janus激酶抑制剂和甲氨蝶呤联合应用对类风湿关节炎患者恶性肿瘤的影响:随机对照试验的系统评价和荟萃分析。

Q1 Medicine Auto-Immunity Highlights Pub Date : 2021-04-28 DOI:10.1186/s13317-021-00153-5
Vinod Solipuram, Akhila Mohan, Roshniben Patel, Ruoning Ni
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引用次数: 18

摘要

背景:类风湿性关节炎(RA)是一种全身性自身免疫性疾病。常用甲氨蝶呤(MTX)联合Janus激酶抑制剂(JAKi)联合治疗。RA患者发生恶性肿瘤的风险增加,然而,目前尚不清楚联合治疗是否与更高的风险相关。目的:评价JAKi联合甲氨蝶呤治疗RA患者与单用甲氨蝶呤相比发生恶性肿瘤的风险。方法:全面检索PubMed、Cochrane和Embase从成立到2020年7月期间接受JAKi和MTX治疗的RA患者的随机对照试验(rct)。主要终点是恶性事件,非黑素瘤性皮肤癌(NMSC)和恶性肿瘤(不包括NMSC),次要终点是严重不良事件(SAE),死亡。采用Mantel-Haenszel随机效应法计算风险比(RR)和95% CI。结果:659篇出版物被筛选,13项随机对照试验共纳入6911例患者。恶性肿瘤差异无统计学意义[RR = 1.42;95% CI (0.59, 3.41)], NMSC [RR = 1.44(0.36, 5.76)]和除NMSC外的恶性肿瘤[RR = 1.12(0.40, 3.13)]均未发现。两组间SAE [RR = 1.15(0.90, 1.47)]和死亡[RR = 1.99(0.75, 5.27)]差异无统计学意义。结论:与单用MTX相比,JAKi联合MTX与恶性肿瘤风险增加无关。与单独使用甲氨蝶呤相比,RA患者的SAE和死亡风险没有增加。
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Effect of janus kinase inhibitors and methotrexate combination on malignancy in patients with rheumatoid arthritis: a systematic review and meta-analysis of randomized controlled trials.

Background: Rheumatoid arthritis (RA) is a systemic autoimmune disease. The combination therapy of methotrexate (MTX) and Janus kinase inhibitor (JAKi) is commonly used. Patients with RA are at increased risk of malignancy, however, it remains unclear whether the combination therapy is associated with a higher risk.

Objective: To assess the malignancy risk among patients with RA receiving combination therapy of JAKi and MTX compared to MTX alone.

Methods: PubMed, Cochrane and Embase were thoroughly searched for randomized controlled trials (RCTs) in patients with RA receiving JAKi and MTX, from inception to July 2020. Primary endpoints were malignancy events, Non melanomatous skin cancer (NMSC) and malignancy excluding NMSC and secondary endpoints were serious adverse events (SAE), deaths. Risk ratio (RR) and 95% CI were calculated using the Mantel-Haenszel random-effect method.

Results: 659 publications were screened and 13 RCTs with a total of 6911 patients were included in the analysis. There was no statistically significant difference in malignancy [RR = 1.42; 95% CI (0.59, 3.41)], neither NMSC [RR = 1.44 (0.36, 5.76)] nor malignancies excluding NMSC [RR = 1.12 (0.40, 3.13)]. No statistically significant difference between the two groups for SAE [RR = 1.15 (0.90, 1.47)] and deaths [RR = 1.99 (0.75, 5.27)] was found.

Conclusion: The adjunction of JAKi to MTX is not associated with an increased risk of malignancy when compared to MTX alone. There is no increased risk of SAE and deaths when compared to MTX alone in patients with RA.

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