首页> 美国卫生研究院文献>British Journal of Cancer >High-dose intensity cyclophosphamide epidoxorubicin vincristine and prednisone by shortened intervals and granulocyte colony-stimulating factor in non-Hodgkins lymphoma: a phase II study.
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High-dose intensity cyclophosphamide epidoxorubicin vincristine and prednisone by shortened intervals and granulocyte colony-stimulating factor in non-Hodgkins lymphoma: a phase II study.

机译:非霍奇金淋巴瘤中间隔时间短的大剂量强度环磷酰胺表阿霉素长春新碱和泼尼松和粒细胞集落刺激因子:II期研究。

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摘要

Twenty patients with non-Hodgkin's lymphoma were treated with a combination of cyclophosphamide (750 mg m(-2), day 1), epidoxorubicin (60 mg m(-2), day 1), vincristine (1.4 mg m(-2), day 1) and prednisone (100 mg m(-2), days 1-5) every 14 days. Shortening of intervals was associated with the prophylactic employment of granulocyte colony-stimulating factor (G-CSF; specifically, filgrastim) administered at a dose of 300 microg subcutaneously from day 6 to day 11. The ratio between actually delivered dose intensity and planned dose intensity was 1.0 in 18 out the 20 patients. Toxicity was acceptable; response rate and survival are in the expected range. The present study demonstrated the feasibility of acceleration of chemotherapy cycles to obtain dose intensification in non-Hodgkin's lymphoma.
机译:20例非霍奇金淋巴瘤患者接受环磷酰胺(750 mg m(-2),第1天),表柔比霉素(60 mg m(-2),第1天),长春新碱(1.4 mg m(-2)联合治疗,第1天)和泼尼松(100 mg m(-2),第1-5天)每14天。间隔时间的缩短与从第6天到第11天皮下注射300微克的预防性应用粒细胞集落刺激因子(G-CSF;特别是非格司亭)有关。实际递送的剂量强度与计划的剂量强度之比20例患者中有18例为1.0。毒性是可以接受的;反应率和生存率均在预期范围内。本研究证明了在非霍奇金淋巴瘤中加速化疗周期以获得剂量强化的可行性。

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