The cost-effectiveness of dapagliflozin versus sulfonylurea as an add-on to metformin in the treatment of Type 2 diabetes mellitus

Diabet Med. 2015 Jul;32(7):890-8. doi: 10.1111/dme.12772. Epub 2015 Apr 30.

Abstract

Aims: To assess the cost-effectiveness of dapagliflozin, a sodium-glucose co-transporter-2 (SGLT-2) inhibitor, compared with a sulfonylurea, when added to metformin for treatment of UK people with Type 2 diabetes mellitus inadequately controlled on metformin alone.

Methods: Clinical inputs sourced from a head-to-head randomized controlled trial (RCT) informed the Cardiff diabetes decision model. Risk equations developed from the United Kingdom Prospective Diabetes Study (UKPDS) were used in conjunction with the clinical inputs to predict disease progression and the incidence of micro- and macrovascular complications over a lifetime horizon. Cost and utility data were generated to present the incremental cost-effectiveness ratio (ICER) for both treatment arms, and sensitivity and scenario analyses were conducted to assess the impact of uncertainty on the final model results.

Results: The dapagliflozin treatment arm was associated with a mean incremental benefit of 0.467 quality-adjusted life years (QALYs) [95% confidence interval (CI): 0.420; 0.665], with an incremental cost of £1246 (95% CI: £613; £1637). This resulted in an ICER point estimate of £2671 per QALY gained. Incremental costs were shown to be insensitive to parameter variation, with only treatment-related weight change having a significant impact on the incremental QALYs. Probabilistic sensitivity analysis determined that dapagliflozin had a 100% probability of being cost-effective at a willingness-to-pay threshold of £20,000 per QALY.

Conclusions: Dapagliflozin in combination with metformin was shown to be a cost-effective treatment option compared with sulfonylurea from a UK healthcare perspective for people with Type 2 diabetes mellitus who are inadequately controlled on metformin monotherapy.

Publication types

  • Clinical Trial, Phase III
  • Comparative Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Benzhydryl Compounds / adverse effects
  • Benzhydryl Compounds / economics
  • Benzhydryl Compounds / therapeutic use*
  • Cohort Studies
  • Cost-Benefit Analysis
  • Diabetes Complications / economics
  • Diabetes Complications / epidemiology
  • Diabetes Complications / prevention & control
  • Diabetes Complications / therapy
  • Diabetes Mellitus, Type 2 / complications
  • Diabetes Mellitus, Type 2 / drug therapy*
  • Diabetes Mellitus, Type 2 / economics
  • Diabetes Mellitus, Type 2 / metabolism
  • Drug Resistance
  • Drug Therapy, Combination / adverse effects
  • Drug Therapy, Combination / economics
  • Female
  • Glucosides / adverse effects
  • Glucosides / economics
  • Glucosides / therapeutic use*
  • Health Care Costs
  • Humans
  • Hyperglycemia / economics
  • Hyperglycemia / prevention & control*
  • Hyperglycemia / therapy
  • Hypoglycemia / chemically induced
  • Hypoglycemia / economics
  • Hypoglycemia / prevention & control*
  • Hypoglycemia / therapy
  • Hypoglycemic Agents / adverse effects
  • Hypoglycemic Agents / economics
  • Hypoglycemic Agents / therapeutic use*
  • Male
  • Metformin / adverse effects
  • Metformin / economics
  • Metformin / therapeutic use*
  • Middle Aged
  • Overweight / economics
  • Overweight / epidemiology
  • Overweight / prevention & control
  • Overweight / therapy
  • Quality-Adjusted Life Years
  • Risk
  • Sodium-Glucose Transport Proteins / antagonists & inhibitors*
  • Sodium-Glucose Transport Proteins / metabolism
  • Sulfonylurea Compounds / adverse effects
  • Sulfonylurea Compounds / economics
  • Sulfonylurea Compounds / therapeutic use
  • United Kingdom / epidemiology
  • Weight Loss / drug effects

Substances

  • Benzhydryl Compounds
  • Glucosides
  • Hypoglycemic Agents
  • Sodium-Glucose Transport Proteins
  • Sulfonylurea Compounds
  • dapagliflozin
  • Metformin