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通过皮下注射粒细胞集落刺激因子并优化治疗剂量和疗程来治疗化疗引起的中性粒细胞减少症。

Treatment of chemotherapy-induced neutropenia by subcutaneously administered granulocyte colony-stimulating factor with optimization of dose and duration of therapy.

作者信息

Morstyn G, Campbell L, Lieschke G, Layton J E, Maher D, O'Connor M, Green M, Sheridan W, Vincent M, Alton K

机构信息

Ludwig Institute for Cancer Research, Royal Melbourne Hospital, Victoria, Australia.

出版信息

J Clin Oncol. 1989 Oct;7(10):1554-62. doi: 10.1200/JCO.1989.7.10.1554.

DOI:10.1200/JCO.1989.7.10.1554
PMID:2789274
Abstract

In patients who have not received extensive prior chemotherapy or radiotherapy, it has been previously demonstrated that granulocyte colony-stimulating factor (G-CSF) abrogated the leukopenia following administration of melphalan (25 mg/m2). This study examined the necessity of a prechemotherapy period of G-CSF administration and the effect of varying the timing and duration of postchemotherapy G-CSF. Initially, patients received 0.3, 1.0, 3.0, and 10 micrograms/kg/d subcutaneously on days 1 to 5 and days 10 to 18. Melphalan was given on day 9. In the next portion of the study melphalan was administered on day 1 and G-CSF, 10 micrograms/kg/d, was administered by subcutaneous infusion on five schedules: (1) days 2 to 13; (2) days 8 to 13; (3) days 2 to 18; (4) days 8 to 18; (5) days -9 to -2 and 2 to 13. G-CSF produced a rapid and sustained elevation in neutrophil levels within 24 hours even when started 8 days after melphalan. This treatment was sufficient to abrogate the neutropenia in patients who had received no prior chemotherapy. It was not necessary to continue G-CSF for more than 7 days. G-CSF did not consistently alter the course of the thrombocytopenia that followed this dose of melphalan. G-CSF was well tolerated, although mild bone pain occurred and was reduced with acetaminophen. One of 22 patients developed cellulitis at an infusion site. We conclude that after melphalan chemotherapy, G-CSF may need to be given for only a short period to prevent chemotherapy-induced neutropenia, and that G-CSF induces a rapid rise in neutrophil levels even when started 8 days after melphalan administration.

摘要

在未接受过广泛的前期化疗或放疗的患者中,先前已经证明粒细胞集落刺激因子(G-CSF)可消除美法仑(25mg/m²)给药后的白细胞减少。本研究探讨了化疗前给予G-CSF的必要性以及改变化疗后G-CSF给药时间和持续时间的影响。最初,患者在第1至5天和第10至18天皮下注射0.3、1.0、3.0和10μg/kg/d。美法仑在第9天给药。在研究的下一部分中,美法仑在第1天给药,G-CSF 10μg/kg/d通过皮下输注按五种方案给药:(1)第2至13天;(2)第8至13天;(3)第2至18天;(4)第8至18天;(5)第-9至-2天和第2至13天。即使在美法仑给药8天后开始使用G-CSF,它也能在24小时内使中性粒细胞水平迅速且持续升高。这种治疗足以消除未接受过前期化疗患者的中性粒细胞减少。持续使用G-CSF超过7天没有必要。G-CSF并未持续改变此剂量美法仑后出现的血小板减少的病程。G-CSF耐受性良好,尽管出现了轻度骨痛,对乙酰氨基酚可减轻疼痛。22例患者中有1例在输注部位发生蜂窝织炎。我们得出结论,美法仑化疗后,可能仅需短期给予G-CSF以预防化疗引起的中性粒细胞减少,并且即使在美法仑给药8天后开始使用G-CSF,也能使中性粒细胞水平迅速升高。

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Treatment of chemotherapy-induced neutropenia by subcutaneously administered granulocyte colony-stimulating factor with optimization of dose and duration of therapy.通过皮下注射粒细胞集落刺激因子并优化治疗剂量和疗程来治疗化疗引起的中性粒细胞减少症。
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