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Home administration of filgrastim (Nivestim?) in primary prophylaxis of chemotherapy-induced febrile neutropenia

机译:非格司亭(Nivestim?)的家庭管理主要用于预防化疗引起的发热性中性粒细胞减少

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Background: The granulocyte-colony stimulating factor (G-CSF) biosimilar filgrastim (Nivestim?) reduces the duration and severity of neutropenia and the frequency of occurrence of febrile neutropenia (FN). Administration of this biosimilar filgrastim and the patient population receiving it at home have not been sufficiently documented in day-to-day medical practice. Insight into home administration may help optimize the management of FN in this setting, potentially at a reduced cost and patient burden vs hospital administration. Materials and methods: This was a prospective, non-interventional, non-comparative, multisite study involving 171 patients across 29 sites treated with at least one dose of filgrastim. Mean age was 59.3 years, and most patients were female and G-CSF-na?ve. The data collected originated from paper-based patient questionnaires and routine documentation by the treating physicians. The primary endpoint was the characterization of patients treated with filgrastim. Secondary endpoints were satisfaction with filgrastim, effectiveness, safety and tolerability, and compliance with prescription. Results: Most patients had solid tumors (95.9%), mainly located in the breast, while 4.7% had malignant hematological disease. Solid tumors were recorded as grade 1 (7.9%), grade 2 (28.0%), grade 3 (45.7%), and grade 4 (3.0%), and the majority of patients classified at TNM Stages I and II. Many patients (71.0%) could self-inject filgrastim and 72.2% found the handling instructions “extremely straightforward and easy to understand” at least once. Nearly all (99.4%) patients found the syringes “easy to use” at least once and 91.7% were willing to continue home administration. The mean patient satisfaction score for home administration was 1.9±0.9, ranging from 1 (very satisfied) to 6 (absolutely dissatisfied). No cases of neutropenia were observed and only one event of FN occurred. Conclusion: Home-based prophylaxis for FN with filgrastim was found to be effective, well tolerated, and well received by patients ( ClinicalTrials.gov Identifier: NCT02956967).
机译:背景:粒细胞集落刺激因子(G-CSF)生物仿制药非格司亭(Nivestim?)减少了中性粒细胞减少症的持续时间和严重程度以及发热性中性粒细胞减少症(FN)的发生频率。在日常医学实践中,尚未充分记录这种生物仿制药非格司亭的给药方法以及在家中接受该药的患者人群。在这种情况下,对家庭管理的深入了解可能有助于优化FN的管理,与医院管理相比,可能会降低成本和减轻患者负担。材料和方法:这是一项前瞻性,非干预,非对照性的多部位研究,涉及171个患者,分布在29个部位,接受了至少一剂非格司亭治疗。平均年龄为59.3岁,大多数患者为女性和G-CSF天真。收集的数据来自治疗医师的纸质患者问卷和常规文档。主要终点是接受非格司亭治疗的患者的特征。次要终点是对非格司亭,有效性,安全性和耐受性以及遵从处方的满意度。结果:多数患者实体瘤(95.9%)主要位于乳腺,而恶性血液病占4.7%。实体瘤记录为1级(7.9%),2级(28.0%),3级(45.7%)和4级(3.0%),并且大多数患者被分类为TNM阶段I和II。许多患者(71.0%)可以自行注射非格司亭,而72.2%的患者至少一次接受了操作说明“极其直接且易于理解”。几乎所有患者(99.4%)至少一次发现注射器“易于使用”,并且91.7%的患者愿意继续家庭给药。家庭管理的平均患者满意度得分为1.9±0.9,范围从1(非常满意)到6(绝对不满意)。没有观察到中性粒细胞减少症的病例,仅发生了一次FN事件。结论:发现在家中对非格司亭进行FN预防是有效的,耐受性良好且深受患者好评(ClinicalTrials.gov标识符:NCT02956967)。

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