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Cost-effectiveness of treating advanced melanoma with tumor-infiltrating lymphocytes based on an international randomized phase 3 clinical trial.
Ten Ham, Renske M T; Rohaan, Maartje W; Jedema, Inge; Kessels, Rob; Stegeman, Wim; Scheepmaker, Walter; Nuijen, Bastiaan; Nijenhuis, Cynthia; Lindenberg, Melanie; Borch, Troels Holz; Monberg, Tine; Donia, Marco; Marie Svane, Inge; van Harten, Wim; Haanen, John; Retel, Valesca P.
Afiliação
  • Ten Ham RMT; Department of Epidemiology & Health Economics, Julius Center for Health Sciences and Primary Care, Utrecht, The Netherlands.
  • Rohaan MW; Division of Psychosocial Research and Epidemiology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Jedema I; Division of Medical Oncology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Kessels R; Division of Molecular Oncology and Immunology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Stegeman W; Department of Biometrics, Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Scheepmaker W; Department of Biometrics, Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Nuijen B; Financial Department, Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Nijenhuis C; Division of Pharmacy & Pharmacology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Lindenberg M; Biotherapeutics Unit, Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Borch TH; Division of Psychosocial Research and Epidemiology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Monberg T; Department of Oncology, National Center for Cancer Immune Therapy, Copenhagen University Hospital, Herlev, Denmark.
  • Donia M; Department of Oncology, National Center for Cancer Immune Therapy, Copenhagen University Hospital, Herlev, Denmark.
  • Marie Svane I; Department of Oncology, National Center for Cancer Immune Therapy, Copenhagen University Hospital, Herlev, Denmark.
  • van Harten W; Department of Oncology, National Center for Cancer Immune Therapy, Copenhagen University Hospital, Herlev, Denmark.
  • Haanen J; Division of Psychosocial Research and Epidemiology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
  • Retel VP; Department of Health Technology and Services Research, University of Twente, Enschede, The Netherlands.
J Immunother Cancer ; 12(3)2024 Mar 26.
Article em En | MEDLINE | ID: mdl-38531663
ABSTRACT

INTRODUCTION:

In a multicenter, open-label randomized phase 3 clinical trial conducted in the Netherlands and Denmark, treatment with ex vivo-expanded tumor-infiltrating lymphocytes (TIL-NKI/CCIT) from autologous melanoma tumor compared with ipilimumab improved progression-free survival in patients with unresectable stage IIIC-IV melanoma after failure of first-line or second-line treatment. Based on this trial, we conducted a cost-utility analysis.

METHODS:

A Markov decision model was constructed to estimate expected costs (expressed in 2021€) and outcomes (quality-adjusted life years (QALYs)) of TIL-NKI/CCIT versus ipilimumab in the Netherlands. The Danish setting was assessed in a scenario analysis. A modified societal perspective was applied over a lifetime horizon. TIL-NKI/CCIT production costs were estimated via activity-based costing. Through sensitivity analyses, uncertainties and their impact on the incremental cost-effectiveness ratio (ICER) were assessed.

RESULTS:

Mean total undiscounted lifetime benefits were 4.47 life years (LYs) and 3.52 QALYs for TIL-NKI/CCIT and 3.33 LYs and 2.46 QALYs for ipilimumab. Total lifetime undiscounted costs in the Netherlands were €347,168 for TIL-NKI/CCIT (including €67,547 for production costs) compared with €433,634 for ipilimumab. Undiscounted lifetime cost in the Danish scenario were €337,309 and €436,135, respectively. This resulted in a dominant situation for TIL-NKI/CCIT compared with ipilimumab in both countries, meaning incremental QALYs were gained at lower costs. Survival probabilities, and utility in progressive disease affected the ICER most.

CONCLUSION:

Based on the data of a randomized phase 3 trial, treatment with TIL-NKI/CCIT in patients with unresectable stage IIIC-IV melanoma is cost-effective and cost-saving, both in the current Dutch and Danish setting. These findings led to inclusion of TIL-NKI/CCIT as insured care and treatment guidelines. Publicly funded development of the TIL-NKI/CCIT cell therapy shows realistic promise to further explore development of effective personalized treatment while warranting economic sustainability of healthcare systems.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Melanoma Limite: Humans Idioma: En Revista: J Immunother Cancer Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Holanda País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Melanoma Limite: Humans Idioma: En Revista: J Immunother Cancer Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Holanda País de publicação: Reino Unido