University Center of Excellence On Nephrologic, Rheumatologic and Rare Diseases (ERK-Net, ERN-Reconnect and RITA-ERN Member) With Nephrology and Dialysis Unit and Center of Immuno-Rheumatology and Rare Diseases (CMID), San Giovanni Bosco Hub Hospital, Department of Clinical and Biological Sciences, University of Turin, 10124, Turin, Italy.
Immunol Res. 2024 Aug;72(4):538-553. doi: 10.1007/s12026-024-09463-y. Epub 2024 Mar 9.
Prompt disease control of flares in patients with systemic lupus erythematosus (SLE) is a priority in treatment strategy planning. However, the long-term dosage-related collateral effects of glucocorticoids (GCs) have pushed researchers towards the identification and utilization of novel biological agents that could both induce and maintain low disease activity and remission, especially in the context of lupus nephritis (LN). This scoping review aims at assessing the current evidence of the potential steroid-sparing effect of biologic therapies by reviewing phase II and phase III randomized, placebo-controlled trials involving SLE/LN patients. A scoping review of the literature was carried out in accordance with PRISMA-ScR recommendations. Risk of bias was assessed through the utilization of the Cochrane Collaboration's tool for randomized controlled trials (RCTs). Eight RCTs met the inclusion criteria and were included in this analysis (treatment drug, 7 belimumab; 1 anifrolumab). Four studies showed a definite steroid-sparing effect (treatment drug, 3 belimumab; 1 anifrolumab), while in the remaining four RCTs, the steroid-sparing effect was not observed. When focusing on phase III trials, the overall quality of the studies resulted fair or good considering the risk of bias. However, a degree of heterogeneity of steroid regimen protocol (considering initial dosage, tapering and rescue treatment allowance) was observed. While a growing body of evidence is supporting the safety and efficacy of biological treatment in SLE, the evidence on their steroid-sparing effect remains scattered. Future research needs to pursue the identification of precise SLE clusters of patients who would benefit most from a specific treatment protocol with a definite steroid-sparing effect.
控制系统性红斑狼疮(SLE)患者的病情发作是治疗策略规划的重点。然而,糖皮质激素(GCs)长期剂量相关的副作用促使研究人员寻找新的生物制剂,这些制剂既能诱导又能维持低疾病活动度和缓解,尤其是在狼疮肾炎(LN)的情况下。本范围综述旨在通过审查涉及 SLE/LN 患者的 II 期和 III 期随机、安慰剂对照试验,评估生物疗法潜在的类固醇节约效应的现有证据。根据 PRISMA-ScR 建议对文献进行了范围综述。通过使用 Cochrane 协作对随机对照试验(RCTs)的工具来评估偏倚风险。八项 RCT 符合纳入标准并纳入本分析(治疗药物,7 个贝利尤单抗;1 个阿尼鲁单抗)。四项研究显示出明确的类固醇节约效应(治疗药物,3 个贝利尤单抗;1 个阿尼鲁单抗),而在其余四项 RCT 中,未观察到类固醇节约效应。当关注 III 期试验时,考虑到偏倚风险,研究的整体质量是公平或良好的。然而,观察到类固醇方案方案(考虑初始剂量、逐渐减少和抢救治疗允许)存在一定程度的异质性。尽管越来越多的证据支持生物治疗在 SLE 中的安全性和有效性,但关于其类固醇节约效应的证据仍然分散。未来的研究需要确定最受益于特定治疗方案和明确类固醇节约效应的精确 SLE 患者聚类。