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抗 TNF 治疗对类风湿关节炎患者角质形成细胞皮肤癌发病率的影响:英国风湿病学会生物制剂登记处的纵向结果。

The influence of anti-TNF therapy upon incidence of keratinocyte skin cancer in patients with rheumatoid arthritis: longitudinal results from the British Society for Rheumatology Biologics Register.

机构信息

Arthritis Research UK Epidemiology Unit, The University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.

出版信息

Ann Rheum Dis. 2012 Jun;71(6):869-74. doi: 10.1136/annrheumdis-2011-200622. Epub 2012 Jan 12.

Abstract

OBJECTIVES

To compare the risk of keratinoctye skin cancer (basal cell carcinoma (BCC) and squamous cell carcinoma (SCC)) in patients treated for rheumatoid arthritis (RA) compared with the general population, and to determine whether anti-tumour necrosis factor (TNF) therapy exacerbates this risk.

METHODS

Patients with RA enrolled in the British Society for Rheumatology Biologics Register, a prospective national cohort established in 2001 to monitor the safety of anti-TNF, were followed until 2008. 11 881 patients treated with anti-TNF were compared with 3629 patients receiving non-biological disease-modifying antirheumatic drugs (nbDMARD). Standardised incidence ratios (SIR) were calculated for each cohort and rates between cohorts were compared using Cox proportional HR, adjusted using inverse probability of treatment weighting.

RESULTS

SIR for skin cancer was increased in both cohorts compared with the English population: SIR 1.72 (95% CI 1.43 to 2.04) anti-TNF; 1.83 (95% CI 1.30 to 2.50) nbDMARD only. In patients without previous skin cancer, BCC incidence per 100 000 patient-years was 342 (95% CI 290 to 402) after anti-TNF and 407 (95% CI 288 to 558) after nbDMARD. HR after anti-TNF adjusted for treatment weighting was 0.95 (95% CI 0.53 to 1.71). SCC incidence per 100 000 patient-years: anti-TNF 53 (95% CI 33 to 79); nbDMARD 43 (95% CI 12 to 110); adjusted HR 1.16 (95% CI 0.35 to 3.84).

CONCLUSIONS

Skin cancers were increased among treated patients with RA. No evidence was found that anti-TNF therapy exacerbates the risk of BCC or SCC but this cannot be excluded. Patients with RA should use sun protection and be monitored for skin cancer.

摘要

目的

比较接受类风湿关节炎(RA)治疗的患者与普通人群相比发生角质细胞皮肤癌(基底细胞癌(BCC)和鳞状细胞癌(SCC))的风险,并确定抗肿瘤坏死因子(TNF)治疗是否会加剧这种风险。

方法

2001 年成立的英国风湿病学会生物制剂注册处是一个前瞻性的全国队列,旨在监测抗 TNF 的安全性,本研究纳入其中的患者接受 RA 治疗,随访至 2008 年。将 11881 例接受抗 TNF 治疗的患者与 3629 例接受非生物改良抗风湿药物(nbDMARD)治疗的患者进行比较。计算了每个队列的标准化发病率比(SIR),并使用 Cox 比例 HR 比较了队列之间的比率,采用逆概率治疗加权进行调整。

结果

与英国人群相比,两个队列的皮肤癌 SIR 均升高:抗 TNF 队列为 1.72(95%CI 1.43 至 2.04),nbDMARD 队列为 1.83(95%CI 1.30 至 2.50)。在无既往皮肤癌的患者中,抗 TNF 治疗后每 100000 患者年的 BCC 发生率为 342(95%CI 290 至 402),nbDMARD 治疗后为 407(95%CI 288 至 558)。经治疗权重调整后的抗 TNF 治疗后 HR 为 0.95(95%CI 0.53 至 1.71)。每 100000 患者年的 SCC 发生率:抗 TNF 队列为 53(95%CI 33 至 79);nbDMARD 队列为 43(95%CI 12 至 110);调整后的 HR 为 1.16(95%CI 0.35 至 3.84)。

结论

接受 RA 治疗的患者皮肤癌发生率升高。没有证据表明抗 TNF 治疗会加剧 BCC 或 SCC 的风险,但不能排除这种可能性。RA 患者应使用防晒措施,并监测皮肤癌。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a61/3371225/e41e5ef3eb17/ard-71-6-0869-fig1.jpg

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