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粒细胞集落刺激因子治疗韦格纳肉芽肿中由环磷酰胺引起的严重中性粒细胞减少症。

Granulocyte colony-stimulating factor treatment for cyclophosphamide-induced severe neutropenia in Wegener's granulomatosis.

作者信息

Hellmich B, Schnabel A, Gross W L

机构信息

Medizinische Universität zu Lübeck, Germany.

出版信息

Arthritis Rheum. 1999 Aug;42(8):1752-6. doi: 10.1002/1529-0131(199908)42:8<1752::AID-ANR26>3.0.CO;2-6.

DOI:10.1002/1529-0131(199908)42:8<1752::AID-ANR26>3.0.CO;2-6
PMID:10446877
Abstract

OBJECTIVE

To examine the efficacy and safety of recombinant human granulocyte colony-stimulating factor (rHuG-CSF) in the treatment of cyclophosphamide (CYC)-induced severe neutropenia (<1,000 neutrophils/microl) in patients with generalized Wegener's granulomatosis (WG).

METHODS

Six WG patients with severe neutropenia due to CYC treatment (group A) were given short-term dosages of rHuG-CSF. Treatment response in these 6 patients was compared with that in 6 WG patients who were matched for age, sex, disease status, and prior treatment and who received supportive treatment only (group B).

RESULTS

The duration of severe neutropenia was significantly shorter in group A patients (4.0+/-0.8 days) than in group B patients (9.0+/-1.3 days; P = 0.03). This was accompanied by fewer bacterial infections (2 versus 4) and fewer nonbacterial infections (0 versus 3) in group A compared with group B patients. Treatment with rHuG-CSF was well tolerated and, notably, no disease flare occurred during treatment and up to 4-6 months after rHuG-CSF administration.

CONCLUSION

Short-term, low-dose rHuG-CSF treatment can substantially shorten the duration of CYC-induced neutropenia and appears to confer significant clinical benefit. Such treatment, aimed at raising the neutrophil count above 1,000/microl, does not appear to carry a high risk of inducing a flare of the vasculitis.

摘要

目的

研究重组人粒细胞集落刺激因子(rHuG-CSF)治疗环磷酰胺(CYC)诱导的广泛性韦格纳肉芽肿(WG)患者严重中性粒细胞减少症(中性粒细胞<1000/微升)的疗效和安全性。

方法

6例因CYC治疗导致严重中性粒细胞减少的WG患者(A组)接受短期剂量的rHuG-CSF治疗。将这6例患者的治疗反应与6例年龄、性别、疾病状态和既往治疗相匹配且仅接受支持治疗的WG患者(B组)进行比较。

结果

A组患者严重中性粒细胞减少的持续时间(4.0±0.8天)明显短于B组患者(9.0±1.3天;P = 0.03)。与B组患者相比,A组患者的细菌感染(2次对4次)和非细菌感染(0次对3次)更少。rHuG-CSF治疗耐受性良好,值得注意的是,在治疗期间以及rHuG-CSF给药后长达4至6个月内均未出现疾病复发。

结论

短期、低剂量的rHuG-CSF治疗可显著缩短CYC诱导的中性粒细胞减少症的持续时间,且似乎具有显著的临床益处。这种旨在将中性粒细胞计数提高到1,000/微升以上的治疗方法似乎不会带来引发血管炎复发的高风险。

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