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dc.contributor.authorSchroeder, BA
dc.contributor.authorKohli, K
dc.contributor.authorO'Malley, RB
dc.contributor.authorKim, TS
dc.contributor.authorJones, RL
dc.contributor.authorPierce, RH
dc.contributor.authorPollack, SM
dc.coverage.spatialUnited States
dc.date.accessioned2022-09-02T14:08:44Z
dc.date.available2022-09-02T14:08:44Z
dc.date.issued2020-01-01
dc.identifierARTN 1710064
dc.identifier1710064
dc.identifier.citationOncoImmunology, 2020, 9 (1), pp. 1710064 -en_US
dc.identifier.issn2162-4011
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/5398
dc.identifier.eissn2162-402X
dc.identifier.eissn2162-402X
dc.identifier.doi10.1080/2162402X.2019.1710064
dc.description.abstractGastrointestinal stromal tumor (GIST) is a devastating disease, especially in the setting of metastasis. The natural progression of GIST has been significantly altered by the development of small molecule tyrosine kinase inhibitors (TKIs), including imatinib, sunitinib, and regorafenib, all of which are FDA approved. However, TKIs are not always well-tolerated, and the refractory disease continues to be a problem. For these reasons, alternative treatments are needed. In this report, we discuss a patient with metastatic wild-type (WT) GIST refractory to multiple TKIs, but with a durable clinical response to the anti-programmed cell death protein 1 (PD-1) antibody, nivolumab. This report suggests that continued research evaluating checkpoint inhibitors in GIST is warranted.
dc.formatElectronic-eCollection
dc.format.extent1710064 -
dc.languageeng
dc.language.isoengen_US
dc.publisherTAYLOR & FRANCIS INCen_US
dc.relation.ispartofOncoImmunology
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0en_US
dc.subjectGIST
dc.subjectImatinib
dc.subjectMetastatic
dc.subjectNivolumab
dc.subjectPD-1
dc.subjectPD-L1
dc.subjectRefractory
dc.subjectSarcoma
dc.subjectWild-Type
dc.subjectDrug Resistance, Neoplasm
dc.subjectGastrointestinal Neoplasms
dc.subjectGastrointestinal Stromal Tumors
dc.subjectHumans
dc.subjectNivolumab
dc.subjectProtein Kinase Inhibitors
dc.titleDurable tumor regression in highly refractory metastatic KIT/PDGFRA wild-type GIST following treatment with nivolumab.en_US
dc.typeJournal Article
dcterms.dateAccepted2019-12-05
dc.date.updated2022-09-02T14:08:00Z
rioxxterms.versionVoRen_US
rioxxterms.versionofrecord10.1080/2162402X.2019.1710064en_US
rioxxterms.licenseref.startdate2020-01-01
rioxxterms.typeJournal Article/Reviewen_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/32002307
pubs.issue1
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/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.publication-statusPublished online
pubs.publisher-urlhttp://dx.doi.org/10.1080/2162402x.2019.1710064
pubs.volume9
dc.contributor.icrauthorJones, Robin
icr.provenanceDeposited by Mr Arek Surman on 2022-09-02. Deposit type is initial. No. of files: 1. Files: Durable tumor regression in highly refractory metastatic iKITPDGFRAi wild-type GIST following treatment with nivolumab.pdf


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