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Efficacy and safety of 'Second Adjuvant' therapy with BRAF/MEK inhibitors after local therapy for recurrent melanoma following adjuvant PD-1 based immunotherapy.
Taylor, Amelia M; McKeown, Janet; Dimitriou, Florentia; Jacques, Sarah K; Zimmer, Lisa; Allayous, Clara; Yeoh, Hui-Ling; Haydon, Andrew; Ressler, Julia M; Galea, Claire; Woodford, Rachel; Kahler, Katharina; Hauschild, Axel; Festino, Lucia; Hoeller, Christoph; Schwarze, Julia K; Neyns, Bart; Wicky, Alexandre; Michielin, Olivier; Placzke, Joanna; Rutkowski, Piotr; Johnson, Douglas B; Lebbe, Celeste; Dummer, Reinhard; Ascierto, Paolo A; Lo, Serigne; Long, Georgina V; Carlino, Matteo S; Menzies, Alexander M.
Afiliación
  • Taylor AM; Melanoma Institute Australia, The University of Sydney, Australia.
  • McKeown J; Melanoma Institute Australia, The University of Sydney, Australia.
  • Dimitriou F; Department of Dermatology, University Hospital of Zurich, Zurich, Switzerland.
  • Jacques SK; Crown Princess Mary Cancer Centre, Westmead and Blacktown Hospitals, Sydney, Australia.
  • Zimmer L; Department of Dermatology, University Hospital Essen, Essen, Germany.
  • Allayous C; Université Paris Cite,AP-HP Dermato-oncology, Cancer institute APHP.nord Paris cité, INSERM U976, Saint Louis Hospital, Paris, France.
  • Yeoh HL; Alfred Health, Melbourne, Australia.
  • Haydon A; Alfred Health, Melbourne, Australia.
  • Ressler JM; Department of Dermatology, Medical University of Vienna, Vienna, Austria.
  • Galea C; Melanoma Institute Australia, The University of Sydney, Australia.
  • Woodford R; Melanoma Institute Australia, The University of Sydney, Australia.
  • Kahler K; University Hospital (UKSH), Campus Kiel, Department of Dermatology, Kiel, Germany.
  • Hauschild A; University Hospital (UKSH), Campus Kiel, Department of Dermatology, Kiel, Germany.
  • Festino L; Melanoma. Cancer Immunotherapy and Development Therapeutics Unit, Istituto Nazionale Tumori IRCCS Fondazione "G. Pascale", Napoli, Italy.
  • Hoeller C; Department of Dermatology, Medical University of Vienna, Vienna, Austria.
  • Schwarze JK; Department of Medical Oncology, Brussels, Belgium.
  • Neyns B; Department of Medical Oncology, Brussels, Belgium.
  • Wicky A; Department of Oncology, Lausanne University Hospital, Lausanne, Switzerland.
  • Michielin O; Precision Oncology Center, Lausanne University Hospital, Switzerland.
  • Placzke J; Department of Soft Tissue/Bone Sarcoma and Melanoma, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
  • Rutkowski P; Department of Soft Tissue/Bone Sarcoma and Melanoma, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
  • Johnson DB; Vanderbilt University Medical Center, Nashville, USA.
  • Lebbe C; Université Paris Cite,AP-HP Dermato-oncology, Cancer institute APHP.nord Paris cité, INSERM U976, Saint Louis Hospital, Paris, France.
  • Dummer R; Department of Dermatology, University Hospital of Zurich, Zurich, Switzerland.
  • Ascierto PA; Melanoma. Cancer Immunotherapy and Development Therapeutics Unit, Istituto Nazionale Tumori IRCCS Fondazione "G. Pascale", Napoli, Italy.
  • Lo S; Melanoma Institute Australia, The University of Sydney, Australia.
  • Long GV; Melanoma Institute Australia, The University of Sydney, Australia; Faculty of Medicine and Health, University of Sydney, Sydney, Australia; Royal North Shore Hospital, Sydney, Australia; Mater Hospital, Sydney, Australia.
  • Carlino MS; Melanoma Institute Australia, The University of Sydney, Australia; Crown Princess Mary Cancer Centre, Westmead and Blacktown Hospitals, Sydney, Australia.
  • Menzies AM; Melanoma Institute Australia, The University of Sydney, Australia; Faculty of Medicine and Health, University of Sydney, Sydney, Australia; Royal North Shore Hospital, Sydney, Australia; Mater Hospital, Sydney, Australia. Electronic address: alexander.menzies@sydney.edu.au.
Eur J Cancer ; 199: 113561, 2024 Mar.
Article en En | MEDLINE | ID: mdl-38278009
ABSTRACT

BACKGROUND:

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).

CONCLUSION:

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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 6_ODS3_enfermedades_notrasmisibles Problema de salud: 6_malignant_skin_melanoma / 6_skin_diseases Asunto principal: Neoplasias Cutáneas / Melanoma Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Eur J Cancer Año: 2024 Tipo del documento: Article País de afiliación: Australia

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 6_ODS3_enfermedades_notrasmisibles Problema de salud: 6_malignant_skin_melanoma / 6_skin_diseases Asunto principal: Neoplasias Cutáneas / Melanoma Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Revista: Eur J Cancer Año: 2024 Tipo del documento: Article País de afiliación: Australia
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