RTI Health Solutions, Research Triangle Park, North Carolina, USA.
AIDS. 2012 Jan 28;26(3):355-64. doi: 10.1097/QAD.0b013e32834e87e6.
To assess the cost-effectiveness of etravirine (INTELENCE), a novel nonnucleoside reverse transcriptase inhibitor, used in combination with a background regimen that included darunavir/ritonavir, from a Canadian Provincial Ministry of Health perspective.
A Markov model with a 3-month cycle time and six health states based on CD4 cell count ranges was developed to follow a hypothetical cohort of treatment-experienced adults with HIV-1 infection through initial and subsequent treatment regimens.
Costs (in 2009 Canadian dollars), utilities, and HIV-related mortality data for each health state as well as non-HIV-related mortality data were estimated from Canadian sources and published literature. Transition probabilities between health states and first-year hospitalization and mortality rates were derived from clinical trial data. Incremental 1-year costs per additional adult with viral load less than 50 copies/ml at 48 weeks and incremental lifetime costs per quality-adjusted life-year (QALY) gained were estimated using a 5% discount rate. Sensitivity and variability analyses and model validation were performed.
Etravirine was associated with an increased probability of achieving less than 50 copies/ml at 48 weeks of 0.205 and an estimated gain of 0.66 discounted (1.48 undiscounted) QALYs over a lifetime. The incremental 1-year cost per additional person with viral load less than 50 copies/ml was $23,862. The lifetime incremental cost per QALY gained was $49,120. For the uncertainty ranges and variability scenarios tested for the lifetime horizon, the cost-effectiveness ratio was between $28,859 and 66,249.
When compared with optimized standard of care including darunavir/ritonavir, adding etravirine represents a cost-effective option for treatment-experienced adults in Canada.
从加拿大省级卫生部门的角度评估依曲韦林(INTELENCE),一种新型非核苷类逆转录酶抑制剂,与包括达芦那韦/利托那韦的背景治疗方案联合使用的成本效益。
采用马尔可夫模型,每 3 个月为一个周期,有 6 种健康状态,依据 CD4 细胞计数范围进行划分,对一组患有 HIV-1 感染的经验治疗成年人患者通过初始和后续治疗方案进行随访。
从加拿大来源和已发表文献中估计了每个健康状态的成本(以 2009 年加元计)、效用值和 HIV 相关死亡率数据,以及非 HIV 相关死亡率数据。健康状态之间的转移概率以及第一年住院和死亡率是从临床试验数据中得出的。采用 5%贴现率,估计了第 48 周病毒载量低于 50 拷贝/ml 的每位成年患者的额外 1 年成本,以及每获得 1 个质量调整生命年(QALY)的终生增量成本。进行了敏感性和变异性分析以及模型验证。
依曲韦林可使第 48 周病毒载量低于 50 拷贝/ml 的概率增加 0.205,估计终生可增加 0.66 个贴现(1.48 个不贴现)QALY。每增加 1 例病毒载量低于 50 拷贝/ml 的患者的额外 1 年成本为 23862 美元。每获得 1 个 QALY 的终生增量成本为 49120 美元。对于终生时间范围内测试的不确定性范围和变异性情况,成本效益比在 28859 美元至 66249 美元之间。
与包括达芦那韦/利托那韦的优化标准治疗相比,依曲韦林对加拿大经验治疗的成年人是一种具有成本效益的选择。