Department of Hematology and Hematopoietic Cell Transplantation, City of Hope National Medical Center, Duarte, CA.
Center for Digestive Health, Penn Medicine Princeton Medical Center, Plainsboro, NJ.
Blood. 2022 Dec 22;140(25):2697-2708. doi: 10.1182/blood.2022016624.
In patients with treatment-naive diffuse large B-cell lymphoma (DLBCL), the POLARIX study (A Study Comparing the Efficacy and Safety of Polatuzumab Vedotin With Rituximab-Cyclophosphamide, Doxorubicin, and Prednisone [R-CHP] Versus Rituximab-Cyclophosphamide, Doxorubicin, Vincristine, and Prednisone [R-CHOP] in Participants With Diffuse Large B-Cell Lymphoma) reported a 6.5% improvement in the 2-year progression-free survival (PFS), with no difference in overall survival (OS) or safety using polatuzumab vedotin, rituximab, cyclophosphamide, doxorubicin, and prednisone (pola-R-CHP) compared with standard rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone (R-CHOP). We evaluated the cost-effectiveness of pola-R-CHP for DLBCL. We modeled a hypothetical cohort of US adults (mean age, 65 years) with treatment-naive DLBCL by developing a Markov model (lifetime horizon) to model the cost-effectiveness of pola-R-CHP and R-CHOP using a range of plausible long-term outcomes. Progression rates and OS were estimated from POLARIX. Outcome measures were reported in incremental cost-effectiveness ratios, with a willingness-to-pay (WTP) threshold of $150 000 per quality-adjusted life-year (QALY). Assuming a 5-year PFS of 69.6% with pola-R-CHP and 62.7% with R-CHOP, pola-R-CHP was cost-effective at a WTP of $150 000 (incremental cost-effectiveness ratio, $84 308/QALY). pola-R-CHP was no longer cost-effective if its 5-year PFS was 66.1% or lower. One-way sensitivity analysis revealed that pola-R-CHP is cost-effective up to a cost of $276 312 at a WTP of $150 000. pola-R-CHP was the cost-effective strategy in 56.6% of the 10 000 Monte Carlo iterations at a WTP of $150 000. If the absolute benefit in PFS is maintained over time, pola-R-CHP is cost-effective compared with R-CHOP at a WTP of $150 000/QALY. However, its cost-effectiveness is highly dependent on its long-term outcomes and costs of chimeric antigen receptor T-cell therapy. Routine usage of pola-R-CHP would add significantly to health care expenditures. Price reductions or identification of subgroups that have maximal benefit would improve cost-effectiveness.
在未经治疗的弥漫性大 B 细胞淋巴瘤 (DLBCL) 患者中,POLARIX 研究报告称,与标准利妥昔单抗、环磷酰胺、多柔比星、长春新碱和泼尼松(R-CHOP)相比,使用泊洛妥珠单抗联合利妥昔单抗、环磷酰胺、多柔比星和泼尼松(pola-R-CHP)可将 2 年无进展生存率(PFS)提高 6.5%,总生存(OS)或安全性无差异。我们评估了 pola-R-CHP 治疗 DLBCL 的成本效益。我们通过开发一个马尔可夫模型(终生)来评估美国成年人(平均年龄 65 岁)未经治疗的 DLBCL 的假设队列,该模型用于根据各种可能的长期结果来模拟 pola-R-CHP 和 R-CHOP 的成本效益。进展率和 OS 是从 POLARIX 中估计的。结果测量报告为增量成本效益比,意愿支付 (WTP) 阈值为每质量调整生命年 (QALY) 150000 美元。假设使用 pola-R-CHP 的 5 年 PFS 为 69.6%,使用 R-CHOP 的 5 年 PFS 为 62.7%,则在 WTP 为 150000 美元时,pola-R-CHP 具有成本效益(增量成本效益比为 84308 美元/QALY)。如果 5 年 PFS 为 66.1%或更低,则 pola-R-CHP 不再具有成本效益。单向敏感性分析表明,在 WTP 为 150000 美元时,pola-R-CHP 的成本效益高达 276312 美元。在 WTP 为 150000 美元时,pola-R-CHP 在 10000 次蒙特卡罗迭代中的 56.6%情况下是具有成本效益的策略。如果 PFS 的绝对获益能够随着时间的推移保持不变,那么与 R-CHOP 相比,pola-R-CHP 在 WTP 为 150000 美元/QALY 时具有成本效益。然而,其成本效益高度依赖于其长期结果和嵌合抗原受体 T 细胞治疗的成本。常规使用 pola-R-CHP 将显著增加医疗保健支出。降低价格或确定具有最大获益的亚组将提高成本效益。