The complement inhibitor eculizumab in paroxysmal nocturnal hemoglobinuria

被引:921
作者
Hillmen, Peter
Young, Neal S.
Schubert, Joerg
Brodsky, Robert A.
Socie, Gerard
Muus, Petra
Roeth, Alexander
Szer, Jeffrey
Elebute, Modupe O.
Nakamura, Ryotaro
Browne, Paul
Risitano, Antonio M.
Hill, Anita
Schrezenmeier, Hubert
Fu, Chieh-Lin
Maciejewski, Jaroslaw
Rollins, Scott A.
Mojcik, Christopher F.
Rother, Russell P.
Luzzatto, Lucio
机构
[1] Gen Infirm, Dept Haematol, Leeds LS1 3EX, W Yorkshire, England
[2] NHLBI, Bethesda, MD 20892 USA
[3] Univ Saarland, Sch Med, D-6650 Homburg, Germany
[4] Johns Hopkins, Sidney Kimmel Comprehens Canc Ctr, Baltimore, MD USA
[5] Hop St Louis, Paris, France
[6] INSERM, Paris, France
[7] Radboud Univ Med Ctr, Nijmegen, Netherlands
[8] Univ Hosp Essen, Essen, Germany
[9] Royal Melbourne Hosp, Melbourne, Vic, Australia
[10] Univ London St Georges Hosp, London, England
[11] City Hope Natl Med Ctr, Beckman Res Inst, Duarte, CA 91010 USA
[12] Univ Dublin Trinity Coll, St James Hosp, Dublin 2, Ireland
[13] Univ Naples Federico II, Naples, Italy
[14] Univ Hosp, Inst Transfus Med, Ulm, Germany
[15] Cleveland Clin Florida, Weston, FL USA
[16] Cleveland Clin Fdn, Taussig Canc Ctr, Cleveland, OH 44195 USA
[17] Alex Pharmaceut, Cheshire, CT USA
[18] Ist Toscano Tumori, Florence, Italy
关键词
D O I
10.1056/NEJMoa061648
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: We tested the safety and efficacy of eculizumab, a humanized monoclonal antibody against terminal complement protein C5 that inhibits terminal complement activation, in patients with paroxysmal nocturnal hemoglobinuria (PNH). METHODS: We conducted a double-blind, randomized, placebo-controlled, multicenter, phase 3 trial. Patients received either placebo or eculizumab intravenously; eculizumab was given at a dose of 600 mg weekly for 4 weeks, followed 1 week later by a 900-mg dose and then 900 mg every other week through week 26. The two primary end points were the stabilization of hemoglobin levels and the number of units of packed red cells transfused. Biochemical indicators of intravascular hemolysis and the patients' quality of life were also assessed. RESULTS: Eighty-seven patients underwent randomization. Stabilization of hemoglobin levels in the absence of transfusions was achieved in 49% (21 of 43) of the patients assigned to eculizumab and none (0 of 44) of those assigned to placebo (P<0.001). During the study, a median of 0 units of packed red cells was administered in the eculizumab group, as compared with 10 units in the placebo group (P<0.001). Eculizumab reduced intravascular hemolysis, as shown by the 85.8% lower median area under the curve for lactate dehydrogenase plotted against time (in days) in the eculizumab group, as compared with the placebo group (58,587 vs. 411,822 U per liter; P<0.001). Clinically significant improvements were also found in the quality of life, as measured by scores on the Functional Assessment of Chronic Illness Therapy-Fatigue instrument (P<0.001) and the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire. Of the 87 patients, 4 in the eculizumab group and 9 in the placebo group had serious adverse events, none of which were considered to be treatment-related; all these patients recovered without sequelae. CONCLUSIONS: Eculizumab is an effective therapy for PNH.
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收藏
页码:1233 / 1243
页数:11
相关论文
共 21 条
  • [1] THE EUROPEAN-ORGANIZATION-FOR-RESEARCH-AND-TREATMENT-OF-CANCER QLQ-C30 - A QUALITY-OF-LIFE INSTRUMENT FOR USE IN INTERNATIONAL CLINICAL-TRIALS IN ONCOLOGY
    AARONSON, NK
    AHMEDZAI, S
    BERGMAN, B
    BULLINGER, M
    CULL, A
    DUEZ, NJ
    FILIBERTI, A
    FLECHTNER, H
    FLEISHMAN, SB
    DEHAES, JCJM
    KAASA, S
    KLEE, M
    OSOBA, D
    RAZAVI, D
    ROFE, PB
    SCHRAUB, S
    SNEEUW, K
    SULLIVAN, M
    TAKEDA, F
    [J]. JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1993, 85 (05) : 365 - 376
  • [2] PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA (PNH) IS CAUSED BY SOMATIC MUTATIONS IN THE PIG-A GENE
    BESSLER, M
    MASON, PJ
    HILLMEN, P
    MIYATA, T
    YAMADA, N
    TAKEDA, J
    LUZZATTO, L
    KINOSHITA, T
    [J]. EMBO JOURNAL, 1994, 13 (01) : 110 - 117
  • [3] Combining anchor and distribution-based methods to derive minimal clinically important differences on the functional assessment of cancer therapy (FACT) anemia and fatigue scales
    Cella, D
    Eton, DT
    Lai, JS
    Peterman, AH
    Merkel, DE
    [J]. JOURNAL OF PAIN AND SYMPTOM MANAGEMENT, 2002, 24 (06) : 547 - 561
  • [4] Fatigue in cancer patients compared with fatigue in the general United States population
    Cella, D
    Lai, JS
    Chang, CH
    Peterman, A
    Slavin, M
    [J]. CANCER, 2002, 94 (02) : 528 - 538
  • [5] Cella D, 1997, MANUAL FUNCTIONAL AS
  • [6] Fayers P, 1995, EORTC QLQ C30 SCORIN
  • [7] HILL A, 2005, BLOOD, V106, pA1046
  • [8] HILL A, 2005, HAEMATOLOGICA S12, V90
  • [9] Effect of eculizumab on hemolysis and transfusion requirements in patients with paroxysmal nocturnal hemoglobinuria
    Hillmen, P
    Hall, C
    Marsh, JCW
    Elebute, M
    Bombara, MP
    Petro, BE
    Cullen, MJ
    Richards, SJ
    Rollins, SA
    Mojcik, CF
    Rother, RP
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2004, 350 (06) : 552 - 559
  • [10] ISOLATION AND CHARACTERIZATION OF A MEMBRANE-PROTEIN FROM NORMAL HUMAN-ERYTHROCYTES THAT INHIBITS REACTIVE LYSIS OF THE ERYTHROCYTES OF PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA
    HOLGUIN, MH
    FREDRICK, LR
    BERNSHAW, NJ
    WILCOX, LA
    PARKER, CJ
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (01) : 7 - 17