Terminal Complement Inhibitor Eculizumab in Adult Patients With Atypical Hemolytic Uremic Syndrome: A Single-Arm, Open-Label Trial

Details

Serval ID
serval:BIB_3742DA836A71
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Terminal Complement Inhibitor Eculizumab in Adult Patients With Atypical Hemolytic Uremic Syndrome: A Single-Arm, Open-Label Trial
Journal
Am J Kidney Dis
Author(s)
Fakhouri F., Hourmant M., Campistol J. M., Cataland S. R., Espinosa M., Gaber A. O., Menne J., Minetti E. E., Provot F., Rondeau E., Ruggenenti P., Weekers L. E., Ogawa M., Bedrosian C. L., Legendre C. M.
ISSN
1523-6838 (Electronic)
ISSN-L
0272-6386
Publication state
Published
Issued date
07/2016
Volume
68
Number
1
Pages
84-93
Language
english
Notes
Fakhouri, Fadi
Hourmant, Maryvonne
Campistol, Josep M
Cataland, Spero R
Espinosa, Mario
Gaber, A Osama
Menne, Jan
Minetti, Enrico E
Provot, Francois
Rondeau, Eric
Ruggenenti, Piero
Weekers, Laurent E
Ogawa, Masayo
Bedrosian, Camille L
Legendre, Christophe M
eng
Clinical Trial, Phase II
Multicenter Study
Am J Kidney Dis. 2016 Jul;68(1):84-93. doi: 10.1053/j.ajkd.2015.12.034. Epub 2016 Mar 21.
Abstract
BACKGROUND: Atypical hemolytic uremic syndrome (aHUS) is a rare genetic life-threatening disease of chronic uncontrolled complement activation leading to thrombotic microangiopathy (TMA) and severe end-organ damage. Eculizumab, a terminal complement inhibitor approved for aHUS treatment, was reported to improve hematologic and renal parameters in 2 prior prospective phase 2 studies. This is the largest prospective study of eculizumab in aHUS to date, conducted in an adult population. STUDY DESIGN: Open-label single-arm phase 2 trial. SETTING & PARTICIPANTS: Patients 18 years or older with aHUS (platelet count <150 x 10(3)/muL, hemoglobin </= lower limit of normal, lactate dehydrogenase >/=1.5 x upper limit of normal [ULN], and serum creatinine >/= ULN) were included in this multicenter multinational study. INTERVENTION: Intravenous eculizumab (900mg/wk for 4 weeks, 1,200mg at week 5 and then every 2 weeks) for 26 weeks. OUTCOMES & MEASUREMENTS: Primary end point was complete TMA response within 26 weeks, defined as hematologic normalization (platelet count >/=150 x 10(3)/muL, LDH </= ULN), and preservation of kidney function (<25% serum creatinine increase from baseline), confirmed by 2 or more consecutive measurements obtained 4 or more weeks apart. RESULTS: 41 patients were treated; 38 (93%) completed 26 weeks of treatment. 30 (73%) were included during their first TMA manifestation. 30 (73%) had complete TMA response. Platelet counts and estimated glomerular filtration rates increased from baseline (P<0.001). All 35 patients on baseline plasma exchange/plasma infusion discontinued by week 26. Of 24 patients requiring baseline dialysis, 5 recovered kidney function before eculizumab initiation and 15 of the remaining 19 (79%) discontinued dialysis during eculizumab treatment. No patients lost existing transplants. Quality-of-life measures were significantly improved. Two patients developed meningococcal infections; both recovered, and 1 remained on eculizumab treatment. LIMITATIONS: Single-arm open-label design. CONCLUSIONS: Results highlight the benefits of eculizumab in adult patients with aHUS: improvement in hematologic, renal, and quality-of-life parameters; dialysis discontinuation; and transplant protection.
Keywords
Adolescent, Adult, Aged, Aged, 80 and over, Antibodies, Monoclonal, Humanized/*therapeutic use, Atypical Hemolytic Uremic Syndrome/*drug therapy, Female, Humans, Male, Middle Aged, Prospective Studies, Remission Induction, Young Adult, *Eculizumab, *Soliris, *TMA response, *adults, *atypical hemolytic uremic syndrome (aHUS), *clinical trial, *hematologic normalization, *hemoglobin, *kidney disease, *lactate dehydrogenase (LDH), *platelet count, *renal function, *terminal complement inhibitor, *thrombotic microangiopathy (TMA)
Pubmed
Create date
01/03/2022 11:18
Last modification date
02/03/2022 7:35
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