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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.
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.
Afiliación
  • Bouwmeester RN; Department of Pediatric Nephrology, Radboud University Medical Center, Amalia Children's Hospital, Radboud Institute for Molecular Life Sciences, Nijmegen, the Netherlands.
  • Duineveld C; Department of Nephrology, Radboud University Medical Center, Radboud Institute for Health Sciences, Nijmegen, the Netherlands.
  • Wijnsma KL; Department of Pediatric Nephrology, Radboud University Medical Center, Amalia Children's Hospital, Radboud Institute for Molecular Life Sciences, Nijmegen, the Netherlands.
  • Bemelman FJ; Department of Nephrology, Amsterdam University Medical Center, Amsterdam, the Netherlands.
  • van der Heijden JW; Department of Nephrology, Amsterdam University Medical Center, Amsterdam, the Netherlands.
  • van Wijk JAE; Department of Nephrology, Amsterdam University Medical Center, Amsterdam, the Netherlands.
  • Bouts AHM; Department of Pediatric Nephrology, Amsterdam University Medical Center, Emma Children's Hospital, Amsterdam, the Netherlands.
  • van de Wetering J; Department of Nephrology, Erasmus Medical Center, Rotterdam, the Netherlands.
  • Dorresteijn E; Department of Pediatric Nephrology, Erasmus Medical Center, Sophia Children's Hospital, Rotterdam, the Netherlands.
  • Berger SP; Department of Nephrology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
  • Gracchi V; Department of Pediatric Nephrology, University Medical Center Groningen, University of Groningen, Beatrix Children's Hospital, Groningen, the Netherlands.
  • van Zuilen AD; Department of Nephrology and Hypertension, University Medical Center Utrecht, Utrecht, the Netherlands.
  • Keijzer-Veen MG; Department of Pediatric Nephrology, University Medical Center Utrecht, Wilhelmina Children's Hospital, Utrecht, the Netherlands.
  • de Vries APJ; Department of Nephrology, Leiden University Medical Center, Leiden, the Netherlands.
  • van Rooij RWG; Department of Pediatric Nephrology, Leiden University Medical Center, Willem-Alexander Children's Hospital, Leiden, the Netherlands.
  • Engels FAPT; Department of Pediatric Nephrology, Maastricht University Medical Center, Maastricht, the Netherlands.
  • Altena W; Dutch Kidney Patient Association, Bussum, the Netherlands.
  • de Wildt R; Dutch Kidney Patient Association, Bussum, the Netherlands.
  • van Kempen E; Dutch Kidney Patient Association, Bussum, the Netherlands.
  • Adang EM; Department for Health Evidence, Radboud University Medical Center, Radboud Institute for Health Sciences, Nijmegen, the Netherlands.
  • Ter Avest M; Department of Pharmacy, Radboud University Medical Center, Radboud Institute for Health Sciences, Nijmegen, the Netherlands.
  • Ter Heine R; Department of Pharmacy, Radboud University Medical Center, Radboud Institute for Health Sciences, Nijmegen, the Netherlands.
  • Volokhina EB; Department of Pediatric Nephrology, Radboud University Medical Center, Amalia Children's Hospital, Radboud Institute for Molecular Life Sciences, Nijmegen, the Netherlands.
  • van den Heuvel LPWJ; Department of Pediatric Nephrology, Radboud University Medical Center, Amalia Children's Hospital, Radboud Institute for Molecular Life Sciences, Nijmegen, the Netherlands.
  • Wetzels JFM; Department of Nephrology, Radboud University Medical Center, Radboud Institute for Health Sciences, Nijmegen, the Netherlands.
  • van de Kar NCAJ; Department of Pediatric Nephrology, Radboud University Medical Center, Amalia Children's Hospital, Radboud Institute for Molecular Life Sciences, Nijmegen, the Netherlands.
Kidney Int Rep ; 8(1): 91-102, 2023 Jan.
Article en En | MEDLINE | ID: mdl-36644349
ABSTRACT

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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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Health_economic_evaluation / Observational_studies / Prognostic_studies Idioma: En Revista: Kidney Int Rep Año: 2023 Tipo del documento: Article País de afiliación: Países Bajos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Tipo de estudio: Health_economic_evaluation / Observational_studies / Prognostic_studies Idioma: En Revista: Kidney Int Rep Año: 2023 Tipo del documento: Article País de afiliación: Países Bajos