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Discontinuation of anti-PD-1 antibody therapy in the absence of disease progression or treatment limiting toxicity: clinical outcomes in advanced melanoma.
Jansen, Y J L; Rozeman, E A; Mason, R; Goldinger, S M; Geukes Foppen, M H; Hoejberg, L; Schmidt, H; van Thienen, J V; Haanen, J B A G; Tiainen, L; Svane, I M; Mäkelä, S; Seremet, T; Arance, A; Dummer, R; Bastholt, L; Nyakas, M; Straume, O; Menzies, A M; Long, G V; Atkinson, V; Blank, C U; Neyns, B.
Afiliación
  • Jansen YJL; Department of Medical Oncology, Universitair Ziekenhuis Brussel, Brussel, Belgium. Electronic address: Yanina.Jansen@uzbrussel.be.
  • Rozeman EA; Department of Medical Oncology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Mason R; Department of Medical Oncology, Princess Alexandra Hospital, Brisbane; Greenslope Oncology, Greenslope Private Hospital, Brisbrane.
  • Goldinger SM; Melanoma Institute Australia and The University of Syndey, Sydney, Australia; Department of Dermatology, University Hospital Zurich, Zurich, Switzerland.
  • Geukes Foppen MH; Department of Medical Oncology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Hoejberg L; Department of Oncology, Odense University Hospital, Odense.
  • Schmidt H; Department of Oncology, Aarhus Universitet, Aarhus, Denmark.
  • van Thienen JV; Department of Medical Oncology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Haanen JBAG; Department of Medical Oncology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Tiainen L; Department of Oncology, Tampere University Hospital, Tampere, Finland.
  • Svane IM; Department of Oncology, Copenhagen University Hospital, Herlev, Denmark.
  • Mäkelä S; Department of Oncology, University of Helsinki, Helsinki, Finland.
  • Seremet T; Department of Medical Oncology, Universitair Ziekenhuis Brussel, Brussel, Belgium.
  • Arance A; Department of Medical Oncology, Hospital Clínic Barcelona, Barcelona, Spain.
  • Dummer R; Department of Dermatology, University Hospital Zurich, Zurich, Switzerland.
  • Bastholt L; Department of Oncology, Odense University Hospital, Odense.
  • Nyakas M; Department of Clinical Cancer Research, Oslo University Hospital, Oslo.
  • Straume O; Department of Oncology, Universitetet Bergen, Bergen, Norway.
  • Menzies AM; Melanoma Institute Australia and The University of Syndey, Sydney, Australia; Department of Medical Oncology, Northern Sydney Cancer Centre, Royal North Shore Hospital, Sydney; Department of Medical Oncology, Mater Hospital, Sydney, Australia.
  • Long GV; Melanoma Institute Australia and The University of Syndey, Sydney, Australia; Department of Medical Oncology, Northern Sydney Cancer Centre, Royal North Shore Hospital, Sydney; Department of Medical Oncology, Mater Hospital, Sydney, Australia.
  • Atkinson V; Greenslope Oncology, Greenslope Private Hospital, Brisbrane; Department of Medical Oncology, Princess Alexandra Hospital, Brisbane.
  • Blank CU; Department of Medical Oncology, The Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Neyns B; Department of Medical Oncology, Universitair Ziekenhuis Brussel, Brussel, Belgium.
Ann Oncol ; 30(7): 1154-1161, 2019 07 01.
Article en En | MEDLINE | ID: mdl-30923820
BACKGROUND: Programmed cell death protein 1 (PD-1) blocking monoclonal antibodies improve the overall survival of patients with advanced melanoma but the optimal duration of treatment has not been established. PATIENTS AND METHODS: This academic real-world cohort study investigated the outcome of 185 advanced melanoma patients who electively discontinued anti-PD-1 therapy with pembrolizumab (N = 167) or nivolumab (N = 18) in the absence of disease progression (PD) or treatment limiting toxicity (TLT) at 14 medical centres across Europe and Australia. RESULTS: Median time on treatment was 12 months (range 0.7-43). The best objective tumour response at the time of treatment discontinuation was complete response (CR) in 117 (63%) patients, partial response (PR) in 44 (24%) patients and stable disease (SD) in 16 (9%) patients; 8 (4%) patients had no evaluable disease (NE). After a median follow-up of 18 months (range 0.7-48) after treatment discontinuation, 78% of patients remained free of progression. Median time to progression was 12 months (range 2-23). PD was less frequent in patients with CR (14%) compared with patients with PR (32%) and SD (50%). Six out of 19 (32%) patients who were retreated with an anti-PD-1 at the time of PD obtained a new antitumour response. CONCLUSIONS: In this real-world cohort of advanced melanoma patients discontinuing anti-PD-1 therapy in the absence of TLT or PD, the duration of anti-PD-1 therapy was shorter when compared with clinical trials. In patients obtaining a CR, and being treated for >6 months, the risk of relapse after treatment discontinuation was low. Patients achieving a PR or SD as best tumour response were at higher risk for progression after discontinuing therapy, and defining optimal treatment duration in such patients deserves further study. Retreatment with an anti-PD-1 at the time of progression may lead to renewed antitumour activity in some patients. CLINICAL TRIAL REGISTRATION: NCT02673970 (https://clinicaltrials.gov/ct2/show/NCT02673970?cond=melanoma&cntry=BE&city=Jette&rank=3).
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Cutáneas / Síndrome de Abstinencia a Sustancias / Protocolos de Quimioterapia Combinada Antineoplásica / Receptor de Muerte Celular Programada 1 / Melanoma Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Oncol Asunto de la revista: NEOPLASIAS Año: 2019 Tipo del documento: Article Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Cutáneas / Síndrome de Abstinencia a Sustancias / Protocolos de Quimioterapia Combinada Antineoplásica / Receptor de Muerte Celular Programada 1 / Melanoma Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Oncol Asunto de la revista: NEOPLASIAS Año: 2019 Tipo del documento: Article Pais de publicación: Reino Unido