IBD Unit, Guy's and St Thomas' Hospital, London, UK.
Department of Medicine, University of British Columbia, Vancouver, Canada.
Aliment Pharmacol Ther. 2022 Oct;56(7):1131-1145. doi: 10.1111/apt.17185. Epub 2022 Aug 22.
Tofacitinib is an oral small molecule Janus kinase inhibitor for the treatment of ulcerative colitis (UC). The induction dose is 10 mg twice daily (b.d.), whilst for maintenance therapy, the lowest effective dose should be used.
To examine published evidence on the two tofacitinib dosing strategies used in UC treatment, including expert interpretation of the data and how they could inform clinical practice.
The use of tofacitinib 5 or 10 mg b.d. was assessed using data from the tofacitinib UC clinical programme in the context of different clinical scenarios. We include experts' opinions on the clinical implications of dose adjustment to inform the benefit/risk of using tofacitinib 5 or 10 mg b.d., based on clinical scenarios and real-world data.
Factors to consider when adjusting the tofacitinib dose include disease severity, comorbidities and previous biological exposure. The endoscopic subscore can determine whether a patient is a good candidate for dose reduction. Following disease relapse, the response can be recaptured in a substantial number of patients with a dose increase. Furthermore, data are now published showing real-world use of tofacitinib and, so far, these are consistent with data from the clinical trials.
Clinicians must consider the benefit/risk balance of tofacitinib 10 versus 5 mg b.d. in terms of dose-related side effects, as well as the safety implications of undertreating active disease. All patients should be closely monitored for disease relapse following dose reduction or interruption for early recapture of response.
托法替尼是一种用于治疗溃疡性结肠炎(UC)的口服小分子 Janus 激酶抑制剂。诱导剂量为 10mg,每日两次(bid),而维持治疗则应使用最低有效剂量。
检查托法替尼治疗 UC 的两种给药方案的已发表证据,包括对数据的专家解释以及如何将其应用于临床实践。
根据不同的临床情况,使用托法替尼 UC 临床项目中的数据评估托法替尼 5mg 或 10mg bid 的使用情况。我们包括专家对剂量调整的临床意义的意见,以根据临床情况和真实世界数据告知使用托法替尼 5mg 或 10mg bid 的获益/风险。
调整托法替尼剂量时需要考虑的因素包括疾病严重程度、合并症和以前的生物治疗暴露。内镜下评分可以确定患者是否适合剂量减少。在疾病复发后,相当数量的患者通过增加剂量可以再次获得缓解。此外,现在已经发表了托法替尼的真实世界使用数据,到目前为止,这些数据与临床试验数据一致。
临床医生必须考虑托法替尼 10mg 与 5mg bid 在剂量相关副作用方面的获益/风险平衡,以及治疗活动性疾病不足的安全性影响。所有患者在剂量减少或中断后都应密切监测疾病复发,以便及早再次获得缓解。