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dc.contributor.authorBorelli, B
dc.contributor.authorFontana, E
dc.contributor.authorGiordano, M
dc.contributor.authorAntoniotti, C
dc.contributor.authorLonardi, S
dc.contributor.authorBergamo, F
dc.contributor.authorPietrantonio, F
dc.contributor.authorMorano, F
dc.contributor.authorTamburini, E
dc.contributor.authorBoccaccino, A
dc.contributor.authorSantini, D
dc.contributor.authorZucchelli, G
dc.contributor.authorPella, N
dc.contributor.authorMaiello, E
dc.contributor.authorPassardi, A
dc.contributor.authorZaniboni, A
dc.contributor.authorUgolini, C
dc.contributor.authorFontanini, G
dc.contributor.authorFalcone, A
dc.contributor.authorNyamundanda, G
dc.contributor.authorSadanandam, A
dc.contributor.authorCremolini, C
dc.date.accessioned2021-03-31T11:04:23Z
dc.date.available2021-03-31T11:04:23Z
dc.date.issued2021-03-03
dc.identifier.citationESMO open, 2021, 6 (2), pp. 100073 - ?
dc.identifier.issn2059-7029
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/4476
dc.identifier.eissn2059-7029
dc.identifier.doi10.1016/j.esmoop.2021.100073
dc.description.abstractIntroduction The consensus molecular subtypes (CMS) demonstrated prognostic value in metastatic colorectal cancer (mCRC). Similarly, a prognostic impact was suggested for the pre-consensus CRCAssigner (CRCA) classifier in early stages. The potential predictive role of these classifiers with regard to the choice of the first-line therapy has not been established. We investigated the prognostic and predictive impact of CMS and CRCA subtypes among mCRC patients treated in the TRIBE2 study.Methods Among 679 randomized patients, 426 and 428 (63%) samples were profiled according to CMS and CRCA classifications, respectively. The prognostic and predictive impact of both CMS and CRCA subtypes was investigated with univariate and multivariate analyses for progression-free survival (PFS), PFS 2 (PFS2), and overall survival (OS).Results Significant associations of CMS and CRCA subtypes with PFS, PFS2, and OS were demonstrated; the CMS classifier confirmed its independent prognostic value in the multivariable model (P value for PFS/PFS2/OS = 0.01/0.07/0.08). The effect of treatment intensification was independent of CMS subtypes (P value for interaction for PFS/PFS2/OS = 0.88/0.75/0.55). A significant interaction effect between CRCA subtypes and treatment arm was demonstrated in PFS (P = 0.02), PFS2 (P = 0.01), and OS (P = 0.008). The benefit of FOLFOXIRI seemed more relevant in the stem-like (PFS, hazard ratio = 0.60; P = 0.03) and mixed subtypes (hazard ratio = 0.44; P = 0.002). These findings were confirmed in a subgroup of patients of the previous TRIBE study.Conclusions We confirmed the independent prognostic role of CMS classification in mCRC independently of RAS/BRAF status. CRCA classification may help identifying subgroups of patients who may derive more benefit from FOLFOXIRI/bevacizumab.
dc.formatPrint-Electronic
dc.format.extent100073 - ?
dc.languageeng
dc.language.isoeng
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.titlePrognostic and predictive impact of consensus molecular subtypes and CRCAssigner classifications in metastatic colorectal cancer: a translational analysis of the TRIBE2 study.
dc.typeJournal Article
dcterms.dateAccepted2021-02-03
rioxxterms.versionVoR
rioxxterms.versionofrecord10.1016/j.esmoop.2021.100073
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2021-03-03
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfESMO open
pubs.issue2
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/Molecular Pathology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology/Systems and Precision Cancer Medicine
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/Molecular Pathology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Molecular Pathology/Systems and Precision Cancer Medicine
pubs.publication-statusPublished
pubs.volume6
pubs.embargo.termsNot known
icr.researchteamSystems and Precision Cancer Medicine
icr.researchteamSystems and Precision Cancer Medicineen_US
dc.contributor.icrauthorSadanandam, Anguraj


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