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
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.
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 10:18
Last modification date
02/03/2022 6:35