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	<title>anti-EGFR &#8211; Grupo TTD</title>
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		<title>Presentado el diseño del estudio TTD 24-07 ARIEL-ENGIC04 en ESMO 2026</title>
		<link>https://grupottd.org/presentado-el-diseno-del-estudio-ariel-engic04-en-esmo-2026/</link>
					<comments>https://grupottd.org/presentado-el-diseno-del-estudio-ariel-engic04-en-esmo-2026/#respond</comments>
		
		<dc:creator><![CDATA[Antonio Martín]]></dc:creator>
		<pubDate>Sun, 25 Oct 2026 16:45:53 +0000</pubDate>
				<category><![CDATA[Eventos]]></category>
		<category><![CDATA[anti-EGFR]]></category>
		<category><![CDATA[Biomarcadores]]></category>
		<category><![CDATA[cáncer colorrectal metastático]]></category>
		<category><![CDATA[Ensayos clínicos]]></category>
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					<description><![CDATA[La profesora Jenny Seligmann, de la Universidad de Leeds (Reino Unido) ha presentado diseño del estudio en progreso TTD 24-07 ARIEL-ENGIC04 titulado "ARIEL-ENGIC04: A biomarker enrichment trial of anti-EGFR agents in right primary tumour location (rPTL), RAS wild-type (RAS-wt) metastatic colorectal cancer (mCRC): A European collaboration", promovido por ENGIC y en el que participa el Grupo TTD, durante el Congreso de ESMO 2026, que se celebra en Madrid del 23 al 27 de octubre.]]></description>
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					<h2 class="elementor-heading-title elementor-size-default">Presentado el diseño del estudio TTD 24-07 ARIEL-ENGIC04 en ESMO 2026</h2>				</div>
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									<p>La profesora Jenny Seligmann, de la Universidad de Leeds (Reino Unido), ha presentado el diseño del estudio en progreso <strong>TTD 24-07 </strong> ARIEL-ENGIC04 titulado &#8220;<strong>ARIEL-ENGIC04: A biomarker enrichment trial of anti-EGFR agents in right primary tumour location (rPTL), RAS wild-type (RAS-wt) metastatic colorectal cancer (mCRC): A European collaboration&#8221;</strong>, promovido por ENGIC y en el que participa el Grupo TTD, durante el Congreso de ESMO 2026, que se celebra en Madrid del 23 al 27 de octubre.</p>								</div>
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						Grupo TTD					</p>
				
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			</item>
		<item>
		<title>Resultados del estudio CR-SEQUENCE del TTD presentados en ESMO GI 2026</title>
		<link>https://grupottd.org/resultados-del-estudio-cr-sequence-del-ttd-presentados-en-esmo-gi-2026/</link>
					<comments>https://grupottd.org/resultados-del-estudio-cr-sequence-del-ttd-presentados-en-esmo-gi-2026/#respond</comments>
		
		<dc:creator><![CDATA[Juan Jose Barea]]></dc:creator>
		<pubDate>Mon, 06 Jul 2026 07:31:53 +0000</pubDate>
				<category><![CDATA[Eventos]]></category>
		<category><![CDATA[anti-EGFR]]></category>
		<category><![CDATA[anti-VEGF]]></category>
		<category><![CDATA[cáncer colorrectal metastásico]]></category>
		<category><![CDATA[CR-SEQUENCE]]></category>
		<category><![CDATA[ESMO GI 2026]]></category>
		<category><![CDATA[localización izquierda]]></category>
		<category><![CDATA[RAS wild-type]]></category>
		<guid isPermaLink="false">https://grupottd.org/?p=13382</guid>

					<description><![CDATA[El Dr. Ramón Salazar, del Instituto Catalán de Oncología, presenta el póster de título “Influence of Primary Tumor Resection timing on survival after sequential therapy in left sided RAS wild type mCRC”.]]></description>
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									<p>El Dr. Salazar, del Instituto Catalán de Oncología, ha presentado el póster de título: “<strong>Influence of Primary Tumor Resection timing on survival after sequential therapy in left‑sided RAS wild‑type mCRC” </strong>en ESMO GI 2026.</p><p>El estudio CR-SEQUENCE aborda una pregunta clínica de gran relevancia práctica: ¿cuál es el orden óptimo de los esquemas de quimioterapia en cáncer colorrectal RAS wild-type de localización izquierda? ¿un tratamiento de quimioterapia con anti-EGFR seguido a la progresión de quimioterapia y anti-VEGF, o bien la secuencia inversa? Los resultados confirman que iniciar con anti-EGFR (Panitumumab) se asocia a un mayor control inicial de la enfermedad en primera línea, con mejoras estadísticamente significativas en SLP y en las tasas de respuesta.</p>								</div>
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			</item>
		<item>
		<title>Resultados estudio CR-SEQUENCE del TTD presentados en ASCO 2026</title>
		<link>https://grupottd.org/resultados-estudio-cr-sequence-del-ttd-presentados-en-asco-2026/</link>
					<comments>https://grupottd.org/resultados-estudio-cr-sequence-del-ttd-presentados-en-asco-2026/#respond</comments>
		
		<dc:creator><![CDATA[Susana Rodríguez]]></dc:creator>
		<pubDate>Tue, 02 Jun 2026 14:00:00 +0000</pubDate>
				<category><![CDATA[Eventos]]></category>
		<category><![CDATA[anti-EGFR]]></category>
		<category><![CDATA[anti-VEGF]]></category>
		<category><![CDATA[ASCO 2026]]></category>
		<category><![CDATA[bevacizumab]]></category>
		<category><![CDATA[cáncer colorrectal metastásico]]></category>
		<category><![CDATA[CR-SEQUENCE]]></category>
		<category><![CDATA[hiperselección molecular]]></category>
		<category><![CDATA[localización izquierda]]></category>
		<category><![CDATA[panitumumab]]></category>
		<category><![CDATA[quimioterapia]]></category>
		<category><![CDATA[RAS wild-type]]></category>
		<category><![CDATA[slp]]></category>
		<guid isPermaLink="false">https://grupottd.org/?p=13192</guid>

					<description><![CDATA[Primer estudio prospectivo europeo que valida la secuencia anti-EGFR → anti-VEGF en CCRm RAS WT izquierdo. Refuerza las guías actuales con evidencia prospectiva de nivel europeo. Pendiente de datos maduros de SG y resultados de biopsias líquidas para definir hiperselección.]]></description>
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					<h2 class="elementor-heading-title elementor-size-default">Resultados estudio CR-SEQUENCE del TTD presentados en ASCO 2026</h2>				</div>
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									<p>En ASCO 2026, el Dr. Ramón Salazar del Instituto Catalán de Oncología presenta los resultados de eficacia del estudio CR-SEQUENCE del grupo TTD, el primer estudio prospectivo aleatorizado europeo que evalúa la secuencia óptima de tratamiento biológico en pacientes con cáncer colorrectal metastásico RAS wild-type con localización izquierda.</p><p>El estudio CR-SEQUENCE aborda una pregunta clínica de gran relevancia práctica: ¿cuál es el orden óptimo de los esquemas de quimioterapia en cáncer colorrectal RAS wild-type de localización izquierda? ¿un tratamiento de quimioterapia con anti-EGFR seguido a la progresión de quimioterapia y anti-VEGF, o bien la secuencia inversa? Los resultados confirman que iniciar con anti-EGFR (Panitumumab) se asocia a un mayor control inicial de la enfermedad en primera línea, con mejoras estadísticamente significativas en SLP y en las tasas de respuesta. El objetivo principal del estudio —porcentaje de pacientes libres de progresión total a los 36 meses— no alcanzó la significación estadística, aunque se observa una diferencia numérica favorable a la secuencia con anti-EGFR. Los datos de supervivencia global son aún inmaduros. Por otro lado, se encuentran pendientes los resultados de las biopsias líquidas seriadas que permitirán en el futuro definir estrategias de hiperselección molecular y cuyos resultados se presentarán próximamente</p>								</div>
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									<p>El CR-SEQUENCE es el primer estudio prospectivo europeo que valida la secuencia terapéutica en CCRm RAS wild-type izquierdo. Aunque el endpoint principal no alcanzó significación estadística, los datos de primera línea refuerzan la recomendación clínica de iniciar con anti-EGFR: la secuencia 1 logra una SLP en primera línea estadísticamente superior (14,1 vs 12,4 meses) y mayor control de la enfermedad. Los datos de supervivencia global son todavía inmaduros, con la base de datos prevista cerrarse en aproximadamente un año. La lectura clínica apunta a que la secuencia anti-EGFR → anti-VEGF optimiza el control inicial de la enfermedad, un beneficio que puede tener impacto en pacientes que no lleguen a recibir segunda línea. Próximamente se presentarán los datos del programa de biopsias líquidas, que podrían permitir la hiperselección negativa de pacientes no candidatos al esquema con anti-EGFR.</p>								</div>
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									<blockquote><p><strong>IMPACTO:</strong> Primer estudio prospectivo europeo que valida la secuencia anti-EGFR → anti-VEGF en CCRm RAS WT izquierdo. Refuerza las guías actuales con evidencia prospectiva de nivel europeo. Pendiente de datos maduros de SG y resultados de biopsias líquidas para definir hiperselección</p></blockquote>								</div>
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		<title>CCRm RAS/BRAF nativo: resultados definitivos a cinco años del ensayo TRIPLETE con mFOLFOXIRI más panitumumab</title>
		<link>https://grupottd.org/ccrm-ras-braf-nativo-resultados-definitivos-a-cinco-anos-del-ensayo-triplete-con-mfolfoxiri-mas-panitumumab/</link>
					<comments>https://grupottd.org/ccrm-ras-braf-nativo-resultados-definitivos-a-cinco-anos-del-ensayo-triplete-con-mfolfoxiri-mas-panitumumab/#respond</comments>
		
		<dc:creator><![CDATA[Susana Rodríguez]]></dc:creator>
		<pubDate>Thu, 16 Apr 2026 10:32:23 +0000</pubDate>
				<category><![CDATA[Artículos comentados]]></category>
		<category><![CDATA[anti-EGFR]]></category>
		<category><![CDATA[cáncer colorrectal metastásico]]></category>
		<category><![CDATA[CCRm]]></category>
		<category><![CDATA[fase-3]]></category>
		<category><![CDATA[mFOLFOXIRI]]></category>
		<category><![CDATA[Oncología digestiva]]></category>
		<category><![CDATA[panitumumab]]></category>
		<category><![CDATA[primera línea]]></category>
		<category><![CDATA[RAS-BRAF nativo]]></category>
		<category><![CDATA[Supervivencia global]]></category>
		<category><![CDATA[TRIPLETE]]></category>
		<category><![CDATA[triplete quimioterapia]]></category>
		<guid isPermaLink="false">https://grupottd.org/?p=12847</guid>

					<description><![CDATA[El ensayo TRIPLETE (JCO 2026) presenta los resultados definitivos con 60 meses de seguimiento de la comparación entre mFOLFOXIRI más panitumumab y mFOLFOX más panitumumab en primera línea de cáncer colorrectal metastásico RAS/BRAF nativo. El objetivo primario —tasa de respuesta objetiva— no mostró diferencias entre brazos (75% vs 78%). El análisis de supervivencia global, objetivo secundario, reveló un beneficio estadísticamente significativo a favor del triplete (41,1 vs 33,3 meses; HR 0,79; p=0,049), sin correlato en supervivencia libre de progresión ni en parámetros de actividad tumoral.]]></description>
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					<h2 class="elementor-heading-title elementor-size-default">CCRm RAS/BRAF nativo: resultados definitivos a cinco años del ensayo TRIPLETE con mFOLFOXIRI más panitumumab</h2>				</div>
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					<p class="elementor-heading-title elementor-size-default">Conca V, Rossini D, Antoniotti C, Lonardi S, Pietrantonio F, Moretto R, Antonuzzo L, Randon G, Lavacchi D, Pozzo C, Marmorino F, Bergamo F, Tamburini E, Passardi A, Fazio R, Murgioni S, Borelli B, Buonadonna A, Germani MM, Formica V, Carullo M, Bordonaro R, Aprile G, Zaniboni A, Masi G, Boni L, Cremolini C.</p>				</div>
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					<p class="elementor-heading-title elementor-size-default">Roberto Morales Giménez. Hospital General Universitario Virgen de la Salud de Elda, Alicante. (Miembro de la Asamblea General del Grupo TTD)</p>				</div>
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									<p>El ensayo TRIPLETE (JCO 2026) presenta los resultados definitivos con 60 meses de seguimiento de la comparación entre mFOLFOXIRI más panitumumab y mFOLFOX más panitumumab en primera línea de cáncer colorrectal metastásico RAS/BRAF nativo. El objetivo primario —tasa de respuesta objetiva— no mostró diferencias entre brazos (75% vs 78%). El análisis de supervivencia global, objetivo secundario, reveló un beneficio estadísticamente significativo a favor del triplete (41,1 vs 33,3 meses; HR 0,79; p=0,049), sin correlato en supervivencia libre de progresión ni en parámetros de actividad tumoral.</p>								</div>
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