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Early Eculizumab Withdrawal in Patients With Atypical Hemolytic Uremic Syndrome in Native Kidneys Is Safe and Cost-Effective: Results of the CUREiHUS Study

INTRODUCTION: The introduction of eculizumab has improved the outcome in patients with atypical hemolytic uremic syndrome (aHUS). The optimal treatment strategy is debated. Here, we report the results of the CUREiHUS study, a 4-year prospective, observational study monitoring unbiased eculizumab dis...

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Autores principales: Bouwmeester, Romy N., Duineveld, Caroline, Wijnsma, Kioa L., Bemelman, Frederike J., van der Heijden, Joost W., van Wijk, Joanna A.E., Bouts, Antonia H.M., van de Wetering, Jacqueline, Dorresteijn, Eiske, Berger, Stefan P., Gracchi, Valentina, van Zuilen, Arjan D., Keijzer-Veen, Mandy G., de Vries, Aiko P.J., van Rooij, Roos W.G., Engels, Flore A.P.T., Altena, Wim, de Wildt, Renée, van Kempen, Evy, Adang, Eddy M., ter Avest, Mendy, ter Heine, Rob, Volokhina, Elena B., van den Heuvel, Lambertus P.W.J., Wetzels, Jack F.M., van de Kar, Nicole C.A.J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9832049/
https://www.ncbi.nlm.nih.gov/pubmed/36644349
http://dx.doi.org/10.1016/j.ekir.2022.10.013
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author Bouwmeester, Romy N.
Duineveld, Caroline
Wijnsma, Kioa L.
Bemelman, Frederike J.
van der Heijden, Joost W.
van Wijk, Joanna A.E.
Bouts, Antonia H.M.
van de Wetering, Jacqueline
Dorresteijn, Eiske
Berger, Stefan P.
Gracchi, Valentina
van Zuilen, Arjan D.
Keijzer-Veen, Mandy G.
de Vries, Aiko P.J.
van Rooij, Roos W.G.
Engels, Flore A.P.T.
Altena, Wim
de Wildt, Renée
van Kempen, Evy
Adang, Eddy M.
ter Avest, Mendy
ter Heine, Rob
Volokhina, Elena B.
van den Heuvel, Lambertus P.W.J.
Wetzels, Jack F.M.
van de Kar, Nicole C.A.J.
author_facet Bouwmeester, Romy N.
Duineveld, Caroline
Wijnsma, Kioa L.
Bemelman, Frederike J.
van der Heijden, Joost W.
van Wijk, Joanna A.E.
Bouts, Antonia H.M.
van de Wetering, Jacqueline
Dorresteijn, Eiske
Berger, Stefan P.
Gracchi, Valentina
van Zuilen, Arjan D.
Keijzer-Veen, Mandy G.
de Vries, Aiko P.J.
van Rooij, Roos W.G.
Engels, Flore A.P.T.
Altena, Wim
de Wildt, Renée
van Kempen, Evy
Adang, Eddy M.
ter Avest, Mendy
ter Heine, Rob
Volokhina, Elena B.
van den Heuvel, Lambertus P.W.J.
Wetzels, Jack F.M.
van de Kar, Nicole C.A.J.
author_sort Bouwmeester, Romy N.
collection PubMed
description INTRODUCTION: The introduction of eculizumab has improved the outcome in patients with atypical hemolytic uremic syndrome (aHUS). The optimal treatment strategy is debated. Here, we report the results of the CUREiHUS study, a 4-year prospective, observational study monitoring unbiased eculizumab discontinuation in Dutch patients with aHUS after 3 months of therapy. METHODS: All pediatric and adult patients with aHUS in native kidneys and a first-time eculizumab treatment were evaluated. In addition, an extensive cost-consequence analysis was conducted. RESULTS: A total of 21 patients were included in the study from January 2016 to October 2020. In 17 patients (81%), a complement genetic variant or antibodies against factor H were identified. All patients showed full recovery of hematological thrombotic microangiopathy (TMA) parameters after the start of eculizumab. A renal response was noted in 18 patients. After a median treatment duration of 13.6 weeks (range 2.1–43.9), eculizumab was withdrawn in all patients. During follow-up (80.7 weeks [0.0–236.9]), relapses occurred in 4 patients. Median time to first relapse was 19.5 (14.3–53.6) weeks. Eculizumab was reinitiated within 24 hours in all relapsing patients. At last follow-up, there were no chronic sequelae, i.e., no clinically relevant increase in serum creatinine (sCr), proteinuria, and/or hypertension in relapsing patients. The low sample size and event rate did not allow to determine predictors of relapse. However, relapses only occurred in patients with a likely pathogenic variant. The cost-effectiveness analysis revealed that the total medical expenses of our population were only 30% of the fictive expenses that would have been made when patients received eculizumab every fortnight. CONCLUSION: It is safe and cost-effective to discontinue eculizumab after 3 months of therapy in patients with aHUS in native kidneys. Larger data registries are needed to determine factors associated with suboptimal kidney function recovery during eculizumab treatment, factors to predict relapses, and long-term outcomes of eculizumab discontinuation.
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spelling pubmed-98320492023-01-12 Early Eculizumab Withdrawal in Patients With Atypical Hemolytic Uremic Syndrome in Native Kidneys Is Safe and Cost-Effective: Results of the CUREiHUS Study Bouwmeester, Romy N. Duineveld, Caroline Wijnsma, Kioa L. Bemelman, Frederike J. van der Heijden, Joost W. van Wijk, Joanna A.E. Bouts, Antonia H.M. van de Wetering, Jacqueline Dorresteijn, Eiske Berger, Stefan P. Gracchi, Valentina van Zuilen, Arjan D. Keijzer-Veen, Mandy G. de Vries, Aiko P.J. van Rooij, Roos W.G. Engels, Flore A.P.T. Altena, Wim de Wildt, Renée van Kempen, Evy Adang, Eddy M. ter Avest, Mendy ter Heine, Rob Volokhina, Elena B. van den Heuvel, Lambertus P.W.J. Wetzels, Jack F.M. van de Kar, Nicole C.A.J. Kidney Int Rep Clinical Research INTRODUCTION: The introduction of eculizumab has improved the outcome in patients with atypical hemolytic uremic syndrome (aHUS). The optimal treatment strategy is debated. Here, we report the results of the CUREiHUS study, a 4-year prospective, observational study monitoring unbiased eculizumab discontinuation in Dutch patients with aHUS after 3 months of therapy. METHODS: All pediatric and adult patients with aHUS in native kidneys and a first-time eculizumab treatment were evaluated. In addition, an extensive cost-consequence analysis was conducted. RESULTS: A total of 21 patients were included in the study from January 2016 to October 2020. In 17 patients (81%), a complement genetic variant or antibodies against factor H were identified. All patients showed full recovery of hematological thrombotic microangiopathy (TMA) parameters after the start of eculizumab. A renal response was noted in 18 patients. After a median treatment duration of 13.6 weeks (range 2.1–43.9), eculizumab was withdrawn in all patients. During follow-up (80.7 weeks [0.0–236.9]), relapses occurred in 4 patients. Median time to first relapse was 19.5 (14.3–53.6) weeks. Eculizumab was reinitiated within 24 hours in all relapsing patients. At last follow-up, there were no chronic sequelae, i.e., no clinically relevant increase in serum creatinine (sCr), proteinuria, and/or hypertension in relapsing patients. The low sample size and event rate did not allow to determine predictors of relapse. However, relapses only occurred in patients with a likely pathogenic variant. The cost-effectiveness analysis revealed that the total medical expenses of our population were only 30% of the fictive expenses that would have been made when patients received eculizumab every fortnight. CONCLUSION: It is safe and cost-effective to discontinue eculizumab after 3 months of therapy in patients with aHUS in native kidneys. Larger data registries are needed to determine factors associated with suboptimal kidney function recovery during eculizumab treatment, factors to predict relapses, and long-term outcomes of eculizumab discontinuation. Elsevier 2022-10-18 /pmc/articles/PMC9832049/ /pubmed/36644349 http://dx.doi.org/10.1016/j.ekir.2022.10.013 Text en © 2022 Published by Elsevier Inc. on behalf of the International Society of Nephrology. https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Clinical Research
Bouwmeester, Romy N.
Duineveld, Caroline
Wijnsma, Kioa L.
Bemelman, Frederike J.
van der Heijden, Joost W.
van Wijk, Joanna A.E.
Bouts, Antonia H.M.
van de Wetering, Jacqueline
Dorresteijn, Eiske
Berger, Stefan P.
Gracchi, Valentina
van Zuilen, Arjan D.
Keijzer-Veen, Mandy G.
de Vries, Aiko P.J.
van Rooij, Roos W.G.
Engels, Flore A.P.T.
Altena, Wim
de Wildt, Renée
van Kempen, Evy
Adang, Eddy M.
ter Avest, Mendy
ter Heine, Rob
Volokhina, Elena B.
van den Heuvel, Lambertus P.W.J.
Wetzels, Jack F.M.
van de Kar, Nicole C.A.J.
Early Eculizumab Withdrawal in Patients With Atypical Hemolytic Uremic Syndrome in Native Kidneys Is Safe and Cost-Effective: Results of the CUREiHUS Study
title Early Eculizumab Withdrawal in Patients With Atypical Hemolytic Uremic Syndrome in Native Kidneys Is Safe and Cost-Effective: Results of the CUREiHUS Study
title_full Early Eculizumab Withdrawal in Patients With Atypical Hemolytic Uremic Syndrome in Native Kidneys Is Safe and Cost-Effective: Results of the CUREiHUS Study
title_fullStr Early Eculizumab Withdrawal in Patients With Atypical Hemolytic Uremic Syndrome in Native Kidneys Is Safe and Cost-Effective: Results of the CUREiHUS Study
title_full_unstemmed Early Eculizumab Withdrawal in Patients With Atypical Hemolytic Uremic Syndrome in Native Kidneys Is Safe and Cost-Effective: Results of the CUREiHUS Study
title_short Early Eculizumab Withdrawal in Patients With Atypical Hemolytic Uremic Syndrome in Native Kidneys Is Safe and Cost-Effective: Results of the CUREiHUS Study
title_sort early eculizumab withdrawal in patients with atypical hemolytic uremic syndrome in native kidneys is safe and cost-effective: results of the cureihus study
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9832049/
https://www.ncbi.nlm.nih.gov/pubmed/36644349
http://dx.doi.org/10.1016/j.ekir.2022.10.013
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