University of Waterloo School of Pharmacy, Waterloo, Ontario, Canada.
Sunnybrook Odette Cancer Centre, Toronto, Ontario, Canada.
Oncologist. 2018 Feb;23(2):225-233. doi: 10.1634/theoncologist.2017-0277. Epub 2017 Oct 11.
Treatment options for patients with platinum-refractory, recurrent, metastatic head and neck squamous cell carcinoma (r/m HNSCC) are limited and prognosis is poor. The recent CheckMate 141 clinical trial demonstrated that nivolumab, an anti-programmed cell death protein 1 monoclonal antibody, was efficacious in extending the median overall survival (OS) in this patient population compared with standard therapies. We conducted a cost-effectiveness analysis to determine whether nivolumab is a cost-effective treatment in this patient population and examined various subgroups to determine for which, if any, the treatment is more cost-effective.
We implemented a state transition model for HNSCC with a patient cohort who had tumor progression 6 months after the last dose of platinum-containing chemotherapy and compared the cost-effectiveness of nivolumab with docetaxel. Treatment effect estimates and adverse event rates were obtained from CheckMate 141. Costs, utilities, and other model inputs were gathered from published sources. We used a Canadian perspective, a 5-year time horizon, and a 1.5% discount rate for the analysis.
Nivolumab extended mean OS by 4 months compared with docetaxel and resulted in fewer treatment-related adverse events, producing an incremental effectiveness of 0.13 quality-adjusted life years (QALY). The incremental cost of treatment with nivolumab was $18,823. At a willingness-to-pay threshold of $100,000/QALY, nivolumab was not a cost-effective treatment option for r/m HNSCC, with an incremental cost-effectiveness ratio of $144,744/QALY. Nivolumab would be cost-effective if its price was reduced by 20%. Our subgroup analysis seemed to indicate that nivolumab might be cost-effective for tumors with expression of programmed death-ligand 1 >5%.
We conclude that although nivolumab offers clinical benefit for the treatment of r/m HNSCC over current regimens, it is not cost-effective based on its list price. We have also established a value-based price estimate for nivolumab to be cost-effective in this patient population. Further study is required to draw a definitive conclusion on biomarkers for cost-effectiveness.
In health care settings in which cost considerations are a constraint on choice of therapy, patient selection should be carefully considered to maintain efficiency in the system. Until a biomarker for response to therapy is identified for nivolumab, this medication is unlikely to be cost-effective for most patients with recurrent, metastatic head and neck squamous cell carcinoma.
铂类耐药、复发、转移性头颈部鳞状细胞癌(r/m HNSCC)患者的治疗选择有限,预后较差。最近的 CheckMate 141 临床试验表明,抗程序性死亡蛋白 1 单克隆抗体纳武利尤单抗可延长此类患者的中位总生存期(OS),与标准治疗相比具有疗效。我们进行了一项成本效益分析,以确定纳武利尤单抗在该患者人群中的治疗是否具有成本效益,并对各种亚组进行了检查,以确定该药物在哪些方面更具成本效益。
我们为接受含铂化疗后 6 个月肿瘤进展的患者实施了头颈部鳞状细胞癌的状态转移模型,并比较了纳武利尤单抗与多西他赛的成本效益。从 CheckMate 141 中获得治疗效果估计和不良事件发生率。成本、效用和其他模型输入均来自已发表的来源。我们使用加拿大视角、5 年时间范围和 1.5%的贴现率进行分析。
与多西他赛相比,纳武利尤单抗延长了平均 OS 4 个月,并减少了治疗相关的不良事件,从而产生了 0.13 个质量调整生命年(QALY)的增量有效性。纳武利尤单抗的增量治疗成本为 18823 美元。在 100000 美元/QALY 的意愿支付阈值下,纳武利尤单抗对 r/m HNSCC 不是一种具有成本效益的治疗选择,增量成本效益比为 144744 美元/QALY。如果纳武利尤单抗的价格降低 20%,则它将具有成本效益。我们的亚组分析似乎表明,对于 PD-L1 表达>5%的肿瘤,纳武利尤单抗可能具有成本效益。
我们的结论是,尽管纳武利尤单抗为 r/m HNSCC 的治疗提供了优于现有方案的临床益处,但根据其定价,它并不具有成本效益。我们还确定了纳武利尤单抗在该患者人群中具有成本效益的基于价值的价格估算。需要进一步研究以确定治疗反应的生物标志物,从而得出明确的成本效益结论。
在考虑成本因素是治疗选择的限制因素的医疗保健环境中,应仔细考虑患者选择,以保持系统的效率。在确定纳武利尤单抗治疗反应的生物标志物之前,该药物对大多数复发、转移性头颈部鳞状细胞癌患者不太可能具有成本效益。