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Pegfilgrastim vs filgrastim in PBSC mobilization for autologous hematopoietic SCT: a systematic review and meta-analysis

机译:培格非司亭vs非格司亭在PBSC动员中用于自体造血SCT的系统评价和荟萃分析

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Trial outcomes comparing cytokine agents for PBSC mobilization in autologous hematopoietic transplant patients have been controversial. We performed a systematic review and meta-analysis of evidence available on pegfilgrastim vs filgrastim in chemocytokine mobilization. Electronic literature searches of PubMed, EMBASE and CENTRAL identified nine articles eligible for qualitative analysis with one randomized controlled trial. Eight articles involving 719 patients were included in the meta-analysis. Results showed similar CD34+ cell collection yields for pegfilgrastim and filgrastim (SDM -0.08, 95% CI: -0.388 to 0.228). On comparison with filgrastim, pegfilgrastim showed a significantly earlier apheresis onset time (SDM: -0.512, 95% CI: -0.973 to -0.050) and reduction in required apheresis procedures (SDM -0.260, 95% CI: -0.466 to -0.054). Times to leukocyte (>= 1.0 x 10(9)/L) and platelet (>= 20 x 10(9)/L) recovery were similar between groups (SDM: 0.015, 95% CI: -0.41 to 0.44 and SDM: 0.309, 95% CI: -0.11 to 0.72, respectively). Both agents were well tolerated and mild bone pain was the most frequently reported adverse event. Pegfilgrastim may be a convenient alternative to filgrastim in PBSC mobilization for multiple myeloma and lymphoma patients, but further studies are required to clarify effects of cytokine dosage and previous cytotoxic exposure in specific subpopulations.
机译:在自体造血移植患者中比较用于PBSC动员的细胞因子药物的试验结果一直存在争议。我们进行了系统的回顾和荟萃分析,证明了在化学细胞因子动员中,pegfilgrastim vs filgrastim可用的证据。在PubMed,EMBASE和CENTRAL的电子文献搜索中,通过一项随机对照试验,确定了9篇符合定性分析要求的文章。荟萃分析包括八篇涉及719名患者的文章。结果显示,pegfilgrastim和filgrastim的CD34 +细胞收集率相似(SDM -0.08,95%CI:-0.388至0.228)。与filgrastim相比,pegfilgrastim的单采单药起效时间显着更早(SDM:-0.512,95%CI:-0.973至-0.050)和所需的单采单药程序减少(SDM -0.260,95%CI:-0.466至-0.054) 。各组之间白细胞恢复时间(> = 1.0 x 10(9)/ L)和血小板恢复时间(> = 20 x 10(9)/ L)(SDM:0.015,95%CI:-0.41至0.44和SDM: 0.309、95%CI:分别为-0.11至0.72)。两种药物均具有良好的耐受性,轻度的骨痛是最常报告的不良事件。在多发性骨髓瘤和淋巴瘤患者的PBSC动员中,培格非司亭可能是非格司亭的便捷替代品,但仍需要进一步的研究来阐明特定因子亚群中细胞因子剂量和先前的细胞毒性暴露的影响。

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