Yin Fan, Liu Xiaolei, He Dongdong, Li Songbo, Feng Xin, Shi Yongquan, Chen Min
State Key Laboratory of Holistic Integrative Management of Gastrointestinal Cancers and National Clinical Research Center for Digestive Diseases, Xijing Hospital of Digestive Diseases, Air Force Military Medical University, Xi'an, China.
Department of Gastroenterology, Guang'an People's Hospital, Guang'an, China.
Clin Transl Sci. 2025 Mar;18(3):e70198. doi: 10.1111/cts.70198.
Patients with refractory inflammatory bowel disease (IBD) face difficulty in the treatment strategy. Combined advanced targeted therapies may obtain higher therapeutic efficacy. However, few studies compare the efficacy and safety of dual biologic therapy (DBT) with biologic small-molecule therapy (BMT) for refractory IBD. We aimed to compare the effectiveness of DBT with BMT. We retrospectively analyzed the data of patients with refractory IBD treated with DBT (n = 22) or BMT (n = 21). The primary outcome was the clinical remission rate at week 12. Secondary outcomes included the clinical response rate, endoscopic response rate, endoscopic remission rate, colectomy rate, and rate of adverse events (AEs) at week 12. At week 12, the clinical remission rates in the DBT group and BMT group were 22.7% and 28.6%, respectively. No statistically significant difference was observed between the two groups (p = 0.661). There were also no statistically significant differences between the DBT group and BMT group in the clinical response rate (68.2% vs. 71.4%, p = 0.817), endoscopic response rate (66.7% vs. 68.8%, p = 1.000), endoscopic remission rate (4.8% vs. 18.8%, p = 0.296) and colectomy rate (4.5% vs. 23.8%, p = 0.167). Two patients (9.5%) in the BMT group and no patients in the DBT group experienced AEs. However, the difference was not statistically significant (p = 0.233). In conclusion, this study revealed that there may be similar effectiveness and safety of DBT and BMT for patients with refractory IBD. Further multi-center, prospective randomized controlled trials are necessary to confirm this conclusion.
难治性炎症性肠病(IBD)患者在治疗策略上面临困难。联合先进的靶向治疗可能会获得更高的治疗效果。然而,很少有研究比较双重生物治疗(DBT)与生物小分子治疗(BMT)用于难治性IBD的疗效和安全性。我们旨在比较DBT和BMT的有效性。我们回顾性分析了接受DBT(n = 22)或BMT(n = 21)治疗的难治性IBD患者的数据。主要结局是第12周时的临床缓解率。次要结局包括第12周时的临床缓解率、内镜缓解率、内镜下缓解率、结肠切除术率和不良事件(AE)发生率。在第12周时,DBT组和BMT组的临床缓解率分别为22.7%和28.6%。两组之间未观察到统计学上的显著差异(p = 0.661)。DBT组和BMT组在临床缓解率(68.2%对71.4%,p = 0.817)、内镜缓解率(66.7%对68.8%,p = 1.000)、内镜下缓解率(4.8%对18.8%,p = 0.296)和结肠切除术率(4.5%对23.8%,p = 0.167)方面也没有统计学上的显著差异。BMT组有2例患者(9.5%)发生AE,DBT组无患者发生AE。然而,差异无统计学意义(p = 0.233)。总之,本研究表明DBT和BMT为难治性IBD患者带来的有效性和安全性可能相似。需要进一步开展多中心、前瞻性随机对照试验来证实这一结论。