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A Multicenter Study Evaluating the Discontinuation of Eculizumab Therapy in Children with Atypical Hemolytic Uremic Syndrome
Background: Atypical hemolytic uremic syndrome (aHUS) is a rare, life-threatening thrombotic microangiopathy (TMA), which has been treated successfully with eculizumab. The optimal duration of eculizumab in treating patients with aHUS remains poorly defined. Methods: We conducted a multicenter retro...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9688604/ https://www.ncbi.nlm.nih.gov/pubmed/36421183 http://dx.doi.org/10.3390/children9111734 |
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author | AlZabali, Saeed AlBatati, Sawsan Rahim, Khawla Faqeehi, Hassan Osman, Abubaker Bamhraz, Abdulaziz Saleh, Mohammed A. Kari, Jameela A. Aloufi, Majed Eid, Loai Nasser, Haydar Imam, Abubakr AlHammadi, Entesar Alkandari, Omar Al Riyami, Mohammed Sethi, Sidharth Licht, Christoph Alhasan, Khalid A. AlAnazi, Abdulkarim |
author_facet | AlZabali, Saeed AlBatati, Sawsan Rahim, Khawla Faqeehi, Hassan Osman, Abubaker Bamhraz, Abdulaziz Saleh, Mohammed A. Kari, Jameela A. Aloufi, Majed Eid, Loai Nasser, Haydar Imam, Abubakr AlHammadi, Entesar Alkandari, Omar Al Riyami, Mohammed Sethi, Sidharth Licht, Christoph Alhasan, Khalid A. AlAnazi, Abdulkarim |
author_sort | AlZabali, Saeed |
collection | PubMed |
description | Background: Atypical hemolytic uremic syndrome (aHUS) is a rare, life-threatening thrombotic microangiopathy (TMA), which has been treated successfully with eculizumab. The optimal duration of eculizumab in treating patients with aHUS remains poorly defined. Methods: We conducted a multicenter retrospective study in the Arabian Gulf region for children of less than 18 years of age who were diagnosed with aHUS and who discontinued eculizumab between June 2013 and June 2021 to assess the rate and risk factors of aHUS recurrence. Results: We analyzed 28 patients with a clinical diagnosis of aHUS who had discontinued eculizumab. The most common reason for the discontinuation of eculizumab was renal and hematological remission (71.4%), followed by negative genetic testing (28.6%). During a median follow-up period of 24 months after discontinuation, 8 patients (28.5%) experienced HUS relapse. The risk factors of recurrence were positive genetic mutations (p = 0.020). On the other hand, there was no significant relationship between the relapse and age of presentation, the need for acute dialysis, the duration of eculizumab therapy before discontinuation, or the timing of eculizumab after the presentation. Regarding the renal outcomes after discontinuation, 23 patients were in remission with normal renal function, while 4 patients had chronic kidney disease (CKD) (three of them had pre-existing chronic kidney disease (CKD) before discontinuation, and one case developed a new CKD after discontinuation) and one patient underwent transplantation. Conclusions: The discontinuation of eculizumab in patients with aHUS is not without risk; it can result in HUS recurrence. Eculizumab discontinuation can be performed with close monitoring of the patients. It is essential to assess risk the factors for relapse before eculizumab discontinuation, in particular in children with a positive complement variant and any degree of residual CKD, as HUS relapse may lead to additional loss of kidney function. Resuming eculizumab promptly after relapse is effective in most patients. |
format | Online Article Text |
id | pubmed-9688604 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96886042022-11-25 A Multicenter Study Evaluating the Discontinuation of Eculizumab Therapy in Children with Atypical Hemolytic Uremic Syndrome AlZabali, Saeed AlBatati, Sawsan Rahim, Khawla Faqeehi, Hassan Osman, Abubaker Bamhraz, Abdulaziz Saleh, Mohammed A. Kari, Jameela A. Aloufi, Majed Eid, Loai Nasser, Haydar Imam, Abubakr AlHammadi, Entesar Alkandari, Omar Al Riyami, Mohammed Sethi, Sidharth Licht, Christoph Alhasan, Khalid A. AlAnazi, Abdulkarim Children (Basel) Article Background: Atypical hemolytic uremic syndrome (aHUS) is a rare, life-threatening thrombotic microangiopathy (TMA), which has been treated successfully with eculizumab. The optimal duration of eculizumab in treating patients with aHUS remains poorly defined. Methods: We conducted a multicenter retrospective study in the Arabian Gulf region for children of less than 18 years of age who were diagnosed with aHUS and who discontinued eculizumab between June 2013 and June 2021 to assess the rate and risk factors of aHUS recurrence. Results: We analyzed 28 patients with a clinical diagnosis of aHUS who had discontinued eculizumab. The most common reason for the discontinuation of eculizumab was renal and hematological remission (71.4%), followed by negative genetic testing (28.6%). During a median follow-up period of 24 months after discontinuation, 8 patients (28.5%) experienced HUS relapse. The risk factors of recurrence were positive genetic mutations (p = 0.020). On the other hand, there was no significant relationship between the relapse and age of presentation, the need for acute dialysis, the duration of eculizumab therapy before discontinuation, or the timing of eculizumab after the presentation. Regarding the renal outcomes after discontinuation, 23 patients were in remission with normal renal function, while 4 patients had chronic kidney disease (CKD) (three of them had pre-existing chronic kidney disease (CKD) before discontinuation, and one case developed a new CKD after discontinuation) and one patient underwent transplantation. Conclusions: The discontinuation of eculizumab in patients with aHUS is not without risk; it can result in HUS recurrence. Eculizumab discontinuation can be performed with close monitoring of the patients. It is essential to assess risk the factors for relapse before eculizumab discontinuation, in particular in children with a positive complement variant and any degree of residual CKD, as HUS relapse may lead to additional loss of kidney function. Resuming eculizumab promptly after relapse is effective in most patients. MDPI 2022-11-11 /pmc/articles/PMC9688604/ /pubmed/36421183 http://dx.doi.org/10.3390/children9111734 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article AlZabali, Saeed AlBatati, Sawsan Rahim, Khawla Faqeehi, Hassan Osman, Abubaker Bamhraz, Abdulaziz Saleh, Mohammed A. Kari, Jameela A. Aloufi, Majed Eid, Loai Nasser, Haydar Imam, Abubakr AlHammadi, Entesar Alkandari, Omar Al Riyami, Mohammed Sethi, Sidharth Licht, Christoph Alhasan, Khalid A. AlAnazi, Abdulkarim A Multicenter Study Evaluating the Discontinuation of Eculizumab Therapy in Children with Atypical Hemolytic Uremic Syndrome |
title | A Multicenter Study Evaluating the Discontinuation of Eculizumab Therapy in Children with Atypical Hemolytic Uremic Syndrome |
title_full | A Multicenter Study Evaluating the Discontinuation of Eculizumab Therapy in Children with Atypical Hemolytic Uremic Syndrome |
title_fullStr | A Multicenter Study Evaluating the Discontinuation of Eculizumab Therapy in Children with Atypical Hemolytic Uremic Syndrome |
title_full_unstemmed | A Multicenter Study Evaluating the Discontinuation of Eculizumab Therapy in Children with Atypical Hemolytic Uremic Syndrome |
title_short | A Multicenter Study Evaluating the Discontinuation of Eculizumab Therapy in Children with Atypical Hemolytic Uremic Syndrome |
title_sort | multicenter study evaluating the discontinuation of eculizumab therapy in children with atypical hemolytic uremic syndrome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9688604/ https://www.ncbi.nlm.nih.gov/pubmed/36421183 http://dx.doi.org/10.3390/children9111734 |
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