Analysis Group, Inc., Los Angeles, CA 90071, USA.
F. Hoffmann-La Roche Ltd, Basel, Switzerland.
J Comp Eff Res. 2020 Oct;9(14):1003-1015. doi: 10.2217/cer-2020-0057. Epub 2020 Oct 8.
To evaluate the cost-effectiveness of polatuzumab vedotin (pola) + bendamustine + rituximab (BR) in relapsed/refractory diffuse large B-cell lymphoma based on the GO29365 trial from a US payer's perspective. A partitioned survival model used progression-free survival and overall survival data from the GO29365 trial. The base case analysis assumed overall survival was informed by progression-free survival; a mixture cure model estimated proportion of long-term survivors. In the base case, pola + BR was cost-effective versus BR at US$35,864 per quality-adjusted life year gained. Probabilistic and one-way sensitivity analyses showed that the findings were robust. Pola + BR is cost-effective versus BR for the treatment of transplant-ineligible relapsed/refractory diffuse large B-cell lymphoma in the US.
评估基于 GO29365 试验的泊洛妥珠单抗联合苯达莫司汀和利妥昔单抗(BR)治疗复发/难治性弥漫性大 B 细胞淋巴瘤的成本效果,从美国支付者角度出发。 采用分区生存模型,利用 GO29365 试验的无进展生存期和总生存期数据。 基础病例分析假设总生存期由无进展生存期推断;混合治愈模型估计长期生存者的比例。 在基础病例中,泊洛妥珠单抗联合 BR 比 BR 每获得一个质量调整生命年的成本增加 35864 美元。概率敏感性分析和单向敏感性分析显示结果具有稳健性。 泊洛妥珠单抗联合 BR 治疗美国不适合移植的复发/难治性弥漫性大 B 细胞淋巴瘤是具有成本效果的。