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dc.contributor.authorTaylor, A. M.-
dc.contributor.authorMcKeown, J.-
dc.contributor.authorDimitriou, F.-
dc.contributor.authorJacques, Sarah-
dc.contributor.authorZimmer, L.-
dc.contributor.authorAllayous, C.-
dc.contributor.authorYeoh, H. L.-
dc.contributor.authorHaydon, A.-
dc.contributor.authorRessler, J. M.-
dc.contributor.authorGalea, C.-
dc.contributor.authorWoodford, R.-
dc.contributor.authorKahler, K.-
dc.contributor.authorHauschild, A.-
dc.contributor.authorFestino, L.-
dc.contributor.authorHoeller, C.-
dc.contributor.authorSchwarze, J. K.-
dc.contributor.authorNeyns, B.-
dc.contributor.authorWicky, A.-
dc.contributor.authorMichielin, O.-
dc.contributor.authorPlaczke, J.-
dc.contributor.authorRutkowski, P.-
dc.contributor.authorJohnson, D. B.-
dc.contributor.authorLebbe, C.-
dc.contributor.authorDummer, R.-
dc.contributor.authorAscierto, P. A.-
dc.contributor.authorLo, S.-
dc.contributor.authorLong, G. V.-
dc.contributor.authorCarlino, Matteo S.-
dc.contributor.authorMenzies, A. M.-
dc.date.accessioned2024-04-26T04:08:10Z-
dc.date.available2024-04-26T04:08:10Z-
dc.date.issued2024-
dc.identifier.citationEuropean Journal of Cancer 199:113561, 2024-
dc.identifier.urihttps://wslhd.intersearch.com.au/wslhdjspui/handle/1/9512-
dc.description.abstractBACKGROUND: Anti-PD-1 antibodies and BRAK/MEK inhibitors (BRAF/MEKi) reduce the risk of recurrence for patients with resected stage III melanoma. BRAFV600-mutated (BRAFmut) melanoma patients who recur with isolated disease following adjuvant therapy may be suitable for 'second adjuvant' treatment after local therapy. We sought to examine the efficacy and safety of 'second adjuvant' BRAF/MEKi. PATIENTS AND METHODS: Patients with BRAFmut melanoma treated with adjuvant PD-1 based immunotherapy who recurred, underwent definitive local therapy and were then treated with adjuvant BRAF/MEKi were identified retrospectively from 13 centres (second adjuvant group). Demographics, disease and treatment characteristics and outcome data were examined. Outcomes were compared to BRAFmut patients who did not receive 'second adjuvant' therapy (no second adjuvant group). RESULTS: 73 patients were included; 61 who received 'second adjuvant' therapy and 12 who did not. Most initially recurred on PD-1 therapy (66%). There were no differences in characteristics between groups. 92% of second adjuvant group received dabrafenib and trametinib and median duration of therapy was 11.8 months (0.4, 34.5). 72% required dose adjustments, 23% had grade 3 + toxicity and 38% permanently discontinued drug due to toxicity. After median 26.1 months (1.9, 56.3) follow-up, recurrence-free survival (RFS) was improved in second adjuvant group versus no second adjuvant group (median 30.8 vs 4 months, HR 0.35; p = 0.014), largely driven by a delay in early recurrence, with no difference in overall survival (p = 0.59). CONCLUSIONS: This is the first study examining outcomes of 'second adjuvant' targeted therapy for melanoma, after failure of adjuvant PD-1 based immunotherapy. Data suggest a short-term improvement in RFS, but at the cost of toxicity. Alternative strategies and more data on sequencing adjuvant therapies are required to improve outcomes-
dc.subjectOncology-
dc.titleEfficacy and safety of 'Second Adjuvant' therapy with BRAF/MEK inhibitors after local therapy for recurrent melanoma following adjuvant PD-1 based immunotherapy-
dc.typeJournal Article-
dc.identifier.doihttps://dx.doi.org/10.1016/j.ejca.2024.113561-
dc.subject.keywordsadjuvants-
dc.subject.keywordsmelanoma-
dc.subject.keywordsradiotherapy-
dc.subject.keywordssurgery-
dc.subject.keywordsdabrafenib-
dc.subject.keywordstrametinib-
dc.identifier.journaltitleEuropean Journal of Cancer-
dc.identifier.departmentOncology-
dc.contributor.wslhdJacques, Sarah-
dc.contributor.wslhdCarlino, Matteo S.-
dc.type.studyortrialMajor Clinical Study-
dc.type.studyortrialRetrospective Study-
dc.identifier.pmid38278009-
dc.identifier.affiliationMelanoma Institute Australia, The University of Sydney, Australia-
dc.identifier.affiliationDepartment of Dermatology, University Hospital of Zurich, Zurich, Switzerland-
dc.identifier.affiliationCrown Princess Mary Cancer Centre, Westmead and Blacktown Hospitals, Sydney, Australia-
dc.identifier.affiliationDepartment of Dermatology, University Hospital Essen, Essen, Germany-
dc.identifier.affiliationUniversite Paris Cite,AP-HP Dermato-oncology, Cancer institute APHP.nord Paris cite, INSERM U976, Saint Louis Hospital, Paris, France-
dc.identifier.affiliationAlfred Health, Melbourne, Australia-
dc.identifier.affiliationDepartment of Dermatology, Medical University of Vienna, Vienna, Austria-
dc.identifier.affiliationUniversity Hospital Melanoma. Cancer Immunotherapy and Development Therapeutics Unit, Istituto Nazionale Tumori IRCCS Fondazione "G. Pascale", Napoli, Italy-
dc.identifier.affiliationDepartment of Medical Oncology, Brussels, Belgium-
dc.identifier.affiliationDepartment of Oncology, Lausanne University Hospital, Lausanne, Switzerland-
dc.identifier.affiliationPrecision Oncology Center, Lausanne University Hospital, Switzerland-
dc.identifier.affiliationDepartment of Soft Tissue/Bone Sarcoma and Melanoma, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland-
dc.identifier.affiliationVanderbilt University Medical Center, Nashville, United States-
dc.identifier.affiliationFaculty of Medicine and Health, University of Sydney, Sydney, Australia-
dc.identifier.affiliationRoyal North Shore Hospital, Sydney, Australia-
dc.identifier.affiliationMater Hospital, Sydney, Australia-
dc.identifier.facilityBlacktown-
dc.identifier.facilityWestmead-
Appears in Collections:Blacktown Mount Druitt Hospital

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