Neeser Kurt, Lübben Georg, Siebert Uwe, Schramm Wendelin
Institute for Medical Informatics and Biostatistics, Basel, Switzerland.
Pharmacoeconomics. 2004;22(5):321-41. doi: 10.2165/00019053-200422050-00006.
Pioglitazone has been approved in Europe for oral combination therapy for type 2 diabetes mellitus. Along with other agents of the thiazolidinedione class, it has a novel intracellular mechanism of action. Clinical trials with pioglitazone have confirmed a strong product profile in terms of control of blood glucose and lipids. However, the drug acquisition cost for pioglitazone is greater than standard medications for type 2 diabetes. Long-term data regarding the cost effectiveness of pioglitazone-based combination therapy are not available.
To evaluate, using a decision analysis model, the cost effectiveness of pioglitazone-based combination therapy compared with relevant alternative medications for the treatment of type 2 diabetes in Germany.
This study compared the clinical effects and costs of pioglitazone 30 mg added to metformin in patients who failed metformin monotherapy and pioglitazone added to a sulphonylurea in patients who failed sulphonylurea monotherapy, with the most relevant treatment alternatives. A published and validated Markov model was adapted to reflect the management of type 2 diabetes. This simulated the number of severe complications occurring and the mean life expectancy of a diabetic cohort, which was based on the overweight group of the UK Prospective Diabetes Study at year 6 of follow-up. Drug treatment costs, other costs for general management of type 2 diabetes and the costs of complications were combined to compute overall lifetime treatment costs from the perspective of the German statutory healthcare system in 2002.
Combination therapy with pioglitazone/metformin was associated with a higher life expectancy (15.2 years) relative to sulphonylurea/metformin (14.9 years) or acarbose/metformin (14.7 years). Likewise, pioglitazone/sulphonylurea (15.5 years) was superior to metformin/sulphonylurea (14.9 years) and acarbose/sulphonylurea (14.8 years). Undiscounted incremental cost-effectiveness ratios in comparison to the next best strategy were euro20,002 per life-year gained (LYG) for pioglitazone/metformin versus sulphonylurea/metformin, and euro8707 per LYG for pioglitazone/sulphonylurea versus metformin/sulphonylurea. After discounting costs and life expectancy at 5% per year, the incremental cost-effectiveness ratio was euro47 636 per LYG for pioglitazone/metformin versus sulphonylurea/metformin, and euro19 745 per LYG for pioglitazone/sulphonylurea versus metformin/sulphonylurea.
In this model, with its underlying assumptions and data, combination therapy with pioglitazone increased life expectancy in overweight type 2 diabetes patients at acceptable cost compared with other well established medications in Germany. These findings should be re-evaluated as soon as additional evidence becomes available from the currently ongoing long-term clinical and economic studies.
吡格列酮已在欧洲获批用于2型糖尿病的口服联合治疗。与其他噻唑烷二酮类药物一样,它具有一种新的细胞内作用机制。吡格列酮的临床试验已证实其在控制血糖和血脂方面具有强大的产品优势。然而,吡格列酮的药物获取成本高于2型糖尿病的标准药物。关于基于吡格列酮的联合治疗的成本效益的长期数据尚不可得。
使用决策分析模型评估在德国,基于吡格列酮的联合治疗与相关替代药物治疗2型糖尿病的成本效益。
本研究比较了在二甲双胍单药治疗失败的患者中加用30毫克吡格列酮和在磺脲类单药治疗失败的患者中加用吡格列酮的临床效果和成本,以及最相关的治疗替代方案。采用一个已发表并经验证的马尔可夫模型来反映2型糖尿病的管理情况。这模拟了发生的严重并发症数量以及糖尿病队列的平均预期寿命,该队列基于英国前瞻性糖尿病研究随访第6年的超重组。将药物治疗成本、2型糖尿病的其他一般管理成本和并发症成本相结合,从2002年德国法定医疗保健系统的角度计算总体终身治疗成本。
与磺脲类/二甲双胍(14.9年)或阿卡波糖/二甲双胍(14.7年)相比,吡格列酮/二甲双胍联合治疗的预期寿命更长(15.2年)。同样,吡格列酮/磺脲类(15.5年)优于二甲双胍/磺脲类(14.9年)和阿卡波糖/磺脲类(14.8年)。与次优策略相比,未贴现的增量成本效益比为:吡格列酮/二甲双胍相对于磺脲类/二甲双胍每获得一个生命年(LYG)为20, 002欧元,吡格列酮/磺脲类相对于二甲双胍/磺脲类每获得一个LYG为8707欧元。在按每年5%对成本和预期寿命进行贴现后,吡格列酮/二甲双胍相对于磺脲类/二甲双胍的增量成本效益比为每获得一个LYG 47, 636欧元,吡格列酮/磺脲类相对于二甲双胍/磺脲类为每获得一个LYG 19, 745欧元。
在该具有其潜在假设和数据的模型中,与德国其他成熟药物相比,吡格列酮联合治疗以可接受的成本提高了超重2型糖尿病患者的预期寿命。一旦从当前正在进行的长期临床和经济研究中获得更多证据,应重新评估这些发现。