Department of Hepatology and Infectious Diseases, Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Department of Pediatrics, Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
JAMA Netw Open. 2021 Apr 1;4(4):e214846. doi: 10.1001/jamanetworkopen.2021.4846.
Atezolizumab plus bevacizumab as a first-line therapy for patients with unresectable or metastatic hepatocellular carcinoma has been shown to improve overall and progression-free survival compared with standard sorafenib treatment. However, because of the high cost of atezolizumab plus bevacizumab, assessment of its value by considering both efficacy and cost is needed.
To evaluate the cost-effectiveness of atezolizumab plus bevacizumab vs sorafenib for patients with unresectable or metastatic hepatocellular carcinoma from a US payer perspective.
DESIGN, SETTING, AND PARTICIPANTS: This economic evaluation was performed from June through September 2020, with a 6-year investment time period. Hypothetical patients were male and female adults 18 years or older who had a diagnosis of locally advanced metastatic or unresectable hepatocellular carcinoma confirmed by histologic or clinical features.
Health care costs (adjusted to 2020 US dollars), life-years, quality-adjusted life-years (QALYs), and incremental cost-effectiveness ratio (ICER) of atezolizumab plus bevacizumab vs sorafenib were examined using a partitioned survival model. One-way deterministic and probabilistic sensitivity analyses were used to examine model uncertainty. The model was also used to estimate price reductions of atezolizumab plus bevacizumab that would achieve more favorable cost-effectiveness.
In the base case analysis of a hypothetical sample of 424 patients, atezolizumab plus bevacizumab was associated with an increase of 0.623 life-years (1.840 vs 1.218 life-years) and 0.484 QALYs (1.412 vs 0.928 QALYs) and with an incremental cost of $156 210 per patient compared with sorafenib. The ICER was $322 500 per QALY (5th to 95th percentile, $149 364-$683 744 per QALY), with 0.6% and 5.1% chance of being cost-effective at willingness-to-pay thresholds of $100 000 and $150 000 per QALY, respectively. The ICER never decreased below $150 000 per QALY in the 1-way sensitivity analyses. To achieve more favorable cost-effectiveness under the thresholds of $150 000 to $100 000 per QALY, the prices of atezolizumab and bevacizumab would need to be reduced by 37% to 47%.
In this economic evaluation, atezolizumab plus bevacizumab was associated with clinical benefit but was not cost-effective compared with sorafenib for first-line treatment of unresectable or metastatic hepatocellular carcinoma from a US payer perspective. A substantial reduction in price for atezolizumab plus bevacizumab would be needed to achieve favorable cost-effectiveness for this new therapy.
阿特珠单抗联合贝伐珠单抗作为不可切除或转移性肝细胞癌患者的一线治疗,与标准索拉非尼治疗相比,已被证明可提高总生存期和无进展生存期。然而,由于阿特珠单抗联合贝伐珠单抗的成本较高,因此需要从美国支付者的角度评估其疗效和成本。
从美国支付者的角度评估阿特珠单抗联合贝伐珠单抗与索拉非尼治疗不可切除或转移性肝细胞癌的成本效益。
设计、地点和参与者:本经济评价于 2020 年 6 月至 9 月进行,投资期限为 6 年。假设患者为 18 岁或以上的男性和女性成年患者,经组织学或临床特征确诊为局部晚期转移性或不可切除的肝细胞癌。
使用分割生存模型评估阿特珠单抗联合贝伐珠单抗与索拉非尼相比的医疗保健成本(调整至 2020 年美元)、寿命年、质量调整寿命年(QALY)和增量成本效益比(ICER)。采用单因素确定性和概率敏感性分析来检验模型的不确定性。该模型还用于估计阿特珠单抗联合贝伐珠单抗的降价幅度,以实现更有利的成本效益。
在 424 例患者的假设样本的基础案例分析中,与索拉非尼相比,阿特珠单抗联合贝伐珠单抗可使寿命年增加 0.623 年(1.840 年比 1.218 年)和 QALY 增加 0.484(1.412 年比 0.928 年),每位患者的增量成本为 156210 美元。ICER 为 322500 美元/QALY(第 5 至 95 百分位为 149364-683744 美元/QALY),在分别为 100000 美元和 150000 美元/QALY 的意愿支付阈值下,分别有 0.6%和 5.1%的可能性具有成本效益。在单因素敏感性分析中,ICER 从未降至 150000 美元/QALY 以下。要在 150000 美元至 100000 美元/QALY 的门槛下获得更有利的成本效益,阿特珠单抗和贝伐珠单抗的价格需要降低 37%至 47%。
在这项经济评价中,与索拉非尼相比,阿特珠单抗联合贝伐珠单抗在治疗不可切除或转移性肝细胞癌的一线治疗中具有临床获益,但从美国支付者的角度来看并不具有成本效益。需要大幅降低阿特珠单抗联合贝伐珠单抗的价格,才能为这种新疗法带来有利的成本效益。