Center of Autoinflammatory Diseases and Immunodeficiencies, Department of Pediatrics and Rheumatology, IRCCS Istituto G. Gaslini, Genova, Italy.
Division of Rheumatology, IRCCS Ospedale Pediatrico Bambino Gesù, Roma, Italy.
J Pediatr. 2023 May;256:18-26.e8. doi: 10.1016/j.jpeds.2022.11.034. Epub 2022 Dec 5.
To analyze, in a cohort of pediatric patients with recurrent pericarditis undergoing anti-interleukin (IL)-1 treatment: the agent and dosing used as first-line treatment, the long-term efficacy of IL-1 blockers, the percentage of patients achieving a drug-free remission, and the presence of variables associated with drug-free remission.
Data were collected from patients' charts. The annualized relapse rate (ARR) was used for evaluation of treatment efficacy, and bivariate logistic regression analysis was used for variables associated with drug-free remission.
Fifty-eight patients, treated between 2008 and 2018, were included in the study (mean follow-up. 2.6 years). Of the 56 patients treated with first-line drugs, 14 not responsive patients were underdosed. Fifty-seven patients were treated with anakinra: the ARR before and during daily treatment was 3.05 and 0.28, respectively (P < .0001); an increase to 0.83 was observed after the reduction/withdrawal of treatment (P < .0001). The switch from anakinra to canakinumab (5 patients) was associated to an increase of the ARR (0.49 vs 1.46), but without statistical significance (P = .215). At last follow-up, only 9 of the 58 patients had withdrawn all treatments. With the limits of a retrospective study and the heterogeneity between the patients enrolled in the study, a shorter duration of treatment with anakinra was the only variable associated with drug-free remission.
This study shows that most pediatric patients with recurrent pericarditis needing IL-1 blockade received an inadequate treatment with first-line agents. The effectiveness of anakinra is supported by this study, but few patients achieved drug-free remission. The different rate of response to anakinra and canakinumab may suggest a possible role of IL-1α in the pathogenesis of recurrent pericarditis.
在接受白细胞介素(IL)-1 治疗的复发性心包炎儿科患者队列中进行分析:作为一线治疗使用的药物和剂量、IL-1 阻滞剂的长期疗效、达到无药物缓解的患者比例,以及与无药物缓解相关的变量。
从患者病历中收集数据。采用年复发率(ARR)评估治疗效果,并采用双变量逻辑回归分析与无药物缓解相关的变量。
研究纳入了 58 名于 2008 年至 2018 年期间接受治疗的患者(平均随访 2.6 年)。在接受一线药物治疗的 56 名患者中,有 14 名未应答患者剂量不足。57 名患者接受了阿那白滞素治疗:在每日治疗前和治疗期间的 ARR 分别为 3.05 和 0.28(P<.0001);在减少/停药后观察到 ARR 增加到 0.83(P<.0001)。从阿那白滞素转换为卡那单抗(5 名患者)与 ARR 增加(0.49 比 1.46)相关,但无统计学意义(P=.215)。最后一次随访时,只有 58 名患者中的 9 名患者已停止所有治疗。由于这是一项回顾性研究的局限性以及研究中患者的异质性,阿那白滞素治疗时间较短是与无药物缓解相关的唯一变量。
本研究表明,大多数需要 IL-1 阻断的复发性心包炎儿科患者接受了一线药物的不充分治疗。阿那白滞素的有效性得到了本研究的支持,但很少有患者达到无药物缓解。阿那白滞素和卡那单抗的不同反应率可能提示白细胞介素-1α在复发性心包炎的发病机制中可能发挥作用。