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Evaluation of the VeriStrat® serum protein test in patients with advanced squamous cell carcinoma of the lung treated with second-line afatinib or erlotinib in the phase III LUX-Lung 8 study.

dc.contributor.authorGadgeel, Shirish
dc.contributor.authorGoss, Glenwood
dc.contributor.authorSoria, Jean-Charles
dc.contributor.authorFelip, Enriqueta
dc.contributor.authorGeorgoulias, Vassilis
dc.contributor.authorLu, Shun
dc.contributor.authorCobo, Manuel
dc.contributor.authorSyrigos, Konstantinos
dc.contributor.authorLee, Ki Hyeong
dc.contributor.authorGoker, Erdem
dc.contributor.authorGuclu, Salih Z
dc.contributor.authorIsla, Dolores
dc.contributor.authorMorabito, Alessandro
dc.contributor.authorDupuis, Nicholas
dc.contributor.authorBuhnemann, Claudia
dc.contributor.authorKramer, Nicole
dc.contributor.authorSolca, Flavio
dc.contributor.authorEhrnrooth, Eva
dc.contributor.authorArdizzoni, Andrea
dc.date.accessioned2023-01-25T09:47:02Z
dc.date.available2023-01-25T09:47:02Z
dc.date.issued2017-05-11
dc.description.abstractIdentification of biomarkers associated with clinical benefit may be crucial in establishing optimal treatment choice for patients with squamous cell carcinoma (SCC) of the lung after first-line chemotherapy. In this study, the ability of the VeriStrat serum protein test to predict differential clinical benefit with afatinib versus erlotinib, and the association of VeriStrat status with clinical outcomes irrespective of EGFR-TKI used, was assessed in a retrospective analysis of the phase III LUX-Lung 8 trial. Pretreatment plasma samples were analyzed using matrix-assisted laser desorption ionization time-of-flight mass spectrometry. Spectra were evaluated to assign a VeriStrat 'Good' (VS-G) or VeriStrat 'Poor' (VS-P) classification. Overall survival (OS), progression-free survival, and other endpoints were assessed with respect to pretreatment VeriStrat status; OS was the primary efficacy variable. Outcomes with other efficacy endpoints were similar. Of 795 patients randomized in LUX-Lung 8, 675 were classified (VS-G: 412; VS-P: 263). In the VS-G group, OS was significantly longer with afatinib versus erlotinib (HR 0.79 [95% CI: 0.63-0.98]). In the VS-P group, there was no significant difference in OS between afatinib and erlotinib (HR 0.90 [0.70-1.16]). However, there was no interaction between VeriStrat classification and treatment group for OS (pinteraction=0.5303). OS was significantly longer in VS-G versus VS-P patients, both in the overall VeriStrat-classified population (HR 0.41 [0.35-0.49]) and afatinib-treated patients (HR 0.40 [0.31-0.51]). Multivariate analysis showed that VeriStrat was an independent predictor of OS in afatinib-treated patients, regardless of ECOG PS or best response to first-line chemotherapy. VS-G classification is strongly associated with favorable survival outcomes with either afatinib or erlotinib compared with VS-P classification. In VS-G patients, survival outcomes with afatinib are superior to those with erlotinib. VeriStrat classification may guide treatment decisions in patients with SCC of the lung.
dc.description.versionSi
dc.identifier.citationGadgeel S, Goss G, Soria JC, Felip E, Georgoulias V, Lu S, et al. Evaluation of the VeriStrat® serum protein test in patients with advanced squamous cell carcinoma of the lung treated with second-line afatinib or erlotinib in the phase III LUX-Lung 8 study. Lung Cancer. 2017 Jul;109:101-108
dc.identifier.doi10.1016/j.lungcan.2017.05.010
dc.identifier.essn1872-8332
dc.identifier.pmid28577938
dc.identifier.unpaywallURLhttp://www.lungcancerjournal.info/article/S016950021730329X/pdf
dc.identifier.urihttp://hdl.handle.net/10668/11269
dc.journal.titleLung cancer (Amsterdam, Netherlands)
dc.journal.titleabbreviationLung Cancer
dc.language.isoen
dc.organizationInstituto de Investigación Biomédica de Málaga-IBIMA
dc.organizationHospital Universitario Virgen de la Victoria
dc.organizationHospital Universitario Regional de Málaga
dc.page.number101-108
dc.provenanceRealizada la curación de contenido 01/04/2025
dc.publisherElsevier
dc.pubmedtypeClinical Trial, Phase III
dc.pubmedtypeJournal Article
dc.pubmedtypeMulticenter Study
dc.pubmedtypeRandomized Controlled Trial
dc.relation.publisherversionhttps://linkinghub.elsevier.com/retrieve/pii/S0169-5002(17)30329-X
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectAfatinib
dc.subjectBiomarker
dc.subjectErlotinib
dc.subjectLUX-lung 8
dc.subjectSquamous cell carcinoma of the lung
dc.subjectVeriStrat
dc.subject.decsClasificación
dc.subject.decsPulmón
dc.subject.decsQuimioterapia
dc.subject.decsEspectrometría de Masas
dc.subject.decsProteínas Sanguíneas
dc.subject.decsCarcinoma de Células Escamosas
dc.subject.meshAfatinib
dc.subject.meshAged
dc.subject.meshAntineoplastic Combined Chemotherapy Protocols
dc.subject.meshBiomarkers, Tumor
dc.subject.meshBlood Proteins
dc.subject.meshCarcinoma, Squamous Cell
dc.subject.meshErlotinib Hydrochloride
dc.subject.meshFemale
dc.subject.meshHematologic Tests
dc.subject.meshHumans
dc.subject.meshLung Neoplasms
dc.subject.meshMale
dc.subject.meshMiddle Aged
dc.subject.meshPredictive Value of Tests
dc.subject.meshQuinazolines
dc.subject.meshRetrospective Studies
dc.subject.meshSpectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization
dc.subject.meshSurvival Analysis
dc.subject.meshTreatment Outcome
dc.titleEvaluation of the VeriStrat® serum protein test in patients with advanced squamous cell carcinoma of the lung treated with second-line afatinib or erlotinib in the phase III LUX-Lung 8 study.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number109
dspace.entity.typePublication

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