Department of Medicine, Medical Practice Evaluation Center, Massachusetts General Hospital, Boston, MA.
Division of Infectious Diseases, Brigham and Women's Hospital, Boston, MA.
J Acquir Immune Defic Syndr. 2020 Feb 1;83(2):148-156. doi: 10.1097/QAI.0000000000002241.
We projected the clinical outcomes, cost-effectiveness, and budget impact of ibalizumab plus an optimized background regimen (OBR) for people with multidrug-resistant (MDR) HIV in the United States.
Using the Cost-Effectiveness of Preventing AIDS Complications microsimulation model and a health care sector perspective, we compared 2 treatment strategies for MDR HIV: (1) IBA + OBR-ibalizumab plus OBR and (2) OBR-OBR alone. Ibalizumab efficacy and cohort characteristics were from trial data: mean age 49 years, 85% male, and mean CD4 150/µL. Six-month viral suppression was 50% with IBA + OBR and 0% with OBR. The ibalizumab loading dose cost $10,500, and subsequent ibalizumab injections cost $8400/month; OBR cost $4500/month. Incremental cost-effectiveness ratios (ICERs) were calculated using discounted (3%/year) quality-adjusted life years (QALYs) and costs. ICERs ≤$100,000/QALY were considered cost-effective. We performed sensitivity analysis on key parameters and examined budget impact.
In the base case, 5-year survival increased from 38% with OBR to 47% with IBA + OBR. Lifetime costs were $301,700/person with OBR and $661,800/person with IBA + OBR; the ICER for IBA + OBR compared with OBR was $260,900/QALY. IBA + OBR was not cost-effective even with 100% efficacy. IBA + OBR became cost-effective at base case efficacy if ibalizumab cost was reduced by ≥88%. For an estimated 12,000 people with MDR HIV in the United States, IBA + OBR increased care costs by $1.8 billion (1.5% of total treatment budget) over 5 years.
For people with MDR HIV lacking other treatment options, ibalizumab will substantially increase survival when effective. Although adding ibalizumab to OBR is not cost-effective, the low number of eligible patients in the United States makes the budget impact relatively small.
我们预测了伊博利珠单抗联合优化背景治疗方案(OBR)治疗美国多重耐药(MDR)HIV 感染者的临床结局、成本效益和预算影响。
使用预防艾滋病并发症成本效益微观模拟模型和医疗保健部门视角,我们比较了 MDR HIV 的 2 种治疗策略:(1)IBA+OBR-伊博利珠单抗联合 OBR 和(2)OBR-OBR 单独治疗。Ibalizumab 的疗效和队列特征来自临床试验数据:平均年龄 49 岁,85%为男性,平均 CD4 细胞计数为 150/μL。IBA+OBR 的 6 个月病毒抑制率为 50%,而 OBR 为 0%。伊博利珠单抗的负荷剂量费用为 10500 美元,随后的伊博利珠单抗注射费用为 8400 美元/月;OBR 每月费用为 4500 美元。采用贴现(3%/年)质量调整生命年(QALY)和成本计算增量成本效益比(ICER)。ICER≤100000 美元/QALY 被认为具有成本效益。我们对关键参数进行了敏感性分析,并考察了预算影响。
在基线情况下,OBR 组的 5 年生存率从 38%提高到 IBA+OBR 组的 47%。OBR 组的终身成本为每人 301700 美元,IBA+OBR 组为每人 661800 美元;与 OBR 相比,IBA+OBR 的 ICER 为 260900 美元/QALY。即使疗效达到 100%,IBA+OBR 也不具有成本效益。如果伊博利珠单抗的成本降低≥88%,则在基线情况下,IBA+OBR 的疗效具有成本效益。在美国,估计有 12000 名 MDR HIV 感染者,IBA+OBR 在 5 年内将增加 18 亿美元(占总治疗预算的 1.5%)的医疗费用。
对于没有其他治疗选择的 MDR HIV 感染者,伊博利珠单抗在有效时可显著提高生存率。尽管将伊博利珠单抗添加到 OBR 中并不具有成本效益,但美国符合条件的患者人数较少,因此预算影响相对较小。