The use of cinacalcet after pediatric renal transplantation: an international CERTAIN Registry analysis.


Journal

Pediatric nephrology (Berlin, Germany)
ISSN: 1432-198X
Titre abrégé: Pediatr Nephrol
Pays: Germany
ID NLM: 8708728

Informations de publication

Date de publication:
09 2020
Historique:
received: 11 11 2019
accepted: 27 03 2020
revised: 18 03 2020
pubmed: 6 5 2020
medline: 16 6 2021
entrez: 6 5 2020
Statut: ppublish

Résumé

Secondary hyperparathyroidism (SHPT) may persist after renal transplantation (RTx), inducing hypophosphatemia and hypercalcemia that precludes the use of vitamin D analogs. The calcimimetic cinacalcet improved plasma calcium and parathyroid hormone (PTH) levels in randomized controlled trials in adults after RTx, but pediatric data are scarce. In this retrospective study, we analyzed 20 pediatric patients from the Cooperative European Paediatric Renal TransplAnt Initiative (CERTAIN) Registry who received cinacalcet after RTx. The results are presented as median and interquartile range (25th-75th percentile). At 13.7 (11.0-16.5) years of age, 20 pediatric patients received a renal allograft. Cinacalcet was introduced at 0.4 (0.3-2.7) years post-transplant at an estimated glomerular filtration rate (eGFR) of 50 (34-66) mL/min/1.73 m This pilot study suggests that cinacalcet as off-label therapy for SHPT after pediatric RTx is efficacious in controlling post-transplant SHPT with acceptable tolerability. Continuing cinacalcet even with normal PTH can lead to dangerous life-threatening hypocalcemia. Therefore, at each subsequent visit, the need to continue cinacalcet must be assessed.

Sections du résumé

BACKGROUND
Secondary hyperparathyroidism (SHPT) may persist after renal transplantation (RTx), inducing hypophosphatemia and hypercalcemia that precludes the use of vitamin D analogs. The calcimimetic cinacalcet improved plasma calcium and parathyroid hormone (PTH) levels in randomized controlled trials in adults after RTx, but pediatric data are scarce.
METHODS
In this retrospective study, we analyzed 20 pediatric patients from the Cooperative European Paediatric Renal TransplAnt Initiative (CERTAIN) Registry who received cinacalcet after RTx. The results are presented as median and interquartile range (25th-75th percentile).
RESULTS
At 13.7 (11.0-16.5) years of age, 20 pediatric patients received a renal allograft. Cinacalcet was introduced at 0.4 (0.3-2.7) years post-transplant at an estimated glomerular filtration rate (eGFR) of 50 (34-66) mL/min/1.73 m
CONCLUSIONS
This pilot study suggests that cinacalcet as off-label therapy for SHPT after pediatric RTx is efficacious in controlling post-transplant SHPT with acceptable tolerability. Continuing cinacalcet even with normal PTH can lead to dangerous life-threatening hypocalcemia. Therefore, at each subsequent visit, the need to continue cinacalcet must be assessed.

Identifiants

pubmed: 32367310
doi: 10.1007/s00467-020-04558-8
pii: 10.1007/s00467-020-04558-8
doi:

Substances chimiques

Calcimimetic Agents 0
Cinacalcet UAZ6V7728S

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1707-1718

Auteurs

Julie Bernardor (J)

Reference Center for Rare Renal Disorders, Reference Center for Rare Disorders of Calcium and Phosphate Metabolism, Department of Pediatric Nephrology, Rheumatology and Dermatology, Femme Mère Enfant Hospital, Bron Cedex, France. bernardor.j@chu-nice.fr.
Department of Pediatric Nephrology, CHU de Nice, Hôpital Archet, 151 Route Saint-Antoine de Ginestière, 06200, Nice, France. bernardor.j@chu-nice.fr.

Claus Peter Schmitt (CP)

Department of Pediatrics I, University Children's Hospital, Im Neuenheimer Feld 430, 69120, Heidelberg, Germany.

Jun Oh (J)

University Medical Center, Hamburg, Germany.

Anne-Laure Sellier-Leclerc (AL)

Reference Center for Rare Renal Disorders, Reference Center for Rare Disorders of Calcium and Phosphate Metabolism, Department of Pediatric Nephrology, Rheumatology and Dermatology, Femme Mère Enfant Hospital, Bron Cedex, France.

Anja Büscher (A)

Pediatric Nephrology, Pediatrics II, University Children's Hospital Essen, Hufelandstrasse 55, 45122, Essen, Germany.

Luca Dello Strologo (L)

Pediatric Nephrology and Renal Transplant Unit, Bambino Gesù Children's Hospital-IRCCS, Piazza S. Onofrio 4, 00165, Rome, Italy.

Gurkan Genc (G)

Pediatric Nephrology Department, Faculty of Medicine, Ondokuz Mayis University, Samsun, Turkey.

Ulrike John (U)

University Children's Hospital-Pediatric Nephrology, Jena, Germany.

Marcus Weitz (M)

Pediatric Nephrology, University Children's Hospital Zurich, Zurich, Switzerland.

Matthias Zirngibl (M)

Pediatric Nephrology, University Children's Hospital, Hoppe-Seyler-Str. 1, 72076, Tübingen, Germany.

Kai Krupka (K)

Department of Pediatrics I, University Children's Hospital, Im Neuenheimer Feld 430, 69120, Heidelberg, Germany.

Burkhard Tönshoff (B)

Department of Pediatrics I, University Children's Hospital, Im Neuenheimer Feld 430, 69120, Heidelberg, Germany.

Justine Bacchetta (J)

Reference Center for Rare Renal Disorders, Reference Center for Rare Disorders of Calcium and Phosphate Metabolism, Department of Pediatric Nephrology, Rheumatology and Dermatology, Femme Mère Enfant Hospital, Bron Cedex, France.

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