Department of Pharmacy, The First Affiliated Hospital of University of Science and Technology of China, Hefei, Anhui, China.
Medical Decision and Economic Group, Department of Pharmacy, Ren Ji Hospital, South Campus, Shanghai Jiaotong University School of Medicine, Shanghai, China.
JAMA Netw Open. 2021 Feb 1;4(2):e210037. doi: 10.1001/jamanetworkopen.2021.0037.
Treatment with atezolizumab plus bevacizumab may prolong overall survival among patients with unresectable hepatocellular carcinoma. However, to our knowledge, the cost-effectiveness of using this high-priced therapy for this indication is currently unknown.
To evaluate the cost-effectiveness of atezolizumab plus bevacizumab to treat unresectable hepatocellular carcinoma from the US payer perspective.
DESIGN, SETTING, AND PARTICIPANTS: This economic evaluation used a partitioned survival model consisting of 3 discrete health states to assess the cost-effectiveness of treatment of hepatocellular carcinoma with atezolizumab plus bevacizumab vs sorafenib. The characteristics of patients in the model were similar to patients in a phase 3, open-label randomized clinical trial (IMbrave150) who had unresectable hepatocellular carcinoma and had not previously received systemic treatment. Key clinical data were generated from the IMbrave150 trial conducted between March 15, 2018, and January 30, 2019, and cost and health preference data were collected from the literature.
Costs, quality-adjusted life-years (QALYs), incremental cost-utility ratios, incremental net health benefits, and incremental net monetary benefits were calculated for the 2 treatment strategies. Subgroup, 1-way sensitivity, and probabilistic sensitivity analyses were performed.
Treatment of hepatocellular carcinoma with atezolizumab plus bevacizumab added 0.530 QALYs and resulted in an incremental cost of $89 807 compared with sorafenib therapy, which had an incremental cost-utility ratio of $169 223 per QALY gained. The incremental net health benefit was -0.068 QALYs, and the incremental net monetary benefit was -$10 202 at a willingness-to-pay threshold of $150 000/QALY. The probabilistic sensitivity analysis indicated that treatment with atezolizumab plus bevacizumab achieved a 35% probability of cost-effectiveness at a threshold of $150 000/QALY. One-way sensitivity analysis revealed that the results were most sensitive to the hazard ratio of overall survival. The subgroup analysis found that treatment with atezolizumab plus bevacizumab was associated with preferred incremental net health benefits in several subgroups, including patients with hepatitis B and C.
Atezolizumab plus bevacizumab treatment is unlikely to be a cost-effective option compared with sorafenib for patients with unresectable hepatocellular carcinoma. Reducing the prices of atezolizumab and bevacizumab may improve cost-effectiveness. The economic outcomes also may be improved by tailoring treatments based on individual patient factors.
阿特珠单抗联合贝伐珠单抗治疗不可切除肝细胞癌患者可能延长总生存期。然而,据我们所知,目前尚不清楚针对该适应症使用这种高价疗法的成本效益。
从美国支付者的角度评估阿特珠单抗联合贝伐珠单抗治疗不可切除肝细胞癌的成本效益。
设计、设置和参与者:本经济学评价采用由 3 个离散健康状态组成的分割生存模型,以评估阿特珠单抗联合贝伐珠单抗治疗肝细胞癌与索拉非尼相比的成本效益。模型中患者的特征与一项 3 期、开放标签、随机临床试验(IMbrave150)中的患者相似,这些患者患有不可切除的肝细胞癌且未接受过系统治疗。关键临床数据来自于 2018 年 3 月 15 日至 2019 年 1 月 30 日期间进行的 IMbrave150 试验,成本和健康偏好数据来自文献。
为两种治疗策略计算了成本、质量调整生命年(QALYs)、增量成本-效用比、增量净健康效益和增量净货币效益。进行了亚组、1 次敏感性和概率敏感性分析。
与索拉非尼治疗相比,阿特珠单抗联合贝伐珠单抗治疗肝细胞癌增加了 0.530 个 QALYs,增量成本为 89807 美元,增量成本-效用比为每获得 1 个 QALY 增加 169223 美元。增量净健康效益为-0.068 QALYs,增量净货币效益为-10202 美元,在 150000 美元/QALY 的支付意愿阈值下。概率敏感性分析表明,在 150000 美元/QALY 的阈值下,阿特珠单抗联合贝伐珠单抗治疗的成本效益达到 35%的可能性。单因素敏感性分析表明,结果对总生存的风险比最敏感。亚组分析发现,在几个亚组中,包括乙型肝炎和丙型肝炎患者,阿特珠单抗联合贝伐珠单抗治疗与更优的增量净健康效益相关。
与索拉非尼相比,阿特珠单抗联合贝伐珠单抗治疗不可切除肝细胞癌患者不太可能是一种具有成本效益的选择。降低阿特珠单抗和贝伐珠单抗的价格可能会提高成本效益。根据个体患者因素定制治疗也可能改善经济结果。