乌达帕替尼加强化粒细胞和单核细胞吸附性血液透析作为难治性溃疡性结肠炎诱导治疗的有效性和安全性。

IF 1.6 Q2 MEDICINE, GENERAL & INTERNAL
Journal of clinical medicine research Pub Date : 2024-05-01 Epub Date: 2024-05-29 DOI:10.14740/jocmr5165
Satoshi Tanida, Shun Sasoh, Takahiro Otani, Yoshimasa Kubota, Tesshin Ban, Tomoaki Ando, Makoto Nakamura, Takashi Joh
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引用次数: 0

摘要

选择性 Janus 激酶 (JAK) 抑制剂或强化粒细胞和单核细胞吸附性剥脱术 (GMA) 的单药治疗仅限于难治性溃疡性结肠炎 (UC) 患者。以前没有任何报道描述过对传统药物和阿达木单抗耐药的顽固性 UC 采用乌达替尼(UPA)加强化 GMA(每周两次)联合疗法的疗效(包括组织病理学评估)和安全性。这项回顾性研究评估了UPA加强化GMA诱导联合疗法对难治性UC患者为期10周的临床和组织病理学疗效。在接受 UPA 加强化 GMA 联合疗法的 8 名患者(中度 UC,n = 1;重度 UC,n = 7)中,50.0% 的患者在 10 周前实现了临床缓解。10周时,组织学内镜下粘膜改善和粘膜愈合的患者比例分别为62.5%和12.5%。在排除一名因不耐受 UPA 而在第 10 周停止治疗的患者后,基线时的平均梅奥评分、内镜子评分和 C 反应蛋白浓度分别为 11.43 ± 0.37、3 ± 0 和 1.29 ± 0.70 mg/dL。10周时的相应值分别为2.28 ± 0.77(P < 0.03)、1.14 ± 0.34(P < 0.03)和0.03 ± 0.008 mg/dL(P < 0.05)。有一名患者出现带状疱疹、肌酐磷酸激酶暂时升高和贫血等不良反应。一名患者在第 4 周因 UPA 引起的暂时性味觉异常而停止了联合治疗。对于常规药物和抗肿瘤坏死因子-α抗体治疗无效的顽固性UC患者,UPA加强化GMA的联合疗法似乎可以达到令人满意的诱导临床缓解和组织病理学改善的效果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Efficacy and Safety of Upadacitinib Plus Intensive Granulocyte and Monocyte Adsorptive Apheresis as Induction for Intractable Ulcerative Colitis.

Monotherapy with a selective Janus kinase (JAK) inhibitor or intensive granulocyte and monocyte adsorptive apheresis (GMA) has been limited to patients with intractable ulcerative colitis (UC). No previous reports have described the efficacy including histopathological evaluations and the safety of combination therapy with upadacitinib (UPA) plus intensive GMA (two sessions per week) for intractable UC showing resistance to conventional agents and adalimumab. This retrospective study evaluated the 10-week clinical and histopathological efficacy of induction combination therapy with UPA plus intensive GMA in patients with intractable UC. Among eight patients (moderate UC, n = 1; severe UC, n = 7) who received combination therapy with UPA plus intensive GMA, 50.0% had achieved clinical remission by 10 weeks. Percentages of patients with histological-endoscopic mucosal improvement and mucosal healing at 10 weeks were 62.5% and 12.5%, respectively. After excluding one patient who discontinued treatment by week 10 because of intolerance for UPA, mean full Mayo score, endoscopic subscore and C-reactive protein concentration at baseline were 11.43 ± 0.37, 3 ± 0 and 1.29 ± 0.70 mg/dL, respectively. Corresponding values at 10 weeks were 2.28 ± 0.77 (P < 0.03), 1.14 ± 0.34 (P < 0.03) and 0.03 ± 0.008 mg/dL (P < 0.05), respectively. Adverse events of herpes zoster, temporary increase in creatinine phosphokinase and anemia were observed in one patient each. One patient discontinued combination therapy at week 4 because of temporary taste abnormality due to UPA. Combination comprising UPA plus intensive GMA appears likely to achieve satisfactory induction of clinical remission and histopathological improvement for patients with intractable UC for whom conventional agents and anti-tumor necrosis factor-α antibody have failed.

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