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Rituximab in chronic lymphocytic leukemia

机译:利妥昔单抗治疗慢性淋巴细胞性白血病

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Rituximab (Rituxan®; iogen Idec, San Diego, CA, USA) is a human-mouse chimeric monoclonal antibody specific for CD20, a surface glycoprotein expressed on B lymphocytes. Administration of rituximab as a single agent to patients with chronic lymphocytic leukemia (CLL) has limited clinical activity, but generally does not eradicate leukemia from the marrow. However, when administered in combination with chemotherapy, rituximab can improve the survival of patients relative to those treated with chemotherapy alone. As a result of this, the US Food and Drug Administration approved the use of rituximab in previously untreated and previously treated CD20-positive CLL in combination with fludarabine monophosphate and cyclophosphamide. The results of clinical studies evaluating the activity of rituximab when used alone or in combination with other antileukemia agents for the treatment of this disease are reviewed here.
机译:利妥昔单抗(Rituxan®; iogen Idec,美国加利福尼亚州圣地亚哥)是对CD20(一种在B淋巴细胞上表达的表面糖蛋白)具有特异性的人-鼠嵌合单克隆抗体。利妥昔单抗作为单一药物给予慢性淋巴细胞性白血病(CLL)患者的临床活动有限,但通常不会从骨髓根除白血病。但是,与化疗联合使用时,利妥昔单抗可以提高患者的生存率。结果,美国食品药品监督管理局批准了利妥昔单抗与氟达拉滨单磷酸酯和环磷酰胺联合用于先前未治疗和先前治疗的CD20阳性CLL中。本文综述了利妥昔单抗单独使用或与其他抗白血病药联合使用治疗该病时的活性评估的临床研究结果。

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