在治疗狼疮的随机对照试验中评估生物制剂的类固醇节约效应:范围界定综述。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2024-08-01 Epub Date: 2024-03-09 DOI:10.1007/s12026-024-09463-y
Savino Sciascia, Silvia Grazietta Foddai, Marta Arbrile, Massimo Radin, Irene Cecchi, Alice Barinotti, Roberta Fenoglio, Dario Roccatello
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引用次数: 0

摘要

及时控制系统性红斑狼疮(SLE)患者的病情发作是治疗策略规划中的首要任务。然而,糖皮质激素(GCs)与剂量相关的长期副作用促使研究人员开始寻找和使用既能诱导又能维持低疾病活动度和缓解的新型生物制剂,尤其是在狼疮肾炎(LN)的情况下。本范围综述旨在通过回顾涉及系统性红斑狼疮/狼疮肾炎患者的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省效应的现有证据。本研究根据 PRISMA-ScR 建议对文献进行了范围界定。利用 Cochrane 协作组织的随机对照试验(RCTs)工具对偏倚风险进行了评估。八项随机对照研究符合纳入标准并被纳入本次分析(治疗药物:7 项贝利木单抗;1 项安非罗单抗)。四项研究显示了明确的类固醇节省效应(治疗药物:3项贝利木单抗;1项安非罗单抗),而在其余四项随机对照试验中,类固醇节省效应未被观察到。在关注III期试验时,考虑到偏倚风险,研究的总体质量为一般或良好。不过,类固醇治疗方案(考虑初始剂量、减量和抢救治疗允许量)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系统性红斑狼疮中的安全性和有效性,但有关其类固醇节省效果的证据仍然很分散。未来的研究需要确定哪些系统性红斑狼疮患者会从具有明确类固醇节省效果的特定治疗方案中获益最多。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assessing the steroid-sparing effect of biological agents in randomized controlled trials for lupus: a scoping review.

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.

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