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dc.contributorUniversitat de Vic - Universitat Central de Catalunya. Facultat de Medicina
dc.contributor.authorTabernero, Josep
dc.contributor.authorGrothey, Axel
dc.contributor.authorVan Cutsem, Eric
dc.contributor.authorWasan, Harpreet
dc.contributor.authorYoshino, Takayuki
dc.contributor.authorDesai, Jayesh
dc.contributor.authorCiardiello, Fortunato
dc.contributor.authorLoupakis, Fotio
dc.contributor.authorHong, Yong Sang
dc.date.accessioned2024-01-31T14:22:07Z
dc.date.available2024-01-31T14:22:07Z
dc.date.created2021
dc.date.issued2021
dc.identifier.citationTabernero, J., Grothey, A., Van Cutsem, E., Yaeger, R., Wasan, H., Yoshino, T., Kopetz, S. (2021). Encorafenib plus cetuximab as a new standard of care for previously treated BRAF V600E-mutant metastatic colorectal cancer: Updated survival results and subgroup analyses from the BEACON study. Journal of clinical oncology official journal of the American Society of Clinical Oncology, 39(4), 273-284. https://doi.org/10.1200/JCO.20.02088es
dc.identifier.issn1527-7755
dc.identifier.urihttp://hdl.handle.net/10854/7720
dc.description.abstractPURPOSE BEACON CRC evaluated encorafenib plus cetuximab with or without binimetinib versus investigators' choice of irinotecan or FOLFIRI plus cetuximab in patients with BRAF V600E-mutant metastatic colorectal cancer (mCRC), after progression on 1-2 prior regimens. In the previously reported primary analysis, encorafenib, binimetinib plus cetuximab (ENCO/BINI/CETUX; triplet) and encorafenib plus cetuximab (ENCO/CETUX; doublet) regimens improved overall survival (OS) and objective response rate (ORR; by blinded central review) versus standard of care. The purpose of this analysis was to report updated efficacy and safety data. METHODS In this open-label, phase III trial, 665 patients with BRAF V600E-mutant mCRC were randomly assigned 1:1:1 to receive triplet, doublet, or control. Primary end points were OS and independently reviewed ORR comparing triplet to control. OS for doublet versus control was a key secondary end point. Updated analyses include 6 months of additional follow-up and ORR for all randomized patients. RESULTS Patients received triplet (n=224), doublet (n=220), or control (n=221). Median OS was 9.3 months (95% CI, 8.2 to 10.8) for triplet and 5.9 months (95% CI, 5.1 to 7.1) for control (hazard ratio [HR], 0.60 [95% CI, 0.47 to 0.75]). Median OS for doublet was 9.3 months (95% CI, 8.0 to 11.3) (HR v control, 0.61 [95% CI, 0.48 to 0.77]). Confirmed ORR was 26.8% (95% CI, 21.1% to 33.1%) for triplet, 19.5% (95% CI, 14.5% to 25.4%) for doublet, and 1.8% (95% CI, 0.5% to 4.6%) for control. Adverse events were consistent with the prior primary analysis, with grade >= 3 adverse events in 65.8%, 57.4%, and 64.2% for triplet, doublet, and control, respectively. CONCLUSION In the BEACON CRC study, encorafenib plus cetuximab improved OS, ORR, and progression-free survival in previously treated patients in the metastatic setting compared with standard chemotherapy. Based on the primary and updated analyses, encorafenib plus cetuximab is a new standard care regimen for previously treated patients with BRAF V600E mCRC. (C) 2021 by American Society of Clinical Oncologyes
dc.description.sponsorshipSupported by the Cancer Center Core Grant P30 CA 008748 to Memorial Sloan-Kettering Cancer Center. The BEACON trial was sponsored by Pfizer and was conducted with support from Merck KGaA Darmstadt, Germany (for sites outside of North America), ONO Pharmaceutical, and Pierre Fabre.EN
dc.formatapplication/pdfes
dc.format.extent13 p.es
dc.language.isoenges
dc.publisherAmerican Society of Clinical Oncologyes
dc.rightsAquest document està subjecte a aquesta llicència Creative Commonses
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/deed.caes
dc.subject.otherCòlon -- Cànceres
dc.subject.otherMetàstasies
dc.titleEncorafenib plus cetuximab as a new standard of care for previously treated BRAF V600E-mutant metastatic colorectal cancer: Updated survival results and subgroup analyses from the BEACON studyes
dc.typeinfo:eu-repo/semantics/articlees
dc.identifier.doihttps://doi.org/10.1200/JCO.20.02088
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses
dc.type.versioninfo:eu-repo/publishedVersiones
dc.indexacioIndexat a WOS/JCRes
dc.indexacioIndexat a SCOPUSes


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