首页> 外文期刊>Leukemia and lymphoma >Fludarabine, cyclophosphamide and rituximab plus granulocyte macrophage colony-stimulating factor as frontline treatment for patients with chronic lymphocytic leukemia.
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Fludarabine, cyclophosphamide and rituximab plus granulocyte macrophage colony-stimulating factor as frontline treatment for patients with chronic lymphocytic leukemia.

机译:氟达拉滨,环磷酰胺和利妥昔单抗加粒细胞巨噬细胞集落刺激因子作为慢性淋巴细胞性白血病患者的一线治疗。

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摘要

Fludarabine, cyclophosphamide and rituximab (FCR), the standard of care for the frontline treatment of patients with chronic lymphocytic leukemia (CLL), is associated with a high rate of neutropenia and infectious complications. Granulocyte macrophage colony-stimulating factor (GM-CSF) reduces myelosuppression and can potentiate rituximab activity. We conducted a clinical trial combining GM-CSF with FCR for frontline treatment of 60 patients with CLL. Eighty-six percent completed all six courses and 18% discontinued GM-CSF for toxicity: grade 3-4 neutropenia was observed in 30% of cycles, and severe infections in 16% of cases. The overall response rate was 100%. Both median event-free survival (EFS) and overall survival (OS) have not been reached. Longer EFS was associated with favorable cytogenetics. GM-CSF led to a lower frequency of infectious complications than in the historical FCR group, albeit similar EFS and OS.
机译:氟达拉滨,环磷酰胺和利妥昔单抗(FCR)是慢性淋巴细胞性白血病(CLL)患者一线治疗的护理标准,与中性粒细胞减少症和感染并发症的发生率高相关。粒细胞巨噬细胞集落刺激因子(GM-CSF)减少骨髓抑制并可以增强利妥昔单抗的活性。我们进行了一项将GM-CSF与FCR结合使用的临床试验,以一线治疗60例CLL。有86%的人完成了全部六个疗程,有18%的人由于毒性停止了GM-CSF:在30%的周期中观察到3-4级中性粒细胞减少,在16%的病例中出现严重感染。总体回应率为100%。中值无事件生存期(EFS)和总体生存期(OS)均未达到。较长的EFS与良好的细胞遗传学有关。尽管EFS和OS相似,但GM-CSF导致的感染并发症发生率比历史FCR组低。

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