类风湿因子滴度(而非 Fc 片段)可能与类风湿性关节炎患者服用抗肿瘤坏死因子药物的存活率密切相关。

Northern clinics of Istanbul Pub Date : 2024-04-25 eCollection Date: 2024-01-01 DOI:10.14744/nci.2023.01643
Huseyin Kaplan, Gizem Cengiz, Isa Cuce, Senem Sas, Emre Senkoy, Mustafa Calis, Orhun Ozturk, Huseyin Demir, Mehmet Kirnap
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引用次数: 0

摘要

目的研究肿瘤坏死因子(TNF)抑制剂中的Fc片段和类风湿因子(RF)滴度对类风湿性关节炎(RA)患者的治疗存活率、疾病活动性和实验室指标的影响:在这项回顾性队列研究中,纳入了在 2017 年 1 月至 2020 年 3 月期间开始接受任何抗肿瘤坏死因子治疗并持续治疗至少 6 个月的 RA 患者。根据患者是否继续或停止治疗,以及抗肿瘤坏死因子结构中是否存在 Fc 部分,分别比较了患者的数据。服用不含Fc片段的certolizumab pegol(CZP)的患者被归入 "不含Fc组"(wo/Fc),而服用其他药物(阿达木单抗、依那西普、戈利木单抗和英夫利昔单抗)的患者被归入 "含Fc组"(w/Fc):在有数据可查的 221 名 RA 患者中,有 52 名患者符合纳入标准并被纳入研究。在治疗的第三个月,wo/Fc 组与 w/Fc 组的 DAS28-CRP 评分有明显差异(p=0.012)。然而,这种差异在治疗的第六个月并没有持续(P=0.384)。根据cox-回归结果,在对其他候选预测因子的影响进行调整后,RF滴度对抗肿瘤坏死因子药物的存活率有显著影响(危险比:1.007 (1.002-1.012),p=0.009):我们的研究结果表明,与 Fc 片段相比,RF 滴度是影响抗肿瘤坏死因子药物存活率的更重要的风险因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Rheumatoid factor titers, but not Fc fragments, may be strongly associated with drug survival of anti-TNF agents in patients with rheumatoid arthritis.

Objective: To investigate the effects of both the Fc fragment in tumor necrosis factor (TNF) inhibitors and rheumatoid factor (RF) titers on treatment survival, disease activity, and laboratory parameters in patients with rheumatoid arthritis (RA).

Methods: In this retrospective cohort study, patients with RA who had started any anti-TNF therapy between January 2017 and March 2020 and who had stayed on this treatment for at least six months were included. The data of the patients were compared separately according to continuation or discontinuation of treatment and the presence or absence of Fc portion in the structure of anti-TNFs. Patients who were taking certolizumab pegol (CZP) without the Fc fragment were placed in the "without Fc group" (wo/Fc), while patients who were taking other drugs (adalimumab, etanercept, golimumab, and infliximab) were placed in the "with Fc group" (w/Fc).

Results: Among the 221 RA patients whose data were available, 52 patients met the inclusion criteria and were included in the study. There was a significant difference in the DAS28-CRP score between wo/Fc group and w/Fc group in the third month of treatment (p=0.012). However, this difference did not persist at the sixth month of treatment (p=0.384). According to the cox-regression results, RF titers were determined to have a significant impact on the drug survival of anti-TNF agents when adjustments were made for the effects of other candidate predictors (Hazard ratio: 1.007 (1.002-1.012), p=0.009).

Conclusion: Our results suggest that compared to the Fc fragment, RF titers were the more important risk factor in survival of anti-TNF drugs.

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