Fust Kelly, Parthan Anju, Maschio Michael, Gu Qing, Li Xiaoyan, Lyman Gary H, Tzivelekis Spiros, Villa Guillermo, Weinstein Milton C
a Health Economics & Outcomes Research, Optum , Boston , MA , USA.
b Health Economics & Outcomes Research, Optum , Burlington , ON , Canada.
Expert Rev Pharmacoecon Outcomes Res. 2017 Feb;17(1):39-52. doi: 10.1080/14737167.2017.1276829. Epub 2017 Jan 20.
We reviewed the evolution of the methods used in cost-effectiveness analyses of granulocyte colony-stimulating factors (G-CSFs) in the primary and secondary prevention of febrile neutropenia (FN) in patients receiving myelosuppressive cancer chemotherapy. Areas covered: FN is a side effect of myelosuppressive chemotherapy associated with significant morbidity, mortality, and costs. The risk of FN may depend on the drugs used within a chemotherapy regimen, and an FN event may cause chemotherapy dose reductions or delays in subsequent cycles. Expert commentary: More recent pharmacoeconomic models have reflected these clinical observations by modeling sequential chemotherapy regimens to account for FN risk on a per-cycle basis, and by accounting for chemotherapy dose reductions and consequent survival losses.
我们回顾了在接受骨髓抑制性癌症化疗的患者中,粒细胞集落刺激因子(G-CSFs)用于发热性中性粒细胞减少症(FN)一级和二级预防的成本效益分析方法的演变。涵盖领域:FN是骨髓抑制性化疗的一种副作用,与显著的发病率、死亡率和成本相关。FN的风险可能取决于化疗方案中使用的药物,并且一次FN事件可能导致化疗剂量减少或后续周期的延迟。专家评论:最近的药物经济学模型通过对序贯化疗方案进行建模以逐周期考虑FN风险,并通过考虑化疗剂量减少及随之而来的生存损失,反映了这些临床观察结果。