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		<title>Estudio LEVIATHAN en segunda línea de carcinoma hepatocelular</title>
		<link>https://grupottd.org/lenvatinib-vs-sorafenib-as-second-line-treatment-post-atezolizumab-plus-bevacizumab-for-hepatocellular-carcinoma-the-leviathan-study/</link>
					<comments>https://grupottd.org/lenvatinib-vs-sorafenib-as-second-line-treatment-post-atezolizumab-plus-bevacizumab-for-hepatocellular-carcinoma-the-leviathan-study/#respond</comments>
		
		<dc:creator><![CDATA[Susana Rodríguez]]></dc:creator>
		<pubDate>Mon, 27 Apr 2026 10:50:49 +0000</pubDate>
				<category><![CDATA[Artículos comentados]]></category>
		<category><![CDATA[Hepatocarcinoma]]></category>
		<category><![CDATA[lenvatinib]]></category>
		<category><![CDATA[observacional]]></category>
		<category><![CDATA[progresión a inmunoterapia]]></category>
		<category><![CDATA[Propensity score matching]]></category>
		<category><![CDATA[Secuencia de tratamiento]]></category>
		<category><![CDATA[Segunda línea]]></category>
		<category><![CDATA[sorafenib]]></category>
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					<description><![CDATA[El estudio Leviathan es un estudio observacional en segunda línea de carcinoma hepatocelular, que en pacientes en progresión a atezolizumab-bevacizumab compara lenvatinib con sorafenib. Al ser un estudio no randomizado se realiza un Propensity Score Matching para minimizar sesgos. Se analizaron 230 pacientes procedentes de una base de datos prospectiva. Su objetivo es evaluar tasas de control de enfermedad y supervivencia global. Lenvatinib obtuvo mejores resultados que sorafenib para todos los ítems analizados.]]></description>
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					<h2 class="elementor-heading-title elementor-size-default">Estudio LEVIATHAN en segunda línea de carcinoma hepatocelular</h2>				</div>
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					<h5 class="elementor-heading-title elementor-size-default">Edición:</h5>				</div>
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					<p class="elementor-heading-title elementor-size-default">Publicación científica 2026</p>				</div>
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					<h4 class="elementor-heading-title elementor-size-default">Fecha:</h4>				</div>
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					<p class="elementor-heading-title elementor-size-default">30 de abril de 2026</p>				</div>
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					<h4 class="elementor-heading-title elementor-size-default">Autores:</h4>				</div>
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					<p class="elementor-heading-title elementor-size-default">Pasquale Lombardi, Jung Sun Kim, Giulia F. Manfredi, Ciro Celsa, Claudia A. M. Fulgenzi, Antonio D’Alessio, Bernardo Stefanini, Niraj C. Doshi, Emily Warmington,Thomas U. Marron, Matthias Pinter, Bernhard Scheiner, Beodeul Kang, Ho Yeong Lim, Wei-Fan Hsu, Brooke Wietharn, Marianna Silletta, Alessandro Parisi, Chun-Yen Lin, Andrea Dalbeni, Gianluca Masi, Martin Schönlein, Johann von Felden, Fabio Piscaglia, Peter R. Galle, Masatoshi Kudo, Tiziana Pressiani, Lorenza Rimassa,Mario Pirisi, Giuseppe Cabibbo, Hong Jae Chon, David J. Pinato</p>				</div>
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					<h4 class="elementor-heading-title elementor-size-default">Autor de la revisión:</h4>				</div>
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					<p class="elementor-heading-title elementor-size-default">Alberto Carral Maseda. Complexo Hospitalario Universitario A Coruña (Miembro de la Asamblea General del Grupo TTD)</p>				</div>
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									<p>El estudio LEVIATHAN es un estudio observacional en segunda línea de carcinoma hepatocelular, que en pacientes en progresión a atezolizumab-bevacizumab compara lenvatinib con sorafenib. Al ser un estudio no randomizado se realiza un Propensity Score Matching para minimizar sesgos. Se analizaron 230 pacientes procedentes de una base de datos prospectiva. Su objetivo es evaluar tasas de control de enfermedad y supervivencia global. Lenvatinib obtuvo mejores resultados que sorafenib para todos los ítems analizados.</p>								</div>
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