Show simple item record

dc.contributor.authorLong, GV
dc.contributor.authorFlaherty, KT
dc.contributor.authorStroyakovskiy, D
dc.contributor.authorGogas, H
dc.contributor.authorLevchenko, E
dc.contributor.authorde Braud, F
dc.contributor.authorLarkin, J
dc.contributor.authorGarbe, C
dc.contributor.authorJouary, T
dc.contributor.authorHauschild, A
dc.contributor.authorChiarion-Sileni, V
dc.contributor.authorLebbe, C
dc.contributor.authorMandalà, M
dc.contributor.authorMillward, M
dc.contributor.authorArance, A
dc.contributor.authorBondarenko, I
dc.contributor.authorHaanen, JBAG
dc.contributor.authorHansson, J
dc.contributor.authorUtikal, J
dc.contributor.authorFerraresi, V
dc.contributor.authorMohr, P
dc.contributor.authorProbachai, V
dc.contributor.authorSchadendorf, D
dc.contributor.authorNathan, P
dc.contributor.authorRobert, C
dc.contributor.authorRibas, A
dc.contributor.authorDavies, MA
dc.contributor.authorLane, SR
dc.contributor.authorLegos, JJ
dc.contributor.authorMookerjee, B
dc.contributor.authorGrob, J-J
dc.date.accessioned2017-05-26T15:34:42Z
dc.date.issued2017-07
dc.identifier.citationAnnals of oncology : official journal of the European Society for Medical Oncology, 2017, 28 (7), pp. 1631 - 1639
dc.identifier.issn0923-7534
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/663
dc.identifier.eissn1569-8041
dc.identifier.doi10.1093/annonc/mdx176
dc.description.abstractBackground Previous analysis of COMBI-d (NCT01584648) demonstrated improved progression-free survival (PFS) and overall survival (OS) with combination dabrafenib and trametinib versus dabrafenib monotherapy in BRAF V600E/K-mutant metastatic melanoma. This study was continued to assess 3-year landmark efficacy and safety after ≥36-month follow-up for all living patients.Patients and methods This double-blind, phase 3 study enrolled previously untreated patients with BRAF V600E/K-mutant unresectable stage IIIC or stage IV melanoma. Patients were randomized to receive dabrafenib (150 mg twice daily) plus trametinib (2 mg once daily) or dabrafenib plus placebo. The primary endpoint was PFS; secondary endpoints were OS, overall response, duration of response, safety, and pharmacokinetics.Results Between 4 May and 30 November 2012, a total of 423 of 947 screened patients were randomly assigned to receive dabrafenib plus trametinib (n = 211) or dabrafenib monotherapy (n = 212). At data cut-off (15 February 2016), outcomes remained superior with the combination: 3-year PFS was 22% with dabrafenib plus trametinib versus 12% with monotherapy, and 3-year OS was 44% versus 32%, respectively. Twenty-five patients receiving monotherapy crossed over to combination therapy, with continued follow-up under the monotherapy arm (per intent-to-treat principle). Of combination-arm patients alive at 3 years, 58% remained on dabrafenib plus trametinib. Three-year OS with the combination reached 62% in the most favourable subgroup (normal lactate dehydrogenase and <3 organ sites with metastasis) versus only 25% in the unfavourable subgroup (elevated lactate dehydrogenase). The dabrafenib plus trametinib safety profile was consistent with previous clinical trial observations, and no new safety signals were detected with long-term use.Conclusions These data demonstrate that durable (≥3 years) survival is achievable with dabrafenib plus trametinib in patients with BRAF V600-mutant metastatic melanoma and support long-term first-line use of the combination in this setting.
dc.formatPrint
dc.format.extent1631 - 1639
dc.languageeng
dc.language.isoeng
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectHumans
dc.subjectMelanoma
dc.subjectSkin Neoplasms
dc.subjectDisease Progression
dc.subjectOximes
dc.subjectImidazoles
dc.subjectPyridones
dc.subjectPyrimidinones
dc.subjectProto-Oncogene Proteins B-raf
dc.subjectAntineoplastic Combined Chemotherapy Protocols
dc.subjectProtein Kinase Inhibitors
dc.subjectDisease-Free Survival
dc.subjectTreatment Outcome
dc.subjectDrug Administration Schedule
dc.subjectRisk Factors
dc.subjectDouble-Blind Method
dc.subjectMutation
dc.subjectTime Factors
dc.subjectKaplan-Meier Estimate
dc.subjectBiomarkers, Tumor
dc.titleDabrafenib plus trametinib versus dabrafenib monotherapy in patients with metastatic BRAF V600E/K-mutant melanoma: long-term survival and safety analysis of a phase 3 study.
dc.typeJournal Article
rioxxterms.versionofrecord10.1093/annonc/mdx176
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by-nc/4.0
rioxxterms.licenseref.startdate2017-07
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfAnnals of oncology : official journal of the European Society for Medical Oncology
pubs.issue7
pubs.notesNo embargo
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/Melanoma and Kidney Cancer
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Melanoma and Kidney Cancer/Melanoma and Kidney Cancer (hon.)
pubs.organisational-group/ICR/Primary Group/Royal Marsden Clinical Units
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/Melanoma and Kidney Cancer
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Melanoma and Kidney Cancer/Melanoma and Kidney Cancer (hon.)
pubs.organisational-group/ICR/Primary Group/Royal Marsden Clinical Units
pubs.publication-statusPublished
pubs.volume28
pubs.embargo.termsNo embargo
icr.researchteamMelanoma and Kidney Canceren_US
dc.contributor.icrauthorLarkin, James
dc.contributor.icrauthorMarsden,


Files in this item

Thumbnail

This item appears in the following collection(s)

Show simple item record

https://creativecommons.org/licenses/by/4.0
Except where otherwise noted, this item's license is described as https://creativecommons.org/licenses/by/4.0