Department of Medicine, Division of Medical Oncology, The Ottawa Hospital and University of Ottawa, Ottawa, Canada; Cancer Therapeutics Program, Ottawa Hospital Research Institute, Ottawa, Canada; Clinical Epidemiology Program, Ottawa Hospital Research Institute and School of Epidemiology and Public Health, University of Ottawa, Ottawa, Canada.
Clinical Epidemiology Program, Ottawa Hospital Research Institute and School of Epidemiology and Public Health, University of Ottawa, Ottawa, Canada.
Breast. 2021 Aug;58:42-49. doi: 10.1016/j.breast.2021.03.012. Epub 2021 Apr 1.
Primary febrile neutropenia (FN) prophylaxis with ciprofloxacin or granulocyte-colony stimulating factors (G-CSF) is recommended with docetaxel-cyclophosphamide (TC) chemotherapy for early-stage breast cancer (EBC). A pragmatic randomised trial compared the superiority of G-CSF to ciprofloxacin and a cost-utility analysis were conducted.
EBC patients receiving TC chemotherapy were randomised to ciprofloxacin or G-CSF. The primary outcome was a composite of FN and non-FN treatment-related hospitalisation. Secondary outcomes included; rates of FN, non-FN treatment-related hospitalisation, chemotherapy dose reductions/delays/discontinuations. Primary analysis was performed with the intention to treat population. Cost-utility analyses were conducted from the Canadian public payer perspective.
458 eligible patients were randomised: 228 to ciprofloxacin and 230 to G-CSF. For the primary endpoint there was non-statistically significant difference (Risk difference = -6.7%, 95%CI = -13.5%-0.1%, p = 0.061) between ciprofloxacin patients (46,20.2%) and G-CSF (31,13.5%). Patients receiving ciprofloxacin were more likely to experience FN (36/228, 15.8% vs 13/230, 5.7%) than patients receiving G-CSF (p < 0.001). Non-FN treatment-related hospitalisation occurred in 40/228 (17.5%) of ciprofloxacin patients vs 28/230 (12.2%) of G-CSF patients (p = 0.12). There were no differences in other secondary outcomes. G-CSF was associated with an incremental cost-effectiveness ratio of C$1,760,796 per one quality-adjusted life year gained.
The primary endpoint of superiority of G-CSF over ciprofloxacin was not demonstrated. While there were reduced FN rates with G-CSF, there were no differences in chemotherapy dose delays/reductions or discontinuations. With the commonly used willingness to pay value of C$50,000/QALY, G-CSF use was not cost-effective compared to ciprofloxacin and deserves scrutiny from the payer perspective.
对于接受多西他赛-环磷酰胺(TC)化疗的早期乳腺癌(EBC)患者,建议使用环丙沙星或粒细胞集落刺激因子(G-CSF)进行原发性发热性中性粒细胞减少症(FN)预防。一项实用随机试验比较了 G-CSF 优于环丙沙星的优越性,并进行了成本效益分析。
接受 TC 化疗的 EBC 患者被随机分配至环丙沙星或 G-CSF 组。主要结局是 FN 和非 FN 治疗相关住院的复合结局。次要结局包括 FN 发生率、非 FN 治疗相关住院率、化疗剂量减少/延迟/中断率。主要分析采用意向治疗人群。成本效益分析从加拿大公共支付方的角度进行。
458 名符合条件的患者被随机分组:228 名接受环丙沙星治疗,230 名接受 G-CSF 治疗。在主要终点方面,环丙沙星组(46 例,20.2%)与 G-CSF 组(31 例,13.5%)之间无统计学显著差异(风险差=-6.7%,95%CI=-13.5%~0.1%,p=0.061)。接受环丙沙星治疗的患者更有可能发生 FN(36/228,15.8%比 13/230,5.7%)(p<0.001)。228 名环丙沙星患者中有 40 名(17.5%)和 230 名 G-CSF 患者中有 28 名(12.2%)发生非 FN 治疗相关住院(p=0.12)。其他次要结局无差异。G-CSF 每获得一个质量调整生命年的增量成本效益比为 1760796 加元。
未证明 G-CSF 优于环丙沙星的主要终点。虽然 G-CSF 降低 FN 发生率,但化疗剂量延迟/减少或中断无差异。使用常用的 50000 加元/QALY 的意愿支付值,与环丙沙星相比,G-CSF 的使用并不具有成本效益,值得从支付方角度进行审查。