Center for Health Outcomes and PharmacoEconomic Research, College of Pharmacy, The University of Arizona, Tucson.
Department of Pharmacy Practice and Science, College of Pharmacy, The University of Arizona, Tucson.
JAMA Dermatol. 2019 Jan 1;155(1):22-28. doi: 10.1001/jamadermatol.2018.3958.
A phase 2 trial comparing talimogene laherparepvec plus ipilimumab vs ipilimumab monotherapy in patients with advanced unresectable melanoma found no differential benefit in progression-free survival (PFS) but noted objective response rates (ORRs) of 38.8% (38 of 98 patients) vs 18.0% (18 of 100 patients), respectively.
To perform an economic evaluation of talimogene laherparepvec plus ipilimumab combination therapy vs ipilimumab monotherapy.
DESIGN, SETTING, AND PARTICIPANTS: For PFS, cost-effectiveness and cost-utility analyses using a 2-state Markov model (PFS vs progression or death) was performed. For ORRs, cost-effectiveness analysis of the incremental cost of 1 additional patient achieving objective response was performed. In this setting based on a US payer perspective (2017 US dollars), participants were patients with advanced unresectable melanoma.
The PFS life-years and PFS quality-adjusted life-years were determined, and the associated incremental cost-effectiveness ratios (ICERs) and incremental cost-utility ratios (ICURs) were estimated. Also estimated was the ICER per 1 additional patient (out of 100 treated patients) achieving objective response. Base-case analyses were validated by sensitivity analyses.
In PFS analyses, the cost of talimogene laherparepvec plus ipilimumab ($494 983) exceeded the cost of ipilimumab monotherapy ($132 950) by $362 033. The ICER was $2 129 606 per PFS life-years, and the ICUR was $2 262 706 per PFS quality-adjusted life-year gained. Probabilistic sensitivity analyses yielded an ICER of $1 481 208 per PFS life-year gained and an ICUR of $1 683 191 per PFS quality-adjusted life-year gained. In 1-way sensitivity analyses, the PFS hazard ratio and the utility of response were the most influential parameters. Talimogene laherparepvec plus ipilimumab has a 50% likelihood of being cost-effective at a willingness-to-pay threshold of $1 683 191 per PFS quality-adjusted life-year gained. In ORR analyses, talimogene laherparepvec plus ipilimumab ($474 904) vs ipilimumab alone ($132 810), a $342 094 difference, yielded an ICER of $1 629 019 per additional patient achieving objective response. In subgroup analyses by disease stage and BRAFV600E mutation status, ICERs ranged from $1 069 044 to $17 104 700 per 1 additional patient achieving objective response.
The cost to gain 1 additional progression-free quality-adjusted life-year, 1 additional progression-free life-year, or to have 1 additional patient attain objective response is about $1.6 million. This amount may be beyond what payers typically are willing to pay. Combination therapy of talimogene laherparepvec plus ipilimumab does not offer an economically beneficial treatment option relative to ipilimumab monotherapy at the population level. This should not preclude treatment for individual patients for whom this regimen may be indicated.
一项比较替莫唑胺拉赫帕维普韦联合伊匹单抗与伊匹单抗单药治疗晚期不可切除黑色素瘤患者的 2 期试验发现,无进展生存期(PFS)无差异获益,但观察到客观缓解率(ORR)分别为 38.8%(98 例患者中的 38 例)和 18.0%(100 例患者中的 18 例)。
对替莫唑胺拉赫帕维普韦联合伊匹单抗与伊匹单抗单药治疗进行经济评估。
设计、设置和参与者:对于 PFS,使用 2 状态马尔可夫模型(PFS 与进展或死亡)进行成本效益和成本效用分析。对于 ORR,进行了额外 1 例患者达到客观缓解的增量成本的成本效益分析。在此基础上,基于美国支付者的角度(2017 年美元),参与者为晚期不可切除黑色素瘤患者。
确定了 PFS 寿命年数和 PFS 质量调整寿命年数,并估计了相关的增量成本效益比(ICER)和增量成本效用比(ICUR)。还估计了每 100 例接受治疗的患者中额外 1 例达到客观缓解的 ICER。通过敏感性分析验证了基本案例分析。
在 PFS 分析中,替莫唑胺拉赫帕维普韦联合伊匹单抗的费用($494983)超过伊匹单抗单药的费用($132950)$362033。ICER 为每 PFS 寿命年 2129606 美元,ICUR 为每 PFS 质量调整寿命年增加 2262706 美元。概率敏感性分析得出的 ICER 为每 PFS 寿命年 1481208 美元,ICUR 为每 PFS 质量调整寿命年 1683191 美元。在 1 种敏感性分析中,PFS 风险比和反应的效用是最具影响力的参数。替莫唑胺拉赫帕维普韦联合伊匹单抗在支付意愿阈值为每 PFS 质量调整寿命年 1683191 美元时,有 50%的可能性具有成本效益。在 ORR 分析中,替莫唑胺拉赫帕维普韦联合伊匹单抗($474904)与伊匹单抗单药($132810)相比,差异为$342094,产生的每额外 1 例患者达到客观缓解的 ICER 为 1629019 美元。在按疾病阶段和 BRAFV600E 突变状态进行的亚组分析中,ICER 范围为每额外 1 例患者达到客观缓解的 1069044 美元至 17104700 美元。
每增加 1 个无进展质量调整寿命年、1 个无进展寿命年或每增加 1 例患者达到客观缓解的成本约为 160 万美元。这一数额可能超出了支付者通常愿意支付的水平。与伊匹单抗单药治疗相比,替莫唑胺拉赫帕维普韦联合伊匹单抗的治疗在人群水平上并没有提供经济上有益的治疗选择。这不应排除为那些可能适合这种治疗方案的患者进行治疗。