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Bloquea un mecanismo protector de las células cancerosas y permite que el sistema inmunitario las destruya. El anticuerpo monoclonal contra la proteína de muerte celular programada 1 (PD-1) bloquea la interacción entre PD-1 y sus ligandos: PD-L1 y PD-L2.</p><p> Los precios de Keytruda se especifican en este listado. Envíe una solicitud para obtener un presupuesto personalizado. </p></div><h2> ¿El pembrolizumab está aprobado por la FDA?</h2><i class=\"fa fa-angle-down\"></i><div class=\"accordion-item-text\"><p> El 23 de mayo de 2017, la Administración de Drogas y Alimentos de EE. UU. otorgó una aprobación acelerada a pembrolizumab (Keytruda), una aprobación más rápida de medicamentos para afecciones graves que satisfacen una necesidad médica no cubierta. La FDA permitió recetar un nuevo fármaco de inmunoterapia para tratar a pacientes cuyos cánceres tienen una característica genética específica (biomarcador). </p></div><h2> <strong>¿Cuáles son las tasas de éxito de Keytruda?</strong></h2><i class=\"fa fa-angle-down\"></i><div class=\"accordion-item-text\"><p> Durante los ensayos clínicos de Keytruda, se lograron los siguientes indicadores:</p><table><tbody class=\"block-green-frame\" style=\"width:100%;\"><tr><td><p> <strong>Período</strong></p></td><td style=\"text-align:center;\"><p style=\"text-align:center;\"> <strong>La tasa de supervivencia de pacientes con 3-4 etapas de cáncer</strong></p></td></tr><tr><td><p> 6 meses</p></td><td><p> 92%</p></td></tr><tr><td><p> 1 año</p></td><td><p> 69%</p></td></tr><tr><td><p> 1,5 años</p></td><td><p> 62%</p></td></tr><tr><td><p> 2 años</p></td><td><p> 58% </p></td></tr></tbody></table></div><h2> ¿Quién produce Keytruda?</h2><i class=\"fa fa-angle-down\"></i><div class=\"accordion-item-text\"><p> El fabricante es Merck &amp; Co., Inc., una compañía farmacéutica estadounidense y una de las compañías farmacéuticas más grandes del mundo. La investigación realizada en Merck ha conducido a la aprobación por parte de la FDA de 63 nuevos medicamentos. La compañía ha desarrollado más medicamentos nuevos que cualquier otra compañía en los EE. UU.</p></div>"},"guide_mc":{"text":"<p>Día 1</p><ul><li> Llegada al país y registro en el alojamiento.</li><li> Prepárese para las pruebas médicas iniciales al día siguiente.</li></ul><p> Dia 2</p><ul><li> Sométete a un hemograma completo con marcadores de cáncer.</li><li> Realice un proteinograma para evaluar sus niveles de proteína.</li></ul><p> Día 3</p><ul><li> Consulta con el oncólogo para analizar los resultados de las pruebas.</li><li> Plan y cronograma de Inmunoterapia con Keytruda (Pembolizumab).</li></ul><p> Día 4-5</p><ul><li> Iniciar Inmunoterapia con Keytruda (Pembolizumab).</li><li> La sesión dura entre 30 minutos y 4 horas.</li><li> No se requiere anestesia para este tratamiento.</li></ul><p> día 6</p><ul><li> Consulta postratamiento con oncólogo.</li><li> Discusión sobre los efectos secundarios y precauciones.</li></ul><p> Día 7</p><ul><li> Descansa y recupérate en tu alojamiento.</li><li> Prepárate para el viaje de regreso a casa.</li></ul><p> Semanas 2-4</p><ul><li> Controle cualquier efecto secundario o reacción.</li><li> Comuníquese con la clínica si surge alguna inquietud.</li></ul><p> <i>Tenga en cuenta que la experiencia de cada paciente puede variar y siempre debe seguir los consejos de su proveedor de atención médica.</i></p>"},"overview":{"text":"<h3>Inmunoterapia con Keytruda (pembolizumab)</h3> <p>Keytruda, una forma de terapia basada en la inmunidad, aprovecha el sistema inmunitario del organismo para atacar y destruir las células cancerosas mediante anticuerpos monoclonales.</p> <div>[<b>Ventajas:</b><span> Ofrece un enfoque dirigido con menos efectos secundarios; los ensayos clínicos muestran una tasa de respuesta del 70% en algunos tipos de cáncer. Adecuado para diversos tipos de cáncer gracias a sus propiedades de modulación inmunitaria.</span></div> <div>[icon-cons<b>]Contras</b><span>: Puede causar efectos adversos relacionados con el sistema inmunitario, como colitis o neumonitis, en hasta un 10% de los pacientes. Eficacia limitada en tumores con baja expresión de PD-L1.</span></div> <div>[icon-efecto<b>]Eficacia</b><span>: Tasa de respuesta del 70% en algunos tipos de cáncer.</span></div> <div>[icon-reloj<b>]Duración:</b><span> Cada sesión dura unos 30 minutos.</span></div> <div>[icon-run<b>]Recuperación:</b><span> No es necesaria.</span></div> <div>[icon-thumbs<b>]Lo mejor para:</b><span> Cánceres con alta expresión de PD-L1, melanoma y cáncer de pulmón no microcítico.</span></div> <div>[icon-price<b>]Precios:</b><span> [txt-país]</span></div>"}}},"relations":{"countries":[{"name":"Alemania","alias":"germany","iso_code":"DE"},{"name":"Azerbaiyán","alias":"azerbaijan","iso_code":"AZ"},{"name":"China","alias":"china","iso_code":"CN"},{"name":"Corea del Sur","alias":"republic-of-korea","iso_code":"KR"},{"name":"Egipto","alias":"egypt","iso_code":"EG"},{"name":"España","alias":"spain","iso_code":"ES"},{"name":"Estados 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