Hospices Civils de Lyon and Université Lyon 1, France.
Haematologica. 2013 Jul;98(7):1107-14. doi: 10.3324/haematol.2012.082412. Epub 2013 May 3.
Anti-CD20-containing chemotherapy regimens have become the standard of care for patients with follicular lymphoma needing cytotoxic therapy. Four randomized trials demonstrated a clinical benefit for patients treated with rituximab. However, no long-term follow up (i.e. > 5 years) of these trials is yet available. Between May 2000 and May 2002, 358 newly diagnosed patients with high tumor burden follicular lymphoma were randomized to receive cyclophosphamide, adriamycin, etoposide and prednisolone plus interferon-α2a or a similar chemotherapy-based regimen plus rituximab, and outcome was up-dated. With a median follow up of 8.3 years, addition of rituximab remained significantly associated with prolonged event-free survival (primary end point) (P=0.0004) with a trend towards a benefit for overall survival (P=0.076). The Follicular Lymphoma International Prognostic Index score was strongly associated with outcome for both event-free and overall survival in univariate analysis and its prognostic value remained highly significant after adjusting for other significant covariates in multivariate models (P<0.0001 and P=0.001, respectively). Considering long-term toxicity, the addition of rituximab in the first-line setting was confirmed as safe with regards to development of secondary malignancies. Long-term follow up of patients with follicular lymphoma treated in the FL2000 study confirms the sustained clinical benefit of rituximab without long-term toxicity.
抗 CD20 化疗方案已成为滤泡性淋巴瘤患者需要细胞毒治疗的标准治疗方法。四项随机试验表明利妥昔单抗治疗的患者具有临床获益。然而,这些试验尚无长期随访(即>5 年)。在 2000 年 5 月至 2002 年 5 月期间,358 例新诊断的高肿瘤负荷滤泡性淋巴瘤患者被随机分为接受环磷酰胺、阿霉素、依托泊苷和泼尼松联合干扰素-α2a 或类似的基于化疗的方案联合利妥昔单抗治疗,并进行了随访。中位随访 8.3 年后,利妥昔单抗的加入仍然与延长无事件生存(主要终点)显著相关(P=0.0004),并且总生存有获益趋势(P=0.076)。滤泡性淋巴瘤国际预后指数评分在单因素分析中与无事件生存和总生存均显著相关,并且在多因素模型中调整其他显著协变量后,其预后价值仍然非常显著(P<0.0001 和 P=0.001)。考虑到长期毒性,利妥昔单抗在一线治疗中的加入被证实是安全的,不会导致继发性恶性肿瘤。FL2000 研究中滤泡性淋巴瘤患者的长期随访证实了利妥昔单抗的持续临床获益,没有长期毒性。