Safety and efficacy of biological agents in the treatment of Systemic Lupus Erythematosus (SLE).

IF 2.1 Q3 RHEUMATOLOGY
Justin Chan, Giles D Walters, Prianka Puri, Simon H Jiang
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引用次数: 0

Abstract

Background: To determine the safety and efficacy of biological agents used in the treatment of systemic lupus erythematosus (SLE) in adults.

Methods: Systematic review and meta-analysis following PRISMA guidelines.

Data sources: MEDLINE (through Pubmed), EMBASE, Cochrane library, Clinicaltrials.gov, Australianclinicaltrials.gov.au, ANZCTR.org.au and WHO International Clinical Trials Registry Platform for studies published from 20 May 2021 and 15 years prior. A grey literature search was performed and completed on 31 May 2021.

Study criteria: Phase II, III or quasi randomised controlled trials, studies with only cerebral or cutaneous lupus were excluded.

Data extraction: Two authors independently screened studies for eligibility, extracted, reviewed data for accuracy, and used the Cochrane tool to assess risk of bias.

Results: Forty-four studies were identified, consisting of 15 groups of drugs and 25 different biological agents, totalling 16,889 patients. The main outcomes assessed included Systemic Lupus Erythematosus Responder Index (SRI), BILAG-Based Composite Lupus Assessment (BICLA) and combined combined/partial renal remission (CRR/PRR). Four groups of biologics were found to improve outcomes. Anti-interferons: Anifrolumab increased BICLA response and SRI 5 to 8, decreased prednisone dosages, with increased herpes zoster infections, but fewer serious adverse events. Sifalimumab improved SRI but also increased herpes zoster infections. Anti BAFF/BLyS and/or APRIL: Belimumab consistently improved SRI 4, decreased prednisone dosages, increased combined CRR/PRR, and had no adverse safety outcomes. Tabalumab increased SRI 5 at 52 weeks with no steroid sparing effect but was associated with increased infusion related adverse events. Telitacicept improved SRI 4 at 52 weeks, with no increased adverse events, though data was rather sparse. Anti CD-20 monoclonal antibody, Obinutuzumab increased combined CRR/PRR at 1 and 2 years. Anti IL12/23 monoclonal antibody, Ustekinumab, increased SRI 4 to 6, but not BICLA at 24 weeks, with no concerning safety outcomes.

Conclusion: Multiple biologic agents are shown in high quality studies to have a significant therapeutic impact on outcomes in SLE.

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生物制剂治疗系统性红斑狼疮(SLE)的安全性和有效性。
背景:确定生物制剂治疗成人系统性红斑狼疮(SLE)的安全性和有效性。方法:遵循PRISMA指南进行系统回顾和荟萃分析。数据来源:MEDLINE(通过Pubmed)、EMBASE、Cochrane图书馆、Clinicaltrials.gov、Australianclinicialtrials.gov.au、ANZCTR.org.au和世界卫生组织国际临床试验注册平台,用于2021年5月20日和15年前发布的研究。2021年5月31日进行并完成了灰色文献检索。研究标准:II期、III期或准随机对照试验,仅排除脑或皮肤狼疮的研究。数据提取:两位作者独立筛选研究的合格性,提取并审查数据的准确性,并使用Cochrane工具评估偏倚风险。结果:确定了44项研究,包括15组药物和25种不同的生物制剂,共16889名患者。评估的主要结果包括系统性红斑狼疮反应者指数(SRI)、基于BILAG的综合狼疮评估(BICLA)和联合/部分肾脏缓解(CRR/PRR)。发现四组生物制剂可以改善疗效。抗干扰素:Anifrolumab增加了BICLA反应和SRI 5至8,减少了泼尼松剂量,带状疱疹感染增加,但严重不良事件较少。西法利单抗改善了SRI,但也增加了带状疱疹感染。抗BAFF/BLyS和/或APRIL:Belimumab持续改善SRI4,减少泼尼松剂量,增加联合CRR/PRR,并且没有不良安全性结果。Tabalumab在52周时增加SRI 5,没有类固醇保留作用,但与输液相关不良事件增加有关。Telitacicept在52周时改善了SRI4,没有增加不良事件,尽管数据相当稀少。抗CD-20单克隆抗体,奥比努珠单抗在1年和2年时增加了CRR/PRR。抗IL12/23单克隆抗体Ustekinumab在24周时将SRI增加到4至6,但没有增加BICLA,没有相关的安全性结果。结论:在高质量的研究中,多种生物制剂对SLE的疗效有显著影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Rheumatology
BMC Rheumatology Medicine-Rheumatology
CiteScore
3.80
自引率
0.00%
发文量
73
审稿时长
15 weeks
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