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Prophylaxis of chemotherapy-induced neutropenia and febrile neutropenia with lipegfilgrastim in 2489 cancer patients: final results from the non-interventional study NADIR

机译:在2489例癌症患者中,用LipegfilGrastim的化疗诱导的中性粒细胞率和Feberile Neveropenia的预防:非介入研究Nadir的最终结果

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Objectives: The non-interventional study (NIS) NADIR (DRKS00005711) evaluated the effectiveness and safety of prophylaxis with lipegfilgrastim, a glycopegylated granulocyte-colony stimulating factor, in 2500 patients undergoing chemotherapy in routine clinical practice. Primary objective was the incidence of chemotherapy-induced severe neutropenia, febrile neutropenia (FN), and neutropenia-associated complications.Methods: NADIR was a prospective NIS conducted in 201 study centers in Germany.Results: The analysis included 2489 patients. Main tumor types were breast cancer (n=1198, 48.1%), lung cancer (n=303, 12.2%), non-Hodgkin lymphoma (NHL; n=337, 13.5%), and prostate cancer (n=111, 4.5%). Nine hundred and ten (36.6%) patients were aged 65years (regarded as elderly patients). Severe neutropenia (CTCAE grade 3/4) was reported in 26.8% (n=666) and 25.2% (n=229) of the total population and elderly patients, respectively. FN was documented in 2.7% (n=68) of the total population vs 3.0% (n=27) of elderly patients. Primary prophylaxis with lipegfilgrastim among patients with high risk of FN (>20%) was documented in 83.5% of the total population and 75.1% of elderly patients. Infections (CTCAE grade 3/4) were documented in 99 patients (4.0%) in the total population vs 47 (5.1%) elderly patients. Fatal infections were reported in 14 (0.6%) patients in the total population vs 11 (1.2%) elderly patients. Overall, most frequent lipegfilgrastim-related adverse events (AEs) included bone pain (8.0%), anemia (3.2%), leucocytosis (2.7%), and thrombocytopenia (2.5%). Of the patients, 18.0% had 1 documented serious AE; none of the fatal events (2.7%) was lipegfilgrastim-related.Conclusions: Lipegfilgrastim administered to patients with solid tumor/NHL undergoing chemotherapy in routine clinical practice showed similar effectiveness and safety compared to the pivotal trials.
机译:目的:非介入研究(NIS)Nadir(DRKS00005711)评估了预防利脂素血浆刺激因子的预防糖蛋白粒细胞刺激因子的有效性和安全性,在常规临床实践中进行化疗的2500名患者。初级目标是化疗诱导的严重中性粒细胞减少症,发热中性蛋白酶(FN)和中性粒细胞凋亡的发病率。方法:Nadir是德国201学习中心进行的一个未来的NIS.Results:分析包括2489名患者。主要肿瘤类型是乳腺癌(n = 1198,48.1%),肺癌(n = 303,12.2%),非霍奇金淋巴瘤(NHL; n = 337,13.5%)和前列腺癌(n = 111,4.5 %)。九百岁(36.6%)患者65岁(被视为老年患者)。报告了26.8%(n = 666)和25.2%(n = 229)的严重中性蛋白(CTCAE 3/4)分别为总人口和老年患者25.2%(n = 229岁)。根据老年患者的总人口与3.0%(n = 27)的2.7%(n = 68),FN记录在2.7%(n = 68)中。患有高风险(> 20%)患者的初级预防患者在总人口的83.5%和75.1%的老年患者中记录。在99名患者(4.0%)中记录了感染(CTCAE级3/4),总人口与47(5.1%)老年患者。致命感染于14例(0.6%)患者总人口与11(1.2%)老年患者。总体而言,最常用的Lipegfilgrastim相关的不良事件(AES)包括骨疼痛(8.0%),贫血(3.2%),白细胞症(2.7%)和血小板减少(2.5%)。患者,18.0%有1名严重AE;没有致命事件(2.7%)是Lipegfilgrastim-相关的。结论:对在常规临床实践中进行化疗的固体瘤/ NHL患者的Lipegfilgrastim,与关键试验相比,与术语临床实践相比类似的有效性和安全性。

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