P468 抗药物抗体与超治疗浓度抗肿瘤坏死因子的相关性

J. Kim, M. Walshe, K. Borowski, R. Milgrom, J. Stempak, S. Lee, K. Croitoru, M. Silverberg
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The drug concentrations were classified as subtherapeutic (IFX: <3 µg/mL; ADA: <5 µg/mL), therapeutic (IFX: 3-8 µg/mL; ADA 5-10 µg/mL), and supratherapeutic (IFX > 8 µg/mL; ADA > 10 µg/mL) concentrations regardless of the timing of blood sample collection. We analysed the relationship between i) drug concentrations and ii) the presence and absence of anti-drug antibodies with use of systemic corticosteroids and anti-TNF discontinuation.\n \n \n \n Of 172 patients (122 CD [70.9%], 44 UC [25.6%], 3 IBD-U [1.7%], and 3 IBD-pouch [1.7%]), the median age was 32.3 years (range, 24.8-42.5), and the median duration of IBD was 9.7 years (range 5.3-15.6). IFX and ADA were used in 81 (47.1%) and 91 (52.9%) patients, respectively, and concurrent usage of immunomodulators and systemic corticosteroids was observed in 39 (22.7%) and 23 (13.4%) patients, respectively. 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引用次数: 0

摘要

抗肿瘤坏死因子-α(anti-TNFα)药物血清浓度低和抗药抗体的存在与炎症性肠病(IBD)治疗效果不佳有关。我们旨在评估同时存在抗药抗体和超治疗药物浓度的患者的预后。 我们前瞻性地招募了正在接受英夫利西单抗(IFX)或阿达木单抗(ADA)维持治疗的 IBD 患者。对血清药物浓度和抗药抗体进行了测定(Anser,Prometheus)。无论血样采集时间如何,药物浓度都被归类为亚治疗浓度(IFX:8 µg/mL;ADA > 10 µg/mL)。我们分析了 i) 药物浓度和 ii) 抗药性抗体的存在与否与使用全身性皮质类固醇激素和停用抗肿瘤坏死因子之间的关系。 在 172 名患者(122 名 CD [70.9%]、44 名 UC [25.6%]、3 名 IBD-U [1.7%] 和 3 名 IBD-袋 [1.7%])中,中位年龄为 32.3 岁(范围为 24.8-42.5),中位 IBD 病程为 9.7 年(范围为 5.3-15.6)。81(47.1%)和 91(52.9%)名患者使用了 IFX 和 ADA,39(22.7%)和 23(13.4%)名患者同时使用了免疫调节剂和系统性皮质类固醇激素。在 74 例(43.0%)、32 例(18.6%)和 66 例(38.4%)患者中分别观察到超治疗浓度、治疗浓度和亚治疗浓度。与没有抗体的患者相比,有抗药抗体的患者(n = 79,45.9%)出现亚治疗药物浓度的频率更高(68.4% vs 12.9%,P < 0.001),而且抗体的存在是停用抗肿瘤坏死因子α药物的独立预测因素(危险比 3.50,95% 置信区间 1.88-6.51,P < 0.001,图 1A)。在亚组分析中,与药物浓度低于治疗水平的患者相比,具有抗药抗体和药物浓度高于治疗水平的患者的药物持续性有改善的趋势,尽管效果不显著(P = 0.099,图 1B)。然而,这组患者的持续用药情况仍然比没有抗体的患者差(P = 0.003)。最后,无论是抗 TNFα 浓度还是抗药抗体的存在,都与 6 个月内是否需要额外使用全身性皮质类固醇无关。 尽管抗肿瘤坏死因子α的药物浓度超过治疗水平,但抗药抗体的存在仍可预测抗肿瘤坏死因子α药物的停药情况。虽然超治疗药物浓度可改善抗肿瘤坏死因子α药物在有抗药抗体患者中的治疗持久性,但其持续时间不如无抗体患者。
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P468 Relevance of anti-drug antibodies in context of supra-therapeutic anti-TNF concentrations
The low serum concentration of anti-tumor necrosis factor-alpha (anti-TNFα) agents and the presence of anti-drug antibodies are related to poor therapeutic outcomes in inflammatory bowel disease (IBD). We aimed to evaluate the prognosis of patients having both antidrug antibodies and supratherapeutic drug concentrations. IBD patients on maintenance infliximab (IFX) or adalimumab (ADA) therapy were prospectively recruited. Serum drug concentrations and antidrug antibodies were measured (Anser, Prometheus). The drug concentrations were classified as subtherapeutic (IFX: <3 µg/mL; ADA: <5 µg/mL), therapeutic (IFX: 3-8 µg/mL; ADA 5-10 µg/mL), and supratherapeutic (IFX > 8 µg/mL; ADA > 10 µg/mL) concentrations regardless of the timing of blood sample collection. We analysed the relationship between i) drug concentrations and ii) the presence and absence of anti-drug antibodies with use of systemic corticosteroids and anti-TNF discontinuation. Of 172 patients (122 CD [70.9%], 44 UC [25.6%], 3 IBD-U [1.7%], and 3 IBD-pouch [1.7%]), the median age was 32.3 years (range, 24.8-42.5), and the median duration of IBD was 9.7 years (range 5.3-15.6). IFX and ADA were used in 81 (47.1%) and 91 (52.9%) patients, respectively, and concurrent usage of immunomodulators and systemic corticosteroids was observed in 39 (22.7%) and 23 (13.4%) patients, respectively. Supratherapeutic, therapeutic, and subtherapeutic concentrations were observed in 74 (43.0%), 32 (18.6%), and 66 (38.4%), respectively. The patients with antidrug antibodies (n = 79, 45.9%) showed a higher frequency of having subtherapeutic drug concentrations (68.4% vs 12.9%, P < 0.001) compared to those without antibodies, and the presence of antibodies was an independent predictor of discontinuation of anti-TNFα agents (hazard ratio 3.50, 95% confidence interval 1.88-6.51, P < 0.001, Fig. 1A). In subgroup analysis, patients with antidrug antibodies and supratherapeutic drug concentration exhibited a tendency to have improved drug persistence compared to those with subtherapeutic drug concentration, albeit insignificantly (P = 0.099, Fig. 1B). However, the persistence in this group was still poorer than that observed in patients without antibodies (P = 0.003). Finally, neither anti-TNFα concentrations nor the presence of antidrug antibodies were associated with the need for additional systemic corticosteroid use within 6 months. The presence of antidrug antibodies can predict the discontinuation of anti-TNFα agents despite supratherapeutic drug levels. While supratherapeutic drug concentration may improve the treatment persistence of anti-TNFα agents in patients with anti-drug antibodies, it does not last as long as in those without antibodies.
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