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dc.contributor.authorLorimer, C
dc.contributor.authorCheng, L
dc.contributor.authorChandler, R
dc.contributor.authorGarcez, K
dc.contributor.authorGill, V
dc.contributor.authorGraham, K
dc.contributor.authorGrant, W
dc.contributor.authorSardo Infirri, S
dc.contributor.authorWadsley, J
dc.contributor.authorWall, L
dc.contributor.authorWebber, N
dc.contributor.authorWong, KH
dc.contributor.authorNewbold, K
dc.coverage.spatialEngland
dc.date.accessioned2022-12-20T10:18:12Z
dc.date.available2022-12-20T10:18:12Z
dc.date.issued2022-11-12
dc.identifierS0936-6555(22)00512-X
dc.identifier.citationClinical Oncology, 2022, pp. S0936-6555(22)00512-X -
dc.identifier.issn0936-6555
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/5609
dc.identifier.eissn1433-2981
dc.identifier.eissn1433-2981
dc.identifier.doi10.1016/j.clon.2022.10.017
dc.description.abstractAIMS: Anaplastic thyroid cancer (ATC) is a rare but aggressive form of thyroid cancer with a median survival of 4 months. Recent advances in molecular profiling have shown that up to half of ATCs harbour the BRAF-V600E mutation. The aim of this study was to provide real-world data and experience on the use of combination therapy dabrafenib and trametinib in patients with BRAF-V600E-mutated advanced ATC. MATERIALS AND METHODS: We retrospectively evaluated patients with confirmed BRAF-V600E-mutated ATC, defined as patients with locally advanced or metastatic ATC with no locoregional, radical treatment options. Outcomes measured were overall survival, progression-free survival, response rate, discontinuation rate, dose reduction rate and toxicity data. RESULTS: Seventeen patients were evaluated and the mean age was 68 years. Ten patients died by the time of censoring. The median duration of follow-up was 12 months (3-43 months). The estimated median overall survival was 6.9 months (95% confidence interval 2.46 months - upper confidence interval not reached) and the median progression-free survival was 4.7 months (95% confidence interval 1.4-7.8 months). Dose interruptions and/or reductions were common, but none of the patients had to permanently discontinue treatment because of toxicities. Severe toxicities (grades 3 and 4) were uncommon. CONCLUSIONS: This study supports the indication of dabrafenib and trametinib in BRAF-V600E-mutated ATC as an effective and well-tolerated treatment in an historically difficult to treat cancer.
dc.formatPrint-Electronic
dc.format.extentS0936-6555(22)00512-X -
dc.languageeng
dc.language.isoeng
dc.publisherELSEVIER SCIENCE LONDON
dc.relation.ispartofClinical Oncology
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectBRAF mutation
dc.subjectanaplastic thyroid cancer
dc.subjectdabrafenib
dc.subjecttrametinib
dc.titleDabrafenib and Trametinib Therapy for Advanced Anaplastic Thyroid Cancer - Real-World Outcomes From UK Centres.
dc.typeJournal Article
dcterms.dateAccepted2022-10-25
dc.date.updated2022-12-14T11:58:37Z
rioxxterms.versionVoR
rioxxterms.versionofrecord10.1016/j.clon.2022.10.017
rioxxterms.licenseref.startdate2022-11-12
rioxxterms.typeJournal Article/Review
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/36379836
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/Cancer Biology
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Cancer Biology/Targeted Therapy
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Targeted Therapy
pubs.organisational-group/ICR/Students
pubs.organisational-group/ICR/Students/PhD and MPhil
pubs.organisational-group/ICR/Students/PhD and MPhil/22/23 Starting Cohort
pubs.publication-statusPublished online
pubs.publisher-urlhttp://dx.doi.org/10.1016/j.clon.2022.10.017
icr.researchteamTargeted Therapy
dc.contributor.icrauthorCheng, Leslie
icr.provenanceDeposited by Dr Leslie Cheng on 2022-12-14. Deposit type is initial. No. of files: 1. Files: s41467-017-00965-y.pdf


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