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Cost-effectiveness of prophylaxis treatment strategies for febrile neutropenia in patients with recurrent ovarian cancer

机译:复发性卵巢癌患者发热性中性粒细胞减少症的预防性治疗策略的成本效益

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Objective Evaluate the cost-effectiveness of primary prophylaxis (PP) or secondary prophylaxis (SP) with pegfilgrastim, filgrastim (6-day and 11-day), or no prophylaxis to reduce the risk of febrile neutropenia (FN) in patients with recurrent ovarian cancer receiving docetaxel or topotecan. Methods A Markov model was used to evaluate the cost-effectiveness of PP vs SP from a US payer perspective. Model inputs, including the efficacy of each strategy (relative risk of FN with prophylaxis compared to no prophylaxis) and mortality, costs, and utility values were estimated from public sources and peer-reviewed publications. Incremental cost-effectiveness was evaluated in terms of net cost per FN event avoided, incremental cost per life-year saved (LYS), and incremental cost per quality-adjusted life-year (QALY) gained over a lifetime horizon. Deterministic and probabilistic sensitivity analyses (DSA and PSA) were conducted. Results For patients receiving docetaxel, the incremental cost-effectiveness ratio (ICER) for PP vs SP with pegfilgrastim was $7900 per QALY gained, and PP with pegfilgrastim dominated all other comparators. For patients receiving topotecan, PP with pegfilgrastim dominated all comparators. Model results were most sensitive to baseline FN risk. PP vs SP with pegfilgrastim was cost effective in 68% and 83% of simulations for docetaxel and in > 99% of simulations for topotecan at willingness-to-pay thresholds of $50,000 and $100,000 per QALY. Conclusions PP with pegfilgrastim should be considered cost effective compared to other prophylaxis strategies in patients with recurrent ovarian cancer receiving docetaxel or topotecan with a high risk of FN.
机译:目的评估培格非司亭,非格司亭(6天和11天)或不进行预防措施以降低复发性卵巢癌患者发热性中性粒细胞减少症(FN)的风险,以评估其主要预防措施(PP)或次要预防措施(SP)的成本效益接受多西他赛或托泊替康的癌症。方法使用马尔可夫模型从美国付款人的角度评估PP与SP的成本效益。模型输入,包括每种策略的功效(FN与预防相比与FN的相对风险相比,预防与否)以及死亡率,成本和实用价值,均来自公共来源和同行评审的出版物。根据避免的每个FN事件的净成本,每个生命年节省的增量成本(LYS)以及生命周期内每个质量调整生命年的增量成本(QALY)来评估增量成本效益。进行了确定性和概率敏感性分析(DSA和PSA)。结果对于接受多西他赛治疗的患者,每接受QALY接受PP与SP联合使用Pegfilgrastim的成本效益比(ICER)为7900美元,而使用Pegfilgrastim的PP主导其他所有比较者。对于接受拓扑替康的患者,pegfilgrastim的PP占所有比较者的比例。模型结果对基线FN风险最敏感。多西他赛的PP与SP联合培格非司汀的模拟在68%和83%的多西他赛模拟中和99%以上的托泊替康模拟中(每个QALY的支付意愿阈值为50,000和100,000美元)具有成本效益。结论与其他预防策略相比,接受多西他赛或托泊替康的FN风险高的患者,与其他预防策略相比,pegfilgrastim的PP应被认为具有成本效益。

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