Department of Oncology, Xiangya Hospital, Central South University, Changsha, China.
Department of Gastroenterology, Xiangya Hospital, Central South University, Changsha, China.
Front Endocrinol (Lausanne). 2022 Jul 14;13:909333. doi: 10.3389/fendo.2022.909333. eCollection 2022.
Two targeted drugs (apatinib and lenvatinib) show clinical efficacy in first-line treatment of Chinese patients with radioactive advanced iodine-refractory differentiated thyroid cancer (RAIR-DTC) and are recommended by the Chinese Society of Clinical Oncology guidelines. Considering the high clinical cost of long-term vascular endothelial growth factor receptor inhibitor administration and to determine which of the two targeted drugs is preferable, we opted to conduct a cost-effectiveness analysis (CEA) and network meta-analysis (NMA).
The results of NMA and CEA included in the two phase III randomized clinical trials REALITY (NCT03048877) and Study-308 (NCT02966093), in which Bayesian NMA and CEA were performed on 243 and 149 Chinese patients, respectively, were retrieved. Overall survival and progression-free survival (PFS) for apatinib versus lenvatinib were determined by NMA. CEA involved the development of a 20-year Markov model to obtain the total cost and quality-adjusted life-years (QALYs), and this was followed by sensitivity and subgroup analyses.
Compared with lenvatinib, apatinib therapy provided a 0.837 improvement in QALY and $6,975 reduction in costs. The hazard ratio of apatinib versus lenvatinib and the cost of the targeted drugs had a significant impact on the model. According to the sensitivity analysis, apatinib was more cost-effective and had no correlation with willingness-to-pay in China. Subgroup analysis showed that apatinib maintained PFS more economically.
NMA and CEA demonstrated that apatinib was more cost-effective compared to lenvatinib in the first-line treatment of Chinese RAIR-DTC patients.
两种靶向药物(阿帕替尼和仑伐替尼)在治疗中国放射性碘难治性分化型甲状腺癌(RAIR-DTC)患者的一线治疗中显示出临床疗效,并被中国临床肿瘤学会指南推荐。考虑到长期血管内皮生长因子受体抑制剂治疗的高临床成本,并确定两种靶向药物中哪种更优,我们选择进行成本效益分析(CEA)和网络荟萃分析(NMA)。
从两项 III 期随机临床试验 REALITY(NCT03048877)和 Study-308(NCT02966093)中检索到包含在 NMA 和 CEA 中的结果,分别对 243 例和 149 例中国患者进行了贝叶斯 NMA 和 CEA。通过 NMA 确定阿帕替尼与仑伐替尼相比的总生存期和无进展生存期(PFS)。CEA 涉及开发一个 20 年的马尔可夫模型,以获得总成本和质量调整生命年(QALYs),然后进行敏感性和亚组分析。
与仑伐替尼相比,阿帕替尼治疗可提高 0.837 的 QALY 并降低 6975 美元的成本。阿帕替尼与仑伐替尼的风险比和靶向药物的成本对模型有显著影响。根据敏感性分析,阿帕替尼在成本效益方面更具优势,在中国与支付意愿无关。亚组分析表明,阿帕替尼在 PFS 方面更具经济性。
NMA 和 CEA 表明,与仑伐替尼相比,阿帕替尼在治疗中国 RAIR-DTC 患者的一线治疗中更具成本效益。