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利妥昔单抗。慢性淋巴细胞白血病:无决定性优势。

Rituximab. Chronic lymphoid leukaemia: no decisive advantage.

出版信息

Prescrire Int. 2010 Apr;19(106):56-8.

Abstract

When treatment is needed for patients with symptomatic chronic lymphoid leukaemia, the standard first-line treatment is oral chlorambucil. Fludarabine has been used more as a second-line option. Rituximab has been authorised for use in both first-line and second-line therapy. We found no randomised trials comparing rituximab versus either chlorambucil or fludarabine. Clinical evaluation of rituximab is mainly based on 2 randomised unblinded trials, comparing cytotoxic chemotherapy, with and without the addition of rituximab, as first-line treatment in 817 patients in one trial and as second-line treatment in 552 patients in the other trial. Most patients were at a relatively early stage of the disease. After a median follow-up of about 2 years, addition of rituximab increased median progression-free survival by about 7 to 10 months. It was also associated with a higher complete response rate (about 10% to 20% higher). Follow-up was too short to reliably estimate the possible impact on overall survival. In the trial of first-line treatment, adverse events were more frequent in the rituximab group (77% versus 62%), especially serious infections (18% versus 15%) and febrile neutropenia (8% versus 6%). In the trial of second-line therapy, there were more fatal adverse events in the rituximab group (13% versus 10%). Rituximab also carries a risk of progressive multifocal leukoencephalopathy. In practice, adding rituximab to other cytotoxic drugs has no proven benefit in previously untreated patients with chronic lymphoid leukaemia. In second-line treatment, the progression-free survival benefit associated with rituximab must be weighed against the increase in adverse effects.

摘要

对于有症状的慢性淋巴细胞白血病患者,若需要进行治疗,标准的一线治疗药物是口服苯丁酸氮芥。氟达拉滨更多地用作二线治疗选择。利妥昔单抗已被批准用于一线和二线治疗。我们未找到比较利妥昔单抗与苯丁酸氮芥或氟达拉滨的随机试验。利妥昔单抗的临床评估主要基于2项非盲随机试验,在一项试验中,将细胞毒性化疗(加或不加利妥昔单抗)作为817例患者的一线治疗,在另一项试验中作为552例患者的二线治疗。大多数患者处于疾病相对早期阶段。经过约2年的中位随访,添加利妥昔单抗使中位无进展生存期延长约7至10个月。它还与更高的完全缓解率相关(高出约10%至20%)。随访时间过短,无法可靠估计对总生存期的可能影响。在一线治疗试验中,利妥昔单抗组不良事件更频繁(77%对62%),尤其是严重感染(18%对15%)和发热性中性粒细胞减少(8%对6%)。在二线治疗试验中,利妥昔单抗组致命不良事件更多(13%对10%)。利妥昔单抗还存在进行性多灶性白质脑病风险。在实际应用中,对于既往未治疗的慢性淋巴细胞白血病患者,在其他细胞毒性药物中添加利妥昔单抗未显示出益处。在二线治疗中,必须权衡利妥昔单抗带来的无进展生存期益处与不良反应增加的情况。

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