Publication: Treatment options beyond immunotherapy in patients with wild-type lung adenocarcinoma: a Delphi consensus.
dc.contributor.author | Isla, D | |
dc.contributor.author | de Castro, J | |
dc.contributor.author | García-Campelo, R | |
dc.contributor.author | Lianes, P | |
dc.contributor.author | Felip, E | |
dc.contributor.author | Garrido, P | |
dc.contributor.author | Paz-Ares, L | |
dc.contributor.author | Trigo, J M | |
dc.date.accessioned | 2023-01-25T13:38:22Z | |
dc.date.available | 2023-01-25T13:38:22Z | |
dc.date.issued | 2019-07-31 | |
dc.description.abstract | 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. 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). 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. To support decision making following progression to immunotherapy-based treatment in patients with advanced wild-type lung adenocarcinoma, a consensus document has been developed. | |
dc.identifier.doi | 10.1007/s12094-019-02191-y | |
dc.identifier.essn | 1699-3055 | |
dc.identifier.pmid | 31368078 | |
dc.identifier.unpaywallURL | https://link.springer.com/content/pdf/10.1007/s12094-019-02191-y.pdf | |
dc.identifier.uri | http://hdl.handle.net/10668/14349 | |
dc.issue.number | 5 | |
dc.journal.title | Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico | |
dc.journal.titleabbreviation | Clin Transl Oncol | |
dc.language.iso | en | |
dc.organization | Hospital Universitario Virgen de la Victoria | |
dc.organization | Instituto de Investigación Biomédica de Málaga-IBIMA | |
dc.page.number | 759-771 | |
dc.pubmedtype | Journal Article | |
dc.rights | Attribution 4.0 International | |
dc.rights.accessRights | open access | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.subject | Accumulated toxicity | |
dc.subject | Chemotherapy | |
dc.subject | Delphi consensus | |
dc.subject | Disease aggressiveness | |
dc.subject | Immunotherapy | |
dc.subject | Lung adenocarcinoma | |
dc.subject | Nintedanib | |
dc.subject | PD-L1 expression | |
dc.subject | Prior treatment | |
dc.subject | Progression-free interval | |
dc.subject | Treatment decisions | |
dc.subject | Tumour mutational burden | |
dc.subject.mesh | Adenocarcinoma of Lung | |
dc.subject.mesh | Antibodies, Monoclonal | |
dc.subject.mesh | Antineoplastic Combined Chemotherapy Protocols | |
dc.subject.mesh | B7-H1 Antigen | |
dc.subject.mesh | Clinical Decision-Making | |
dc.subject.mesh | Consensus | |
dc.subject.mesh | Delphi Technique | |
dc.subject.mesh | Disease Progression | |
dc.subject.mesh | Docetaxel | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Immunotherapy | |
dc.subject.mesh | Indoles | |
dc.subject.mesh | Lung Neoplasms | |
dc.subject.mesh | Mutation | |
dc.subject.mesh | Spain | |
dc.title | Treatment options beyond immunotherapy in patients with wild-type lung adenocarcinoma: a Delphi consensus. | |
dc.type | research article | |
dc.type.hasVersion | VoR | |
dc.volume.number | 22 | |
dspace.entity.type | Publication |