Public Health Sciences Division, Fred Hutchinson Cancer Research Center and University of Washington Department of Medicine, Seattle, WA 98109, USA.
Value Health. 2009 Mar-Apr;12(2):217-25. doi: 10.1111/j.1524-4733.2008.00434.x. Epub 2008 Jul 31.
Prophylaxis with granulocyte colony-stimulating factor (G-CSF) reduces the risk of febrile neutropenia (FN) in patients receiving myelosuppressive chemotherapy. We estimated the incremental cost-effectiveness of G-CSF pegfilgrastim primary (starting in cycle 1 and continuing in subsequent cycles of chemotherapy) versus secondary (only after an FN event) prophylaxis in women with early-stage breast cancer receiving myelosuppressive chemotherapy with a >or=20% FN risk.
A decision-analytic model was constructed from a health insurer's perspective with a lifetime study horizon. The model considers direct medical costs and outcomes related to reduced FN and potential survival benefits because of reduced FN-related mortality. Inputs for the model were obtained from the medical literature. Sensitivity analyses were conducted across plausible ranges in parameter values.
The incremental cost-effectiveness ratio (ICER) of pegfilgrastim as primary versus secondary prophylaxis was $48,000/FN episode avoided. Adding survival benefit from avoiding FN mortality yielded an ICER of $110,000/life-year gained (LYG) or $116,000/quality-adjusted life-year (QALY) gained. The most influential factors included FN case-fatality, FN relative risk reduction from primary prophylaxis, and age at diagnosis.
Compared with secondary prophylaxis, the cost-effectiveness of pegfilgrastim as primary prophylaxis may be equivalent or superior to other commonly used supportive care interventions for women with breast cancer. Further assessment of the direct impact of G-CSF on short- and long-term survival is needed to substantiate these findings.
粒细胞集落刺激因子(G-CSF)预防可降低接受骨髓抑制化疗的患者发生发热性中性粒细胞减少症(FN)的风险。我们评估了 G-CSF 培非格司亭原(起始于第 1 周期且持续于化疗的后续周期)与继发(仅在 FN 事件后)预防在接受>20%FN 风险的骨髓抑制化疗的早期乳腺癌女性中的增量成本效益。
从保险公司的角度构建了一个具有终生研究时间的决策分析模型。该模型考虑了降低 FN 相关的直接医疗成本和潜在的生存获益,这些获益可能归因于降低 FN 相关死亡率。模型的输入数据来自医学文献。在参数值的合理范围内进行了敏感性分析。
培非格司亭原与继发预防相比,FN 每避免一个 FN 事件的增量成本效益比(ICER)为 48000 美元。加入 FN 死亡率降低的生存获益后,ICER 为 110000 美元/LYG 或 116000 美元/QALY 获益。最具影响力的因素包括 FN 病死率、FN 相对风险降低率和诊断时的年龄。
与继发预防相比,培非格司亭原作为预防的成本效益可能与乳腺癌女性常用的其他支持性护理干预相当或更优。需要进一步评估 G-CSF 对短期和长期生存的直接影响,以证实这些发现。