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dc.contributor.authorSmrke, A
dc.contributor.authorGennatas, S
dc.contributor.authorHuang, P
dc.contributor.authorJones, RL
dc.date.accessioned2020-07-03T11:19:46Z
dc.date.issued2020-08-01
dc.identifier.citationFuture oncology (London, England), 2020, 16 (22), pp. 1639 - 1646
dc.identifier.issn1479-6694
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/3795
dc.identifier.eissn1744-8301
dc.identifier.doi10.2217/fon-2020-0348
dc.description.abstractGastrointestinal stromal tumors (GIST) can be molecularly classified based on different subtypes including mutations in KIT and PDGFRA. Patients with PDGFRA mutations are an important subgroup that commonly arise in the stomach and are associated with a more indolent disease course. Importantly, the most common PDGFRA molecular subtype, the D842V mutation in exon 18 of the gene which alters the activation loop, is imatinib insensitive in in vitro studies. Poor responses to imatinib have been seen clinically compared with PDGFRA exon 18 non-D842V-mutated GIST. Avapritinib (BLU-285) is a potent KIT and PDGFRA-specific tyrosine kinase inhibitor which has shown >90% response rates in patients with PDGFRA exon 18 D842V-mutated GIST. Results from the Phase I trial of avapritinib have indicated that this drug should be the standard of care for patients with PDGFRA exon 18 D842V-mutated GIST.
dc.formatPrint-Electronic
dc.format.extent1639 - 1646
dc.languageeng
dc.language.isoeng
dc.publisherFUTURE MEDICINE LTD
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.titleAvapritinib in the treatment of PDGFRA exon 18 mutated gastrointestinal stromal tumors.
dc.typeJournal Article
rioxxterms.versionofrecord10.2217/fon-2020-0348
rioxxterms.licenseref.urihttps://creativecommons.org/licenses/by/4.0
rioxxterms.licenseref.startdate2020-08
rioxxterms.typeJournal Article/Review
dc.relation.isPartOfFuture oncology (London, England)
pubs.issue22
pubs.notesNot known
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.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.volume16
pubs.embargo.termsNot known
icr.researchteamMolecular and Systems Oncology
dc.contributor.icrauthorHuang, Paul


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