Efficacy and safety of emapalumab in macrophage activation syndrome.


Journal

Annals of the rheumatic diseases
ISSN: 1468-2060
Titre abrégé: Ann Rheum Dis
Pays: England
ID NLM: 0372355

Informations de publication

Date de publication:
06 2023
Historique:
received: 18 12 2022
accepted: 02 02 2023
medline: 15 5 2023
pubmed: 1 4 2023
entrez: 31 3 2023
Statut: ppublish

Résumé

Macrophage activation syndrome (MAS) is a severe, life-threatening complication of systemic juvenile idiopathic arthritis (sJIA) and adult-onset Still's disease (AOSD). The objective of this study was to confirm the adequacy of an emapalumab dosing regimen in relation to interferon-γ (IFNγ) activity by assessing efficacy and safety. The efficacy outcome was MAS remission by week 8, based on clinical and laboratory criteria. We studied emapalumab, a human anti-IFNγ antibody, administered with background glucocorticoids, in a prospective single-arm trial involving patients who had MAS secondary to sJIA or AOSD and had previously failed high-dose glucocorticoids, with or without anakinra and/or ciclosporin. The study foresaw 4-week treatment that could be shortened or prolonged based on investigator's assessment of response. Patients entered a long-term (12 months) follow-up study. Fourteen patients received emapalumab. All patients completed the trial, entered the long-term follow-up and were alive at the end of follow-up. The investigated dosing regimen, based on an initial loading dose followed by maintenance doses, was appropriate, as shown by rapid neutralisation of IFNγ activity, demonstrated by a prompt decrease in serum C-X-C motif chemokine ligand 9 (CXCL9) levels. By week 8, MAS remission was achieved in 13 of the 14 patients at a median time of 25 days. Viral infections and positive viral tests were observed. Neutralisation of IFNγ with emapalumab was efficacious in inducing remission of MAS secondary to sJIA or AOSD in patients who had failed high-dose glucocorticoids. Screening for viral infections should be performed, particularly for cytomegalovirus. NCT02069899 and NCT03311854.

Identifiants

pubmed: 37001971
pii: ard-2022-223739
doi: 10.1136/ard-2022-223739
pmc: PMC10314091
doi:

Substances chimiques

Emapalumab 0
Antibodies, Monoclonal 0
Glucocorticoids 0

Banques de données

ClinicalTrials.gov
['NCT02069899', 'NCT03311854']

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

857-865

Commentaires et corrections

Type : CommentIn

Informations de copyright

© Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: FDB: consultant and research grants from AbbVie, Sobi, Pfizer, Roche, Sanofi, Novartis, Novimmune; AAG: consultant for Novartis, AB2 Bio, Novimmune, Sobi; PAB: consultant for Sobi, Novartis, Roche, UCB; CB, MP, GM: none declared; DE: speaker bureau for Sobi; CP: speaker bureau for Sobi; GS: consultant for Novartis, Sobi, Novimmune, AB2 Bio; PQ: consultant for AbbVie, Chugai-Roche, Lilly, Novartis, Pfizer, Sobi and speaker bureau for AbbVie, Chugai-Roche, Lilly, Novartis, Pfizer, Sobi; JA: consultant for Sobi, Novartis, Roche, Pfizer, AbbVie, GSK; CL: consultant for Sobi; RF: previously employed by Sobi; VA: previously employed by Sobi; MB: previously employed by Sobi; PJ: consultant for Sobi; CdM: consultant for Sobi, previously employed by Sobi.

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Auteurs

Fabrizio De Benedetti (F)

Division of Rheumatology, Ospedale Pediatrico Bambino Gesù, IRCCS, Rome, Italy fabrizio.debenedetti@opbg.net.

Alexei A Grom (AA)

Division of Rheumatology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, USA.

Paul A Brogan (PA)

University College London Great Ormond Street Institute of Child Health, London, UK.

Claudia Bracaglia (C)

Division of Rheumatology, Ospedale Pediatrico Bambino Gesù, IRCCS, Rome, Italy.

Manuela Pardeo (M)

Division of Rheumatology, Ospedale Pediatrico Bambino Gesù, IRCCS, Rome, Italy.

Giulia Marucci (G)

Division of Rheumatology, Ospedale Pediatrico Bambino Gesù, IRCCS, Rome, Italy.

Despina Eleftheriou (D)

University College London Great Ormond Street Institute of Child Health, London, UK.

Charalampia Papadopoulou (C)

University College London Great Ormond Street Institute of Child Health, London, UK.

Grant S Schulert (GS)

Division of Rheumatology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati, OH, USA.

Pierre Quartier (P)

Pediatric Immuno-Hematology and Rheumatology Unit, RAISE Rare Disease Reference Centre, Hopital Universitaire Necker-Enfants Malades, Assistance Publique-Hopitaux de Paris, Paris, France.
Université Paris-Cité, Paris, France.

Jordi Antón (J)

Pediatric Rheumatology, Hospital Sant Joan de Deu, Barcelona, Spain.
Faculty of Medicine, Universitat de Barcelona, Barcelona, Spain.

Christian Laveille (C)

Calvagone Sarl, Liergues, France.

Rikke Frederiksen (R)

Swedish Orphan Biovitrum AG (Sobi), Basel, Switzerland.

Veronica Asnaghi (V)

Swedish Orphan Biovitrum AG (Sobi), Basel, Switzerland.

Maria Ballabio (M)

Swedish Orphan Biovitrum AG (Sobi), Basel, Switzerland.

Philippe Jacqmin (P)

MnS Modelling and Simulation, Dinant, Belgium.

Cristina de Min (C)

Swedish Orphan Biovitrum AG (Sobi), Basel, Switzerland.

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