P611 Relation between AntiTNF levels during the induction and clinical and radiological outcomes in perianal Crohn´s disease

C Amiama Roig, C Suarez Ferrer, E Martin Arranz, J L Rueda Garcia, M Sánchez Azofra, J Poza Cordón, I Gonzalez Diaz, C Amor Costa, M D Martín-Arranz
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Abstract

Background Perianal Crohn's disease(PCD) significantly impacts quality of life with poor long-term prognosis. Anti-tumor necrosis factor(anti-TNF) therapy improves fistula closure rates. However, achieving permanent closure remains challenging. Our aim is to evaluate the relation between antiTNF(infliximab (IFX) and adalimumab(ADA) serum concentrations at induction(w2 and 6), and clinical and radiological outcomes at w24 and w52 Methods We conducted a single tertiary center, retrospective, cohort study including patients with an established diagnosis of PCD treated with antiTNF because of perianal activity. Variables related to their PCD(phenotype, location, fistulas type) were collected. Regarding treatment, we collected serum levels at week 2,6,24 and 52, concomitant treatment and setons presence. We defined clinical response as the absence of drainage on physical examination and clinical remission as the absence of external fistula openings. Radiological response was defined as the absence of T2 hypersignal, gadolinium enhancement, abscess and proctitis in pelvic MRI Results 65 patients were included, baseline characteristics are in Table1. None of the demographic characteristics collected were statistically significant related to clinical or radiological response although non smokers(p=0.01), ileal(p=0.02) and non-stricturing disease(p=0.01) had statistically significant higher drug levels. Taking into account the clinical response at w52, IFX mean levels at w2 were 25.8µg/mL(SD 4.1) in non responders and 30.9µg/mL(SD 14) in responders(p=0.39). At w6 they were 17.2µg/mL(SD 12.2) and 19.4µg/mL(SD 13.8) respectively(p=0.7). ADA mean levels at w2 were 13.3µg/mL(SD 7.7) in non responders and 14µg/mL(SD 6.3) in responders(p=0.87). At w6 they were 10.1µg/mL(SD 3.3) and 12µg/mL(SD 6.1) respectively(p= 0.59). For radiological response at w52 IFX mean levels at w2 were 27µg/mL(SD 15.3) in non responders and 32.7µg/mL(SD 14.5) in responders(p=0.45). At w6 the mean levels were 15.9µg/mL(SD 6.7) and 23.7µg/mL(SD 14.8) respectively(p=0.27). In ADA group the mean levels at w2 were 14.8µg/mL(SD 7.6) in responders and only one patient did not respond. At w6 ADA mean levels were 12.3µg/mL(SD 5.9) in non responders and 12.7µg/mL(SD 6.2) in responders(p=0.94). Early response at w24 was related with a long-term response at w52, 89.9% of the patients who responded at w52, had already responded at w24. Conclusion In our study we observed that almost 90% of the patients who had an early response also responded at w52, so trying to achieve an early response should be an aim in clinical practice. Despite the limited number of patients, our study shows a trend in the relationship between higher antiTNF levels and clinical and radiological response rates
P611 肛周克罗恩病诱导期间抗肿瘤坏死因子水平与临床和放射学结果的关系
背景肛周克罗恩病(PCD)严重影响生活质量,且长期预后不良。抗肿瘤坏死因子(anti-TNF)疗法可提高瘘管闭合率。然而,实现永久闭合仍具有挑战性。我们的目的是评估抗肿瘤坏死因子(英夫利昔单抗(IFX)和阿达木单抗(ADA))在诱导期(第2天和第6天)的血清浓度与第24天和第52天的临床和放射学结果之间的关系。 我们进行了一项单一三级中心的回顾性队列研究,研究对象包括确诊为因肛周活动而接受抗肿瘤坏死因子治疗的 PCD 患者。我们收集了与 PCD 相关的变量(表型、位置、瘘管类型)。在治疗方面,我们收集了第 2、6、24 和 52 周的血清水平、同时接受的治疗以及是否存在setons。我们将体格检查无引流定义为临床反应,将无外瘘开口定义为临床缓解。放射学反应的定义是盆腔磁共振成像中没有 T2 超信号、钆增强、脓肿和直肠炎。尽管非吸烟者(P=0.01)、回肠(P=0.02)和非狭窄性疾病(P=0.01)患者的药物水平较高,但所收集的人口统计学特征与临床或放射学反应均无显著相关性。考虑到第 52 周时的临床反应,第 2 周时无反应者的 IFX 平均水平为 25.8µg/mL(SD 4.1),有反应者为 30.9µg/mL(SD 14)(P=0.39)。在第 6 个月时,它们分别为 17.2µg/mL(SD 12.2) 和 19.4µg/mL(SD 13.8)(P=0.7)。第 2 个月时,无应答者的 ADA 平均水平为 13.3µg/mL(SD 7.7),有应答者为 14µg/mL(SD 6.3)(P=0.87)。第 6 个月时,它们分别为 10.1µg/mL(SD 3.3) 和 12µg/mL(SD 6.1)(P= 0.59)。对于放射学反应,在第 52 周时,无反应者的 IFX 平均水平为 27µg/mL(SD 15.3),有反应者为 32.7µg/mL(SD 14.5)(P=0.45)。第 6 个月时的平均水平分别为 15.9µg/mL(SD 6.7)和 23.7µg/mL(SD 14.8)(P=0.27)。在 ADA 组中,第 2 个月时有反应者的平均水平为 14.8µg/mL(标准差 7.6),只有一名患者没有反应。第 6 个月时,无应答者的 ADA 平均水平为 12.3µg/mL(SD 5.9),有反应者为 12.7µg/mL(SD 6.2)(P=0.94)。第 24 个月时的早期反应与第 52 个月时的长期反应相关,第 52 个月时有反应的患者中有 89.9% 在第 24 个月时已经有反应。结论 在我们的研究中,我们观察到近 90% 的早期反应患者在第 52 个月时也有反应,因此在临床实践中应将努力实现早期反应作为目标。尽管患者人数有限,但我们的研究表明,抗肿瘤坏死因子水平越高,临床和放射学反应率之间的关系就越趋于一致。
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