Outcomes of MIS-C patients treated with anakinra: a retrospective multicenter national study.

COVID-19 MIS-C SARS-CoV2 multisystem inflammatory syndrome pediatrics

Journal

Frontiers in pediatrics
ISSN: 2296-2360
Titre abrégé: Front Pediatr
Pays: Switzerland
ID NLM: 101615492

Informations de publication

Date de publication:
2023
Historique:
received: 03 01 2023
accepted: 27 07 2023
medline: 7 9 2023
pubmed: 7 9 2023
entrez: 7 9 2023
Statut: epublish

Résumé

The treatment of multisystem inflammatory syndrome in children unresponsive to first-line therapies (IVIG and/or steroids) is challenging. The effectiveness of IL-1 receptor antagonist, anakinra, is debated. We conducted an anonymous retrospective multicenter study on MIS-C patients treated with anakinra in Italy from January 2020 to February 2021. Our study outcomes included the percentage of patients who required further therapeutic step-up, the percentage of patients who experienced fever resolution within 24 h and a reduction of CRP by half within 48 h, and the percentage of patients who developed Coronary Artery Anomalies (CAA) during follow-up. 35 cases of MIS-C were treated in 10 hospitals. Of these, 13 patients started anakinra while in the ICU, and 22 patients started anakinra in other wards. 25 patients (71.4%) were treated with corticosteroids at a starting dose 2-30 mg/Kg/day plus IVIG (2 g/Kg), 10 patients (28.6%) received only corticosteroids without IVIG. Anakinra was administered intravenously to all patients in Group A (mean dose 8 mg/Kg/day), and subcutaneously in Group B (mean dose 4 mg/Kg/day). Only two patients required further treatment step-up and no patients developed CAA after receiving anakinra. The most commonly observed side effect was an increase in ALT, occurring in 17.1% of patients. In this retrospective cohort of severe MIS-C patients treated with anakinra we report favorable clinical outcomes with a low incidence of side effects. The simultaneous use of steroids ± IVIG in these patients hinders definitive conclusions regarding the need of IL-1 inhibition in MIS-C treatment.

Sections du résumé

Background UNASSIGNED
The treatment of multisystem inflammatory syndrome in children unresponsive to first-line therapies (IVIG and/or steroids) is challenging. The effectiveness of IL-1 receptor antagonist, anakinra, is debated.
Patients and methods UNASSIGNED
We conducted an anonymous retrospective multicenter study on MIS-C patients treated with anakinra in Italy from January 2020 to February 2021. Our study outcomes included the percentage of patients who required further therapeutic step-up, the percentage of patients who experienced fever resolution within 24 h and a reduction of CRP by half within 48 h, and the percentage of patients who developed Coronary Artery Anomalies (CAA) during follow-up.
Results UNASSIGNED
35 cases of MIS-C were treated in 10 hospitals. Of these, 13 patients started anakinra while in the ICU, and 22 patients started anakinra in other wards. 25 patients (71.4%) were treated with corticosteroids at a starting dose 2-30 mg/Kg/day plus IVIG (2 g/Kg), 10 patients (28.6%) received only corticosteroids without IVIG. Anakinra was administered intravenously to all patients in Group A (mean dose 8 mg/Kg/day), and subcutaneously in Group B (mean dose 4 mg/Kg/day). Only two patients required further treatment step-up and no patients developed CAA after receiving anakinra. The most commonly observed side effect was an increase in ALT, occurring in 17.1% of patients.
Conclusions UNASSIGNED
In this retrospective cohort of severe MIS-C patients treated with anakinra we report favorable clinical outcomes with a low incidence of side effects. The simultaneous use of steroids ± IVIG in these patients hinders definitive conclusions regarding the need of IL-1 inhibition in MIS-C treatment.

Identifiants

pubmed: 37675397
doi: 10.3389/fped.2023.1137051
pmc: PMC10478576
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1137051

Informations de copyright

© 2023 Licciardi, Covizzi, Dellepiane, Olivini, Mastrolia, Lo Vecchio, Monno, Tardi, Mauro, Alessio, Filocamo, Cattalini, Taddio, Caorsi, Marseglia, LaTorre, Campana, Simonini, Ravelli and Montin.

Déclaration de conflit d'intérêts

GF is a consultant for SOBI, GS and MM received an unrestricted educational Grant from SOBI, for a project not related to MIS-C. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Références

Lancet Rheumatol. 2022 May;4(5):e329-e337
pubmed: 35368387
Crit Care. 2021 Apr 7;25(1):131
pubmed: 33827651
Arthritis Rheumatol. 2023 Aug;75(8):1466-1476
pubmed: 36908050
Front Pediatr. 2020 Nov 30;8:576912
pubmed: 33330276
Front Pharmacol. 2017 Mar 28;8:163
pubmed: 28400731
Circulation. 2017 Apr 25;135(17):e927-e999
pubmed: 28356445
Front Pediatr. 2021 Jan 05;8:594127
pubmed: 33469522
J Pediatric Infect Dis Soc. 2020 Jul 13;9(3):393-398
pubmed: 32463092
Eur J Pediatr. 2021 Jul;180(7):2019-2034
pubmed: 33599835
Front Pediatr. 2021 Dec 20;9:783745
pubmed: 34988039
Nat Med. 2022 May;28(5):1050-1062
pubmed: 35177862
Front Pediatr. 2021 Feb 23;8:624248
pubmed: 33708752
Cell. 2020 Nov 12;183(4):968-981.e7
pubmed: 32966765
Arthritis Rheumatol. 2022 Apr;74(4):e1-e20
pubmed: 35118829
Expert Opin Biol Ther. 2022 Jan;22(1):1-5
pubmed: 34766862
Ital J Pediatr. 2021 Feb 8;47(1):24
pubmed: 33557873
Pediatrics. 2020 Aug;146(2):
pubmed: 32439816
Front Pediatr. 2022 Aug 18;10:942455
pubmed: 36061383

Auteurs

Francesco Licciardi (F)

Division of Pediatric Immunology and Rheumatology, Department of Public Health and Pediatrics, "Regina Margherita" Children Hospital, University of Turin, Turin, Italy.

Carlotta Covizzi (C)

Division of Pediatric Immunology and Rheumatology, Department of Public Health and Pediatrics, "Regina Margherita" Children Hospital, University of Turin, Turin, Italy.

Marta Dellepiane (M)

Division of Pediatric Immunology and Rheumatology, Department of Public Health and Pediatrics, "Regina Margherita" Children Hospital, University of Turin, Turin, Italy.

Nicole Olivini (N)

Pediatrics Unit, University Department of Pediatrics (DEAPG), Bambino Gesù Children's Hospital-IRCCS, Rome, Italy.

Maria Vincenza Mastrolia (MV)

Rheumatology Unit, Department of Paediatrics, Meyer Children's Hospital, University of Florence, Florence, Italy.

Andrea Lo Vecchio (A)

Section of Paediatrics, Department of Translational Medical Sciences, University of Naples Federico II, Naples, Italy.

Viviana Monno (V)

Pediatric Rheumatology Section, Department of Pediatrics, Giovanni XXIII Pediatric Hospital, Bari, Italy.

Maria Tardi (M)

Rheumatology Unit, Department of Pediatrics, Santobono Pausilipon Children Hospital, Naples, Italy.

Angela Mauro (A)

COVID Unit, Emergency Department, Santobono-Pausilipon Children Hospital, Naples, Italy.

Maria Alessio (M)

Section of Paediatrics, Department of Translational Medical Sciences, University of Naples Federico II, Naples, Italy.

Giovanni Filocamo (G)

Pediatric Rheumatology, Fondazione IRCCS Cà Granda Ospedale Maggiore Policlinico, Milano, Italy.

Marco Cattalini (M)

Spedali Civili, Unità di Immunologia e Reumatologia Pediatrica, Clinica Pediatrica dell'Università di Brescia, Brescia, Italy.

Andrea Taddio (A)

Institute for Maternal and Child Health "IRCCS Burlo Garofolo", Trieste and University of Trieste, Trieste, Italy.

Roberta Caorsi (R)

Clinica Pediatrica e Reumatologia, IRCCS Istituto Giannina Gaslini, Genoa, Italy.

Gian Luigi Marseglia (GL)

Pediatric Clinic Foundation IRCCS Policlinico S. Matteo, University of Pavia, Pavia, Italy.

Francesco La Torre (F)

Pediatric Rheumatology Section, Department of Pediatrics, Giovanni XXIII Pediatric Hospital, Bari, Italy.

Andrea Campana (A)

Pediatrics Unit, University Department of Pediatrics (DEAPG), Bambino Gesù Children's Hospital-IRCCS, Rome, Italy.

Gabriele Simonini (G)

Rheumatology Unit, Department of Paediatrics, Meyer Children's Hospital, University of Florence, Florence, Italy.

Angelo Ravelli (A)

Clinica Pediatrica e Reumatologia, IRCCS Istituto Giannina Gaslini, Genoa, Italy.

Davide Montin (D)

Division of Pediatric Immunology and Rheumatology, Department of Public Health and Pediatrics, "Regina Margherita" Children Hospital, University of Turin, Turin, Italy.

Classifications MeSH