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dc.contributor.authorD., Isla
dc.contributor.authorJ., de Castro
dc.contributor.authorGarcía Campelo, María del Rosario 
dc.contributor.authorP., Lianes
dc.contributor.authorE., Felip
dc.contributor.authorP., Garrido
dc.contributor.authorL., Paz-Ares
dc.contributor.authorJ.M., Trigo
dc.date.accessioned2022-02-01T12:59:10Z
dc.date.available2022-02-01T12:59:10Z
dc.date.issued2019
dc.identifier.issn1699-048X
dc.identifier.otherhttps://www.ncbi.nlm.nih.gov/pubmed/31368078es
dc.identifier.urihttp://hdl.handle.net/20.500.11940/16048
dc.description.abstractPURPOSE: Immunotherapy-based approaches are standard first-line treatments for advanced/metastatic lung cancer or for chemoradiotherapy consolidation in locally advanced disease. Uncertainty on how to treat patients at disease progression prompted us to develop a consensus document on post-immunotherapy options in Spain for patients with advanced wild-type lung adenocarcinoma. METHODS: After extensive literature review, a 5-member scientific committee generated 33 statements in 4 domains: general aspects (n = 4); post-durvalumab in locally advanced disease (n = 6); post-first-line immunotherapy +/- chemotherapy in advanced/metastatic disease (n = 11); and post-first-line platinum-based chemotherapy in advanced/metastatic disease (n = 12). A panel of 26 lung cancer experts completed 2 Delphi iterations through an online platform rating their degree of agreement/disagreement (first-round scale 1-5 and second-round scale 1-4, 1 = strongly disagree, 4/5 = strongly agree) for each statement. Second-round consensus: >/= 70% of responses were in categories 1/2 (disagreement) or 3/4 (agreement). RESULTS: Consensus was reached for 2/33 statements in the first Delphi round and in 29/31 statements in the second round. Important variables informing treatment at disease progression with an immunotherapy-based treatment include: disease aggressiveness, previous treatment, accumulated toxicity, progression-free interval, PD-L1 expression, and tumour mutational burden. A platinum-based chemotherapy should follow a first-line immunotherapy treatment without chemotherapy. Treatment with docetaxel + nintedanib may be appropriate post-durvalumab in refractory patients or following progression to first-line chemotherapy + immunotherapy, or second-line chemotherapy after first-line immunotherapy, or first-line chemotherapy in some patients with low/negative PD-L1 expression, or second-line immunotherapy after first-line chemotherapy. CONCLUSIONS: To support decision making following progression to immunotherapy-based treatment in patients with advanced wild-type lung adenocarcinoma, a consensus document has been developed.en
dc.language.isoenges
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.meshMutation*
dc.subject.meshImmunotherapy*
dc.subject.meshLung Neoplasms*
dc.subject.meshHumans*
dc.subject.meshConsensus*
dc.subject.meshAntibodies*
dc.subject.meshIndoles*
dc.subject.meshDisease Progression*
dc.subject.meshAntineoplastic Combined Chemotherapy Protocols*
dc.titleTreatment options beyond immunotherapy in patients with wild-type lung adenocarcinoma: a Delphi consensusen
dc.typeArtigoes
dc.identifier.doi10.1007/s12094-019-02191-y
dc.identifier.pmid31368078
dc.identifier.sophos33946
dc.issue.number5es
dc.journal.titleClinical & Translational Oncologyes
dc.organizationServizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de A Coruña - Complexo Hospitalario Universitario de A Coruña::Oncoloxía médicaes
dc.page.initial759es
dc.page.final771es
dc.relation.publisherversionhttps://link.springer.com/content/pdf/10.1007/s12094-019-02191-y.pdfes
dc.rights.accessRightsopenAccesses
dc.subject.decsmutación*
dc.subject.decsprotocolos de quimioterapia antineoplásica combinada*
dc.subject.decsinmunoterapia*
dc.subject.decsconsenso*
dc.subject.decshumanos*
dc.subject.decsanticuerpos*
dc.subject.decsneoplasias pulmonares*
dc.subject.decsprogresión de la enfermedad*
dc.subject.decsindoles*
dc.subject.keywordCHUACes
dc.typefidesArtículo Originales
dc.typesophosArtículo Originales
dc.volume.number22es


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Atribución 4.0 Internacional
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