Show simple item record

dc.contributor.authorGoggin, C
dc.contributor.authorStansfeld, A
dc.contributor.authorMahalingam, P
dc.contributor.authorThway, K
dc.contributor.authorSmith, MJ
dc.contributor.authorHuang, P
dc.contributor.authorJones, RL
dc.contributor.authorNapolitano, A
dc.coverage.spatialEngland
dc.date.accessioned2022-09-27T11:47:08Z
dc.date.available2022-09-27T11:47:08Z
dc.date.issued2022-07-26
dc.identifier.citationFuture Oncology, 2022, 18 (26), pp. 2967 - 2978
dc.identifier.issn1479-6694
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/5507
dc.identifier.eissn1744-8301
dc.identifier.eissn1744-8301
dc.identifier.doi10.2217/fon-2022-0226
dc.description.abstractOver the past 20 years, the management of gastrointestinal stromal tumors has acted as an important model in the advancement of molecularly targeted therapies for solid tumors. The success of imatinib has established it as a lasting therapy in the management of early-stage and advanced disease in the first-line setting. Imatinib resistance inevitably develops, resulting in the need for further lines of therapy. Ripretinib is an orally administered switch-control tyrosine kinase inhibitor, specifically developed to target both primary and secondary KIT and PDGFRα resistance mutations. Herein, the authors discuss the molecular rationale, the preclinical evidence and the clinical use of ripretinib in the treatment of gastrointestinal stromal tumors in the advanced stages of disease.
dc.formatPrint-Electronic
dc.format.extent2967 - 2978
dc.languageeng
dc.language.isoeng
dc.publisherFUTURE MEDICINE LTD
dc.relation.ispartofFuture Oncology
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectDCC-2618
dc.subjectGIST
dc.subjectINTRIGUE
dc.subjectINVICTUS
dc.subjectKIT
dc.subjectPDGFR
dc.subjectresistance mutation
dc.subjectripretinib
dc.subjectAntineoplastic Agents
dc.subjectDrug Approval
dc.subjectDrug Resistance, Neoplasm
dc.subjectGastrointestinal Neoplasms
dc.subjectGastrointestinal Stromal Tumors
dc.subjectHumans
dc.subjectImatinib Mesylate
dc.subjectMutation
dc.subjectNaphthyridines
dc.subjectProtein Kinase Inhibitors
dc.subjectProto-Oncogene Proteins c-kit
dc.subjectUrea
dc.titleRipretinib in advanced gastrointestinal stromal tumors: an overview of current evidence and drug approval.
dc.typeJournal Article
dcterms.dateAccepted2022-06-24
dc.date.updated2022-09-27T11:46:23Z
rioxxterms.versionVoR
rioxxterms.versionofrecord10.2217/fon-2022-0226
rioxxterms.licenseref.startdate2022-07-26
rioxxterms.typeJournal Article/Review
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/35880452
pubs.issue26
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/Molecular and Systems Oncology
pubs.publication-statusPublished
pubs.publisher-urlhttp://dx.doi.org/10.2217/fon-2022-0226
pubs.volume18
icr.researchteamTranslational Sarcoma, Melanoma and Rare Tumour Surgery
icr.researchteamMol and Systems Oncology
dc.contributor.icrauthorSmith, Myles
dc.contributor.icrauthorHuang, Paul
icr.provenanceDeposited by Mr Arek Surman on 2022-09-27. Deposit type is initial. No. of files: 1. Files: fon-2022-0226.pdf


Files in this item

Thumbnail

This item appears in the following collection(s)

Show simple item record

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