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对于阵发性夜间血红蛋白尿患者,依库珠单抗给药间隔超过17天可能与突破性溶血的更高风险相关。

Eculizumab Dosing Intervals Longer than 17 Days May Be Associated with Greater Risk of Breakthrough Hemolysis in Patients with Paroxysmal Nocturnal Hemoglobinuria.

作者信息

Nakayama Hirokazu, Usuki Kensuke, Echizen Hirotoshi, Ogawa Ryuichi, Orii Takao

机构信息

Department of Pharmacy, NTT Medical Center Tokyo.

出版信息

Biol Pharm Bull. 2016;39(2):285-8. doi: 10.1248/bpb.b15-00703.

Abstract

Eculizumab given bi-weekly is widely recommended for the treatment of paroxysmal nocturnal hemoglobinuria (PNH). We undertook a retrospective analysis on the medical records of 763 dosings of 14 PNH patients to investigate whether a threshold would exist in dosing intervals associated with breakthrough hemolysis. We identified 12 events of breakthrough hemolysis in 4 patients. Multivariate logistic regression and receiver operating characteristics (ROC) analysis revealed a significant association between increased risk of breakthrough hemolysis and prolonged dosing intervals of 17 days or more and concomitant inflammation: odds ratios (OR) and 95% confidence intervals (CIs) were 1.6 (1.3-2.0, p<0.01) and 5.5 (1.3-22.8, p=0.02), respectively. ROC analysis showed that the best cut-off dosing interval discriminating breakthrough hemolysis was 16.5 days. We consider that eculizumab dosing intervals longer than 17 days may be associated with an increased risk for developing breakthrough hemolysis in patients with PNH.

摘要

每两周一次给予依库珠单抗被广泛推荐用于治疗阵发性睡眠性血红蛋白尿(PNH)。我们对14例PNH患者的763次给药病历进行了回顾性分析,以调查与突破性溶血相关的给药间隔是否存在阈值。我们在4例患者中识别出12次突破性溶血事件。多因素逻辑回归和受试者工作特征(ROC)分析显示,突破性溶血风险增加与给药间隔延长17天或更长时间以及合并炎症之间存在显著关联:优势比(OR)和95%置信区间(CI)分别为1.6(1.3 - 2.0,p<0.01)和5.5(1.3 - 22.8,p = 0.02)。ROC分析表明,区分突破性溶血的最佳给药间隔临界值为16.5天。我们认为,依库珠单抗给药间隔超过17天可能与PNH患者发生突破性溶血的风险增加有关。

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