Wirth Daniel, Dass Ramesh, Hettle Robert
Health Economics & Market Access, Janssen-Cilag GmbH, Johnson & Johnson Platz 1, 41470, Neuss, Germany.
Janssen-Cilag Ltd, High Wycombe, UK.
BMC Health Serv Res. 2017 Mar 8;17(1):182. doi: 10.1186/s12913-017-2118-2.
Treatment of multidrug-resistant tuberculosis (MDR-TB) is complex, lengthy, and involves a minimum of four drugs termed a background regimen (BR), that have not previously been prescribed or that have proven susceptible to patient sputum culture isolates. In recent years, promising new treatment options have emerged as add-on therapies to a BR. The aim of this study was to evaluate the long-term costs and effectiveness of adding the novel or group 5 interventions bedaquiline, delamanid, and linezolid to a background regimen (BR) of drugs for the treatment of adult patients with pulmonary multidrug-resistant tuberculosis (MDR-TB), within their marketing authorisations, from a German healthcare cost-effectiveness perspective.
A cohort-based Markov model was developed to simulate the incremental cost-effectiveness ratio of bedaquiline plus BR, delamanid plus BR, or linezolid plus BR versus BR alone in the treatment of MDR-TB, over a 10-year time horizon. Effectiveness of treatment was evaluated in Quality-Adjusted Life-Years (QALYs) and Life-Years Gained (LYG), using inputs from clinical trials for bedaquiline and delamanid and from a German observational study for linezolid. Cost data were obtained from German Drug Directory costs (€/2015), published literature, and expert opinion. A 3% yearly discount rate was applied. Probabilistic and deterministic sensitivity analyses were conducted.
The total discounted costs per-patient were €85,575 for bedaquiline plus BR, €81,079 for delamanid plus BR, and €80,460 for linezolid plus BR, compared with a cost of €60,962 for BR alone. The total discounted QALYs per-patient were 5.95 for bedaquiline plus BR, 5.36 for delamanid plus BR, and 3.91 for linezolid plus BR, compared with 3.68 for BR alone. All interventions were therefore associated with higher QALYs and higher costs than BR alone, with incremental costs per QALY gained of €22,238 for bedaquiline, €38,703 for delamanid, and €87,484 for linezolid, versus BR alone. In a fully incremental analysis, bedaquiline plus BR was the most cost-effective treatment option at thresholds greater than €22,000 per QALY gained. In probabilistic analyses, the probability that bedaquiline plus BR was the most cost-effective treatment strategy at a willingness-to-pay threshold of €30,000 was 54.5%, compared with 22.9% for BR alone, 18.2% for delamanid plus BR, and 4.4% for linezolid.
In Germany, the addition of bedaquiline, delamanid, or linezolid to a BR would result in QALY gains over BR alone. Based on this analysis, bedaquiline is likely to be the most cost-effective intervention for the treatment of MDR-TB, when added to a BR regimen at thresholds greater than €22,000 per QALY.
耐多药结核病(MDR-TB)的治疗复杂、疗程长,且至少需要四种药物组成基础治疗方案(BR),这些药物此前未被使用过或已被证明对患者痰液培养分离菌敏感。近年来,作为基础治疗方案的附加疗法,出现了一些有前景的新治疗选择。本研究的目的是从德国医疗成本效益的角度,评估在药品上市许可范围内,将新型或第5组干预措施贝达喹啉、地拉米啶和利奈唑胺添加到治疗成年耐多药肺结核(MDR-TB)患者的基础治疗方案(BR)中的长期成本和效果。
建立了一个基于队列的马尔可夫模型,以模拟在10年时间范围内,贝达喹啉联合BR、地拉米啶联合BR或利奈唑胺联合BR与单独使用BR治疗MDR-TB的增量成本效益比。使用贝达喹啉和地拉米啶的临床试验数据以及利奈唑胺的德国观察性研究数据,以质量调整生命年(QALYs)和获得的生命年(LYG)评估治疗效果。成本数据来自德国药品目录成本(€/2015)、已发表文献和专家意见。采用3%的年贴现率。进行了概率和确定性敏感性分析。
与单独使用BR的成本€60,962相比,贝达喹啉联合BR的每位患者总贴现成本为€85,575,地拉米啶联合BR为€81,079,利奈唑胺联合BR为€80,460。与单独使用BR的3.68相比,贝达喹啉联合BR的每位患者总贴现QALYs为5.95,地拉米啶联合BR为5.36,利奈唑胺联合BR为3.91。因此,所有干预措施与单独使用BR相比,均能带来更高的QALYs和更高的成本,与单独使用BR相比,贝达喹啉每获得一个QALY的增量成本为€22,238,地拉米啶为€38,703,利奈唑胺为€87,484。在全面增量分析中,当每获得一个QALY的阈值大于€22,000时,贝达喹啉联合BR是最具成本效益的治疗选择。在概率分析中,在支付意愿阈值为€30,000时,贝达喹啉联合BR是最具成本效益治疗策略的概率为54.5%,单独使用BR为22.9%,地拉米啶联合BR为18.2%,利奈唑胺为4.4%。
在德国,将贝达喹啉、地拉米啶或利奈唑胺添加到BR中,与单独使用BR相比,可带来QALY的增加。基于此分析,当添加到BR方案中且每QALY阈值大于€22,000时,贝达喹啉可能是治疗MDR-TB最具成本效益的干预措施。