Department of Pathology and Laboratory Medicine, UCSD School of Medicine, San Diego, CA, USA.
Clin Rheumatol. 2012 Apr;31(4):631-6. doi: 10.1007/s10067-011-1895-y. Epub 2011 Nov 18.
The 2008 edition of the WHO Classification of Tumours of Haematopoietic and Lymphoid tissues recognizes a new diagnostic entity termed "other iatrogenic immunodeficiency-associated lymphoproliferative disorders" highlighting lymphomas arising in patients treated with immunosuppressive agents for autoimmune disorders. The role of antitumor necrosis factor alpha therapy (anti-TNFα) and lymphoma risk in rheumatoid arthritis (RA) patients remains unclear; therefore, the goal of our study was to determine whether anti-TNFα therapy is associated with iatrogenic lymphomas. A meta-analysis of all randomized controlled clinical trials published (2000-2009) in RA patients receiving anti-TNFα therapy was performed. Fourteen studies fulfilled all search criteria and included 2,306 control patients and 5,179 patients treated with anti-TNFα therapy, namely etanercept, adalumimab, and infliximab. Clinical information including the number of patients, age, gender, lymphoma rates, and follow-up time was recorded. The overall rate and rate differences were analyzed using the DerSimonian and Laird method. Of the control group, four (4/2,306, 0.17%) patients developed hematolymphoid neoplasms. Eleven (11/5,179, 0.21%) patients receiving anti-TNFα therapy developed lymphomas. The adjusted overall rates are 0.36 lymphomas per 1,000 person-years in patients who did not receive anti-TNFα therapy versus 1.65 lymphomas per 1,000 person-years in patients who received anti-TNFα therapy. The corresponding 95% confidence interval for this rate difference is (-0.214, 2.79). The adjusted rate difference is 1.29 lymphomas per 1,000 person-years (95% CI, -0.21, 2.8; p value = 0.093). The corresponding p value is p = 0.0928. There is a suggestion of increased lymphomas in the treated group, with the predominant subset being B-cell lymphomas. Since the outcome of lymphoma is rare, it does not reach statistical significance of p < 0.05.
2008 年版世界卫生组织造血和淋巴组织肿瘤分类中确定了一个新的诊断实体,称为“其他医源性免疫缺陷相关淋巴增生性疾病”,突出了在自身免疫性疾病患者中接受免疫抑制药物治疗后发生的淋巴瘤。抗肿瘤坏死因子 α 治疗(抗 TNFα)和淋巴瘤风险在类风湿关节炎(RA)患者中的作用尚不清楚;因此,我们的研究目标是确定抗 TNFα 治疗是否与医源性淋巴瘤相关。对所有已发表的(2000-2009 年)接受抗 TNFα 治疗的 RA 患者的随机对照临床试验进行了荟萃分析。14 项研究符合所有检索标准,包括 2306 例对照患者和 5179 例接受抗 TNFα 治疗的患者,即依那西普、阿达木单抗和英夫利昔单抗。记录了包括患者数量、年龄、性别、淋巴瘤发生率和随访时间在内的临床信息。使用 DerSimonian 和 Laird 方法分析了总体发生率和发生率差异。在对照组中,有 4 例(4/2306,0.17%)患者发生血液淋巴系统肿瘤。11 例(11/5179,0.21%)接受抗 TNFα 治疗的患者发生淋巴瘤。未接受抗 TNFα 治疗的患者每 1000 人年发生 0.36 例淋巴瘤,接受抗 TNFα 治疗的患者每 1000 人年发生 1.65 例淋巴瘤。该差异的相应 95%置信区间为(-0.214,2.79)。调整后的率差为每 1000 人年 1.29 例淋巴瘤(95%CI,-0.21,2.8;p 值=0.093)。相应的 p 值为 p=0.0928。治疗组中淋巴瘤的发生率略有增加,主要亚组为 B 细胞淋巴瘤。由于淋巴瘤的结局罕见,因此未达到 p<0.05 的统计学意义。