica end&#243;crina, sendo que a informa&#231;&#227;o referente ao estado de RE/RP n&#227;o foi recolhida. Tamb&#233;m n&#227;o foram recolhidos dados quanto ao <i>status</i> HER2 nem quanto &#224; utiliza&#231;&#227;o de inibidores da via HER2. A utiliza&#231;&#227;o de quimioterapia n&#227;o foi diferente entre os dois bra&#231;os mas a utiliza&#231;&#227;o de taxanos foi baixa. Assim a generaliza&#231;&#227;o da conclus&#227;o dos autores dever&#225; ser cautelosa. </p>     <p>De forma semelhante, no ensaio ACOSOGZ0011 n&#227;o foram reportadas diferen&#231;as quanto &#224; terap&#234;utica adjuvante utilizada entre os bra&#231;os do estudo: 96% dos doentes submetidos a EA realizaram algum tipo de tratamento adjuvante e 97% dos doentes que n&#227;o realizaram EA; 58% dos doentes no bra&#231;o de EA e 58% no bra&#231;o sem EA realizaram quimioterapia; 46% dos doentes no bra&#231;o de EA e 47% no bra&#231;o sem EA realizaram terap&#234;utica end&#243;crina<sup>9</sup>.</p>     <p>Neste contexto importa real&#231;ar que em alguns estudos, os tumores HER2 positivos e tumores triplo negativos foram associados a um aumento do risco de recorr&#234;ncia regional quando comparados com outras histologias<sup>39,40</sup>. Na pr&#225;tica cl&#237;nica, os resultados do ensaio AMAROS e ACOSOGZ0011 ser&#227;o dificilmente extrapolados para o subgrupo de doentes com tumores HER2 e triplo negativo pela sua baixa representatividade. De qualquer forma nestes dois subgrupos o impacto do estadio axilar, por si s&#243;, como fator decisivo para realiza&#231;&#227;o de tratamento adjuvante sist&#233;mico, seria s&#243; importante no contexto de tumores mais pequenos.</p>     <p>No grupo de doentes com doen&#231;a hormonodependente a utiliza&#231;&#227;o de plataformas gen&#243;micas como seja OncotypeDX&#174; e Mammaprint&#174; t&#234;m vindo a ser estudada. Estas ferramentas moleculares providenciam informa&#231;&#227;o progn&#243;stica e/ou preditiva sendo que as <i>guidelines</i> da ESMO sugerem a sua utiliza&#231;&#227;o como forma de identifica&#231;&#227;o de doentes com doen&#231;a regional a quem, potencialmente, ser&#225; de considerar omitir terap&#234;utica com quimioterapia. Neste subgrupo de doentes em rela&#231;&#227;o aos quais se pode considerar a omiss&#227;o de quimioterapia, ser&#225; seguro omitir tamb&#233;m EA? A decis&#227;o de tratamento adjuvante, atualmente, deve ser emanada em sede de reuni&#227;o multidisciplinar articulando as diferentes modalidades terap&#234;uticas de forma a n&#227;o promover o sobre-tratamento nem o sub-tratamento.<b>&#160;&#160; </b></p>     <p><b>Conclus&#227;o</b></p>     <p>Estes estudos demonstram que a taxa de recidiva axilar em doentes com axila clinicamente negativa &#233; baixa, mesmo em casos de BGS positiva sem EA. &#201; consensual que, a BGS continua a ser a t&#233;cnica <i>goldstandard</i> para avalia&#231;&#227;o da axila clinicamente negativa. Perante uma BGS negativa, com micromet&#225;stases ou CTI, n&#227;o se recomenda o EA. Na presen&#231;a de macromet&#225;stase sem rotura capsular parece seguro a omiss&#227;o de EA em doentes com mais de 50 anos com pT1, RE positivos, um g&#226;nglio sentinela positivo, submetidas a tumorectomia com RT mam&#225;ria programada. </p>     <p>Do aprofundamento de mais estudos espera-se a resposta a diversas perguntas: sobre protocolos personalizados de RT, sobre a possibilidade de evitar o EA nas mulheres submetidas a mastectomia, sobre contributos nas controv&#233;rsias no que respeita &#224; quimioterapia neoadjuvante ou sobre o que fazer perante confirma&#231;&#227;o pr&#233;-operat&#243;ria de invas&#227;o de um ou dois g&#226;nglios em doentes que cumpram os crit&#233;rios de inclus&#227;o do ensaio ACOSOGZ0011. </p>     <p>Na linha do exposto, outra pergunta l&#243;gica sobressai: podemos evitar a BGS em alguns subgrupos de doentes? Est&#225; em curso no IEO o &#171;SOUND trial&#187; que pretende avaliar se a BGS pode ser evitada em mulheres mais velhas, tumores pequenos com axila clinicamente e ecograficamente negativa e se a escolha de terap&#234;utica adjuvante pode ser feita mediante a biologia do tumor sem a informa&#231;&#227;o do estadiamento patol&#243;gico axilar.</p>     <p>&#160;Os &#250;ltimos consensos de &#171;St. Gallen&#187; (2013) recomendam a omiss&#227;o de EA no caso de BGS com micromet&#225;stases e admitem que possa n&#227;o haver benef&#237;cio no EA nos doentes que cumpram os crit&#233;rios de inclus&#227;o do ensaio ACOSOGZ0011.</p>     <p>Em 2014 a ASCO<sup>41</sup> atualizou as suas recomenda&#231;&#245;es no que respeita &#224; cirurgia da axila. Segundo estas recomenda&#231;&#245;es em doentes com BGS, em que no m&#225;ximo, dois g&#226;nglios estejam envolvidos e que esteja prevista a realiza&#231;&#227;o de tumorectomia e RT mam&#225;ria &#233; de um modo geral recomendada a omiss&#227;o de EA. </p>     ]]></body>
<body><![CDATA[<p>Perante tantas d&#250;vidas, elegemos como conclus&#227;o &#250;ltima a certeza de que o doente tem que ser visto de forma hol&#237;stica devendo a proposta cir&#250;rgica ser inclu&#237;da num &#171;pacote&#187; global de tratamento. Atualmente, consideramos que a realiza&#231;&#227;o de EA deve ser suprimida em casos selecionados. Lembramos que o estadiamento axilar &#233; um dos principais fatores de progn&#243;stico podendo interferir na escolha de terap&#234;utica adjuvante e que o EA pode ser importante no controlo regional da doen&#231;a e influenciar positivamente a recidiva &#224; dist&#226;ncia.</p>     <p>Novos progressos no conhecimento da biologia tumoral, apontam para novos argumentos nesta mat&#233;ria e se &#233; prov&#225;vel que o EA se mantenha &#250;til na elimina&#231;&#227;o de doen&#231;a metast&#225;tica axilar clinicamente importante, j&#225; o seu papel na axila clinicamente negativa ir&#225; ser de marcador de progn&#243;stico.</p>     <p>&nbsp;</p>     <p><b>REFER&#202;NCIAS BIBLIOGR&#193;FICAS</b></p>     <!-- ref --><p>1. Halsted WS. The results of radical operations for the cure of cancer of the breast. Ann Surg. 1907; 46:1-5.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1858755&pid=S1646-5830201600030000700001&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>     <!-- ref --><p>2. Veronesi U, Saccozzi R, Del Vecchio M, Banfi A, Clemente C, De Lena M, Gallus G, Greco M, Luini A, Marubini E, Muscolino G, Rilke F, Salvadori B, Zecchini A and Zucali R. Comparing radical mastectomy with quadrantectomy, axillary dissection, and radiotherapy in patients with small cancers of the breast. N Engl J Med 1981; 305:6-11.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1858757&pid=S1646-5830201600030000700002&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>     <!-- ref --><p>3. Fisher B, Bauer M, Margolese R, Poisson R, Pilch Y, Redmond C, Fisher E, Wolmark N, Deutsch M, Montague E, Saffer E, Wickerham L, Lerner H, Glass A, Shibata H, Deckers P, Ketcham A, Oishi R, and Russell I. Five-year results of a randomized clinical trial comparing total mastectomy and segmental mastectomy with or without radiation in the treatment of breast cancer. N Engl J Med 1985;312:665-673.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1858759&pid=S1646-5830201600030000700003&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>     ]]></body>
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<body><![CDATA[<p>24. Galimberti V, Manika A , Maisonneuve P, Corso G, Salazar Moltrasio L, Intra M, Gentilini O, Veronesi P, Pagani G, Rossi E, Bottiglieri L, Viale G, Rotmensz N, De Cicco C, Grana CM, Sangalli C and Luini A. Long-term follow-up of 5262 breast cancer patients with negative sentinel node and no axillary dissection confirms low rate of axillary disease. EJSO 2014;40:1203-1208.</p>     <p>25. Tjan-Heijnen VC and de Boer M. Minimal lymph node involvement and outcome of breast cancer. The results of the Dutch MIRROR study. Discov Med. 2009;8:137-139.</p>     <!-- ref --><p>26. Fougo JL, Dinis-Ribeiro M, Dias T, Castro F, Reis P, Giesteira L, Ara&#250;jo C. O impacto do conceito de G&#226;nglio Sentinela na sobreviv&#234;ncia livre de doen&#231;a e global e na recorr&#234;ncia axilar de doentes com Cancro da Mama. Revista Portuguesa de Cirurgia. 2013;24:9-17.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1858783&pid=S1646-5830201600030000700026&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>     <p>27. Cserni G, Gregori D, Merletti F, Sapino A, Mano MP, Ponti A, Sandrucci S, Balt&#225;s B and Bussolati G. Meta-analysis of non-sentinel node metastases associated with micrometastatic sentinel nodes in breast cancer.Br J Surg. 2004;91:1245-1252.</p>     <p>28. Yi M, Giordano SH, Meric-Bernstam F, Mittendorf EA, Kuerer HM, Hwang RF, Bedrosian I, Rourke L and Hunt KK. Trends in and outcomes from sentinel lymph node biopsy (SLNB) alone vs SLNB with axillary lymph node dissection for node-positive breast cancer patients: experience from the SEER database. Ann Surg Oncol 2010 Oct;17 Suppl 3:343-351.</p>     <p>29. Bilimoria K, Bentrem D, Hansen N Bethke KP, Rademaker AW, Ko CY, Winchester DP and Winchester DJ. Comparison of Sentinel Lymph Node Biopsy Alone and Completion Axillary Lymph Node Dissection for Node-Positive Breast Cancer. J Clin Oncol 2009; 27:2946-2953.</p>     <!-- ref --><p>30. Bevilacqua JL, Kattan MW, Fey JV, Cody HS 3rd, Borgen PI, Van Zee KJ. Doctor, what are my chances of having a positive sentinel node? A validated nomogram for risk estimation. J Clin Oncol. 2007;25:3670-3679.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1858788&pid=S1646-5830201600030000700030&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>     <p>31. Kohrt HE, Olshen RA, Bermas HR, Goodson W, Wood D, Henry S, Rouse R, Bailey L, Philben V, Dirbas F, Dunn J, Johnson D, Wapnir I, Carlson R, Stockdale F,Hansen N and Jeffrey S. New models and online calculator for predicting non-sentinel lymph node status in sentinel lymph node positive breast cancer patients. BMC Cancer 2008; 8:66.</p>     ]]></body>
<body><![CDATA[<p>32. Jagsi R, Chadha M, Moni J, Ballman K, Laurie F, Buchholz TA, Giuliano A and Haffty BG. Radiation field design on the ACOSOG Z0011 (Alliance) trial. J Clin Oncol 2014;14:1-7.</p>     <!-- ref --><p>33. Darby S, McGale P, Correa C, Taylor C, Arriagada R, Clarke M, Cutter D, Davies C, Ewertz M, Godwin J, Gray R, Pierce L, Whelan T, Wang Y, Peto R; Early Breast Cancer Trialists&#8217; Collaborative Group. Effect of radiotherapy after breast conserving surgery on 10-year recurrence and 15-year breast cancer death: meta-analysis of individual patient data for 10,801 women in 17 randomised trials. Lancet 2011; 378:1707-1716.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=1858792&pid=S1646-5830201600030000700033&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>     <p>34. Clarke M, Collins R, Darby S, Davies C, Elphinstone P, Evans E, Godwin J, Gray R, Hicks C, James S, MacKinnon E, McGale P, McHugh T, Peto R, Taylor C and Wang Y; Early Breast Cancer Trialists&#8217; Collaborative Group (EBCTCG). Effects of radiotherapy and of differences in the extent of surgery for early breast cancer on local recurrence and 15-year survival: an overview of the randomised trials. Lancet 2005&nbsp;; 366:2087-2106.</p>     <p>35. Louis-Sylvestre C, Clough K, Asselain B, Vilcoq JR, Salmon RJ, Campana F and Fourquet A. Axillary treatment in conservative management of operable breast cancer: dissection or radiotherapy? Results of a randomized study with 15 years of follow-up. J Clin Oncol 2004; 22: 97-101.</p>     <p>36. Hoebers FJ, Borger JH, Hart AA, Peterse JL, Th EJ and Lebesque JV. Primary axillary radiotherapy as axillary treatment in breast conserving therapy for patients with breast carcinoma and clinically negative axillary lymph nodes. Cancer 2000; 88: 1633-1642.</p>     <p>37. Perou CM, Sorlie T, Eisen MB, van de Rijn M, Jeffrey SS, Rees CA, Pollack JR, Ross DT, Johnsen H, Akslen LA, Fluge O, Pergamenschikov A, Williams C, Zhu SX, L&#248;nning PE, B&#248;rresen-Dale AL, Brown PO and Botstein D. Molecular portraits of human breast tumours. Nature 2000; 406: 747-752.</p>     <p>38. Straver M, Meijnen P, Tienhoven G, van de Velde CJ, Mansel RE, Bogaerts J, Demonty G, Duez N, Cataliotti L, Klinkenbijl J, Westenberg HA, van der Mijle H, Hurkmans C and Rutgers EJ. Role of Axillary Clearance After a Tumor-Positive Sentinel Node in the Administration of Adjuvant Therapy in Early Breast Cancer. J Clin Oncol 2010 ; 28:731-737.</p>     <p>39. Gabos Z, Thoms J, Ghosh S, Hanson J, Desch&#234;nes J, Sabri S and Abdulkarim B. The association between biological subtypeand locoregional recurrence in newly diagnosed breast cancer. Breast Cancer Res Treat 2010; 124: 187-194.</p>     <p>40. Nguyen PL, Taghian AG, Katz MS, Niemierko A, Abi Raad RF, Boon WL, Bellon JR, Wong JS, Smith BL and Harris JR. Breast cancer subtype approximated by estrogen receptor, progesterone receptor, and HER-2 is associated with local and distant recurrence after breast-conserving therapy. J Clin Oncol 2008; 26: 2373-2378.</p>     ]]></body>
<body><![CDATA[<p>41. Lyman G, Temin S, Edge S, Newman L, Turner R, Weaver D, Benson III A, Bosserman L, Burstein H, Cody III H, Hayman J, Perkins C, Podoloff D and Giuliano AE. Sentinel Lymph Node Biopsy for Patients With Early-Stage Breast Cancer: American Society of Clinical Oncology Clinical Practice Guideline. March 24, 2014.</p>     <p>&nbsp;</p>     <p><a href="#topc0">Endere&ccedil;o para correspond&ecirc;ncia</a> | <a href="#topc0">Direcci&oacute;n para correspondencia</a> | <a href="#topc0">Correspondence</a><a name="c0"></a></p>     <p> Sara Lince Valadares</p>     <p>E-mail: <a href="mailto:slincevaladares@gmail.com">slincevaladares@gmail.com</a> </p>     <p>&nbsp;</p>     <p><b>Recebido em: </b>9/2/2015</p>     <p><b>Aceite para publica&#231;&#227;o: </b>28/6/2015</p>      ]]></body><back>
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