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丹可泊治疗阵发性睡眠性血红蛋白尿症患者的安全性和疗效:系统评价和荟萃分析。

Safety and efficacy of danicopan in patients with paroxysmal nocturnal hemoglobinuria: a systematic review and meta-analysis.

机构信息

Hamidiye International School of Medicine, University of Health Sciences, Istanbul, Turkey.

Department of Medical Pharmacology, Hamidiye Faculty of Medicine, University of Health Sciences, Istanbul, Turkey.

出版信息

Expert Rev Hematol. 2024 Nov;17(11):819-831. doi: 10.1080/17474086.2024.2422558. Epub 2024 Oct 28.

Abstract

INTRODUCTION

Paroxysmal nocturnal hemoglobinuria (PNH) is a rare disease characterized by complement-mediated intravascular hemolysis (IVH). Current treatments like Eculizumab and Ravulizumab have limitations, with many patients still requiring transfusions. This study aimed to investigate the safety and efficacy of the new emergent treatment called Danicopan.

METHODS

We systematically searched five electronic databases - Epistemonikos, Web of Science, Medline, Scopus, and ClinicalTrials - to ensure comprehensive coverage. The systematic review was conducted following the PRISMA guidelines, ensuring methodological rigor.

RESULTS

Four studies were eligible for inclusion, all of them were multicenter trials with 79 patients studied. Treatment with Danicopan led to a notable improvement in hemoglobin levels and a decrease in reticulocyte counts. However, LDH levels did not significantly change after treatment. Additionally, there was a significant increase in GPI-deficient erythrocytes but not in GPI-deficient granulocytes. Total and direct bilirubin levels showed significant differences between treatment groups, and there was an improvement in FACIT scores from baseline.

CONCLUSIONS

Our systematic review and meta-analysis support the potential of Danicopan as a viable therapeutic option for PNH patients. The targeted inhibition of factor D within the complement system by Danicopan demonstrates both safety and efficacy in managing PNH, as evidenced by our findings.

REGISTRATION

This paper was registered with the PROSPERO database (CRD42024499375).

摘要

简介

阵发性夜间血红蛋白尿症(PNH)是一种罕见的疾病,其特征是补体介导的血管内溶血(IVH)。目前的治疗方法,如依库珠单抗和拉维珠单抗,存在局限性,许多患者仍需要输血。本研究旨在探讨一种新出现的治疗方法丹诺昔单抗的安全性和疗效。

方法

我们系统地检索了五个电子数据库——Epistemonikos、Web of Science、Medline、Scopus 和 ClinicalTrials,以确保全面覆盖。系统评价按照 PRISMA 指南进行,确保方法学严谨。

结果

有四项研究符合纳入标准,均为多中心试验,共纳入 79 例患者。丹诺昔单抗治疗可显著提高血红蛋白水平,降低网织红细胞计数。然而,治疗后乳酸脱氢酶(LDH)水平没有显著变化。此外,糖基磷脂酰肌醇(GPI)缺陷型红细胞显著增加,但 GPI 缺陷型粒细胞没有增加。总胆红素和直接胆红素水平在治疗组之间存在显著差异,且 FACIT 评分自基线有所改善。

结论

我们的系统评价和荟萃分析支持丹诺昔单抗作为 PNH 患者一种可行的治疗选择。丹诺昔单抗靶向抑制补体系统中的因子 D,在管理 PNH 方面表现出安全性和疗效,这一点从我们的研究结果中可以得到证实。

登记号

本文在 PROSPERO 数据库(CRD42024499375)进行了登记。

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