Institute for Technology Assessment, Massachusetts General Hospital, Boston.
Massachusetts General Hospital Cancer Center, Boston.
JAMA Netw Open. 2019 Sep 4;2(9):e1911952. doi: 10.1001/jamanetworkopen.2019.11952.
Immune checkpoint inhibitor combination therapy has recently become the standard of care for first-line treatment of metastatic nonsquamous non-small cell lung cancer. The implications of these first-line treatments are considerable, given the potential population of patients eligible to receive them and their high cost.
To evaluate the cost-effectiveness of adding atezolizumab to bevacizumab, carboplatin, and paclitaxel as a first-line treatment strategy for patients with metastatic nonsquamous non-small cell lung cancer in the United States.
DESIGN, SETTING, AND PARTICIPANTS: In this economic evaluation, a primary microsimulation model was developed to assess atezolizumab combination vs bevacizumab, carboplatin, and paclitaxel alone in the first line (base case 1). A secondary model was developed to assess these treatments along with pembrolizumab combination and platinum doublet chemotherapy (base case 2). Treatment strategies and other simulated conditions were based on those from the IMpower150 and KEYNOTE-189 clinical trials. The study perspective was the US health care sector. One million patients with metastatic nonsquamous non-small cell lung cancer were simulated for each treatment group. This study was performed from February 2019 through May 2019.
Incremental cost-effectiveness ratios were compared with a willingness-to-pay threshold of $100 000 per quality-adjusted life-year (QALY).
In base case 1, in which 1 million patients were simulated, treating with bevacizumab, carboplatin, and paclitaxel in the first line was associated with a mean cost of $112 551 (95% CI, $112 450-$112 653) and a mean survival of 1.48 QALYs (95% CI, 1.47-1.48 QALYs) per patient. Atezolizumab plus bevacizumab, carboplatin, and paclitaxel was associated with a mean cost of $244 166 (95% CI, $243 864-$244 468) and a mean survival of 2.13 QALYs (95% CI, 2.12-2.13 QALYs) per patient, for an estimated incremental cost-effectiveness ratio of $201 676 per QALY (95% CI, $198 105-$205 355 per QALY). In base case 2, in which 1 million patients were simulated, pembrolizumab combination therapy was associated with a mean cost of $226 282 (95% CI, $226 007-$226 557) and a mean survival of 2.45 QALYs (95% CI, 2.44-2.46 QALYs) per patient. Pembrolizumab combination dominated atezolizumab plus bevacizumab, carboplatin, and paclitaxel, leading to an incremental cost-effectiveness ratio of $116 698 per QALY (95% CI, $115 088-$118 342 per QALY) between pembrolizumab combination and bevacizumab, carboplatin, and paclitaxel. Atezolizumab combination was not cost-effective at a willingness-to-pay threshold of $100 000 per QALY.
In this simulated model economic analysis, atezolizumab combination was not cost-effective compared with bevacizumab, carboplatin, and paclitaxel and provided suboptimal incremental benefit compared with cost vs pembrolizumab combination for first-line treatment. Although atezolizumab combination therapy provides clinical benefits, price reductions may be necessary for this treatment strategy to become cost-effective.
重要性:免疫检查点抑制剂联合治疗最近已成为转移性非鳞状非小细胞肺癌一线治疗的标准治疗方法。鉴于有资格接受这些一线治疗的患者人群以及其高昂的成本,这些一线治疗的意义重大。
目的:评估在转移性非鳞状非小细胞肺癌患者中,添加阿特珠单抗联合贝伐珠单抗、卡铂和紫杉醇作为一线治疗策略的成本效益。
设计、设置和参与者:在这项经济评估中,开发了一个主要的微观模拟模型,以评估在转移性非鳞状非小细胞肺癌患者中,阿特珠单抗联合贝伐珠单抗、卡铂和紫杉醇作为一线治疗的情况(基础案例 1)。还开发了一个二级模型,以评估这些治疗方法与帕博利珠单抗联合和铂类双药化疗(基础案例 2)的联合应用。治疗策略和其他模拟条件基于 IMpower150 和 KEYNOTE-189 临床试验。研究的观点是美国医疗保健部门。为每个治疗组模拟了 100 万名转移性非鳞状非小细胞肺癌患者。本研究于 2019 年 2 月至 2019 年 5 月进行。
主要结果和措施:比较了增量成本效益比与 100000 美元/QALY 的意愿支付阈值。
结果:在基础案例 1 中,模拟了 100 万名患者,贝伐珠单抗、卡铂和紫杉醇一线治疗的平均成本为 112551 美元(95%CI,112450-112653 美元),平均生存时间为 1.48 QALY(95%CI,1.47-1.48 QALY)/患者。阿特珠单抗联合贝伐珠单抗、卡铂和紫杉醇的平均成本为 244166 美元(95%CI,243864-244468 美元),平均生存时间为 2.13 QALY(95%CI,2.12-2.13 QALY)/患者,估计增量成本效益比为 201676 美元/QALY(95%CI,198105-205355 美元/QALY)。在基础案例 2 中,模拟了 100 万名患者,帕博利珠单抗联合治疗的平均成本为 226282 美元(95%CI,226007-226557 美元),平均生存时间为 2.45 QALY(95%CI,2.44-2.46 QALY)/患者。帕博利珠单抗联合治疗在成本效益上优于阿特珠单抗联合贝伐珠单抗、卡铂和紫杉醇,导致在帕博利珠单抗联合治疗与贝伐珠单抗、卡铂和紫杉醇之间,增量成本效益比为 116698 美元/QALY(95%CI,115088-118342 美元/QALY)。在 100000 美元/QALY 的意愿支付阈值下,阿特珠单抗联合治疗不具有成本效益。
结论和相关性:在这个模拟模型经济分析中,与贝伐珠单抗、卡铂和紫杉醇相比,阿特珠单抗联合治疗不具有成本效益,与帕博利珠单抗联合治疗相比,提供的增量效益不佳,且成本较高。尽管阿特珠单抗联合治疗提供了临床益处,但可能需要降低价格才能使这种治疗策略具有成本效益。