Literature DB >> 24656451

Discontinuation of eculizumab maintenance treatment for atypical hemolytic uremic syndrome: a report of 10 cases.

Gianluigi Ardissino1, Sara Testa2, Ilaria Possenti2, Francesca Tel2, Fabio Paglialonga2, Stefania Salardi2, Silvana Tedeschi2, Mirco Belingheri2, Massimo Cugno2.   

Abstract

Atypical hemolytic uremic syndrome (aHUS) is a life-threatening thrombotic microangiopathy, and as many as 70% of patients with aHUS have mutations in the genes encoding complement regulatory proteins. Eculizumab, a humanized recombinant monoclonal antibody targeting C5, has been used successfully in patients with aHUS since 2009. The standard maintenance treatment requires life-long eculizumab therapy, but the possibility of discontinuation has not yet been tested systematically. We report the safety of discontinuing eculizumab treatment in 10 patients who stopped treatment with the aim of minimizing the risk of adverse reactions, reducing the risk of meningitis, and improving quality of life while also reducing the considerable treatment costs. Disease activity was monitored closely at home by means of urine dipstick testing for hemoglobin. During the cumulative observation period of 95 months, 3 of the 10 patients experienced relapse within 6 weeks of discontinuation, but then immediately resumed treatment and completely recovered. Our experience supports the possibility of discontinuing eculizumab therapy with strict home monitoring for early signs of relapse in patients with aHUS who achieve stable remission.
Copyright © 2014 National Kidney Foundation, Inc. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Atypical hemolytic uremic syndrome; discontinuation; eculizumab

Mesh:

Substances:

Year:  2014        PMID: 24656451     DOI: 10.1053/j.ajkd.2014.01.434

Source DB:  PubMed          Journal:  Am J Kidney Dis        ISSN: 0272-6386            Impact factor:   8.860


  70 in total

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Authors:  Samuel A Merrill; Robert A Brodsky
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2018-11-30

Review 2.  Complementopathies.

Authors:  Andrea C Baines; Robert A Brodsky
Journal:  Blood Rev       Date:  2017-02-06       Impact factor: 8.250

3.  Eculizumab reduces complement activation, inflammation, endothelial damage, thrombosis, and renal injury markers in aHUS.

Authors:  Roxanne Cofiell; Anjli Kukreja; Krystin Bedard; Yan Yan; Angela P Mickle; Masayo Ogawa; Camille L Bedrosian; Susan J Faas
Journal:  Blood       Date:  2015-04-01       Impact factor: 22.113

4.  Eculizumab in pregnancy-associated atypical hemolytic uremic syndrome: insights for optimizing management.

Authors:  Erika De Sousa Amorim; Miquel Blasco; Luis Quintana; Manel Sole; Santiago Rodríguez de Cordoba; Josep Maria Campistol
Journal:  J Nephrol       Date:  2015-02-25       Impact factor: 3.902

5.  Eculizumab cessation in atypical hemolytic uremic syndrome.

Authors:  Samuel A Merrill; Zachary D Brittingham; Xuan Yuan; Alison R Moliterno; C John Sperati; Robert A Brodsky
Journal:  Blood       Date:  2017-05-01       Impact factor: 22.113

Review 6.  Atypical hemolytic uremic syndrome.

Authors:  Vahid Afshar-Kharghan
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2016-12-02

7.  Optimal duration of treatment with eculizumab in atypical hemolytic uremic syndrome (aHUS)-a question to be addressed in a scientific way.

Authors:  Gema Ariceta
Journal:  Pediatr Nephrol       Date:  2019-01-28       Impact factor: 3.714

8.  Two cases of atypical hemolytic uremic syndrome (aHUS) and eosinophilic granulomatosis with polyangiitis (EGPA): a possible relationship.

Authors:  Mercedes Cao; Tamara Ferreiro; Bruna N Leite; Francisco Pita; Luis Bolaños; Francisco Valdés; Angel Alonso; Eduardo Vázquez; Juan Mosquera; María Trigás; Santiago Rodríguez
Journal:  CEN Case Rep       Date:  2017-03-01

Review 9.  Advances and challenges in the management of complement-mediated thrombotic microangiopathies.

Authors:  Jean-Claude Davin; Nicole C A J van de Kar
Journal:  Ther Adv Hematol       Date:  2015-08

10.  Efficacy and safety of eculizumab in childhood atypical hemolytic uremic syndrome in Japan.

Authors:  Naoko Ito; Hiroshi Hataya; Ken Saida; Yoshiro Amano; Yoshihiko Hidaka; Yaeko Motoyoshi; Toshiyuki Ohta; Yasuhiro Yoshida; Chikako Terano; Tadashi Iwasa; Wataru Kubota; Hidetoshi Takada; Toshiro Hara; Yoshihiro Fujimura; Shuichi Ito
Journal:  Clin Exp Nephrol       Date:  2015-07-09       Impact factor: 2.801

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