Long‐term follow‐up of anti‐infliximab antibodies in radiographic axial spondyloarthritis patients: a marker of drug survival and tapering

医学 英夫利昔单抗 相伴的 逐渐变细 内科学 甲氨蝶呤 胃肠病学 队列 外科 类风湿性关节炎 肿瘤坏死因子α 计算机图形学(图像) 计算机科学
作者
Clarissa Queiroz Pimentel,Ana Cristina Medeiros‐Ribeiro,Andréa Yukie Shimabuco,Percival D. Sampaio‐Barros,Júlio César Bertacini de Moraes,Cláudia Goldenstein-Schainberg,Célio Roberto Gonçalves,Elaine Pires Leon,Léonard de Vinci Kanda Kupa,Sandra Gofinet Pasoto,Nádia Emi Aikawa,Clóvis A. Silva,Eloísa Bonfá,Carla Gonçalves Schahin Saad
出处
期刊:Arthritis & rheumatology [Wiley]
标识
DOI:10.1002/art.42923
摘要

Objectives To evaluate the influence of anti‐infliximab antibodies (anti‐IFX) on 3 different points of care: response/tolerance to infliximab (IFX), tapering strategy, and in a subsequent treatment with a second tumor necrosis factor inhibitor (TNFi). Methods A prospective cohort of 60 radiographic axial spondyloarthritis (r‐axSpA) patients under IFX were evaluated retrospectively regarding clinical/laboratorial data, IFX levels and anti‐IFX, at baseline, after 6, 12‐14, 22‐24, 48‐54, 96‐102 weeks and before tapering or switching. Results Anti‐IFX were detected in 27 (45%) patients, of whom 23 (85.1%) became positive in the first year of IFX treatment. In comparison to negative anti‐IFX group, anti‐IFX positive patients demonstrated the following: less use of methotrexate (MTX) as a concomitant treatment to IFX (5 [18.5%] vs. 14 [42.4%]; p=0.048); more infusion reactions at 22‐24 weeks (p=0.020) and 48‐54 weeks (p=0.034); more treatment failures (p=0.028) at 48‐54 weeks; reduced overall IFX survival (p<0.001); and lower sustained responses (p=0.044). Of note, positive anti‐IFX patients exhibited a shorter tapering survival (9.9 months [95% CI 4.0‐15.8] vs 63.4 months [95% CI 27.9‐98.8]; p=0.004) in comparison with negative anti‐IFX patients. Conversely, for patients who failed IFX, positive anti‐IFX patients had better clinical response to the second TNFi at 3 (15 [83.3%] vs. 3 [27.3%]; p=0.005) and 6 months (15 [83.3%] vs. 4 [36.4%]; p=0.017) than the negative anti‐IFX patients after switching. Conclusions This study provided novel data that anti‐IFX is a parameter for reduced tapering survival, reinforcing its detection to guide clinical decision. Additionally, we confirmed in a long‐term cohort the anti‐IFX association with worse IFX performance and as predictor of 2 nd TNFi good clinical response.

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