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dc.contributor.authorGennatas, S
dc.contributor.authorChamberlain, F
dc.contributor.authorSmrke, A
dc.contributor.authorStewart, J
dc.contributor.authorHayes, A
dc.contributor.authorRoden, L
dc.contributor.authorMessiou, C
dc.contributor.authorKowa, J-Y
dc.contributor.authorEstival, A
dc.contributor.authorChauhan, D
dc.contributor.authorThway, K
dc.contributor.authorFisher, C
dc.contributor.authorvan der Graaf, WTA
dc.contributor.authorJones, RL
dc.contributor.authorBenson, C
dc.coverage.spatialEngland
dc.date.accessioned2022-09-01T09:26:34Z
dc.date.available2022-09-01T09:26:34Z
dc.date.issued2020-10-02
dc.identifier.citationThe Oncologist, 2020, 25 (12), pp. e2013 - e2016en_US
dc.identifier.issn1083-7159
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/5363
dc.identifier.eissn1549-490X
dc.identifier.eissn1549-490X
dc.identifier.doi10.1002/ONCO.13516
dc.description.abstractINTRODUCTION: Desmoid tumors (DT) are rare collagen-forming tumors that can exhibit locally aggressive patterns of behavior. The aim of this study was to evaluate the efficacy and safety of treatment of DT with single-agent oral vinorelbine. MATERIALS AND METHODS: A retrospective review of patients treated with vinorelbine 90 mg orally on days 1, 8, and 15 of a 28-day cycle from January 2004 to July 2019 was performed. Response was assessed using RECIST version 1.1. Descriptive statistics were employed. RESULTS: A total of 29 patients were included. Response rate was 20.7% (6/29), and clinical benefit rate (response by RECIST 1.1 and/or clinical symptom improvement) was 65.5% (19/29). No patient experienced grade 3 or above toxicity. Common toxicities were grade 1-2 nausea (14/26, 48.3%), fatigue (9/26, 31.0%), and diarrhea (4/26, 13.8%). CONCLUSION: Single-agent oral vinorelbine is an effective, safe, and well-tolerated treatment for DT. It represents a new oral alternative for management of DT.
dc.formatPrint-Electronic
dc.format.extente2013 - e2016
dc.languageeng
dc.language.isoengen_US
dc.publisherWILEYen_US
dc.relation.ispartofThe Oncologist
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.subjectAdministration, Oral
dc.subjectAntineoplastic Combined Chemotherapy Protocols
dc.subjectFibromatosis, Aggressive
dc.subjectHumans
dc.subjectRetrospective Studies
dc.subjectTreatment Outcome
dc.subjectVinblastine
dc.subjectVinorelbine
dc.titleA Timely Oral Option: Single-Agent Vinorelbine in Desmoid Tumors.en_US
dc.typeJournal Article
dcterms.dateAccepted2020-08-24
dc.date.updated2022-09-01T09:26:08Z
rioxxterms.versionVoRen_US
rioxxterms.versionofrecord10.1002/ONCO.13516en_US
rioxxterms.licenseref.startdate2020-10-02
rioxxterms.typeJournal Article/Reviewen_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/32918789
pubs.issue12
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/Sarcoma Clinical Trials (R Jones)
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging
pubs.organisational-group/ICR/Primary Group/Royal Marsden Clinical Units
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Clinical Studies/Sarcoma Clinical Trials (R Jones)/Sarcoma Clinical Trials (R Jones) (hon.)
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Radiotherapy and Imaging/Sarcoma and Melanoma Surgery
pubs.publication-statusPublished
pubs.volume25
icr.researchteamSarcoma&Melanoma Surgeryen_US
dc.contributor.icrauthorHayes, Andrew
dc.contributor.icrauthorMessiou, Christina
dc.contributor.icrauthorJones, Robin
icr.provenanceDeposited by Mr Arek Surman on 2022-09-01. Deposit type is initial. No. of files: 1. Files: A Timely Oral Option Single-Agent Vinorelbine in Desmoid Tumors.pdf


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