Liao Weiting, Xu Huiqiong, Hutton David, Wu Qiuji, Yang Yang, Feng Mingyang, Lei Wanting, Bai Liangliang, Li Junying, Li Qiu
Department of Medical Oncology, Cancer Center, West China Hospital, Sichuan University, Chengdu, China.
West China Biomedical Big Data Center, Sichuan University, Chengdu, China.
Ther Adv Med Oncol. 2024 Sep 18;16:17588359241274625. doi: 10.1177/17588359241274625. eCollection 2024.
The HIMALAYA trial found that durvalumab plus tremelimumab significantly prolonged progression-free survival and overall survival in patients with unresectable hepatocellular carcinoma (HCC) compared with sorafenib.
This study aimed to investigate the cost-effectiveness of durvalumab plus tremelimumab compared with sorafenib in the first-line HCC setting.
A Markov model-based cost-effectiveness analysis.
We created a Markov model to compare healthcare costs and clinical outcomes of HCC patients treated with durvalumab plus tremelimumab in the first-line setting compared with sorafenib. We estimated transition probabilities from randomized trials. Lifetime direct healthcare costs, quality-adjusted life-years (QALYs), and incremental cost-effectiveness ratios were calculated for first-line durvalumab plus tremelimumab compared with sorafenib from a US payer's perspective.
In the base case, first-line durvalumab plus tremelimumab was associated with an improvement of 0.29 QALYs compared with sorafenib. While both treatment strategies were associated with considerable lifetime expenditures, first-line durvalumab plus tremelimumab was less expensive than sorafenib ($188,405 vs $218,584). The incremental net monetary benefit for durvalumab plus tremelimumab versus sorafenib was $72,762 (valuing QALYs at $150,000 each). The results of durvalumab plus tremelimumab were better in terms of costs and health outcomes in patients with HBV-related HCC and high alpha-fetoprotein levels.
First-line durvalumab plus tremelimumab was estimated to be dominant for the treatment of unresectable HCC compared with sorafenib from a US payer's perspective.
喜马拉雅试验发现,与索拉非尼相比,度伐利尤单抗联合曲美木单抗可显著延长不可切除肝细胞癌(HCC)患者的无进展生存期和总生存期。
本研究旨在探讨在一线HCC治疗中,度伐利尤单抗联合曲美木单抗与索拉非尼相比的成本效益。
基于马尔可夫模型的成本效益分析。
我们创建了一个马尔可夫模型,以比较一线使用度伐利尤单抗联合曲美木单抗与索拉非尼治疗的HCC患者的医疗成本和临床结局。我们从随机试验中估算转移概率。从美国医保支付方的角度计算一线使用度伐利尤单抗联合曲美木单抗与索拉非尼相比的终身直接医疗成本、质量调整生命年(QALY)和增量成本效益比。
在基础病例中,与索拉非尼相比,一线使用度伐利尤单抗联合曲美木单抗可使QALY提高0.29。虽然两种治疗策略都与相当高的终身支出相关,但一线使用度伐利尤单抗联合曲美木单抗的成本低于索拉非尼(188,405美元对218,584美元)。度伐利尤单抗联合曲美木单抗相对于索拉非尼的增量净货币效益为72,762美元(每个QALY价值150,000美元)。在乙肝相关HCC和高甲胎蛋白水平的患者中,度伐利尤单抗联合曲美木单抗在成本和健康结局方面的结果更好。
从美国医保支付方的角度来看,估计一线使用度伐利尤单抗联合曲美木单抗治疗不可切除HCC比索拉非尼更具优势。