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Treatment of eculizumab refractory paroxysmal nocturnal hemoglobinuria: A systematic review about current treatment options and future direction

Objectives: C5 inhibitors such as eculizumab and ravulizumab are the first-line treatment in the management of paroxysmal nocturnal hemoglobinuria (PNH). However, some patients develop novel symptoms as part of their treatment with eculizumab, and the disease is termed as eculizumab refractory PNH. The aim of this study was to conduct a systematic review on the available treatment modalities for the management of eculizumab refractory PNH.

Methods: Two authors independently searched two databases according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines. A total of 70 studies were obtained: 4 out 70 studies were found to meet the inclusion criteria.

Results: Four studies were found to meet the inclusion criteria of our study. Two studies were published in 2021 and two studies were published in 2020. All four studies were multicenter clinical trials. Two studies were phase III clinical trials, one study was a phase II clinical trial, and one study was a phase I clinical trial. Two studies were about pegcetacoplan, one was about danicopan, and one was about iptacopan.

Conclusion: Based upon the findings of our systematic review, we recommend an individualized treatment plan based on the mechanism of eculizumab refractoriness and the mechanism of PNH breakthrough. This recommendation is subject to the available resources and clinical expertise available at different hospitals. More studies using study designs such as randomized controlled trials comparing multiple drugs should be performed to accurately assess the different medications and aid in designing guidelines of the management of eculizumab refractory PNH.

 

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Title: A Systematic Review of Treatment Modalities for Eculizumab Refractory Paroxysmal Nocturnal Hemoglobinuria (PNH)

Objective: The objective of this study was to conduct a systematic review of the available treatment modalities for the management of eculizumab refractory PNH, a condition in which patients develop novel symptoms despite treatment with eculizumab.

Methods: The study followed the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. Two authors independently searched two databases to identify relevant studies. Inclusion criteria were applied, resulting in the selection of four studies from a total of 70 identified studies.

Results: The systematic review identified four studies that met the inclusion criteria. Two studies were published in 2021, and two were published in 2020. All four studies were multicenter clinical trials. Among them, two studies were phase III clinical trials, one was a phase II clinical trial, and one was a phase I clinical trial. The identified studies investigated the efficacy of three different drugs: pegcetacoplan, danicopan, and iptacopan.

Conclusion: Based on the findings of the systematic review, the authors recommend an individualized treatment plan for eculizumab refractory PNH, taking into account the mechanism of eculizumab refractoriness and the underlying mechanism of PNH breakthrough. The implementation of this recommendation should consider the available resources and clinical expertise at different hospitals. The authors also emphasize the need for further studies, particularly randomized controlled trials comparing multiple drugs, to more accurately assess the efficacy of different medications and assist in developing management guidelines for eculizumab refractory PNH.

Related Products

Cat.No. Product Name Information
S0803 Danicopan Danicopan is a potent, selective and orally active inhibitor of factor D with Kd of 0.54 nM for human Factor D. Danicopan inhibits alternative pathway of complement (APC) activity, and has potential to block the alternative pathway of complement in paroxysmal nocturnal hemoglobinuria (PNH) and atypical hemolytic uremic syndrome (aHUS).

Related Targets

Complement System