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Rituximab: as first-line maintenance therapy following rituximab-containing therapy for follicular lymphoma.

机译:利妥昔单抗:作为含利妥昔单抗的滤泡性淋巴瘤治疗后的一线维持治疗。

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摘要

Rituximab is a recombinant chimeric murine/human monoclonal IgG(1-kappa) antibody. It binds specifically to the CD20 antigen on normal and malignant B lymphocytes and produces complement-dependent and antibody-dependent cytotoxicity and induces apoptosis in these cells. Prolonged treatment with rituximab in patients with follicular lymphoma results in a sustained reduction in circulating B lymphocytes. Two years of single-agent maintenance therapy with rituximab significantly prolonged progression-free survival (primary endpoint) compared with observation in patients with follicular lymphoma who were responsive to first-line induction therapy with rituximab plus chemotherapy. Furthermore, maintenance therapy with rituximab significantly delayed the time to the next antilymphoma treatment and the next chemotherapy compared with observation in these patients. Rituximab had an acceptable tolerability profile as single-agent maintenance therapy in patients with follicular lymphoma with no new or unexpected adverse events compared with induction therapy.
机译:利妥昔单抗是一种重组嵌合鼠/人单克隆IgG(1-kappa)抗体。它与正常和恶性B淋巴细胞上的CD20抗原特异性结合,并产生补体依赖性和抗体依赖性细胞毒性,并诱导这些细胞的凋亡。滤泡性淋巴瘤患者长期使用利妥昔单抗治疗可导致循环B淋巴细胞持续减少。与对利妥昔单抗加化疗的一线诱导治疗有反应的滤泡性淋巴瘤患者相比,利妥昔单抗单药维持治疗的两年显着延长了无进展生存期(主要终点)。此外,与这些患者的观察结果相比,利妥昔单抗维持治疗显着延迟了下次抗淋巴瘤治疗和下次化疗的时间。与单药维持治疗相比,利妥昔单抗在滤泡性淋巴瘤患者中的诱导耐受性与诱导治疗相比没有新的或意外的不良事件。

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