Almeida Antonio M, Bedrosian Camille, Cole Alexander, Muus Petra, Schrezenmeier Hubert, Szer Jeff, Rosse Wendell F
Serviço de Hematologia, Instituto Português de Oncologia de Lisboa, Francisco Gentil, Lisbon, Portugal.
Alexion Pharma International, New Haven, Connecticut, USA.
Intern Med J. 2017 Sep;47(9):1026-1034. doi: 10.1111/imj.13523.
Eculizumab reduces intravascular haemolysis and improves disease symptoms in patients with paroxysmal nocturnal haemoglobinuria (PNH).
To characterise, in a real-world setting, the effect of eculizumab in patients with haemolytic PNH (lactase dehydrogenase (LDH) ≥ 1.5 upper limit of normal) and no history of red blood cell transfusion, including those with high disease activity (HDA).
Three populations from the International PNH Registry were studied: (i) non-transfused, untreated; (ii) non-transfused, eculizumab-treated and (iii) transfused, eculizumab-treated (≥1 transfusions in 6 months prior to eculizumab initiation). Using multivariate linear regression, the primary outcome was mean absolute change from baseline to 6 months in LDH (U/L) in non-transfused patients who were treated with eculizumab versus those who remained untreated. Secondary outcomes were mean changes in functional assessment of chronic illness therapy (FACIT)-Fatigue and European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire (EORTC-QLQ)-C30 Fatigue scores from baseline to last available assessment.
The study population included (i) 144 non-transfused, untreated patients; (ii) 45 non-transfused, eculizumab-treated patients and (iii) 105 transfused, eculizumab-treated patients. Of these, 136/144, 43/45 and 99/105 had HDA respectively. Compared with untreated patients, non-transfused, treated patients had greater absolute reduction in LDH (-1318.8 vs -39.4; P < 0.001) and greater percentage reduction in LDH (-69.9 vs -1.6%; P < 0.001). Clinically meaningful improvements in FACIT-Fatigue (73.7 vs 24.6%, respectively) and in EORTC-QLQ-C30 (84.2 vs 33.3%, respectively) were observed. Non-transfused, treated patients with HDA had significantly reduced LDH levels (P < 0.001) and clinically meaningful improvements in FACIT-Fatigue (P = 0.003) and EORTC-QLQ-C30 (P = 0.020) versus untreated patients.
Significant LDH reduction and clinically meaningful improvement in fatigue were observed in patients with PNH and HDA treated with eculizumab versus untreated patients, irrespective of transfusion history.
依库珠单抗可减少阵发性夜间血红蛋白尿(PNH)患者的血管内溶血并改善疾病症状。
在真实世界环境中,描述依库珠单抗对溶血型PNH(乳酸脱氢酶(LDH)≥正常上限1.5倍)且无红细胞输血史患者的影响,包括那些疾病活动度高(HDA)的患者。
对国际PNH注册研究中的三个人群进行了研究:(i)未输血、未治疗的患者;(ii)未输血、接受依库珠单抗治疗的患者;(iii)接受输血、接受依库珠单抗治疗的患者(在开始使用依库珠单抗前6个月内至少输血1次)。使用多变量线性回归,主要结局是接受依库珠单抗治疗的未输血患者与未接受治疗的未输血患者从基线到6个月时LDH(单位/升)的平均绝对变化。次要结局是从基线到最后一次可用评估时慢性病治疗功能评估(FACIT)-疲劳量表和欧洲癌症研究与治疗组织生活质量问卷(EORTC-QLQ)-C30疲劳量表的平均变化。
研究人群包括:(i)144例未输血、未治疗的患者;(ii)45例未输血、接受依库珠单抗治疗的患者;(iii)105例接受输血、接受依库珠单抗治疗的患者。其中,分别有136/144、43/45和99/105例患者有HDA。与未治疗的患者相比,未输血且接受治疗的患者LDH的绝对降低幅度更大(-1318.8 vs -39.4;P<0.001),LDH的降低百分比也更大(-69.9 vs -1.6%;P<0.001)。观察到FACIT-疲劳量表(分别为73.7% vs 24.6%)和EORTC-QLQ-C30(分别为84.2% vs 33.3%)有具有临床意义的改善。与未治疗的患者相比,未输血且接受治疗的HDA患者的LDH水平显著降低(P<0.001),FACIT-疲劳量表(P=0.003)和EORTC-QLQ-C30(P=0.020)有具有临床意义的改善。
与未治疗的患者相比,接受依库珠单抗治疗的PNH和HDA患者无论输血史如何,均观察到LDH显著降低且疲劳有具有临床意义的改善。