<?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>0034-7434</journal-id>
<journal-title><![CDATA[Revista Colombiana de Obstetricia y Ginecología]]></journal-title>
<abbrev-journal-title><![CDATA[Rev Colomb Obstet Ginecol]]></abbrev-journal-title>
<issn>0034-7434</issn>
<publisher>
<publisher-name><![CDATA[Federación Colombiana de Obstetricia y GinecologíaRevista Colombiana de Obstetricia y Ginecología]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S0034-74342016000200005</article-id>
<article-id pub-id-type="doi">10.18597/rcog.385</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Manejo quirúrgico del cáncer epitelial de ovario: Guía de práctica clinica de la Asociación Colombiana de Ginecólogos Oncólogos (ASCGO)]]></article-title>
<article-title xml:lang="en"><![CDATA[Surgical management of epithelial ovarian cancer: Clinical Practice Guideline of the Colombian Association of Gynaecologic Oncologists (ASCGO)]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Acosta-Peñaloza]]></surname>
<given-names><![CDATA[Jesús Antonio]]></given-names>
</name>
<xref ref-type="aff" rid="A01"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[González-Castañeda]]></surname>
<given-names><![CDATA[Mauricio]]></given-names>
</name>
<xref ref-type="aff" rid="A02"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Fernández-Mercado]]></surname>
<given-names><![CDATA[Robinson]]></given-names>
</name>
<xref ref-type="aff" rid="A03"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ramírez-Salazar]]></surname>
<given-names><![CDATA[Heydi Marina]]></given-names>
</name>
<xref ref-type="aff" rid="A04"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Ruiz-Povea]]></surname>
<given-names><![CDATA[Jaime Fernando]]></given-names>
</name>
<xref ref-type="aff" rid="A04"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Sanabria-Serrano]]></surname>
<given-names><![CDATA[Daniel]]></given-names>
</name>
<xref ref-type="aff" rid="A06"/>
</contrib>
</contrib-group>
<aff id="A01">
<institution><![CDATA[,Instituto Nacional de Cancerología ESE Asociación Colombiana de Ginecólogos Oncólogos ]]></institution>
<addr-line><![CDATA[Bogotá ]]></addr-line>
<country>Colombia</country>
</aff>
<aff id="A02">
<institution><![CDATA[,Instituto Nacional de Cancerología ESE Asociación Colombiana de Ginecólogos Oncólogos ]]></institution>
<addr-line><![CDATA[Bogotá ]]></addr-line>
<country>Colombia</country>
</aff>
<aff id="A03">
<institution><![CDATA[,Asociación Colombiana de Ginecólogos Oncólogos Misión Médica Ltda. ]]></institution>
<addr-line><![CDATA[Barranquilla ]]></addr-line>
<country>Colombia</country>
</aff>
<aff id="A04">
<institution><![CDATA[,Asociación Colombiana de Ginecólogos Oncólogos Fundación Clínica Valle del Lili ]]></institution>
<addr-line><![CDATA[Cali ]]></addr-line>
<country>Colombia</country>
</aff>
<aff id="A05">
<institution><![CDATA[,Asociación Colombiana de Ginecólogos Oncólogos Oncólogos de Occidente ]]></institution>
<addr-line><![CDATA[Manizales ]]></addr-line>
<country>Colombia</country>
</aff>
<aff id="A06">
<institution><![CDATA[,Asociación Colombiana de Ginecólogos Oncólogos Fundación Santa Fe de Bogotá ]]></institution>
<addr-line><![CDATA[Bogotá ]]></addr-line>
<country>Colombia</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>06</month>
<year>2016</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>06</month>
<year>2016</year>
</pub-date>
<volume>67</volume>
<numero>2</numero>
<fpage>120</fpage>
<lpage>146</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_arttext&amp;pid=S0034-74342016000200005&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_abstract&amp;pid=S0034-74342016000200005&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.org.co/scielo.php?script=sci_pdf&amp;pid=S0034-74342016000200005&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Introducción: el cáncer epitelial de ovario constituye la primera causa de muerte por cáncer ginecológico a nivel mundial. En Colombia cada año se presentan 8,7 casos nuevos por cada 100.000 mujeres y se registran más de 800 muertes por causa de esta enfermedad. La cirugía constituye el pilar de manejo de las pacientes con cáncer epitelial de ovario, su realización oportuna y la adecuada combinación con otras estrategias terapéuticas busca erradicar la enfermedad o, en los estados avanzados, lograr volúmenes tumorales microscópicos para mejorar el pronóstico. El objetivo de este trabajo consiste en desarrollar recomendaciones basadas en la evidencia para el diagnóstico y tratamiento quirúrgico integral del cáncer epitelial de ovario en población colombiana. Materiales y métodos: guía de práctica clínica basada en la evidencia, desarrollada por un panel de expertos de la Asociación Colombiana de Ginecólogos Oncólogos. La Sociedad definió y validó un total de 33 preguntas de interés para el manejo quirúrgico integral. Se llevó a cabo una revisión de literatura de guías de práctica clínica y se actualizó la evidencia de las guías fuente usando revisiones de literatura y estudios primarios experimentales y observacionales acordes con la naturaleza de cada pregunta. Finalmente, se discutieron y validaron las recomendaciones en la Asociación mediante un método participativo tipo panel de expertos. Resultados: se resumen las recomendaciones basadas en la mejor evidencia disponible para la detección temprana y el diagnóstico del cáncer epitelial de ovario, el manejo quirúrgico en estados tempranos y avanzados de la enfermedad, el seguimiento y manejo de las recaídas, así como el manejo con intención paliativa. Conclusiones: esta GPC fue desarrollada utilizando procedimientos sistemáticos y la mejor evidencia disponible. Se espera que tenga un impacto positivo en el manejo y los desenlaces de las pacientes que padecen de esta enfermedad.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Introduction: Epithelial ovarian cancer is the primary cause of death from gynaecological cancer in the world. In Colombia, every year there are 8.7 new cases for 100,000 women and more than 800 deaths as a result of this disease. Surgery is the mainstay for management of patients with epithelial ovarian cancer. The aim, when performed in a timely fashion and in combination with the right therapeutic strategies, is to eradicate the disease or, in advanced stages, to achieve microscopic tumour volumes in order to improve prognosis. The objective of this work is to develop evidence-based recommendations for the diagnosis and comprehensive surgical treatment of epithelial ovarian cancer in the Colombian population. Materials and methods: Evidence-based clinical practice guideline developed by an expert panel from the Colombian Association of Gynaecologic Oncologists. A total of 33 questions of interest for comprehensive surgical management were defined and validated in the Society. A review of the literature on clinical practice guidelines was conducted. The evidence of the source guidelines was updated using reviews of the literature and primary experimental and observational studies according to the nature of each question. Finally, the recommendations were discussed and validated in the Association using a participatory expert panel method. Results: A summary of recommendations of the best available evidence for early detection and diagnosis of epithelial ovarian cancer, surgical management of early and late stages of the disease, follow-up and management of recurrences, as well as management with palliative goals. Conclusions: This CPG was developed using systematic procedures and the best available evidence. It is expected to have a positive impact on management and outcomes of patients suffering from this disease.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[neoplasias ováricas]]></kwd>
<kwd lng="es"><![CDATA[diagnóstico]]></kwd>
<kwd lng="es"><![CDATA[procedimientos quirúrgicos de citorreducción]]></kwd>
<kwd lng="es"><![CDATA[Guía de Práctica Clínica]]></kwd>
<kwd lng="en"><![CDATA[Ovarian neoplasms]]></kwd>
<kwd lng="en"><![CDATA[diagnosis]]></kwd>
<kwd lng="en"><![CDATA[cytoreductive surgical procedure]]></kwd>
<kwd lng="en"><![CDATA[Clinical Practice Guideline]]></kwd>
</kwd-group>
</article-meta>
</front><body><![CDATA[  <font face="verdana" size="2">     <p>DOI: <a href="http://dx.doi.org/10.18597/rcog.385" target="_blank">http://dx.doi.org/10.18597/rcog.385</a></p> <font size="4">    <center><b>Manejo quir&uacute;rgico del c&aacute;ncer epitelial de ovario: Gu&iacute;a de pr&aacute;ctica clinica de la Asociaci&oacute;n Colombiana de Ginec&oacute;logos Onc&oacute;logos  (ASCGO)</b></center></font></p>     <p>    <center>    <p>Jes&uacute;s Antonio Acosta-Pe&ntilde;aloza, MD<sup>1</sup>, Mauricio Gonz&aacute;lez-Casta&ntilde;eda, MD<sup>2</sup>, Robinson Fern&aacute;ndez-Mercado, MD<sup>3</sup>, Heydi Marina Ram&iacute;rez-Salazar, MD<sup>4</sup>, Jaime Fernando Ruiz-Povea, MD<sup>5</sup>, Daniel Sanabria-Serrano, MD<sup>6</sup> Colaboradores Grupo Desarrollador de la Gu&iacute;a*</p></center></p>     <p>    <center>    <p>Recibido: marzo 14/16 - Aceptado: junio 9/16</p></center></p>     <p><sup>1</sup> Ginec&oacute;logo onc&oacute;logo, Asociaci&oacute;n Colombiana de Ginec&oacute;logos Onc&oacute;logos; Instituto Nacional de Cancerolog&iacute;a ESE, Bogot&aacute; (Colombia). <a href="mailto:jesacosta3@gmail.com">jesacosta3@gmail.com</a>     ]]></body>
<body><![CDATA[<p><sup>2</sup> Ginec&oacute;logo onc&oacute;logo, Asociaci&oacute;n Colombiana de Ginec&oacute;logos Onc&oacute;logos, Instituto Nacional de Cancerolog&iacute;a ESE, Bogot&aacute; (Colombia).     <p><sup>3</sup> Ginec&oacute;logo onc&oacute;logo, Asociaci&oacute;n Colombiana de Ginec&oacute;logos Onc&oacute;logos, Bogot&aacute; (Colombia); Misi&oacute;n M&eacute;dica Ltda., Barranquilla (Colombia).     <p><sup>4</sup> Ginec&oacute;loga onc&oacute;loga, Asociaci&oacute;n Colombiana de Ginec&oacute;logos Onc&oacute;logos, Bogot&aacute; (Colombia); Fundaci&oacute;n Cl&iacute;nica Valle de Lili, Cali (Colombia).     <p><sup>5</sup> Ginec&oacute;logo onc&oacute;logo, Asociaci&oacute;n Colombiana de Ginec&oacute;logos Onc&oacute;logos; Onc&oacute;logos de Occidente, Manizales (Colombia).     <p><sup>6</sup> Ginec&oacute;logo onc&oacute;logo, Asociaci&oacute;n Colombiana de Ginec&oacute;logos Onc&oacute;logos; Fundaci&oacute;n Santa Fe de Bogot&aacute;, Bogot&aacute; (Colombia).</p>     <p>* Colaboradores Grupo desarrollador de la Gu&iacute;a. Lista completa al final del documento.</p>     <p><b>RESUMEN</b></p>     <p><b>Introducci&oacute;n:</b> el c&aacute;ncer epitelial de ovario constituye la primera causa de muerte por c&aacute;ncer ginecol&oacute;gico a nivel mundial. En Colombia cada a&ntilde;o se presentan 8,7 casos nuevos por cada 100.000 mujeres y se registran m&aacute;s de 800 muertes por causa de esta enfermedad. La cirug&iacute;a constituye el pilar de manejo de las pacientes con c&aacute;ncer epitelial de ovario, su realizaci&oacute;n oportuna y la adecuada combinaci&oacute;n con otras estrategias terap&eacute;uticas busca erradicar la enfermedad o, en los estados avanzados, lograr vol&uacute;menes tumorales microsc&oacute;picos para mejorar el pron&oacute;stico. El objetivo de este trabajo consiste en desarrollar recomendaciones basadas en la evidencia para el diagn&oacute;stico y tratamiento quir&uacute;rgico integral del c&aacute;ncer epitelial de ovario en poblaci&oacute;n colombiana.</p>     <p><b>Materiales y m&eacute;todos:</b> gu&iacute;a de pr&aacute;ctica cl&iacute;nica basada en la evidencia, desarrollada por un panel de expertos de la Asociaci&oacute;n Colombiana de Ginec&oacute;logos Onc&oacute;logos. La Sociedad defini&oacute; y valid&oacute; un total de 33 preguntas de inter&eacute;s para el manejo quir&uacute;rgico integral. Se llev&oacute; a cabo una revisi&oacute;n de literatura de gu&iacute;as de pr&aacute;ctica cl&iacute;nica y se actualiz&oacute; la evidencia de las gu&iacute;as fuente usando revisiones de literatura y estudios primarios experimentales y observacionales acordes con la naturaleza de cada pregunta.  Finalmente,  se  discutieron  y  validaron las recomendaciones en la Asociaci&oacute;n mediante un m&eacute;todo participativo tipo panel de expertos. </p>     <p><b>Resultados: </b>se resumen las recomendaciones basadas en la mejor evidencia disponible para la detecci&oacute;n temprana y el diagn&oacute;stico del c&aacute;ncer epitelial de ovario, el manejo quir&uacute;rgico en estados tempranos y avanzados de la enfermedad, el seguimiento y manejo de las reca&iacute;das, as&iacute; como el manejo con intenci&oacute;n paliativa.</p>     ]]></body>
<body><![CDATA[<p><b>Conclusiones:</b> esta GPC fue desarrollada utilizando procedimientos sistem&aacute;ticos y la mejor evidencia disponible. Se espera que tenga un impacto positivo en el manejo y los desenlaces de las pacientes que padecen de esta enfermedad.</p>     <p><b>Palabras clave:</b> neoplasias ov&aacute;ricas, diagn&oacute;stico, procedimientos quir&uacute;rgicos de citorreducci&oacute;n, Gu&iacute;a de Pr&aacute;ctica Cl&iacute;nica.</p> <font size="4">    <center><b>Surgical management of epithelial ovarian cancer: Clinical Practice Guideline of the Colombian Association of Gynaecologic Oncologists (ASCGO)</b></center></font></p>     <p><b>ABSTRACT</b></p>     <p><b>Introduction:</b> Epithelial ovarian cancer is the primary cause of death from gynaecological cancer in the world. In Colombia, every year there are 8.7 new cases for 100,000 women and more than 800 deaths as a result of this disease. Surgery is the mainstay for management of patients with epithelial ovarian cancer. The aim, when performed in a timely fashion and in combination with the right therapeutic strategies, is to eradicate the disease or, in advanced stages, to achieve microscopic tumour volumes in order to improve prognosis. The objective of this work is to develop evidence-based recommendations for the diagnosis and comprehensive surgical treatment of epithelial ovarian cancer in the Colombian population. </p>     <p><b>Materials and methods: </b>Evidence-based clinical practice guideline developed by an expert panel from the Colombian Association of Gynaecologic Oncologists. A total of 33 questions of interest for comprehensive surgical management were defined and validated in the Society. A review of the literature on clinical practice guidelines was conducted. The evidence of the source guidelines was updated using reviews of the literature and primary experimental and observational studies according to the nature of each question. Finally, the recommendations were discussed and validated in the Association using a participatory expert panel method.</p>     <p><b>Results:</b> A summary of recommendations of the best available evidence for early detection and diagnosis of epithelial ovarian cancer, surgical management of early and late stages of the disease, follow-up and management of recurrences, as well as management with palliative goals. </p>     <p><b>Conclusions:</b> This CPG was developed using systematic procedures and the best available evidence. It is expected to have a positive impact on management and outcomes of patients suffering from this disease.</p>     <p><b>Key words:</b> Ovarian neoplasms, diagnosis, cytoreductive surgical procedure, Clinical Practice Guideline.</p>     <p><b>OBJETIVO Y ALCANCE DE LA GU&Iacute;A</b></p>     ]]></body>
<body><![CDATA[<p>Formular y difundir recomendaciones basadas en la evidencia para el diagn&oacute;stico de masas anexiales y el tratamiento quir&uacute;rgico del c&aacute;ncer epitelial de ovario en mujeres mayores de 18 a&ntilde;os en Colombia, como estrategia para mejorar la calidad en la atenci&oacute;n, reducir la variabilidad en el manejo de la entidad y y disminuir la mortalidad en estas pacientes.</p>     <p>La gu&iacute;a valora aspectos desde el diagn&oacute;stico de masas anexiales hasta algunos del manejo paliativo del c&aacute;ncer epitelial de  ovario  (CEO),  por  tanto, los usuarios son m&eacute;dicos generales, ginec&oacute;logos y ginec&oacute;logos onc&oacute;logos.</p>     <p>Las recomendaciones formuladas en el documento se dirigen a dos poblaciones espec&iacute;ficas:</p>     <p>- Mujeres mayores de 18 a&ntilde;os con masa anexial en proceso diagn&oacute;stico.</p>     <p>- Mujeres mayores de 18 a&ntilde;os con diagn&oacute;stico de c&aacute;ncer epitelial de ovario en cualquier estadio.</p>     <p><b>INTRODUCCI&Oacute;N</b></p>     <p>El c&aacute;ncer epitelial de ovario ocupa el cuarto puesto en frecuencia entre todas las enfermedades malignas de las mujeres despu&eacute;s de los c&aacute;nceres de mama, cuello uterino y endometrio, sin embargo, constituye la primera causa de muerte por c&aacute;ncer ginecol&oacute;gico en el mundo (1). En Colombia cada a&ntilde;o se presentan 8,7 casos nuevos por cada 100.000 mujeres (2) y se estima que alrededor de 800 muertes anuales se producen a causa de la enfermedad (3).</p>     <p>Esta neoplasia se comporta como una enfermedad heterog&eacute;nea, que incluye varios tipos histol&oacute;gicos, con distintos grados de diferenciaci&oacute;n (1). El c&aacute;ncer epitelial representa el 90 % de todas las neoplasias malignas del ovario en poblaci&oacute;n general (4), siendo el tipo histol&oacute;gico m&aacute;s frecuente el seroso papilar, seguido por los tipos mucinoso, endometrioide, de c&eacute;lulas claras, transicional, mixto y los tumores indiferenciados (5).</p>     <p>A pesar de que la supervivencia a 5 a&ntilde;os en los estadios tempranos (FIGO I y II) (<a href="/img/revistas/rcog/v67n2/v67n2a05t1.jpg" target="_blank">tabla 1</a>) es superior al 80 % en comparaci&oacute;n con los estadios m&aacute;s tard&iacute;os (FIGO III y IV) (tabla 1), la mortalidad global de la enfermedad es elevada, debido a que cerca del 70 % de las pacientes se diagnostican en estadios avanzados (6). Esto se debe principalmente a que los estadios tempranos son asintom&aacute;ticos o se manifiestan con s&iacute;ntomas inespec&iacute;ficos, lo que hace que la enfermedad pase desapercibida en sus estadios iniciales, y a las dificultades existentes para un adecuado diagn&oacute;stico precoz (7).</p>     <p>Aunque el impacto de la quimioterapia en la supervivencia de la enfermedad ha sido sustancial, la evoluci&oacute;n de las t&eacute;cnicas quir&uacute;rgicas en la cirug&iacute;a de citorreducci&oacute;n primaria con el fin de lograr vol&uacute;menes tumorales microsc&oacute;picos m&iacute;nimos es el factor pron&oacute;stico m&aacute;s importante (8). El uso de abordajes quir&uacute;rgicos ultrarradicales ha cobrado importancia en el manejo de las pacientes (9), as&iacute; como su combinaci&oacute;n con reg&iacute;menes de quimioterapia (10), para lograr mejores resultados en t&eacute;rminos de supervivencia. Otras consideraciones importantes proceden del manejo quir&uacute;rgico de los estadios tempranos, en especial las relacionadas con la preservaci&oacute;n de la fertilidad, el manejo conservador, as&iacute; como el papel de la cirug&iacute;a m&iacute;nimamente invasiva.</p>     ]]></body>
<body><![CDATA[<p>El presente documento resume un conjunto de recomendaciones basadas en la evidencia y formuladas por un panel de expertos de la Asociaci&oacute;n Colombiana de Ginec&oacute;logos Onc&oacute;logos,  sobre las alternativas diagn&oacute;sticas y terap&eacute;uticas para el manejo quir&uacute;rgico integral del c&aacute;ncer epitelial de ovario (CEO). La revisi&oacute;n detallada de la evidencia se describe con mayor detalle en la <i>Gu&iacute;a de Pr&aacute;ctica Cl&iacute;nica para el manejo quir&uacute;rgico del c&aacute;ncer epitelial de ovario </i>(11)<i>.</i></p>     <p><b>MATERIALES Y M&Eacute;TODOS</b></p>     <p>Se realiz&oacute; un proceso de adaptaci&oacute;n y actualizaci&oacute;n de gu&iacute;as, con formulaci&oacute;n de recomendaciones mediante un panel de expertos integrado por especialistas seleccionados por la Asociaci&oacute;n Colombiana de Ginec&oacute;logos Onc&oacute;logos (ASCGO). En una primera instancia se defini&oacute; el grupo desarrollador de la gu&iacute;a, el cual estaba integrado por un panel de seis expertos cl&iacute;nicos procedentes de diferentes regiones del pa&iacute;s y por un grupo de profesionales con experiencia en la s&iacute;ntesis y el uso de evidencia en c&aacute;ncer.</p>     <p>Se definieron 33 preguntas de inter&eacute;s cl&iacute;nico para el manejo quir&uacute;rgico integral, las cuales fueron consultadas y validadas en una conferencia nacional con especialistas cl&iacute;nicos de la Asociaci&oacute;n. Las preguntas incluidas abordaron aspectos relacionados con la detecci&oacute;n y el diagn&oacute;stico del c&aacute;ncer epitelial de ovario, el manejo quir&uacute;rgico en estados tempranos y avanzados de la enfermedad, la combinaci&oacute;n de la cirug&iacute;a con otras modalidades como la quimioterapia, el seguimiento posterior al manejo primario, el diagn&oacute;stico y tratamiento de las reca&iacute;das posterior al manejo primario, y el manejo con intenci&oacute;n paliativa.</p>     <p>Se llev&oacute; a cabo una revisi&oacute;n de literatura en dos etapas. En la primera se buscaron gu&iacute;as de pr&aacute;ctica cl&iacute;nica basadas en evidencia que incluyeran las preguntas de inter&eacute;s. Las principales fuentes de informaci&oacute;n fueron las bases de datos de la Red Internacional de Gu&iacute;as (GIN, por su sigla en ingl&eacute;s)(12) y el repositorio de gu&iacute;as National Guideline Clearinghouse (NGC) de Estados Unidos (13). Se utilizaron t&eacute;rminos de b&uacute;squeda relacionados con &quot;c&aacute;ncer de ovario&quot;, &quot;neoplasias del ovario&quot;, &quot;tumores del ovario&quot; y &quot;c&aacute;ncer epitelial de ovario&quot;, no se realizaron restricciones por idioma, fuente o grupo desarrollador. A partir de las referencias encontradas, se seleccionaron gu&iacute;as de pr&aacute;ctica cl&iacute;nica que hubieran sido publicadas entre enero de 2010 y diciembre de 2014. El cuerpo de gu&iacute;as encontradas se complement&oacute; con nuevas referencias citadas en los documentos hallados y mediante una b&uacute;squeda de literatura gris disponible en el buscador Google Acad&eacute;mico. Se pregunt&oacute; a expertos cl&iacute;nicos sobre la existencia de otras gu&iacute;as o consensos.</p>     <p>Del total de 25 documentos que fueron seleccionados y calificados con la herramienta AGREE II (14), se emplearon 13 gu&iacute;as de pr&aacute;ctica cl&iacute;nica con sus tablas de evidencia como fuente de informaci&oacute;n (15-27). Se extrajeron las recomendaciones en una matriz dise&ntilde;ada para tal fin, que permit&iacute;a registrar la evidencia fuente referenciada por cada desarrollador. Para garantizar la vigencia y exhaustividad de la evidencia, en una segunda etapa se llevaron a cabo revisiones de literatura dirigidas a identificar publicaciones posteriores a la fecha de b&uacute;squeda de cada gu&iacute;a fuente, se seleccionaron revisiones sistem&aacute;ticas, ensayos cl&iacute;nicos aleatorizados para las preguntas de intervenci&oacute;n y, en algunos casos, estudios observacionales anal&iacute;ticos cuando no se encontraba mejor evidencia disponible. La evidencia fue recuperada de Medline, Embase y Cochrane Library.</p>     <p>Se construyeron tablas y res&uacute;menes de evidencia para cada pregunta, y se formularon recomendaciones preliminares para cada una de ellas por parte de los expertos cl&iacute;nicos participantes; estas recomendaciones fueron revisadas y discutidas en una conferencia tipo panel de expertos organizada por la Asociaci&oacute;n. El grado de fuerza de cada recomendaci&oacute;n se estableci&oacute; de acuerdo con el nivel de la evidencia de la cual proviene (<a href="/img/revistas/rcog/v67n2/v67n2a05t2.jpg" target="_blank">tabla 2</a>). Las recomendaciones finales y la evidencia que la soporta, as&iacute; como las herramientas empleadas, pueden ser consultadas en detalle en la publicaci&oacute;n completa de la gu&iacute;a (11).</p>     <p>El presente trabajo se desarroll&oacute; por expertos cl&iacute;nicos, de acuerdo con las consideraciones &eacute;ticas para la investigaci&oacute;n en humanos, garantizando la veracidad de los resultados y la idoneidad de los investigadores.</p>     <p><b>RESULTADOS</b></p>     <p>A continuaci&oacute;n se presentan las recomendaciones de acuerdo con cada pregunta realizada. En la <a href="/img/revistas/rcog/v67n2/v67n2a05t3.jpg" target="_blank">tabla 3</a> se resumen las recomendaciones clave.</p>     ]]></body>
<body><![CDATA[<p><b>Detecci&oacute;n temprana y diagn&oacute;stico del c&aacute;ncer epitelial de ovario</b></p>     <p><i><b>1. &iquest;Cu&aacute;les son los factores de riesgo asociados al c&aacute;ncer epitelial de ovario (CEO)? (24,  28-34)</b></i></p>     <p>Es necesario conocer e identificar los factores de riesgo para c&aacute;ncer de ovario en mujeres por encima de los 30 a&ntilde;os, y en especial aquellas mayores de 50 a&ntilde;os, para poder orientar su estudio en casos justificados.</p>     <p>Los factores de riesgo para desarrollar c&aacute;ncer epitelial de ovario son:</p>     <p>- Nuliparidad</p>     <p>- Menarquia temprana</p>     <p>- Menopausia tard&iacute;a</p>     <p>- Raza blanca</p>     <p>- Edad (mayores de 50 a&ntilde;os)</p>     <p>- Ubicaci&oacute;n geogr&aacute;fica (Norteam&eacute;rica y norte de Europa)</p>     ]]></body>
<body><![CDATA[<p>- Historia familiar</p>     <p>- Historia personal de c&aacute;ncer de seno</p>     <p>- Factores &eacute;tnicos</p>     <p>No se ha comprobado que el uso de terapia de reemplazo hormonal, terapias de fertilidad, o el uso de talco sean factores de riesgo para el desarrollo de esta neoplasia.</p>     <p><i>Punto de buena pr&aacute;ctica cl&iacute;nica</i></p>     <p><i><b>2. &iquest;Cu&aacute;les son los signos y s&iacute;ntomas asociados con la presentaci&oacute;n del CEO? (15, 35-50)</b></i></p>     <p> Mujeres que asisten a la pr&aacute;ctica m&eacute;dica general, que presenten uno o m&aacute;s s&iacute;ntomas de distensi&oacute;n abdominal con o sin dolor abdominal, dolor p&eacute;lvico, sensaci&oacute;n de llenura, dificultad para comer o s&iacute;ntomas urinarios, en los &uacute;ltimos tres meses, y que hayan requerido consultas repetidas, deben ser evaluadas para descartar un diagn&oacute;stico de c&aacute;ncer de ovario, en especial si son mayores de 50 a&ntilde;os.</p>     <p>A toda paciente con presencia de ascitis, masa abdominal o masa p&eacute;lvica palpada en el examen m&eacute;dico o por la paciente, se le debe descartar un c&aacute;ncer de ovario.</p>     <p><i>Punto de buena pr&aacute;ctica cl&iacute;nica</i></p>     <p><i><b>3. &iquest;Cu&aacute;l es la utilidad diagn&oacute;stica de los &iacute;ndices de malignidad (&iacute;ndice de riesgo de malignidad, ROMA) y los marcadores tumorales (CA125, HE4, ACE) para la aproximaci&oacute;n diagn&oacute;stica de las pacientes con masa p&eacute;lvica? (15, 17-19, 23, 24, 26, 27, 51-56)</b></i></p>     ]]></body>
<body><![CDATA[<p>- Se recomienda utilizar los &iacute;ndices de riesgo de malignidad que combinan por lo menos dos pruebas para diferenciar entre una masa anexial benigna o maligna y as&iacute; orientar su manejo.</p>     <p>- Se recomienda utilizar el &iacute;ndice de riesgo de malignidad que tiene en cuenta los hallazgos del ultrasonido, el estado de menopausia y el valor del CA 125 con un punto de corte de 200 UI/ mL (ver <a href="/img/revistas/rcog/v67n2/v67n2a05a1.jpg" target="_blank">Anexo 1</a>).</p>     <p>- En menores de 40 a&ntilde;os con masas complejas de ovario se deben solicitar otros marcadores (ACE, alfa FP, Beta HCG, LDH) para descartar tumores germinales o metast&aacute;sicos.</p>     <p>- El algoritmo ROMA muestra buen rendimiento diagn&oacute;stico en mujeres posmenop&aacute;usicas para diferenciar entre una masa ov&aacute;rica benigna y una maligna; sin embargo, su uso est&aacute; limitado a aquellos centros en donde es posible medir el marcador s&eacute;rico HE4.</p>     <p><i>Fuerza de la recomendaci&oacute;n: moderada</i></p>     <p><i><b>4. &iquest;Cu&aacute;l es la utilidad diagn&oacute;stica del estudio imagenol&oacute;gico con ecograf&iacute;a transvaginal o ecograf&iacute;a transabdominal para el diagn&oacute;stico de masa p&eacute;lvica? (15, 18, 23, 24, 26, 27, 51, 53, 57-59)</b></i></p>     <p>El examen primario de elecci&oacute;n para confirmar una masa p&eacute;lvica debe ser el ultrasonido transvaginal o, si no es posible, transabdominal.</p>           <p>- Si se encuentra disponible, es mejor realizarlo con t&eacute;cnica 3D para caracterizar las lesiones.</p>     <p>- No se recomienda utilizar resonancia magn&eacute;tica como primera opci&oacute;n para el diagn&oacute;stico de una masa p&eacute;lvica, pues su sensibilidad y especificidad son similares a las del ultrasonido, pero su costo es mucho m&aacute;s elevado. Su uso solo est&aacute; recomendado en caso de que no sea posible caracterizar la lesi&oacute;n por ultrasonido.</p>     <p>- Se recomienda el uso de la tomograf&iacute;a axial computarizada (TAC) para evaluar la presencia de enfermedad extrap&eacute;lvica y caracterizarla.</p>     ]]></body>
<body><![CDATA[<p><i>Fuerza de la recomendaci&oacute;n: moderada</i></p>     <p><b>Consejer&iacute;a gen&eacute;tica familiar</b></p>     <p><i><b>5. &iquest;Qu&eacute; pacientes deben ser remitidas a consejer&iacute;a gen&eacute;tica familiar? (26, 28, 51)</b></i></p>     <p>Se recomienda remitir a consejer&iacute;a gen&eacute;tica a aquellas mujeres con antecedentes personales o familiares de parientes en primero o segundo grado que hayan presentado c&aacute;ncer relacionado (seno, ovario o S. de Lynch). Especialmente si hay familiares que sean portadores de mutaciones BRCA 1 o 2.</p>     <p><i>Punto de buena pr&aacute;ctica cl&iacute;nica</i></p>     <p><b>Generalidades del manejo quir&uacute;rgico inicial del c&aacute;ncer epitelial de ovario (<a href="/img/revistas/rcog/v67n2/v67n2a05f1.jpg" target="_blank">figura 1</a>)</b></p>     <p><i><b>6. &iquest;Qu&eacute; debe hacer el cirujano no onc&oacute;logo(ginec&oacute;logo general, cirujano general) ante el hallazgo incidental de c&aacute;ncer de ovario? (24, 60)</b></i></p>     <p>Frente al hallazgo incidental de c&aacute;ncer de ovario se recomienda:</p>     <p>- Registrar cuidadosamente todos los hallazgos en el protocolo intraoperatorio, tomar una biopsia y enviarla a patolog&iacute;a.</p>     <p>- Remitir a la paciente a un equipo multidisciplinario especializado en c&aacute;ncer ginecol&oacute;gico.</p>     ]]></body>
<body><![CDATA[<p>- Abstenerse de realizar procedimientos con cirug&iacute;as citorreductoras hasta que la paciente tenga confirmaci&oacute;n histol&oacute;gica y se planee una intervenci&oacute;n adecuada para su diagn&oacute;stico histol&oacute;gico espec&iacute;fico.</p>     <p><i>Fuerza de la recomendaci&oacute;n: moderada</i></p>     <p><i><b>7. &iquest;Cu&aacute;les son los criterios cl&iacute;nicos para la remisi&oacute;n de la paciente con sospecha de CEO al ginec&oacute;logo  onc&oacute;logo?  (15,  18,  23,  25,  60-64)</b></i></p>      <p>Se recomienda remitir a ginecolog&iacute;a oncol&oacute;gica a toda paciente con sospecha cl&iacute;nica de c&aacute;ncer de ovario, bien sea por estudios imagenol&oacute;gicos o de marcadores  tumorales,  para  manejo  multidisciplinario.</p>     <p>- Pacientes con estudios de ultrasonido sospechosos de c&aacute;ncer  de  ovario,  CA  125  mayor de 200 UI/mL y ascitis deben ser remitidas a ginecolog&iacute;a oncol&oacute;gica.</p>     <p>- Se recomienda el uso del &iacute;ndice de malignidad de Jacobs IRM 1 para clasificar los casos.</p>     <p><i>Fuerza de la recomendaci&oacute;n: moderada</i></p>     <p><i><b>8. &iquest;Cu&aacute;l es la efectividad y seguridad de la salpingooforectom&iacute;a bilateral (SOB) profil&aacute;ctica en pacientes posmenop&aacute;usicas con y sin factores de  riesgo?  (17,  18,  23,  26,  65-82)</b></i></p>     <p>La salpingooforectom&iacute;a bilateral est&aacute; recomendada en mujeres con mutaciones BRCA1 y BRCA2, idealmente en edades entre 35 y 40 a&ntilde;os y con paridad satisfecha. La edad puede modificarse de acuerdo con la edad m&aacute;s temprana de diagn&oacute;stico familiar de c&aacute;ncer.</p>     <p>En mujeres posmenop&aacute;usicas sin factores de riesgo no hay informaci&oacute;n suficiente que permita recomendar o no su utilizaci&oacute;n. Se recomienda informar a las pacientes sobre el potencial riesgo-beneficio de la salpingooforectom&iacute;a bilateral de forma individual.</p>     ]]></body>
<body><![CDATA[<p><i>Fuerza de la recomendaci&oacute;n: moderada</i></p>     <p><i><b>9. &iquest;Cu&aacute;l es el papel de la salpingectom&iacute;a profil&aacute;ctica en paciente sin riesgo? (83-91)</b></i></p>     <p>Para mujeres con riesgo promedio de c&aacute;ncer de ovario, quienes son llevadas a histerectom&iacute;a por condiciones benignas, no hay estudios que permitan establecer una recomendaci&oacute;n sobre el uso de la pr&aacute;ctica de salpingectom&iacute;a bilateral. Sin embargo, series de casos no han mostrado efectos adversos mayores al realizar este tipo de intervenciones.</p>     <p><i>Fuerza de la recomendaci&oacute;n: d&eacute;bil</i></p>     <p><i><b>10. &iquest;Cu&aacute;les son los pasos que se deben seguir para la clasificaci&oacute;n intraquir&uacute;rgica de las pacientes con c&aacute;ncer de ovario? (15, 18, 23, 24,92-99)</b></i></p>     <p>Se recomienda realizar laparotom&iacute;a de estadificaci&oacute;n exhaustiva, la cual incluye laparotom&iacute;a mediana para permitir la evaluaci&oacute;n detallada del abdomen y la pelvis; histerectom&iacute;a abdominal total; salpingooforectom&iacute;a bilateral y omentectom&iacute;a infrac&oacute;lica; biopsias de cualquier dep&oacute;sito peritoneal; biopsias aleatorias del peritoneo p&eacute;lvico y abdominal; y la evaluaci&oacute;n de ganglios linf&aacute;ticos retroperitoneales mediante una resecci&oacute;n ganglionar en caso de compromiso macrosc&oacute;pico o linfadenectom&iacute;a p&eacute;lvica y paraa&oacute;rtica completa en caso de no encontrar lesi&oacute;n macrosc&oacute;pica, siempre que se logre citorreducci&oacute;n completa en la cavidad abdominal.</p>     <p>Procedimientos m&iacute;nimamente invasivos pueden ser utilizados en sospecha de estadios tempranos en pacientes seleccionados, y deben ser realizados por ginec&oacute;logos onc&oacute;logos con experiencia.</p>     <p><i>Fuerza de la recomendaci&oacute;n: moderada</i></p>     <p><i><b>11. &iquest;Cu&aacute;les son los criterios prequir&uacute;rgicos para definir entre citorreducci&oacute;n primaria y quimioterapia  neoadyuvante?  (100,  101)</b></i></p>     <p>Se recomienda considerar la quimioterapia neoadyuvante en aquellas pacientes con compromiso severo de su estado general, o en aquellos estadios IIIC o IV, en los cuales no es posible garantizar una citorreducci&oacute;n completa.</p>     ]]></body>
<body><![CDATA[<p>- Aplicable en los casos que requieren una resecci&oacute;n intestinal mayor de 1,5 m o m&uacute;ltiples resecciones  intestinales.</p>     <p>- En caso de met&aacute;stasis intrahep&aacute;tica o extraabdominal no resecable.</p>     <p>- En caso de tumor mayor de 2 cm alrededor de la arteria mesent&eacute;rica superior o detr&aacute;s de la porta hep&aacute;tica.</p>     <p><i>Punto de buena pr&aacute;ctica cl&iacute;nica</i></p>     <p><i><b>12. &iquest;Cu&aacute;l debe ser el abordaje oncol&oacute;gico de la paciente con c&aacute;ncer de ovario y cirug&iacute;a previa incompleta?  (15)</b></i></p>     <p>Para las pacientes con cirug&iacute;a previa o estadificaci&oacute;n incompleta se recomienda:</p>     <p>- En presuntos estadios IA o IB, grado I, completar cirug&iacute;a y realizar estadificaci&oacute;n quir&uacute;rgica.</p>     <p>- En presuntos estadios IA o IB, grados II o III, o c&eacute;lulas claras, completar cirug&iacute;a y realizar estadificaci&oacute;n  quir&uacute;rgica.</p>     <p>- En presuntos estadios II, III, IV, realizar cirug&iacute;a de reducci&oacute;n del tumor si hay sospecha de enfermedad residual potencialmente resecable. Si se sospecha enfermedad residual no resecable, realizar quimioterapia neoadyuvante y considerar la realizaci&oacute;n de cirug&iacute;a de intervalo.</p>     <p><i>Nota:</i> considere cirug&iacute;a previa incompleta si existe: &uacute;tero intacto, anexo intacto, omentum no removido, documentaci&oacute;n de estatificaci&oacute;n incompleta, enfermedad residual, potencialmente resecable, carcinoma invasivo oculto que se encontr&oacute; en el momento de la cirug&iacute;a de reducci&oacute;n del riesgo.</p>     ]]></body>
<body><![CDATA[<p><i>Punto de buena pr&aacute;ctica cl&iacute;nica</i></p>     <p><i><b>13. &iquest;Cu&aacute;les son las indicaciones y contraindicaciones de la cirug&iacute;a m&iacute;nimamente invasiva en el manejo quir&uacute;rgico de c&aacute;ncer de ovario?  (15,  19,  23-25,  27,  102-111)</b></i></p>     <p>- La laparoscopia es la v&iacute;a preferible para la SOB profil&aacute;ctica indicada en la mujer con riesgo hereditario de CEO. La laparoscopia puede ser la v&iacute;a de acceso para pacientes con aparente CEO en estadios tempranos.</p>     <p>- La laparoscopia se puede utilizar como cirug&iacute;a reestadificadora en pacientes con cirug&iacute;a previa incompleta y aparente estadio temprano.</p>     <p>- En caso de sospecha de irresecabilidad por estudios imagenol&oacute;gicos, la laparoscopia puede utilizarse para la verificaci&oacute;n de resecabilidad o irresecabilidad para el inicio de quimioterapia neoadyuvante. Deben describirse juiciosamente los hallazgos en la descripci&oacute;n. Se pueden utilizar &iacute;ndices validados en la literatura.</p>     <p>- La laparoscopia no muestra diferencia en evoluci&oacute;n oncol&oacute;gica comparada con cirug&iacute;a abierta en  tumores  infiltrantes  en  estadios  tempranos o tumores <i>borderline</i>.</p>     <p>- La laparoscopia puede ser considerada en cirug&iacute;a preservadora de la fertilidad.</p>     <p>- La laparoscopia debe ser discutida con el paciente y elegirse de acuerdo con preferencias de la paciente y del cirujano.</p>     <p>- En caso de decidirse la v&iacute;a laparosc&oacute;pica, esta siempre debe ser realizada por un ginec&oacute;logo onc&oacute;logo.</p>     <p><i>Fuerza de la recomendaci&oacute;n: moderada</i></p>     ]]></body>
<body><![CDATA[<p><b>Manejo del c&aacute;ncer epitelial de ovario en estadios tempranos (<a href="/img/revistas/rcog/v67n2/v67n2a05f1.jpg" target="_blank">figura 1</a>)</b></p>     <p><i><b>14. &iquest;Cu&aacute;l es la efectividad del manejo quir&uacute;rgico en estadios tempranos? (15, 21, 23-25, 27, 93, 112-113)</b></i></p>             <p class="s10" style="padding-top: 1pt;padding-left: 5pt;line-height: 106%;text-align: left;">En  estadios  tempranos  el  manejo  est&aacute;ndar  recomendado es la cirug&iacute;a, la cual incluye:</p>     <p>- Incisi&oacute;n mediana infraumbilical.</p>     <p>- Toma de muestra de ascitis o, en su ausencia, lavados peritoneales.</p>     <p>- Histerectom&iacute;a abdominal + salpingooforectom&iacute;a bilateral.</p>     <p>- Resecci&oacute;n de lesiones peritoneales sospechosas o biopsias peritoneales aleatorias en caso de no evidencia de lesi&oacute;n macrosc&oacute;pica.</p>     <p>- Omentectom&iacute;a  infrac&oacute;lica.</p>     <p>- Linfadenectom&iacute;a p&eacute;lvica y paraa&oacute;rtica.</p>     <p>En pacientes con deseo gen&eacute;sico se recomienda salpingooforectom&iacute;a  unilateral.</p>     ]]></body>
<body><![CDATA[<p>La v&iacute;a laparosc&oacute;pica puede considerarse para el diagn&oacute;stico y la estadificaci&oacute;n, y ser parte del tratamiento en estadios tempranos; sin  embargo, son necesarios estudios aleatorizados y controlados.</p>     <p><i>Fuerza de la recomendaci&oacute;n: moderada</i></p>     <p><i><b>15. &iquest;Cu&aacute;les son los sitios para la toma de muestra de la citolog&iacute;a intraoperatoria? (114) Se debe tomar una muestra de l&iacute;quido asc&iacute;tico para citolog&iacute;a. En ausencia de ascitis, se tomar&aacute; muestra para citolog&iacute;a con suero fisiol&oacute;gico de: fondo de saco anterior, fondo de saco posterior, goteras parietoc&oacute;licas derecha e izquierda y citolog&iacute;a de c&uacute;pulas diafragm&aacute;ticas.</b></i></p>     <p><i>Punto de buena pr&aacute;ctica cl&iacute;nica</i></p>     <p><i><b>16. &iquest;Cu&aacute;l debe ser el esquema para la toma de biopsias peritoneales? (17, 23-25, 115-117) La toma de biopsias peritoneales incluye:</b></i></p>     <p>- Visualizar y palpar todas las superficies peritoneales.</p>     <p>- Resecar todas las adherencias sospechosas y no sospechosas.</p>     <p>- En ausencia de evidencia macrosc&oacute;pica de tumor, se deben tomar biopsias peritoneales aleatorias en fondo de saco anterior, fondo de saco posterior, goteras parietoc&oacute;licas y c&uacute;pula diafragm&aacute;tica (raspado para citolog&iacute;a).</p>     <p><i>Fuerza de la recomendaci&oacute;n: d&eacute;bil</i></p>     <p><i><b>17.&iquest;Cu&aacute;l es el papel de la apendicectom&iacute;a en el manejo de la paciente con c&aacute;ncer de ovario? (23-25, 118-122)</b></i></p>     ]]></body>
<body><![CDATA[<p>- Se debe realizar apendicectom&iacute;a en caso de eviden- cia macrosc&oacute;pica de compromiso tumoral. Tambi&eacute;n se recomienda este procedimiento en tumores mucinosos y seudomixoma peritoneal.</p>     <p><i>Fuerza de la recomendaci&oacute;n: d&eacute;bil</i></p>     <p><i><b>18. &iquest;Cu&aacute;l es la efectividad y seguridad de la linfadenectom&iacute;a radical frente al muestreo ganglionar en estadios tempranos?(15, 25, 94, 96)</b></i></p>     <p>Se recomienda realizar linfadenectom&iacute;a p&eacute;lvica y paraa&oacute;rtica en las pacientes con c&aacute;ncer epitelial de ovario en estadios tempranos.</p>     <p><i>Fuerza de la recomendaci&oacute;n: moderada</i></p>     <p><i><b>19. &iquest;Cu&aacute;les son las indicaciones y rol de la biopsia por congelaci&oacute;n durante el abordaje quir&uacute;rgico? (18, 23, 27, 96, 112, 123-125)</b></i></p>     <p>Se recomienda el uso de la biopsia por congelaci&oacute;n para confirmar enfermedad maligna y desarrollar un algoritmo de manejo individual.</p>     <p>- Se deben considerar las limitaciones de la misma en casos de tumores con bajo riesgo de malignidad.</p>     <p>- Las pacientes que deseen mantener potencialmente la fertilidad deben tener una evaluaci&oacute;n intraoperatoria con biopsia por congelaci&oacute;n.</p>     <p>- En cirug&iacute;a de preservaci&oacute;n de la fertilidad se puede realizar (si es t&eacute;cnicamente factible) si los resultados de la biopsia por congelaci&oacute;n son positivos para tumor maligno de c&eacute;lulas germinales, c&aacute;ncer epitelial de ovario estadio I o tumores <i>borderline</i>.</p>     ]]></body>
<body><![CDATA[<p>Se debe evitar hacer procedimientos radicales sin biopsia por congelaci&oacute;n en casos en los que exista duda.</p>     <p><i>Fuerza de la recomendaci&oacute;n: moderada</i></p>     <p><i><b>20. &iquest;Cu&aacute;l es la indicaci&oacute;n de quimioterapia posoperatoria en estadios tempranos?(15, 23-25, 95, 123, 126)</b></i></p>     <p>Se recomienda el uso de adyuvancia en estadios IA (G3), IB (G2, G3), IC y IIA, en tumores de c&eacute;lulas claras en cualquier grado o estadio, durante tres a seis (6) ciclos con quimioterapia complementaria.</p>     <p><i>Fuerza de la recomendaci&oacute;n: moderada</i></p>     <p><b>Condiciones especiales (<a href="/img/revistas/rcog/v67n2/v67n2a05f2.jpg" target="_blank">figura 2</a>)</b></p>     <p><i><b>21.&iquest;Cu&aacute;l es el manejo quir&uacute;rgico de la paciente con diagn&oacute;stico de CEO borderline? (22, 23, 27, 127-133)</b></i></p>     <p>En mujeres con cirug&iacute;a completa la paciente debe ser llevada a observaci&oacute;n. En caso de cirug&iacute;a incompleta, evaluar el deseo de fertilidad.</p>     <p>En mujeres menores de 40 a&ntilde;os debe considerarse cirug&iacute;a conservadora de fertilidad si la paciente lo desea.</p>     <p>- En caso de cirug&iacute;a conservadora de fertilidad:</p>     ]]></body>
<body><![CDATA[<p>&bull; SOU (para tumor unilateral). Considerar cistectom&iacute;a en caso de compromiso bilateral.</p>     <p>&bull; Exploraci&oacute;n de cavidad (resecci&oacute;n de implantes).</p>     <p>- En caso de no preservaci&oacute;n de fertilidad</p>     <p>&bull; Histerectom&iacute;a abdominal.</p>     <p>&bull; SOB.</p>     <p>&bull; Exploraci&oacute;n cavidad (resecci&oacute;n de implantes).</p>     <p>Se debe realizar citorreducci&oacute;n completa en caso de reca&iacute;das.</p>     <p>La laparoscopia es una opci&oacute;n posible para el manejo de los tumores <i>borderline</i>.</p>     <p><i>Fuerza de la recomendaci&oacute;n: d&eacute;bil</i></p>     <p><i><b>22. &iquest;Cu&aacute;les son las condiciones para realizar cirug&iacute;a conservadora de fertilidad en paciente con CEO en estadios iniciales? (18, 23-25, 27, 128,130, 134-141)</b></i></p>     ]]></body>
<body><![CDATA[<p>La cirug&iacute;a conservadora de fertilidad puede tenerse en cuenta en mujeres menores de 40 a&ntilde;os que deseen paridad, con estadios IA (grados I y II) y IC (grado 1).</p>     <p>- La paciente debe recibir informaci&oacute;n completa del procedimiento y posibles desenlaces.</p>     <p>- Debe incluirse estadificaci&oacute;n completa de la enfermedad como parte del procedimiento.</p>     <p>- En casos seleccionados se sugiere utilizar la v&iacute;a laparosc&oacute;pica.</p>     <p>- Debe considerarse completar cirug&iacute;a cuando est&eacute; satisfecho el deseo de paridad.</p>     <p><i>Fuerza de la recomendaci&oacute;n: moderada</i></p>     <p><b>Manejo del c&aacute;ncer epitelial de ovario en estadios avanzados (<a href="/img/revistas/rcog/v67n2/v67n2a05f1.jpg" target="_blank">figura 1</a>)</b></p>     <p><i><b>23. &iquest;Cu&aacute;l es la efectividad y seguridad de la cirug&iacute;a ultrarradical en el manejo de la paciente con CEO avanzado? (9, 10, 15, 18-20, 23-25,94, 142-149)</b></i></p>     <p>Se recomienda  la  cirug&iacute;a  como  manejo  est&aacute;ndar inicial de la paciente con c&aacute;ncer epitelial de ovario, con el objetivo de clasificar la enfermedad y <i>lograr una citorreducci&oacute;n completa.</i></p>     <p>La cirug&iacute;a radical  debe  incluir: histerectom&iacute;a abdominal, salpingooforectom&iacute;a bilateral, omentectom&iacute;a, linfadenectom&iacute;a p&eacute;lvica y paraa&oacute;rtica, resecci&oacute;n de superficies peritoneales, resecciones intestinales, resecciones hep&aacute;ticas, cola de p&aacute;ncreas y esplenectom&iacute;a. Estas cinco &uacute;ltimas solo en caso de evidencia de tumor macrosc&oacute;pico de estos &oacute;rganos.</p>     ]]></body>
<body><![CDATA[<p><i>Fuerza de la recomendaci&oacute;n: moderada</i></p>     <p><i><b>24. &iquest;Cu&aacute;les son las estrategias para lograr una citorreducci&oacute;n completa u &oacute;ptima en pacientes con CEO avanzado? (9, 18, 23-25, 142, 143, 150, 151)</b></i></p>     <p>Se recomienda la citorreducci&oacute;n completa como objetivo quir&uacute;rgico, para lo cual se prefiere el abordaje ultrarradical en pacientes con CEO avanzado.</p>     <p>Se recomienda acceder al abdomen superior como parte del abordaje ultrarradical, para lo cual es indispensable desarrollar equipos de trabajo multidisciplinarios.</p>     <p><i>Fuerza de la recomendaci&oacute;n: moderada</i></p>     <p><i><b>25. &iquest;Cu&aacute;l es la efectividad y seguridad de la linfadenectom&iacute;a en la paciente con CEO avanzado? (Opini&oacute;n de expertos)</b></i></p>     <p>Se recomienda hacer linfadenectom&iacute;a p&eacute;lvica y paraa&oacute;rtica en pacientes con c&aacute;ncer epitelial de ovario en estadio avanzado solamente cuando se logre la citorreducci&oacute;n completa o exista evidencia de compromiso ganglionar (im&aacute;genes o palpaci&oacute;n).</p>     <p><i>Fuerza de la recomendaci&oacute;n: fuerte</i></p>     <p><i><b>26. &iquest;Cu&aacute;les son las indicaciones y el alcance de la citorreducci&oacute;n secundaria en pacientes con CEO?  (18,  24,  25,  152-158)</b></i></p>     <p>Se recomienda la citorreducci&oacute;n secundaria en pacientes sensibles al platino que recaen en forma loco-regional seis meses o m&aacute;s posteriores al tratamiento   primario.</p>     ]]></body>
<body><![CDATA[<p>El objetivo debe ser la citorreducci&oacute;n completa.</p>     <p><i>Fuerza de la recomendaci&oacute;n: moderada</i></p>     <p><i><b>27. &iquest;Cu&aacute;l es el momento adecuado durante la quimioterapia neoadyuvante para realizar la cirug&iacute;a de intervalo? (9, 15, 18, 23-25, 101,159-162)</b></i></p>     <p>Se sugiere la neoadyuvancia como alternativa terap&eacute;utica en el grupo de pacientes de alta comorbilidad, estadios IIIC/IV, o en aquellos que cumplan los criterios de Leuven para irresecabilidad.</p>     <p>No existe consenso o evidencia acerca del n&uacute;mero de ciclos de quimioterapia previos a la cirug&iacute;a de intervalo.</p>     <p>Al terminar el 3 o 4 ciclo de quimioterapia se debe realizar evaluaci&oacute;n cl&iacute;nica e imagenol&oacute;gica y CA125 si este ha estado elevado previamente, con el fin de decidir la cirug&iacute;a de intervalo.</p>     <p><i>Fuerza de la recomendaci&oacute;n: fuerte</i></p>     <p><i><b>28. &iquest;Cu&aacute;les son las indicaciones de la quimioterapia intraperitoneal en estadios avanzados?   (18-20,   25,   163-169)</b></i></p>     <p>La quimioterapia intraperitoneal (IP) debe considerarse de forma individual, en casos de c&aacute;ncer epitelial de ovario avanzados (estadio III o m&aacute;s), en consenso con oncolog&iacute;a cl&iacute;nica, el paciente y su familia, en pacientes con citorreducci&oacute;n &oacute;ptima atendidas en centros especializados con capacidad de manejo integral.</p>     <p>Se recomienda limitar el uso de quimioterapia intraperitoneal hipert&eacute;rmica (HIPEC) en el abordaje primario o en la reca&iacute;da del CEO a pacientes en estados avanzados atendidas en centros especializados exclusivamente en el marco de estudios cl&iacute;nicos.</p>     ]]></body>
<body><![CDATA[<p><i>Fuerza de la recomendaci&oacute;n: fuerte</i></p>     <p><b>Seguimiento y manejo de las reca&iacute;das</b></p>     <p><i><b>29. &iquest;Cu&aacute;l es el esquema adecuado para el seguimiento en las pacientes tratadas por CEO? (18,  23-25,  170,  171)</b></i></p>     <p>En cada visita de seguimiento debe realizarse una historia cl&iacute;nica y un examen f&iacute;sico completos, incluyendo el examen p&eacute;lvico. Si no hay s&iacute;ntomas sugestivos de reca&iacute;da (similares a los de un tumor primario), no hay obligatoriedad de tomar ning&uacute;n examen paracl&iacute;nico. De acuerdo con lo hallado en la entrevista o el examen f&iacute;sico puede, en cada caso, ser necesario ordenar niveles de CA125 u otros marcadores tumorales cuando aplique (como ant&iacute;geno carcinoembrionario), particularmente si estuvieron elevados anteriormente, y en aquellos casos en los que se considere que con una detecci&oacute;n temprana es posible una citorreducci&oacute;n secundaria ben&eacute;fica para la paciente; as&iacute; mismo, se debe considerar tomar im&aacute;genes diagn&oacute;sticas (rayos X, ecograf&iacute;a, resonancia magn&eacute;tica, tomograf&iacute;a axial, PET-CT).</p>     <p>En caso sugestivo de reca&iacute;da se recomienda valorar a la paciente en junta multidisciplinaria. Las visitas de seguimiento tras el tratamiento deben ser realizadas cada 3-4 meses los primeros dos a&ntilde;os, cada 6 meses entre el tercer y quinto a&ntilde;o y anualmente a partir del quinto a&ntilde;o.</p>     <p><i>Punto de buena pr&aacute;ctica cl&iacute;nica</i></p>     <p>En los casos en los cuales sea realizada quimioterapia adyuvante, el control debe realizarse tambi&eacute;n por el ginec&oacute;logo onc&oacute;logo con periodicidad bimestral mientras se est&aacute; realizando su administraci&oacute;n.</p>     <p>Fuerza de la recomendaci&oacute;n: moderada</p>     <p><i><b>30. &iquest;C&oacute;mo se define la reca&iacute;da posterior al tratamiento en pacientes con CEO? (23, 171)</b></i></p>     <p>La reca&iacute;da posterior al tratamiento en pacientes con CEO hace referencia a la aparici&oacute;n de la enfermedad despu&eacute;s del tratamiento primario. Esta puede ser clasificada como cl&iacute;nica o serol&oacute;gica.</p>     ]]></body>
<body><![CDATA[<p>. Reca&iacute;da cl&iacute;nica. Aparici&oacute;n de s&iacute;ntomas sugestivos de la enfermedad (similares a los del tumor primario) o atribuidos a localizaciones secundarias, con evidencia de tumor en el examen cl&iacute;nico o en las im&aacute;genes que se practiquen.</p>     <p>. Reca&iacute;da  serol&oacute;gica</p>     <p>- Pacientes con elevaci&oacute;n del CA125 antes del tratamiento en quienes se haya normalizado: elevaci&oacute;n igual o superior a 70 UI/mL en dos muestras tomadas con al menos una semana de diferencia1 (dos veces el valor superior normal).</p>     <p>- Pacientes con elevaci&oacute;n del CA125 antes del tratamiento en quienes nunca se normaliz&oacute;: elevaci&oacute;n de dos veces el nadir (valor m&iacute;nimo alcanzado) en dos muestras tomadas con al menos una semana de diferencia.</p>     <p>- Pacientes con valores normales de CA125 antes del tratamiento: elevaci&oacute;n igual o superior a 70 UI/mL en dos muestras tomadas con al menos una semana de diferencia.</p>     <p><i>Punto de buena pr&aacute;ctica cl&iacute;nica</i></p>     <p><i><b>31. &iquest;C&oacute;mo debe ser el estudio y manejo de la reca&iacute;da exclusivamente serol&oacute;gica en pacientes con  CEO?  (18,  23,  171-179)</b></i></p>     <p>En casos de reca&iacute;da serol&oacute;gica deben tomarse estudios imagenol&oacute;gicos conducentes a identificar la localizaci&oacute;n y extensi&oacute;n de la enfermedad recurrente con el objetivo de planear la conducta subsecuente. Resultan de utilidad la TAC abdominop&eacute;lvica con contraste, y de t&oacute;rax, la resonancia magn&eacute;tica y la tomograf&iacute;a por emisi&oacute;n de positrones en combinaci&oacute;n con la TAC (PET-CT). En todos los casos se recomienda definir en una junta m&eacute;dica multidisciplinaria la conducta que se debe seguir.</p>     <p>En caso de documentarse una reca&iacute;da exclusivamente serol&oacute;gica, sin evidencia de representaci&oacute;n cl&iacute;nica ni imagenol&oacute;gica, en pacientes con c&aacute;ncer de ovario, la paciente debe ser evaluada por una junta m&eacute;dica que incluya las especialidades de ginecolog&iacute;a oncol&oacute;gica y oncolog&iacute;a cl&iacute;nica, y que formule una recomendaci&oacute;n ante las circunstancias individuales. Las posibilidades de manejo de esta condici&oacute;n pueden seguir diferentes recomendaciones tales como postergar el inicio de tratamiento hasta que existan manifestaciones cl&iacute;nicas (s&iacute;ntomas) o considerar otras opciones como el inicio de tratamiento con quimioterapia, terapia hormonal, o la incorporaci&oacute;n de la paciente en ensayos cl&iacute;nicos.</p>     <p><i>Punto de buena pr&aacute;ctica cl&iacute;nica</i></p>     ]]></body>
<body><![CDATA[<p><b>Manejo paliativo del c&aacute;ncer epitelial de ovario</b></p>     <p><i><b>32. &iquest;Cu&aacute;les son los criterios para declarar una paciente como no susceptible de manejo con intenci&oacute;n curativa y remitir a cuidado paliativo? (23,   180)</b></i></p>     <p>En las pacientes con persistencia, progresi&oacute;n de la enfermedad o toxicidad limitante, debe decidirse si ser&aacute;n sometidas a otras l&iacute;neas de quimioterapia o se reorienta la intenci&oacute;n del tratamiento hacia el control de los s&iacute;ntomas y cuidados de soporte. Estas pacientes tambi&eacute;n podr&iacute;an incluirse en ensayos cl&iacute;nicos donde est&eacute;n disponibles.</p>     <p><i>Punto de buena pr&aacute;ctica cl&iacute;nica</i></p>     <p><i><b>33. &iquest;C&oacute;mo debe ser el manejo paliativo de la obstrucci&oacute;n intestinal en la paciente con CEO avanzado?   (18,   180-186)</b></i></p>     <p>Los procedimientos de intenci&oacute;n paliativa en las pacientes con c&aacute;ncer de ovario deben realizarse para el tratamiento de situaciones espec&iacute;ficas y cuando se considere que ofrecer&aacute;n un beneficio cl&iacute;nico significativo. La cirug&iacute;a para obstrucci&oacute;n intestinal debe ser realizada solo en casos de obstrucci&oacute;n mec&aacute;nica y no de manera preventiva. Debe evitarse realizar cirug&iacute;a para obstrucci&oacute;n intestinal ante situaciones como enfermedad metast&aacute;sica difusa demostrada en cirug&iacute;a previa, compromiso intestinal proximal, enfermedad metast&aacute;sica masiva palpable, ascitis severa r&aacute;pidamente recurrente o la oposici&oacute;n de la paciente. Debe considerarse tambi&eacute;n evitarla en casos de compromiso extraabdominal extenso y en pacientes con mal estado funcional o nutricional.</p>     <p><i>Fuerza de la recomendaci&oacute;n: fuerte</i></p>     <p><b>ACTUALIZACI&Oacute;N DE LAS RECOMENDACIONES</b></p>     <p>El grupo desarrollador de la gu&iacute;a recomienda hacer la actualizaci&oacute;n de las recomendaciones en un periodo no mayor a cuatro a&ntilde;os a partir de la fecha de publicaci&oacute;n del presente documento, o cuando exista nueva evidencia que pueda cambiar las recomendaciones  formuladas.</p>     <p><b>DECLARACI&Oacute;N DE CONFLICTOS DE INTER&Eacute;S Y FINANCIACI&Oacute;N</b></p>     ]]></body>
<body><![CDATA[<p>En las diferentes actividades, los participantes en el desarrollo de la gu&iacute;a declararon no tener alg&uacute;n conflicto de inter&eacute;s que pudiera interferir en las actividades y la formulaci&oacute;n de recomendaciones. En todo el proceso los integrantes del grupo desarrollador y los participantes en el proyecto realizaron la declaraci&oacute;n escrita y firmada de potenciales conflictos de inter&eacute;s, los cuales han sido analizados y se encuentran a disposici&oacute;n de los interesados.</p>     <p>Los recursos para el desarrollo de la gu&iacute;a y del presente art&iacute;culo provienen de una subvenci&oacute;n para investigaci&oacute;n y soporte log&iacute;stico de Productos Roche S.A. La entidad financiadora garantiz&oacute; total independencia de las acciones y opiniones de los expertos del panel, especialistas participantes y grupo de apoyo metodol&oacute;gico.</p>     <p><b>Nota:</b> este art&iacute;culo hace parte de la versi&oacute;n completa de  la  &quot;Gu&iacute;a  de  pr&aacute;ctica cl&iacute;nica (GPC) para el manejo quir&uacute;rgico del c&aacute;ncer epitelial de ovario en Colombia. Bogot&aacute;&quot; (11). Este documento es publicado con autorizaci&oacute;n de la Asociaci&oacute;n Colombiana de Ginec&oacute;logos Onc&oacute;logos y el Instituto para la Evaluaci&oacute;n de la Calidad y Atenci&oacute;n en Salud (IECAS).</p>     <p><b>*REPRESENTANTES DEL GRUPO DESARROLLADOR DE LA GU&Iacute;A</b></p>     <p>Jes&uacute;s Antonio Acosta-Pe&ntilde;aloza, MD. Ginec&oacute;logo onc&oacute;logo, Asociaci&oacute;n Colombiana de Ginec&oacute;logos Onc&oacute;logos; Instituto Nacional de Cancerolog&iacute;a ESE, Bogot&aacute; (Colombia). <a href="mailto:jesacosta3@gmail.com">jesacosta3@gmail.com</a></p>     <p>Mauricio Gonz&aacute;lez-Casta&ntilde;eda, MD. Ginec&oacute;logo onc&oacute;logo, Asociaci&oacute;n Colombiana de Ginec&oacute;logos Onc&oacute;logos, Instituto Nacional de Cancerolog&iacute;a ESE, Bogot&aacute; (Colombia).</p>     <p>Robinson Fern&aacute;ndez-Mercado, MD. Ginec&oacute;logo onc&oacute;logo, Asociaci&oacute;n Colombiana de Ginec&oacute;logos Onc&oacute;logos, Bogot&aacute; (Colombia); Misi&oacute;n M&eacute;dica Ltda., Barranquilla (Colombia).</p>     <p>Heydi Marina Ram&iacute;rez-Salazar, MD. Ginec&oacute;loga onc&oacute;loga, Asociaci&oacute;n Colombiana de Ginec&oacute;logos Onc&oacute;logos, Bogot&aacute; (Colombia); Fundaci&oacute;n Cl&iacute;nica Valle de Lili, Cali (Colombia).</p>     <p>Jaime Fernando Ruiz-Povea, MD. Ginec&oacute;logo onc&oacute;logo, Asociaci&oacute;n Colombiana de Ginec&oacute;logos Onc&oacute;logos; Onc&oacute;logos de Occidente, Manizales (Colombia).</p>     <p>Daniel Sanabria-Serrano, MD. Ginec&oacute;logo onc&oacute;logo, Asociaci&oacute;n Colombiana de Ginec&oacute;logos Onc&oacute;logos; Fundaci&oacute;n Santa Fe de Bogot&aacute;, Bogot&aacute; (Colombia).</p>     ]]></body>
<body><![CDATA[<p>Carolina Sandoval-Salinas. Bacteri&oacute;loga; Especialista en Epidemiolog&iacute;a general, Instituto para la Evaluaci&oacute;n de la Calidad y la Atenci&oacute;n en Salud (IECAS), Bogot&aacute; (Colombia).</p>     <p>Giancarlo Buitrago-Guti&eacute;rrez, MD, MSc. M&eacute;dico cirujano; MSc en Epidemiolog&iacute;a cl&iacute;nica; MSc en Econom&iacute;a, Instituto para la Evaluaci&oacute;n de la Calidad y la Atenci&oacute;n en Salud (IECAS), Bogot&aacute; (Colombia).</p>     <p>Juan Sebasti&aacute;n Castillo-Londo&ntilde;o, MD, MSc. M&eacute;dico cirujano; MSc en Epidemiolog&iacute;a cl&iacute;nica; MSc en Salud p&uacute;blica. Instituto para la Evaluaci&oacute;n de la Calidad y la Atenci&oacute;n en Salud (IECAS), Bogot&aacute; (Colombia).</p>     <p><b>REVISI&Oacute;N DE LA GU&Iacute;A</b></p>     <p>Grupo Cl&iacute;nica Ginecolog&iacute;a, Instituto Nacional de Cancerolog&iacute;a.</p>     <p><b>REFERENCIAS</b></p>     <!-- ref --><p>1. Wei W, Dizon D, Vathipadiekal V, Birrer MJ. Ovarian Cancer: genomic analysis. Annals of Oncology. 2013;24(suppl10):S7-S10.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=2702606&pid=S0034-7434201600020000500001&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>     <!-- ref --><p>2. Ulusoy S, AKbayir O, Nomanoglu C, Ulusoy N, Odabas E, Gulkilik A. The risk of malignancy index in discrimination of adnexal masses. Int J Gynaecol Obstet.    2007;96:186-91.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=2702608&pid=S0034-7434201600020000500002&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>     ]]></body>
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<body><![CDATA[<!-- ref --><p>20. National Institute of Clinical Excellence NICE. Ovarian Cancer : Evidence Update January 2013. A summary of selected new evidence relevant to NICE clinical guideline 122, &quot;The recognition and initial management of ovarian cancer&quot; (2011) Evidence. Manchester; 2013.    &nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;[&#160;<a href="javascript:void(0);" onclick="javascript: window.open('/scielo.php?script=sci_nlinks&ref=2702640&pid=S0034-7434201600020000500020&lng=','','width=640,height=500,resizable=yes,scrollbars=1,menubar=yes,');">Links</a>&#160;]<!-- end-ref --></p>     <!-- ref --><p>21. National Institute of Clinical Excellence NICE. Quality standard for ovarian cancer. 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