托法替尼在治疗儿童急性严重结肠炎中的作用

Guillermo Alejandro Costaguta, Chloé Girard, Véronique Groleau, Kelly Grzywacz, Martha Heather Dirks, Colette Deslandres
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Results Six patients were included with Pediatric Ulcerative Colitis Activity Index (PUCAI) scores ranging from 65 to 85 on admission, and 35 to 85 before tofacitinib was started (P 0.07). Median response time was 72 h. A median decrease of 40 points in PUCAI was noted (P 0.00001). Mean length of stay was 18 days with discharge 9 days after tofacitinib introduction. Haemoglobin, albumin, fecal calprotectin, and CRP improved after tofacitinib (P 0.02, P 0.02, P 0.025, and P 0.01, respectively). The mean follow-up was 8.5 months, four patients achieved complete remission and only one had a recrudescence of symptoms (P 0.01). One patient had a systemic Epstein-Barr virus infection prior to tofacitinib therapy, which resolved with rituximab treatment. No other complications were noted. Conclusions Tofacitinib response is rapid and impressive in children suffering from ASC, and the safety profile appears comparable to or better than other available treatments. 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摘要

急性严重结肠炎(ASC)发生在高达15%的儿童溃疡性结肠炎,具有很高的发病率和死亡率。治疗包括大剂量类固醇、英夫利昔单抗和挽救性治疗。不幸的是,多达20%的患者可能由于治疗失败而需要紧急结肠切除术。我们报告使用托法替尼治疗6例患者的经验。方法对我院电子病历资料进行回顾性分析。我们纳入了所有ASC和治疗失败的患者,在这些患者中,托法替尼被用作挽救性治疗。记录反应、并发症和病程。结果6例患者入院时儿童溃疡性结肠炎活动指数(PUCAI)评分为65 ~ 85分,托法替尼开始治疗前为35 ~ 85分(P < 0.07)。中位反应时间为72 h, PUCAI中位下降40分(P 0.00001)。使用托法替尼后平均住院时间为18天,出院时间为9天。托法替尼治疗后,血红蛋白、白蛋白、粪便钙保护蛋白和CRP均有改善(分别为P < 0.02、P < 0.02、P < 0.025和P < 0.01)。平均随访8.5个月,4例患者完全缓解,1例复发(p0.01)。1例患者在托法替尼治疗前出现系统性eb病毒感染,经利妥昔单抗治疗后消退。未发现其他并发症。结论:托法替尼对ASC患儿的反应迅速且令人印象深刻,其安全性似乎与其他可用治疗相当或更好。在未来,托法替尼应该整合到儿科方案中。
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The Role of Tofacitinib in the Treatment of Acute Severe Colitis in Children
Abstract Objectives Acute severe colitis (ASC) occurs in up to 15 percent of children with ulcerative colitis, with a high index of morbidity and mortality. Treatment includes high-dose steroids, infliximab, and salvage therapies. Unfortunately, up to 20 percent of patients may need an urgent colectomy due to treatment failure. We report our experience using tofacitinib for the treatment of six patients. Methods A retrospective review of our medical electronic records was conducted. We included every patient with ASC and treatment failure, in whom tofacitinib was used as a salvage therapy. Response, complications, and disease course were noted. Results Six patients were included with Pediatric Ulcerative Colitis Activity Index (PUCAI) scores ranging from 65 to 85 on admission, and 35 to 85 before tofacitinib was started (P 0.07). Median response time was 72 h. A median decrease of 40 points in PUCAI was noted (P 0.00001). Mean length of stay was 18 days with discharge 9 days after tofacitinib introduction. Haemoglobin, albumin, fecal calprotectin, and CRP improved after tofacitinib (P 0.02, P 0.02, P 0.025, and P 0.01, respectively). The mean follow-up was 8.5 months, four patients achieved complete remission and only one had a recrudescence of symptoms (P 0.01). One patient had a systemic Epstein-Barr virus infection prior to tofacitinib therapy, which resolved with rituximab treatment. No other complications were noted. Conclusions Tofacitinib response is rapid and impressive in children suffering from ASC, and the safety profile appears comparable to or better than other available treatments. In the future, tofacitinib should be integrated into pediatric protocols.
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