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Treatment options beyond immunotherapy in patients with wild-type lung adenocarcinoma: a Delphi consensus
dc.contributor.author | D., Isla | |
dc.contributor.author | J., de Castro | |
dc.contributor.author | García Campelo, María del Rosario | |
dc.contributor.author | P., Lianes | |
dc.contributor.author | E., Felip | |
dc.contributor.author | P., Garrido | |
dc.contributor.author | L., Paz-Ares | |
dc.contributor.author | J.M., Trigo | |
dc.date.accessioned | 2022-02-01T12:59:10Z | |
dc.date.available | 2022-02-01T12:59:10Z | |
dc.date.issued | 2019 | |
dc.identifier.issn | 1699-048X | |
dc.identifier.other | https://www.ncbi.nlm.nih.gov/pubmed/31368078 | es |
dc.identifier.uri | http://hdl.handle.net/20.500.11940/16048 | |
dc.description.abstract | PURPOSE: 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.iso | eng | es |
dc.rights | Atribución 4.0 Internacional | * |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | * |
dc.subject.mesh | Mutation | * |
dc.subject.mesh | Immunotherapy | * |
dc.subject.mesh | Lung Neoplasms | * |
dc.subject.mesh | Humans | * |
dc.subject.mesh | Consensus | * |
dc.subject.mesh | Antibodies | * |
dc.subject.mesh | Indoles | * |
dc.subject.mesh | Disease Progression | * |
dc.subject.mesh | Antineoplastic Combined Chemotherapy Protocols | * |
dc.title | Treatment options beyond immunotherapy in patients with wild-type lung adenocarcinoma: a Delphi consensus | en |
dc.type | Artigo | es |
dc.identifier.doi | 10.1007/s12094-019-02191-y | |
dc.identifier.pmid | 31368078 | |
dc.identifier.sophos | 33946 | |
dc.issue.number | 5 | es |
dc.journal.title | Clinical & Translational Oncology | es |
dc.organization | Servizo Galego de Saúde::Estrutura de Xestión Integrada (EOXI)::EOXI de A Coruña - Complexo Hospitalario Universitario de A Coruña::Oncoloxía médica | es |
dc.page.initial | 759 | es |
dc.page.final | 771 | es |
dc.relation.publisherversion | https://link.springer.com/content/pdf/10.1007/s12094-019-02191-y.pdf | es |
dc.rights.accessRights | openAccess | es |
dc.subject.decs | mutación | * |
dc.subject.decs | protocolos de quimioterapia antineoplásica combinada | * |
dc.subject.decs | inmunoterapia | * |
dc.subject.decs | consenso | * |
dc.subject.decs | humanos | * |
dc.subject.decs | anticuerpos | * |
dc.subject.decs | neoplasias pulmonares | * |
dc.subject.decs | progresión de la enfermedad | * |
dc.subject.decs | indoles | * |
dc.subject.keyword | CHUAC | es |
dc.typefides | Artículo Original | es |
dc.typesophos | Artículo Original | es |
dc.volume.number | 22 | es |