Wu Hongzhen, Lu Yi, Su Yun, Su Tao, Zhang Min, Zhi Min, Yao Jiayin
Department of Gastroenterology, The Sixth Affiliated Hospital of Sun Yat-Sen University, Guangzhou, Guangdong, 515000, People's Republic of China.
Biomedical Innovation Center, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, 515000, People's Republic of China.
J Inflamm Res. 2025 Aug 21;18:11463-11477. doi: 10.2147/JIR.S534439. eCollection 2025.
Inflammatory Bowel Disease presents significant management challenges, particularly in pediatric and elderly populations with refractory conditions. Despite advances in biologic therapies, current treatments remain limited with inconsistent response rates. This study investigated Upadacitinib efficacy in Asian adolescent and elderly populations with refractory IBD.
This single-center, retrospective cohort study examined 21 patients at the Sixth Affiliated Hospital of Sun Yat-sen University: 11 pediatric refractory CD patients (aged 9-17) and 10 elderly refractory UC patients (aged 60+). Diagnoses were confirmed via comprehensive criteria including clinical symptoms, biomarkers, endoscopic findings, histological examination, and radiological results. Patients had refractory IBD, defined as failure of at least two biologic agents with distinct mechanisms or comorbid psychosocial complications impairing disease management.
Pediatric CD patients showed remarkable efficacy, with 72.7% achieving steroid-free clinical remission at week 12, maintained at 57.1% by week 24, and reaching 88.9% at final follow-up. Endoscopic remission improved from 50% at week 12 to 57.1% at final follow-up. Elderly UC patients showed modest outcomes, with 20% achieving clinical remission throughout the study. Laboratory parameters demonstrated significant improvements, particularly in C-reactive protein and albumin levels. The safety profile was generally favorable with minimal adverse events. Teenage CD patients experienced minor dermatological side effects, while UC patients showed no significant adverse events. One serious pneumonia case in the elderly group highlighted potential infection risks.
This pioneering Asian study provides critical insights into UPA's potential as alternative treatment for challenging IBD cases in adolescent and elderly populations, demonstrating different efficacy and safety profiles across age groups and contributing evidence for personalized medicine approaches in managing refractory IBD.
炎症性肠病带来了重大的管理挑战,尤其是在患有难治性疾病的儿童和老年人群中。尽管生物疗法取得了进展,但目前的治疗方法仍然有限,缓解率不一致。本研究调查了乌帕替尼在亚洲青少年和老年难治性炎症性肠病患者中的疗效。
这项单中心回顾性队列研究在中山大学附属第六医院检查了21名患者:11名儿童难治性克罗恩病患者(9 - 17岁)和10名老年难治性溃疡性结肠炎患者(60岁以上)。通过包括临床症状、生物标志物、内镜检查结果、组织学检查和放射学结果在内的综合标准确诊。患者患有难治性炎症性肠病,定义为至少两种具有不同作用机制的生物制剂治疗失败,或伴有损害疾病管理的合并心理社会并发症。
儿童克罗恩病患者显示出显著疗效,72.7%的患者在第12周实现无类固醇临床缓解,到第24周维持在57.1%,最终随访时达到88.9%。内镜缓解率从第12周的50%提高到最终随访时的57.1%。老年溃疡性结肠炎患者的结果一般,整个研究期间有20%的患者实现临床缓解。实验室参数显示有显著改善,尤其是C反应蛋白和白蛋白水平。安全性总体良好,不良事件极少。青少年克罗恩病患者出现轻微的皮肤副作用,而溃疡性结肠炎患者未出现显著不良事件。老年组的一例严重肺炎病例突出了潜在的感染风险。
这项开创性的亚洲研究为乌帕替尼作为青少年和老年人群中具有挑战性的炎症性肠病病例的替代治疗方法的潜力提供了重要见解,证明了不同年龄组的疗效和安全性特征不同,并为难治性炎症性肠病的个性化医疗方法提供了证据。