Medicina Interna e Medicina d'Urgenza, Ospedali Riuniti di Ancona, Ancona, Italy.
Clinica Medica, Università Politecnica delle Marche, Ancona, Italy.
Rheumatology (Oxford). 2021 Apr 6;60(4):1640-1650. doi: 10.1093/rheumatology/keab046.
To analyse the available evidence about the use of rituximab (RTX) and other biologic agents in eosinophilic granulomatosis with polyangiitis (EGPA) patients and to provide useful findings to inform the design of future, reliable clinical trials.
A systematic review was performed. A systematic search was conducted in PubMed/MEDLINE, Scopus, Web of Science and the Cochrane library databases on RTX, and an extensive literature search was conducted on other biologic agents.
Forty-five papers pertinent to our questions were found: 16 retrospective cohort studies, 8 case series, 3 prospective cohort studies and 18 single case reports, for a total of 368 EGPA patients. More than 80% of evaluable patients achieved complete or partial remission with a tendency towards a higher rate of complete response in the pANCA-positive subgroup.
Although the majority of the evaluable EGPA patients treated with RTX appears to achieve complete remission, we strongly believe that a number of sources of heterogeneity impair a clear interpretation of results and limit their transferability in clinical practice. Differences in design, enrolment criteria, outcome definition and measurement make a comparison among data obtained from studies on RTX and other biologic agents unreliable.
分析在嗜酸性肉芽肿伴多血管炎(EGPA)患者中使用利妥昔单抗(RTX)和其他生物制剂的现有证据,并提供有用的发现,为未来可靠的临床试验设计提供信息。
进行了系统评价。在 PubMed/MEDLINE、Scopus、Web of Science 和 Cochrane 图书馆数据库中对 RTX 进行了系统搜索,并对其他生物制剂进行了广泛的文献搜索。
发现了 45 篇与我们的问题相关的论文:16 项回顾性队列研究、8 项病例系列研究、3 项前瞻性队列研究和 18 项单病例报告,共涉及 368 名 EGPA 患者。超过 80%的可评估患者达到完全或部分缓解,pANCA 阳性亚组的完全缓解率较高。
尽管大多数接受 RTX 治疗的可评估 EGPA 患者似乎达到了完全缓解,但我们强烈认为,许多异质性来源影响了对结果的清晰解释,并限制了其在临床实践中的可转移性。在设计、入组标准、结局定义和测量方面的差异使得比较 RTX 和其他生物制剂研究的数据不可靠。