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dc.contributor.authorLarkin, J
dc.contributor.authorMarais, R
dc.contributor.authorPorta, N
dc.contributor.authorGonzalez de Castro, D
dc.contributor.authorParsons, L
dc.contributor.authorMessiou, C
dc.contributor.authorStamp, G
dc.contributor.authorThompson, L
dc.contributor.authorEdmonds, K
dc.contributor.authorSarker, S
dc.contributor.authorBanerji, J
dc.contributor.authorLorigan, P
dc.contributor.authorEvans, TRJ
dc.contributor.authorCorrie, P
dc.contributor.authorMarshall, E
dc.contributor.authorMiddleton, MR
dc.contributor.authorNathan, P
dc.contributor.authorNicholson, S
dc.contributor.authorOttensmeier, C
dc.contributor.authorPlummer, R
dc.contributor.authorBliss, J
dc.contributor.authorValpione, S
dc.contributor.authorTurajlic, S
dc.coverage.spatialUnited States
dc.date.accessioned2024-07-03T14:23:34Z
dc.date.available2024-07-03T14:23:34Z
dc.date.issued2024-03-19
dc.identifier101435
dc.identifierS2666-3791(24)00058-2
dc.identifier.citationCell Reports Medicine, 2024, 5 (3), pp. 101435 -en_US
dc.identifier.issn2666-3791
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/6293
dc.identifier.eissn2666-3791
dc.identifier.eissn2666-3791
dc.identifier.doi10.1016/j.xcrm.2024.101435
dc.identifier.doi10.1016/j.xcrm.2024.101435
dc.description.abstractMucosal (MM) and acral melanomas (AM) are rare melanoma subtypes of unmet clinical need; 15%-20% harbor KIT mutations potentially targeted by small-molecule inhibitors, but none yet approved in melanoma. This multicenter, single-arm Phase II trial (NICAM) investigates nilotinib safety and activity in KIT mutated metastatic MM and AM. KIT mutations are identified in 39/219 screened patients (18%); of 29/39 treated, 26 are evaluable for primary analysis. Six patients were alive and progression free at 6 months (local radiology review, 25%); 5/26 (19%) had objective response at 12 weeks; median OS was 7.7 months; ddPCR assay correctly identifies KIT alterations in circulating tumor DNA (ctDNA) in 16/17 patients. Nilotinib is active in KIT-mutant AM and MM, comparable to other KIT inhibitors, with demonstrable activity in nonhotspot KIT mutations, supporting broadening of KIT evaluation in AM and MM. Our results endorse further investigations of nilotinib for the treatment of KIT-mutated melanoma. This clinical trial was registered with ISRCTN (ISRCTN39058880) and EudraCT (2009-012945-49).
dc.formatPrint-Electronic
dc.format.extent101435 -
dc.languageeng
dc.language.isoengen_US
dc.publisherElsevier BVen_US
dc.relation.ispartofCell Reports Medicine
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.subjectKIT mutation
dc.subjectacral
dc.subjectliquid biopsy
dc.subjectmelanoma
dc.subjectmucosal
dc.subjecttyrosine kinase inhibitor
dc.subjectHumans
dc.subjectMelanoma
dc.subjectAntineoplastic Agents
dc.subjectProto-Oncogene Proteins c-kit
dc.subjectSkin Neoplasms
dc.subjectPyrimidines
dc.titleNilotinib in KIT-driven advanced melanoma: Results from the phase II single-arm NICAM trial.en_US
dc.typeJournal Article
dcterms.dateAccepted2024-01-26
dc.date.updated2024-07-03T14:22:51Z
rioxxterms.versionVoRen_US
rioxxterms.versionofrecord10.1016/j.xcrm.2024.101435en_US
rioxxterms.licenseref.startdate2024-03-19
rioxxterms.typeJournal Article/Reviewen_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/38417447
pubs.issue3
pubs.organisational-groupICR
pubs.organisational-groupICR/Primary Group
pubs.organisational-groupICR/Primary Group/ICR Divisions
pubs.organisational-groupICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-groupICR/Primary Group/ICR Divisions/Clinical Studies/Clinical Trials & Statistics Unit
pubs.publication-statusPublished
pubs.publisher-urlhttp://dx.doi.org/10.1016/j.xcrm.2024.101435
pubs.volume5
icr.researchteamClin Trials & Stats Uniten_US
dc.contributor.icrauthorPorta, Nuria
dc.contributor.icrauthorBliss, Judith
icr.provenanceDeposited by Mr Arek Surman on 2024-07-03. Deposit type is initial. No. of files: 1. Files: Nilotinib in KIT-driven advanced melanoma Results from the phase II single-arm NICAM trial.pdf


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