Vamvakas E C, Pineda A A
Blood Transfusion Service, Massachusetts General Hospital, Boston 02114, USA.
J Clin Apher. 1997;12(2):74-81. doi: 10.1002/(sici)1098-1101(1997)12:2<74::aid-jca4>3.0.co;2-6.
Cytokines that improve granulocyte collection yields have recently become available, and may lead to a new series of trials of granulocyte transfusion (GTX) therapy. We conducted a meta-analysis of studies of prophylactic GTX in order to identify the determinants of efficacy of this intervention, and to assist in the design of future trials of GTX for the treatment of patients with overwhelming infection.
Randomized controlled trials of the efficacy of prophylactic GTX published in English in 1970-1995 were retrieved, and eight studies were eligible for analysis. Summary relative odds (RR) of bacterial or fungal infection, death, or death from infection in transfused patients vs. controls were computed for patient subsets defined on the basis of dose of granulocytes transfused, assessment of leukocyte compatibility, duration of neutropenia, and infection rate of controls. The random-effects method was used for all analyses.
Assessment of leukocyte compatibility prior to the transfusion, dose of granulocytes transfused, and duration of neutropenia in enrolled patients could account, respectively, for the variation in findings across published reports in terms of all three, two, and one of the outcome measures studied. Transfusion of adequate doses of compatible leukocytes significantly reduced the relative risk (RR) of infection, death, and death from infection in transfused patients vs. controls (RR = 0.075, RR = 0.224, and RR = 0.168, respectively; P < 0.05).
Two necessary elements in the design of future trials of therapeutic GTX should be the transfusion of high doses of granulocytes and the provision of leukocytes that are crossmatch-compatible with the recipient's serum.
近年来出现了一些能够提高粒细胞采集量的细胞因子,这可能会引发一系列新的粒细胞输注(GTX)治疗试验。我们对预防性GTX的研究进行了荟萃分析,以确定该干预措施疗效的决定因素,并为未来治疗严重感染患者的GTX试验设计提供帮助。
检索1970 - 1995年以英文发表的预防性GTX疗效的随机对照试验,有八项研究符合分析条件。针对根据输注粒细胞剂量、白细胞相容性评估、中性粒细胞减少持续时间以及对照组感染率定义的患者亚组,计算输注患者与对照组相比细菌或真菌感染、死亡或感染相关死亡的汇总相对比值(RR)。所有分析均采用随机效应方法。
输注前白细胞相容性评估、输注粒细胞剂量以及入选患者的中性粒细胞减少持续时间,分别可以解释已发表报告中在所研究的三项、两项和一项结局指标方面研究结果的差异。输注足够剂量的相容白细胞可显著降低输注患者与对照组相比感染、死亡及感染相关死亡的相对风险(RR分别为0.075、0.224和0.168;P < 0.05)。
未来治疗性GTX试验设计中的两个必要要素应该是输注高剂量粒细胞以及提供与受者血清交叉配型相容的白细胞。