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重组人粒细胞巨噬细胞集落刺激因子用于高级别非霍奇金淋巴瘤联合化疗后——一项随机试验研究

Recombinant human granulocyte-macrophage colony-stimulating factor after combined chemotherapy in high-grade non-Hodgkin's lymphoma--a randomised pilot study.

作者信息

Bergmann L, Karakas T, Knuth A, Lautenschläger G, Mitrou P S, Hoelzer D

机构信息

Medical Clinic III, University Hospital, Frankfurt, Germany.

出版信息

Eur J Cancer. 1995 Dec;31A(13-14):2164-8. doi: 10.1016/0959-8049(95)00195-6.

Abstract

High-grade non-Hodgkin's lymphomas (NHL) can potentially be cured with combination chemotherapy, although the optimum schedules still have to be defined. Clinical trials with intensive chemotherapy are predominantly limited by myelosuppression. Here, haematopoetic growth factors open up the possibility of reducing chemotherapy-associated toxicities. In this randomised pilot study, we investigated the effects of a recombinant human granulocyte-macrophage colony-stimulating factor (rhGM-CSF) following combined chemotherapy with vincristine, doxorubicin, cyclophosphamide, prednisone and etoposide (VACPE). A total of 35 patients with high-grade NHLs were randomised to receive either rhGM-CSF or placebo during the first two chemotherapy cycles and rhGM-CSF for all following cycles. rhGM-CSF was administered at a dosage of 5 micrograms/kg for 10 days or until neutrophils were > 1/nl following chemotherapy. The analyses revealed a significant reduction of neutropenia and duration of neutropenia in the rhGM-CSF group. Adverse events were rare and generally mild apart from one anaphylactoid reaction. No effects of rhGM-CSF were observed concerning the platelet nadir or duration of thrombocytopenia. The benefit of rhGM-CSF for response induction and survival via rhGM-CSF-supported dose intensification remains to be determined.

摘要

高级别非霍奇金淋巴瘤(NHL)通过联合化疗有可能治愈,尽管最佳方案仍有待确定。强化化疗的临床试验主要受骨髓抑制的限制。在此,造血生长因子为降低化疗相关毒性提供了可能性。在这项随机试验研究中,我们调查了重组人粒细胞巨噬细胞集落刺激因子(rhGM-CSF)在与长春新碱、阿霉素、环磷酰胺、泼尼松和依托泊苷(VACPE)联合化疗后的效果。总共35例高级别NHL患者被随机分组,在前两个化疗周期接受rhGM-CSF或安慰剂,随后所有周期均接受rhGM-CSF。rhGM-CSF以5微克/千克的剂量给药10天,或直至化疗后中性粒细胞>1/微升。分析显示rhGM-CSF组中性粒细胞减少和中性粒细胞减少持续时间显著降低。除了1例类过敏反应外,不良事件罕见且一般较轻。未观察到rhGM-CSF对血小板最低点或血小板减少持续时间有影响。rhGM-CSF通过支持剂量强化对诱导缓解和生存的益处仍有待确定。

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