Sequential treatment approaches in the management of BRAF wild-type advanced melanoma: a cost-effectiveness analysis

Immunotherapy. 2018 Oct;10(14):1241-1252. doi: 10.2217/imt-2018-0085. Epub 2018 Sep 3.

Abstract

Aim: To evaluate the cost-effectiveness of treatment sequences with checkpoint inhibitors in patients with BRAF wild-type melanoma.

Materials & methods: Using a discrete event simulation model, cost and health outcomes were estimated. Pooled data from CheckMate 067/069 trials were used to calculate survival outcomes including treatment-free interval extrapolated over a patient's lifetime. Costs accounted for treatment, administration, toxicity, and disease management.

Results: First-line anti-PD-1 + anti-CTLA-4 initiating sequences had the highest estimated mean survival gain (7.6-7.7 years), driven by a longer estimated mean treatment-free interval (5.3 years). Incremental costs per incremental quality-adjusted life year gained for anti-PD-1 + anti-CTLA-4 followed by chemotherapy were US$30,955 versus anti-PD-1 initiating sequences, within the willingness-to-pay threshold.

Conclusion: Anti-PD-1 + anti-CTLA-4 initiating sequences for BRAF wild-type melanoma are cost-effective versus anti-PD-1.

Keywords: economic models; ipilimumab; nivolumab.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antibodies, Monoclonal / economics*
  • Antibodies, Monoclonal / therapeutic use
  • CTLA-4 Antigen / antagonists & inhibitors
  • Clinical Trials as Topic
  • Computer Simulation*
  • Cost-Benefit Analysis
  • Drug Therapy, Combination
  • Health Care Costs
  • Humans
  • Immunotherapy / economics*
  • Immunotherapy / methods
  • Ipilimumab / economics*
  • Ipilimumab / therapeutic use
  • Medicare
  • Melanoma / drug therapy*
  • Melanoma / economics
  • Melanoma / mortality
  • Models, Economic
  • Mutation / genetics
  • Nivolumab / economics*
  • Nivolumab / therapeutic use
  • Programmed Cell Death 1 Receptor / antagonists & inhibitors
  • Proto-Oncogene Proteins B-raf / genetics
  • Skin Neoplasms / drug therapy*
  • Skin Neoplasms / economics
  • Skin Neoplasms / mortality
  • Survival Analysis
  • United States

Substances

  • Antibodies, Monoclonal
  • CTLA-4 Antigen
  • Ipilimumab
  • PDCD1 protein, human
  • Programmed Cell Death 1 Receptor
  • Nivolumab
  • BRAF protein, human
  • Proto-Oncogene Proteins B-raf