Department of Pharmaceutical Regulatory Science and Pharmacoeconomics, School of Pharmacy, Nanjing Medical University, Nanjing, Jiangsu Province, China.
Center for Global Health, School of Public Health, Nanjing Medical University, Nanjing, Jiangsu Province, China.
Int J Clin Pharm. 2024 Oct;46(5):1189-1199. doi: 10.1007/s11096-024-01752-8. Epub 2024 May 30.
BACKGROUND: Camrelizumab combined with rivoceranib has been proven effective for treating unresectable hepatocellular carcinoma (uHCC). However, their higher prices than sorafenib could impose a substantial economic burden on patients. AIM: This study aimed to evaluate the relative cost-effectiveness of the combination of camrelizumab and rivoceranib versus sorafenib as first-line therapy for patients with uHCC from the perspective of the US and Chinese payers. METHOD: Using data from the CARES-310 trial, a partitioned survival model (PSM) was developed, considering the perspectives of the US and Chinese payers. The model employed a 15-year time horizon and a biweekly cycle. Direct medical costs and utility data were collected from previous studies and open-access databases. Primary outcomes included quality-adjusted life years (QALYs) and the incremental cost-effectiveness ratio (ICER). Price simulations, sensitivity analyses, and subgroup analyses were conducted. RESULTS: The ICER for the US and China was $122,388.62/QALY and $30,410.56/QALY, respectively, falling below the willingness-to-pay (WTP) thresholds of $150,000/QALY for the US and $35,898.87/QALY for China. Price simulations indicated the cost-effectiveness of camrelizumab plus rivoceranib when the price of camrelizumab (200 mg) remained below $6275.19 in the US and $558.09 in China. The primary determinant of cost-effectiveness in both regions was the cost of camrelizumab. CONCLUSION: The combination of camrelizumab and rivoceranib is a cost-effective first-line therapy for uHCC in both the US and China. Lowering their prices could significantly influence their cost-effectiveness and accessibility to patients. These findings will guide clinicians in treating uHCC and help decision-makers formulate value-based drug pricing strategies.
背景:卡瑞利珠单抗联合雷莫芦单抗已被证实对治疗不可切除肝细胞癌(uHCC)有效。然而,与索拉非尼相比,其价格更高,可能会给患者带来沉重的经济负担。
目的:本研究旨在从美国和中国支付者的角度评估卡瑞利珠单抗联合雷莫芦单抗与索拉非尼作为 uHCC 一线治疗的相对成本效益。
方法:使用 CARES-310 试验数据,建立了一个分割生存模型(PSM),同时考虑了美国和中国支付者的观点。该模型采用了 15 年的时间范围和双周周期。直接医疗成本和效用数据来自先前的研究和开放获取数据库。主要结果包括质量调整生命年(QALY)和增量成本效益比(ICER)。进行了价格模拟、敏感性分析和亚组分析。
结果:美国和中国的 ICER 分别为 122388.62 美元/QALY 和 30410.56 美元/QALY,均低于美国 150000 美元/QALY 和中国 35898.87 美元/QALY 的支付意愿(WTP)阈值。价格模拟表明,当卡瑞利珠单抗(200mg)在美国的价格低于 6275.19 美元,在中国的价格低于 558.09 美元时,卡瑞利珠单抗联合雷莫芦单抗具有成本效益。这两个地区成本效益的主要决定因素是卡瑞利珠单抗的成本。
结论:卡瑞利珠单抗联合雷莫芦单抗是美国和中国 uHCC 的一种具有成本效益的一线治疗方法。降低它们的价格将显著影响它们的成本效益和对患者的可及性。这些发现将指导临床医生治疗 uHCC,并帮助决策者制定基于价值的药物定价策略。
Expert Rev Pharmacoecon Outcomes Res. 2024-6
Therap Adv Gastroenterol. 2025-1-2
Expert Rev Pharmacoecon Outcomes Res. 2022-10