Green M D, Koelbl H, Baselga J, Galid A, Guillem V, Gascon P, Siena S, Lalisang R I, Samonigg H, Clemens M R, Zani V, Liang B C, Renwick J, Piccart M J
Royal Melbourne Hospital, Melbourne, Australia.
Ann Oncol. 2003 Jan;14(1):29-35. doi: 10.1093/annonc/mdg019.
We evaluated the efficacy of a single fixed 6 mg dose of pegfilgrastim (a pegylated version of filgrastim) per cycle of chemotherapy, compared with daily administration of filgrastim, in the provision of neutrophil support.
Patients (n = 157) were randomized to receive either a single 6 mg subcutaneous (s.c.) injection of pegfilgrastim or daily 5 mg/kg s.c. injections of filgrastim, after doxorubicin and docetaxel chemotherapy (60 mg/m(2) and 75 mg/m(2), respectively). Duration of grade 4 neutropenia, depth of neutrophil nadir, incidence of febrile neutropenia, time to neutrophil recovery and safety information were recorded.
A single 6 mg injection of pegfilgrastim was as effective as daily injections of filgrastim for all efficacy measures for all cycles. The mean duration of grade 4 neutropenia in cycle 1 was 1.8 and 1.6 days for the pegfilgrastim and filgrastim groups, respectively. Results for all efficacy end points in cycles 2-4 were consistent with the results from cycle 1. A trend towards a lower incidence of febrile neutropenia was noted across all cycles with pegfilgrastim compared with filgrastim (13% versus 20%, respectively). A single fixed dose of pegfilgrastim was as safe and well tolerated as standard daily filgrastim.
A single fixed dose of pegfilgrastim administered once per cycle of chemotherapy was comparable to multiple daily injections of filgrastim in safely providing neutrophil support during myelosuppressive chemotherapy. Pegfilgrastim may have utility in other clinical settings of neutropenia.
我们评估了每周期化疗单次固定剂量6毫克聚乙二醇化非格司亭(非格司亭的聚乙二醇化版本)与每日注射非格司亭相比,在提供中性粒细胞支持方面的疗效。
患者(n = 157)在接受阿霉素和多西他赛化疗(分别为60毫克/平方米和75毫克/平方米)后,被随机分配接受单次皮下注射6毫克聚乙二醇化非格司亭或每日皮下注射5毫克/千克非格司亭。记录4级中性粒细胞减少的持续时间、中性粒细胞最低点深度、发热性中性粒细胞减少的发生率、中性粒细胞恢复时间和安全性信息。
对于所有周期的所有疗效指标,单次注射6毫克聚乙二醇化非格司亭与每日注射非格司亭效果相同。在第1周期,聚乙二醇化非格司亭组和非格司亭组4级中性粒细胞减少的平均持续时间分别为1.8天和1.6天。第2 - 4周期所有疗效终点的结果与第1周期一致。与非格司亭相比,聚乙二醇化非格司亭在所有周期中发热性中性粒细胞减少的发生率有降低趋势(分别为13%和20%)。单次固定剂量的聚乙二醇化非格司亭与标准每日注射非格司亭一样安全且耐受性良好。
在骨髓抑制性化疗期间,每周期化疗单次给予固定剂量的聚乙二醇化非格司亭在安全提供中性粒细胞支持方面与每日多次注射非格司亭相当。聚乙二醇化非格司亭可能在其他中性粒细胞减少的临床环境中有用。