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非格司亭用于治疗中性粒细胞减少症并支持HIV感染中骨髓抑制性药物的剂量调整。G-CSF 92105研究组。

Filgrastim to treat neutropenia and support myelosuppressive medication dosing in HIV infection. G-CSF 92105 Study Group.

作者信息

Hermans P, Rozenbaum W, Jou A, Castelli F, Borleffs J, Gray S, Ward N, Gori A, De Bona A, Ferré C, Loncà M, Lang J M, Ammassari A, Clumeck N

机构信息

Department of Infectious Diseases, Saint-Pierre University Hospital, Brussels, Belgium.

出版信息

AIDS. 1996 Dec;10(14):1627-33. doi: 10.1097/00002030-199612000-00006.

Abstract

BACKGROUND

Patients with HIV infection frequently experience disease or treatment-related myelosuppression leading to neutropenia. Neutropenia often leads to dose-reduction or discontinuation of important myelosuppressive therapy.

OBJECTIVE

To examine the efficacy and safety of filgrastim for reversing neutropenia and determine the effect of this on use of myelosuppressive medications.

DESIGN

Open-label, non-comparative, multicentre study in 200 HIV-positive patients with neutropenia [absolute neutrophil count (ANC) < 1.0 x 10(9)/l]. Filgrastim was started at 1 microgram/kg/day subcutaneously for 28 days. This initial treatment phase was followed by a maintenance phase, using 300 micrograms on 1-7 days/week. In both phases the dose of filgrastim was adjusted to achieve an ANC of 2-5 x 10(9)/l.

RESULTS

Filgrastim reversed neutropenia in 98% of patients (ANC > or = 2 x 10(9)/l), with a median time to reversal of 2 days (range 1-16) and a median dose of 1 microgram/kg/day (range 0.5-10). Most patients (96%) achieved reversal of neutropenia with a filgrastim dose of < or = 300 micrograms/day (< or = 1 vial/day). Normal ANCs were then maintained with a median of 1 microgram/kg/day (range 0.22-10.6) during the treatment phase and 3 x 300 micrograms vials/week (range 1-7) during the maintenance phase. Ganciclovir, zidovudine, co-trimoxazole and pyrimethamine were the drugs most frequently considered to be causing neutropenia, and 83% of patients received one or more of these in the study. Filgrastim allowed > 80% of patients to increase or maintain dose-levels of these four medications or add them to their therapy. The number of these four medications received per patient increased by > 20% during filgrastim therapy. Filgrastim was well tolerated. CD4, CD8 and total lymphocyte counts all increased slightly, and there was no difference in HIV-1 p24 antigen levels.

CONCLUSION

Filgrastim rapidly reverses neutropenia and maintains normal ANC in patients with HIV infection. This allows greater use of myelosuppressive medications without the potentially life-threatening complications of neutropenia.

摘要

背景

HIV感染患者经常经历与疾病或治疗相关的骨髓抑制,导致中性粒细胞减少。中性粒细胞减少常常导致重要的骨髓抑制治疗药物剂量减少或停药。

目的

研究非格司亭逆转中性粒细胞减少的疗效和安全性,并确定其对骨髓抑制药物使用的影响。

设计

一项开放标签、非对照、多中心研究,纳入200例中性粒细胞减少的HIV阳性患者[绝对中性粒细胞计数(ANC)<1.0×10⁹/L]。非格司亭起始剂量为1微克/千克/天,皮下注射,共28天。初始治疗阶段之后是维持阶段,每周1 - 7天使用300微克。在两个阶段,均调整非格司亭剂量以使ANC达到2 - 5×10⁹/L。

结果

非格司亭使98%的患者中性粒细胞减少得到逆转(ANC≥2×10⁹/L),逆转的中位时间为2天(范围1 - 16天),中位剂量为1微克/千克/天(范围0.5 - 10)。大多数患者(96%)使用剂量≤300微克/天(≤1支/天)的非格司亭实现了中性粒细胞减少的逆转。然后在治疗阶段,以中位剂量1微克/千克/天(范围0.22 - 10.6)维持正常ANC,在维持阶段,以每周3×300微克(范围1 - 7)维持。更昔洛韦、齐多夫定、复方新诺明和乙胺嘧啶是最常被认为导致中性粒细胞减少的药物,83%的患者在研究中接受了其中一种或多种药物治疗。非格司亭使80%以上的患者能够增加或维持这四种药物的剂量水平,或将它们添加到治疗方案中。在非格司亭治疗期间,每位患者接受的这四种药物数量增加了20%以上。非格司亭耐受性良好。CD4、CD8和总淋巴细胞计数均略有增加,HIV - 1 p24抗原水平无差异。

结论

非格司亭能迅速逆转HIV感染患者的中性粒细胞减少并维持正常ANC。这使得在无中性粒细胞减少这一潜在危及生命并发症的情况下,能更多地使用骨髓抑制药物。

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