Matrix45, Tucson, AZ, USA.
Coherus BioSciences, Inc, Redwood City, CA, USA.
J Med Econ. 2024;27(sup3):1-8. doi: 10.1080/13696998.2024.2331905. Epub 2024 Apr 8.
To estimate, in the setting of recurrent or metastatic nasopharyngeal carcinoma (R/M NPC) for an assumed 1,207 incident US cases in 2024, (1) the cost-efficiency of a toripalimab-gemcitabine-cisplatin regimen compared to a similar pembrolizumab regimen; and (2) the budget-neutral expanded access to additional toripalimab cycles and regimens afforded by the accrued savings.
Simulation modeling utilized two cost inputs (wholesale acquisition cost (WAC) at market entry and an toripalimab price point of 80% of pembrolizumab average sales price (ASP)) and drug administration costs over 1 and 2 years of treatment with treatment rates ranging from 45% to 90%. In the absence of trial data for pembrolizumab-gemcitabine-cisplatin in R/M NPC, it is assumed that such a regimen would be comparable to toripalimab-gemcitabine-cisplatin in efficacy and safety.
In the models utilizing the WAC, toripalimab saves $2,223 per patient per cycle and $40,014 over 1 year of treatment ($77,805 over 2 years). Extrapolated to the 1,207-patient panel, estimated 1-year savings range from $21,733,702 (45% treatment rate) to $43,467,404 (90% rate). Reallocating these savings permits budget-neutral expanded access to an additional 2,359 (45% rate) to 4,717 (90% rate) toripalimab maintenance cycles or to an additional 126 (45% rate) to 252 (90%) full 1-year toripalimab regimens with all agents. Two-year savings range from $42,259,976 (45% rate) to $84,519,952 (90% rate). Reallocating these efficiencies provides expanded access, ranging from an additional 4,586 (45% rate) to 9,172 (90% rate) toripalimab cycles or to an additional 128-257 full 2-year toripalimab regimens. The ASP model showed similar results.
This simulation demonstrates that treatment with toripalimab generates savings that enable budget-neutral funding for up to an additional 252 regimens with toripalimab-gemcitabine-cisplatin for one full year, the equivalent of approximately 21% of the 2024 incident cases of R/M NPC in the US.
在假设 2024 年美国有 1207 例复发性或转移性鼻咽癌(R/M NPC)新发病例的情况下,(1)评估与类似的 pembrolizumab 方案相比,toripalimab-吉西他滨-顺铂方案的成本效益;(2)通过累计节省的资金,为额外的 toripalimab 周期和方案提供预算中性的扩大准入。
模拟模型使用了两个成本投入(市场进入时的批发采购成本(WAC)和 toripalimab 价格为 pembrolizumab 平均销售价格(ASP)的 80%)以及 1 年和 2 年治疗期间的药物管理成本,治疗率从 45%到 90%不等。由于没有 pembrolizumab-吉西他滨-顺铂在 R/M NPC 中的试验数据,假设该方案在疗效和安全性方面与 toripalimab-吉西他滨-顺铂相当。
在使用 WAC 的模型中,toripalimab 每个患者每个周期节省 2223 美元,1 年治疗节省 40014 美元(2 年治疗节省 77805 美元)。在 1207 例患者组中,估计 1 年的节省范围从 21733702 美元(45%的治疗率)到 43467404 美元(90%的治疗率)。重新分配这些节省的资金,可以为额外的 2359 个(45%的治疗率)到 4717 个(90%的治疗率)toripalimab 维持周期或额外的 126 个(45%的治疗率)到 252 个(90%的治疗率)全年度的 toripalimab 方案提供预算中性的扩大准入。两年的节省范围从 42259976 美元(45%的治疗率)到 84519952 美元(90%的治疗率)。重新分配这些效率可以提供额外的准入,范围从额外的 4586 个(45%的治疗率)到 9172 个(90%的治疗率)toripalimab 周期,或额外的 128-257 个全年度的 toripalimab 方案。ASP 模型显示了类似的结果。
这项模拟表明,使用 toripalimab 治疗可产生节省,为 toripalimab-吉西他滨-顺铂方案提供预算中性的资金,最多可再进行一年的 252 个方案,相当于美国 2024 年 R/M NPC 新发病例的约 21%。