Discontinuation of Eculizumab Maintenance Treatment for Atypical Hemolytic Uremic Syndrome: A Report of 10 Cases
Adult
Male
Adolescent
Drug-Related Side Effects and Adverse Reactions
Hemoglobinuria
Antibodies, Monoclonal, Humanized
03 medical and health sciences
0302 clinical medicine
Cost of Illness
Recurrence
Humans
Child
Atypical hemolytic uremic syndrome; eculizumab; discontinuation
Atypical Hemolytic Uremic Syndrome
Monitoring, Physiologic
Remission Induction
Infant
Middle Aged
3. Good health
Complement Inactivating Agents
Treatment Outcome
Child, Preschool
Quality of Life
Female
DOI:
10.1053/j.ajkd.2014.01.434
Publication Date:
2014-03-22T00:22:27Z
AUTHORS (9)
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.
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