Covic Andreea, Caruntu Irina Draga, Burlacu Alexandru, Giusca Simona Eliza, Covic Adrian, Stefan Anca Elena, Brinza Crischentian, Ismail Gener
Nephrology Department, Dialysis and Renal Transplant Center, "Dr. C.I. Parhon" University Hospital, 700503 Iasi, Romania.
Faculty of Medicine, 'Grigore T. Popa' University of Medicine, 700115 Iasi, Romania.
J Clin Med. 2023 Oct 27;12(21):6806. doi: 10.3390/jcm12216806.
(1) Background. Hepatitis C infection often leads to extrahepatic manifestations, including cryoglobulinemic vasculitis. This systematic review aimed to assess the efficacy and safety of rituximab in treating hepatitis C-associated cryoglobulinemic vasculitis. (2) Methods. Following PRISMA guidelines, databases were searched for relevant studies. Eligibility criteria included studies on hepatitis C-associated cryoglobulinemic vasculitis treated with rituximab. (3) Results. Nine studies met the eligibility criteria and were included in this analysis. Rituximab was commonly administered at 375 mg/m weekly for one month. The results consistently demonstrated the efficacy of rituximab, whether as a standalone treatment or as part of a therapeutic regimen. The combination of rituximab with Peg-IFN-α and ribavirin significantly increased the complete response rate compared to Peg-IFN-α and ribavirin alone (54.5% vs. 33.3%, < 0.05). The 3-year sustained response rate was notably higher in the rituximab combination group (83.3% vs. 40%). In another trial, rituximab achieved remission in 83.3% of patients at 6 months, compared to only 8.3% in the control group. The efficacy of rituximab was supported by long-term experience, with clinical benefits in patients with severe cryoglobulinemic vasculitis, including those resistant to standard therapies. Mild adverse events were generally reported, with rare severe reactions in some studies. (4) Conclusions: In conclusion, rituximab appeared to be effective and safe in managing hepatitis C-associated cryoglobulinemic vasculitis, either alone or with antiviral therapy.
(1) 背景。丙型肝炎感染常导致肝外表现,包括冷球蛋白血症性血管炎。本系统评价旨在评估利妥昔单抗治疗丙型肝炎相关冷球蛋白血症性血管炎的疗效和安全性。(2) 方法。按照PRISMA指南,检索数据库以查找相关研究。纳入标准包括关于用利妥昔单抗治疗丙型肝炎相关冷球蛋白血症性血管炎的研究。(3) 结果。9项研究符合纳入标准并纳入本分析。利妥昔单抗通常以375mg/m²每周给药一次,共给药1个月。结果一致表明利妥昔单抗的疗效,无论是作为单一治疗还是作为治疗方案的一部分。与单独使用聚乙二醇干扰素-α和利巴韦林相比,利妥昔单抗与聚乙二醇干扰素-α和利巴韦林联合使用显著提高了完全缓解率(54.5%对33.3%,P<0.05)。利妥昔单抗联合治疗组的3年持续缓解率明显更高(83.3%对40%)。在另一项试验中,利妥昔单抗在6个月时使83.3%的患者病情缓解,而对照组仅为8.3%。利妥昔单抗的疗效得到长期经验的支持,对严重冷球蛋白血症性血管炎患者,包括对标准疗法耐药的患者有临床益处。一般报告的是轻度不良事件,在一些研究中有罕见的严重反应。(4) 结论:总之,利妥昔单抗单独或与抗病毒治疗联合应用于治疗丙型肝炎相关冷球蛋白血症性血管炎似乎是有效且安全的。