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<rdf:RDF xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#" xmlns:dc="http://purl.org/dc/elements/1.1/"><rdf:Description rdf:about="https://dirros.openscience.si/IzpisGradiva.php?id=12623"><dc:title>Sequential treatment with afatinib and osimertinib in patients with EGFR mutation-positive non-small-cell lung cancer : an observational study</dc:title><dc:creator>Hochmair,	Maximilian J	(Avtor)
	</dc:creator><dc:creator>Morabito,	Alessandro	(Avtor)
	</dc:creator><dc:creator>Hao,	Desiree	(Avtor)
	</dc:creator><dc:creator>Yang,	Cheng-Ta	(Avtor)
	</dc:creator><dc:creator>Soo,	Ross A	(Avtor)
	</dc:creator><dc:creator>Yang,	James C-H	(Avtor)
	</dc:creator><dc:creator>Gucalp,	Rasim	(Avtor)
	</dc:creator><dc:creator>Halmos,	Balazs	(Avtor)
	</dc:creator><dc:creator>Wang,	Lara	(Avtor)
	</dc:creator><dc:creator>Golembesky,	Amanda	(Avtor)
	</dc:creator><dc:creator>Märten,	Angela	(Avtor)
	</dc:creator><dc:creator>Čufer,	Tanja	(Avtor)
	</dc:creator><dc:subject>lung neoplasms -- therapy</dc:subject><dc:subject>non-small-cell lung cancer</dc:subject><dc:subject>afatinib</dc:subject><dc:subject>osimertinib</dc:subject><dc:subject>epidermal growth factor receptor</dc:subject><dc:subject>EGFR</dc:subject><dc:subject>observational study</dc:subject><dc:description>Aim: To assess outcomes in patients with EGFR mutation-positive (Del19, L858R) non-small-cell lung cancer receiving sequential afatinib and osimertinib in a real-world clinical setting. Materials &amp; methods: In this retrospective, observational, multicenter study, patients (n = 204) had T790M-positive disease following first-line afatinib and started osimertinib treatment [&gt;/=]10 months prior to data entry. Primary outcome was time on treatment. Results: Overall median time on treatment was 27.6 months (90% CI: 25.9-31.3), 30.3 months (90% CI: 27.6-44.5) in Del19-positive patients and 46.7 months (90% CI: 26.8-not reached) in Asians. The 2-year overall survival was 78.9%. Conclusion: In real-world clinical practice, sequential afatinib and osimertinib facilitates prolonged, chemotherapy-free treatment in patients with T790M acquired resistance, and is a potentially attractive strategy, especially for Del19-positive tumors.</dc:description><dc:publisher>Future Medicine Ltd</dc:publisher><dc:date>2018</dc:date><dc:date>2020-11-09 11:24:15</dc:date><dc:type>Neznano</dc:type><dc:identifier>12623</dc:identifier><dc:language>sl</dc:language><dc:rights>2018 Maximilian Hochmair</dc:rights></rdf:Description></rdf:RDF>
