Ross S D, DiGeorge A, Connelly J E, Whiting G W, McDonnell N
MetaWorks, Inc., Boston, Massachusetts 02210, USA.
Pharmacotherapy. 1998 Nov-Dec;18(6):1290-7.
We performed a literature search for all clinical studies reporting outcomes in patients with the acquired immunodeficiency syndrome (AIDS) receiving granulocyte-macrophage colony-stimulating factor (GM-CSF) for any indication. Safety outcomes included human immunodeficiency virus replication, immune status, and frequency of opportunistic infections and neoplasms. Data were synthesized qualitatively. We identified 22 studies (274 patients): 12 addressed AIDS neutropenia, 8 AIDS cancer therapy, and 2 opportunistic infections. Viral burden was assessed by serum p24Ag in 15 studies. Nine reported no change in levels, three net decreases, and three net increases. All studies showing net increases involved patients receiving GM-CSF without a concurrent antiretroviral. The CD4 counts were unchanged in 5 studies, increased in 3, and not reported in 14. The incidence of neoplasms or new opportunistic infections was low. The literature suggests no increased risk of viral replication or clinical deterioration in patients with AIDS who take GM-CSF concurrently with zidovudine.
我们对所有报告接受粒细胞巨噬细胞集落刺激因子(GM-CSF)用于任何适应症的获得性免疫缺陷综合征(AIDS)患者结局的临床研究进行了文献检索。安全性结局包括人类免疫缺陷病毒复制、免疫状态以及机会性感染和肿瘤的发生频率。对数据进行了定性综合分析。我们识别出22项研究(274例患者):12项针对艾滋病中性粒细胞减少症,8项针对艾滋病癌症治疗,2项针对机会性感染。15项研究通过血清p24抗原评估病毒载量。9项报告水平无变化,3项净下降,3项净上升。所有显示净上升的研究均涉及未同时接受抗逆转录病毒治疗而接受GM-CSF的患者。5项研究中CD4细胞计数无变化,3项升高,14项未报告。肿瘤或新的机会性感染的发生率较低。文献表明,同时服用GM-CSF和齐多夫定的艾滋病患者病毒复制或临床恶化风险未增加。