Huang Ang, Zhu Yun, Liu Shuhong, Sun Ying, Liu Zherui, Liang Qing-Sheng, Zhao Jun, Chang Bin-Xia, Bi Jing-Feng, Liu Jiang-Tao, Zhai Xing-Ran, Xie Huan, Li Ning, Tian Hui, Han Lin, Zhuang Yingjie, Ma Hongbin, Teng Guang-Ju, Zhang Wei, Aithal Guruprasad P, Ji Dong, Zhao Jingmin, Zou Zhengsheng
Senior Department of Hepatology, the Fifth Medical Center of PLA General Hospital, Beijing, China.
Department of Gastroenterology and Hepatology, the First Medical Center of PLA General Hospital, Beijing, China.
Liver Int. 2024 Jun;44(6):1435-1447. doi: 10.1111/liv.15899. Epub 2024 Mar 14.
The use of corticosteroids in chronic drug-induced liver injury (DILI) is an important issue. Our previous randomized controlled trial showed that patients with chronic DILI benefited from a 48-week steroid stepwise reduction (SSR) regimen. However, it remains unclear whether a shorter course of therapy can achieve similar efficacy. In this study, we aimed to assess whether a 36-week SSR can achieve efficacy similar to that of 48-week SSR.
A randomized open-label trial was performed. Eligible patients were randomly assigned to the 36- or 48-week (1:1) SSR group. Liver biopsies were performed at baseline and at the end of treatment. The primary outcome was the proportion of patients with relapse rate (RR). The secondary outcomes were improvement in liver histology and safety.
Of the 90 participants enrolled, 84 (87.5%) completed the trial, and 62 patients (68.9%) were women. Hepatocellular damage was observed in 53.4% of the cohort. The RR was 7.1% in the 36-week SSR group but 4.8% in the 48-week SSR group, as determined by per-protocol set analysis (p = 1.000). Significant histological improvements in histological activity (93.1% vs. 92.9%, p = 1.000) and fibrosis (41.4% vs. 46.4%, p = .701) were observed in both the groups. Biochemical normalization time did not differ between the two groups. No severe adverse events were observed.
Both the 36- and 48-week SSR regimens demonstrated similar biochemical response and histological improvements with good safety, supporting 36-week SSR as a preferable therapeutic choice (ClinicalTrials.gov, NCT03266146).
在慢性药物性肝损伤(DILI)中使用皮质类固醇是一个重要问题。我们之前的随机对照试验表明,慢性DILI患者从48周的类固醇逐步减量(SSR)方案中获益。然而,尚不清楚较短疗程的治疗是否能达到相似的疗效。在本研究中,我们旨在评估36周的SSR是否能达到与48周SSR相似的疗效。
进行了一项随机开放标签试验。符合条件的患者被随机分配到36周或48周(1:1)的SSR组。在基线和治疗结束时进行肝活检。主要结局是复发率(RR)患者的比例。次要结局是肝脏组织学改善和安全性。
在纳入的90名参与者中,84名(87.5%)完成了试验,62名患者(68.9%)为女性。队列中53.4%观察到肝细胞损伤。根据符合方案集分析确定,36周SSR组的RR为7.1%,而48周SSR组为4.8%(p = 1.000)。两组均观察到组织学活性(93.1%对92.9%,p = 1.000)和纤维化(41.4%对46.4%,p = 0.701)有显著的组织学改善。两组之间生化指标恢复正常的时间没有差异。未观察到严重不良事件。
36周和48周的SSR方案均显示出相似的生化反应和组织学改善,且安全性良好,支持将36周SSR作为更优的治疗选择(ClinicalTrials.gov,NCT03266146)。