Department of Clinical Pharmacy, Skaggs School of Pharmacy and Pharmaceutical Sciences, University of Colorado Anschutz Medical Campus, Aurora.
Institute for Clinical and Economic Review, Boston, Massachusetts.
JAMA Netw Open. 2019 Feb 1;2(2):e190035. doi: 10.1001/jamanetworkopen.2019.0035.
Axicabtagene ciloleucel, a chimeric antigen receptor T-cell therapy, represents a new and potentially curative treatment option for B-cell lymphoma. It is expected to have long-term survival benefits; however, long-term survival data are limited.
To estimate the long-term survival and cost-effectiveness of axicabtagene ciloleucel for treatment of relapsed or refractory B-cell lymphoma.
DESIGN, SETTING, AND PARTICIPANTS: Economic evaluation study using a survival analysis that digitized and extrapolated survival curves published in the ZUMA-1 trial (Safety and Efficacy of KTE-C19 in Adults With Refractory Aggressive Non-Hodgkin Lymphoma), which enrolled patients between November 2015 and September 2016 and had a maximum follow-up of 24 months. Five different survival models (standard parametric, flexible parametric, 2 mixture cure models, and a flexible parametric mixture model) were used to extrapolate the survival curves to a lifetime horizon from January through June 2018. A cost-effectiveness analysis, from both a trial-based and lifetime horizon, was also conducted to inform the value of this novel therapy. The model was based on data from 111 patients with B-cell lymphoma who were enrolled in the ZUMA-1 trial.
One-time administration of axicabtagene ciloleucel compared with chemotherapy.
Undiscounted and discounted life-years (LYs) and quality-adjusted life-years (QALYs), total costs, and incremental costs per LY and QALY gained.
The modeled cohort of 111 patients started at 58 years of age. At the end of the trial, treatment with axicabtagene ciloleucel resulted in 0.48 more LYs and 0.34 more QALYs than chemotherapy, producing a cost-effectiveness estimate of $896 600 per QALY for public payers and $1 615 000 per QALY for commercial payers. Extrapolated long-term survival for patients treated with axicabtagene ciloleucel ranged from 2.83 to 9.19 discounted LYs and from 2.07 to 7.62 discounted QALYs. Incrementally, treatment with axicabtagene ciloleucel was associated with 1.89 to 5.82 discounted LYs and 1.52 to 4.90 discounted QALYs vs chemotherapy. With the use of these incremental estimates of survival, cost-effectiveness estimates ranged from $82 400 to $230 900 per QALY gained for public payers and from $100 400 to $289 000 per QALY gained for commercial payers.
Treatment with axicabtagene ciloleucel appears to be associated with incremental gains in survival over chemotherapy. The range in projected long-term survival was wide and reflected uncertainty owing to limited follow-up data. Cost-effectiveness is associated with long-term survival, with further evidence needed to reduce uncertainty.
嵌合抗原受体 T 细胞疗法 axicabtagene ciloleucel 代表了 B 细胞淋巴瘤的一种新的潜在治愈性治疗选择。预计它具有长期生存获益;然而,长期生存数据有限。
估计 axicabtagene ciloleucel 治疗复发性或难治性 B 细胞淋巴瘤的长期生存和成本效益。
设计、设置和参与者:使用生存分析的经济评估研究,该研究数字化并外推了在 ZUMA-1 试验(KTE-C19 在难治性侵袭性非霍奇金淋巴瘤成人中的安全性和疗效)中发表的生存曲线,该试验纳入了 2015 年 11 月至 2016 年 9 月间的患者,最长随访时间为 24 个月。使用了 5 种不同的生存模型(标准参数、灵活参数、2 种混合治愈模型和灵活参数混合模型),将生存曲线从 2018 年 1 月至 6 月的终身期限进行外推。还进行了基于试验和终身期限的成本效益分析,以提供这种新疗法的价值信息。该模型基于 111 名 B 细胞淋巴瘤患者的数据,这些患者参加了 ZUMA-1 试验。
单次给予 axicabtagene ciloleucel 与化疗相比。
未贴现和贴现寿命年(LY)和质量调整寿命年(QALY)、总费用以及每获得 LY 和 QALY 的增量成本。
111 名患者的模型队列年龄为 58 岁。在试验结束时,与化疗相比,接受 axicabtagene ciloleucel 治疗可获得 0.48 个 LY 和 0.34 个 QALY,公共支付者的成本效益估计为每 QALY 896600 美元,商业支付者为每 QALY 1615000 美元。接受 axicabtagene ciloleucel 治疗的患者的长期生存预期范围为 2.83 至 9.19 个贴现 LY 和 2.07 至 7.62 个贴现 QALY。增量上,与化疗相比,axicabtagene ciloleucel 治疗与 1.89 至 5.82 个贴现 LY 和 1.52 至 4.90 个贴现 QALY 相关。使用这些生存增量估计值,公共支付者的成本效益估计范围为每 QALY 82400 至 230900 美元,商业支付者的成本效益估计范围为每 QALY 100400 至 289000 美元。
接受 axicabtagene ciloleucel 治疗似乎与化疗相比具有生存获益的增量。预测的长期生存范围很广,反映了由于随访数据有限而导致的不确定性。成本效益与长期生存相关,需要进一步的证据来降低不确定性。