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dc.contributor.authorReck, M
dc.contributor.authorKerr, KM
dc.contributor.authorGrohé, C
dc.contributor.authorManegold, C
dc.contributor.authorPavlakis, N
dc.contributor.authorPaz-Ares, L
dc.contributor.authorHuber, RM
dc.contributor.authorPopat, S
dc.contributor.authorThatcher, N
dc.contributor.authorPark, K
dc.contributor.authorHilberg, F
dc.contributor.authorBarrueco, J
dc.contributor.authorKaiser, R
dc.date.accessioned2020-06-09T12:02:50Z
dc.date.issued2019-04
dc.identifier.citationFuture oncology (London, England), 2019, 15 (12), pp. 1363 - 1383
dc.identifier.issn1479-6694
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/3716
dc.identifier.eissn1744-8301
dc.identifier.doi10.2217/fon-2018-0948
dc.description.abstractA substantial proportion of patients with nononcogene-addicted non-small-cell lung cancer (NSCLC) has 'aggressive disease', as reflected in short time to progression or lack of disease control with initial platinum-based chemotherapy. Recently, clinical correlates of aggressive disease behavior during first-line therapy have been shown to predict greater benefit from addition of nintedanib to second-line docetaxel in adenocarcinoma NSCLC. Positive predictive effects of aggressive disease have since been reported with other anti-angiogenic agents (ramucirumab and bevacizumab), while such features may negatively impact on outcomes with nivolumab in nonsquamous NSCLC with low PD-L1 expression. Based on a review of the clinical data, we recommend aggressive nonsquamous NSCLC should be defined by progression within <6-9 months of first-line treatment initiation.
dc.formatPrint-Electronic
dc.format.extent1363 - 1383
dc.languageeng
dc.language.isoeng
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectLung
dc.subjectHumans
dc.subjectCarcinoma, Non-Small-Cell Lung
dc.subjectLung Neoplasms
dc.subjectDisease Progression
dc.subjectIndoles
dc.subjectAntineoplastic Combined Chemotherapy Protocols
dc.subjectAntibodies, Monoclonal
dc.subjectDisease-Free Survival
dc.subjectPatient Selection
dc.subjectTime Factors
dc.subjectAntibodies, Monoclonal, Humanized
dc.subjectBevacizumab
dc.subjectDocetaxel
dc.titleDefining aggressive or early progressing nononcogene-addicted non-small-cell lung cancer: a separate disease entity?
dc.typeJournal Article
rioxxterms.versionofrecord10.2217/fon-2018-0948
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2019-04
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfFuture oncology (London, England)
pubs.issue12
pubs.notesNot known
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Thoracic Oncology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Thoracic Oncology/Thoracic Oncology (hon.)
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Thoracic Oncology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Thoracic Oncology/Thoracic Oncology (hon.)
pubs.publication-statusPublished
pubs.volume15
pubs.embargo.termsNot known
icr.researchteamThoracic Oncologyen_US
dc.contributor.icrauthorPopat, Sanjay


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