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
Department of Infectious Diseases, Saint-Pierre University Hospital, Brussels, Belgium.
AIDS. 1996 Dec;10(14):1627-33. doi: 10.1097/00002030-199612000-00006.
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.
To examine the efficacy and safety of filgrastim for reversing neutropenia and determine the effect of this on use of myelosuppressive medications.
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.
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.
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.
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。
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。
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。
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。
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。