Hôpital Bicêtre, Institut Pour la Santé et Recherche Médicale (INSERM) U 1012, Université Paris-Sud 11, Le Kremlin Bicêtre, France.
Ann Rheum Dis. 2011 Nov;70(11):1895-904. doi: 10.1136/ard.2010.149419. Epub 2011 Sep 1.
This project was undertaken to assess the risk of malignancy in patients with rheumatoid arthritis treated with tumour necrosis factor inhibitors (TNFi) in clinical practice, as recorded in prospective, observational studies.
The authors undertook comprehensive searches of MEDLINE, EMBASE, the Cochrane Database of Systematic Reviews and American College of Rheumatology, European League against Rheumatism and British Society for Rheumatology conference abstracts according to a prespecified protocol.
The searches identified 2039 full-text papers and 1979 conference abstracts, of which 21 full texts and eight abstracts met the inclusion criteria. The pooled estimate for the risk of all-site malignancy from seven studies was 0.95 (95% CI 0.85 to 1.05). Two studies reported there was no evidence that longer exposure to TNFi agents increased the risk of malignancy. In patients with previous malignancies there was a higher risk of a new/recurring malignancy. This risk was not increased further by exposure to TNFi, although CI were wide. Results from four studies showed that patients treated with TNFi have a significantly increased risk of developing a non-melanoma skin cancer (1.45, 95% CI 1.15 to 1.76). In addition, patients are at an increased risk of developing melanoma, as the pooled estimate from two studies was 1.79 (95% CI 0.92 to 2.67). The pooled estimate for the risk of lymphoma was 1.11 (95% CI 0.70 to 1.51).
This systematic review and meta-analysis shows that TNFi treatments do not increase the risk of malignancy, particularly lymphoma. However, they do appear to increase the risk of skin cancer, including melanoma.
本项目旨在评估在临床实践中使用肿瘤坏死因子抑制剂 (TNFi) 治疗类风湿关节炎患者的恶性肿瘤风险,该评估基于前瞻性观察性研究。
作者根据预设方案,全面检索了 MEDLINE、EMBASE、Cochrane 系统评价数据库以及美国风湿病学会、欧洲抗风湿病联盟和英国风湿病学会会议摘要。
检索共确定了 2039 篇全文论文和 1979 篇会议摘要,其中 21 篇全文和 8 篇摘要符合纳入标准。来自 7 项研究的汇总估计值显示,所有部位恶性肿瘤的风险为 0.95(95%CI 0.85 至 1.05)。两项研究报告称,没有证据表明更长时间暴露于 TNFi 药物会增加恶性肿瘤的风险。在有既往恶性肿瘤的患者中,新发/复发性恶性肿瘤的风险更高。虽然 CI 较宽,但 TNFi 暴露并未进一步增加这种风险。四项研究的结果表明,接受 TNFi 治疗的患者发生非黑色素瘤皮肤癌的风险显著增加(1.45,95%CI 1.15 至 1.76)。此外,由于两项研究的汇总估计值为 1.79(95%CI 0.92 至 2.67),患者发生黑色素瘤的风险也增加。来自两项研究的汇总估计值为 1.11(95%CI 0.70 至 1.51),提示淋巴瘤的风险增加。
本系统评价和荟萃分析表明,TNFi 治疗不会增加恶性肿瘤的风险,特别是淋巴瘤。然而,它们似乎确实会增加皮肤癌(包括黑色素瘤)的风险。