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dc.contributor.authorLarkin, J.en
dc.contributor.authorMarais, Richarden
dc.contributor.authorPorta, N.en
dc.contributor.authorde Castro, D. G.en
dc.contributor.authorParsons, L.en
dc.contributor.authorMessiou, C.en
dc.contributor.authorStamp, G.en
dc.contributor.authorThompson, L.en
dc.contributor.authorEdmonds, K.en
dc.contributor.authorSarker, S.en
dc.contributor.authorBanerji, J.en
dc.contributor.authorLorigan, Paulen
dc.contributor.authorEvans, T. R. J.en
dc.contributor.authorCorrie, P.en
dc.contributor.authorMarshall, E.en
dc.contributor.authorMiddleton, M. R.en
dc.contributor.authorNathan, P.en
dc.contributor.authorNicholson, S.en
dc.contributor.authorOttensmeier, C.en
dc.contributor.authorPlummer, R.en
dc.contributor.authorBliss, J.en
dc.contributor.authorValpione, Saraen
dc.contributor.authorTurajlic, S.en
dc.date.accessioned2024-06-27T07:20:59Z
dc.date.available2024-06-27T07:20:59Z
dc.date.issued2024en
dc.identifier.citationLarkin J, Marais R, Porta N, de Castro DG, Parsons L, Messiou C, et al. Nilotinib in KIT-driven advanced melanoma: Results from the phase II single-arm NICAM trial. CELL REPORTS MEDICINE. 2024 MAR 19;5(3). PubMed PMID: WOS:001217979200001. English.en
dc.identifier.pmid38417447en
dc.identifier.doi10.1016/j.xcrm.2024.101435en
dc.identifier.urihttp://hdl.handle.net/10541/626947
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).en
dc.language.isoenen
dc.relation.urlhttps://dx.doi.org/10.1016/j.xcrm.2024.101435en
dc.titleNilotinib in KIT-driven advanced melanoma: Results from the phase II single-arm NICAM trialen
dc.typeArticleen
dc.contributor.departmentCancer Research UK Manchester Institute, The University of Manchester, Manchester, UK; Division of Cancer Sciences, Unviersity of Manchester, Manchester; The Christie NHS Foundation Trust, Manchester, UKen
dc.identifier.journalCell Reports Medicineen
dc.description.noteen]
refterms.dateFOA2024-06-28T16:25:28Z


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