Publication:
Treatment strategy optimization for patients with non-small-cell lung cancer harboring EGFR mutation: a Delphi consensus.

dc.contributor.authorIsla, D
dc.contributor.authorde Castro, J
dc.contributor.authorGarcía-Campelo, R
dc.contributor.authorMajem, M
dc.contributor.authorVicente, D
dc.contributor.authorJuan-Vidal, O
dc.date.accessioned2023-02-09T10:37:34Z
dc.date.available2023-02-09T10:37:34Z
dc.date.issued2020-11-18
dc.description.abstractTo stablish a consensus on the treatment strategy for advanced non-small-cell lung cancer (aNSCLC) with epidermal growth factor receptor mutation (EGFRm) in Spain. After a systematic literature review, the scientific committee developed 33 statements in 4 fields: molecular diagnosis (10 items); histologic profile and patient clinical characteristics (7 items); first-line (1L) treatment in EGFRm aNSCLC (8 items); and subsequent-line treatment (8 items). A panel of 31 experts completed 2 Delphi online questionnaires rating their degree of agreement/disagreement for each statement through a 1-9 range scale (1-3 = disagree, 7-9 = agree). Consensus was reached if 2/3 of the participants are in the median range. In the first Delphi round consensus was achieved for 24/33 of the statements. One of the assertions was deleted, proceeding to a second round with the eight remaining questions with no consensus or in the range of indeterminacy. Determination of the EGFR status from tissue and analysis of the different biomarkers are two important variables that influenced treatment decision in patients with aNSCLC. 1L treatment should be the best therapeutic option, independently of the subsequent lines of treatment. For patients with the most common activating mutations osimertinib was considered the most efficient and safe 1L option. In case of disease progression, a new biopsy was needed. A consensus document is proposed to optimize the treatment strategy for untreated patients with a NSCLC with EGFR sensitizing mutations.
dc.identifier.doi10.1007/s12094-020-02518-0
dc.identifier.essn1699-3055
dc.identifier.pmcPMC8192379
dc.identifier.pmid33210237
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8192379/pdf
dc.identifier.unpaywallURLhttps://link.springer.com/content/pdf/10.1007/s12094-020-02518-0.pdf
dc.identifier.urihttp://hdl.handle.net/10668/16631
dc.issue.number7
dc.journal.titleClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico
dc.journal.titleabbreviationClin Transl Oncol
dc.language.isoen
dc.organizationHospital Universitario Virgen Macarena
dc.page.number1304-1313
dc.pubmedtypeJournal Article
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectDelphi
dc.subjectEpidermal growth factor receptor
dc.subjectNon–small-cell lung cancer
dc.subjectTirosine kinase inhibitors
dc.subject.meshCarcinoma, Non-Small-Cell Lung
dc.subject.meshConsensus
dc.subject.meshDelphi Technique
dc.subject.meshErbB Receptors
dc.subject.meshHumans
dc.subject.meshLung Neoplasms
dc.subject.meshMutation
dc.titleTreatment strategy optimization for patients with non-small-cell lung cancer harboring EGFR mutation: a Delphi consensus.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number23
dspace.entity.typePublication

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