Clinical benefit of eculizumab in patients with no transfusion history in the International Paroxysmal Nocturnal Haemoglobinuria Registry

被引:20
|
作者
Almeida, Antonio M. [1 ]
Bedrosian, Camille [2 ]
Cole, Alexander [3 ]
Muus, Petra [5 ]
Schrezenmeier, Hubert [6 ,7 ,8 ]
Szer, Jeff [9 ,10 ]
Rosse, Wendell F. [4 ]
机构
[1] Inst Portugues Oncol Francisco Gentil, Serv Hematol, Lisbon, Portugal
[2] Alexion Pharma Int, New Haven, CT USA
[3] Alexion Pharma Int, Lexington, MA USA
[4] Duke Univ, Med Ctr, Durham, NC USA
[5] Radboudumc, Nijmegen, Netherlands
[6] German Red Cross Blood Transfus Serv Baden Wurtte, Inst Clin Transfus Med & Immunogenet, Baden Baden, Germany
[7] Univ Hosp Ulm, Ulm, Germany
[8] Univ Ulm, Inst Transfus Med, Ulm, Germany
[9] Royal Melbourne Hosp, Melbourne, Vic, Australia
[10] Univ Melbourne, Melbourne, Vic, Australia
关键词
paroxysmal nocturnal haemoglobinuria; eculizumab; transfusion; high disease activity; outcome; COMPLEMENT INHIBITOR ECULIZUMAB; THROMBOSIS; VALIDATION;
D O I
10.1111/imj.13523
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Eculizumab reduces intravascular haemolysis and improves disease symptoms in patients with paroxysmal nocturnal haemoglobinuria (PNH). Aims: 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). Methods: 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. Results: The study population included (i) 144 non-transfused, untreated patients; (ii) 45 non-transfused, eculizumab-treated patients and (iii) 105 transfused, eculizumabtreated 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. Conclusion: 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.
引用
收藏
页码:1026 / 1034
页数:9
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