Expert Clinical Management of Severe Immune-Related Adverse Events: Results from a Multicenter Survey on Hot Topics for Management.

acute kidney injury immune checkpoint inhibitors immune-related hepatitis immunotherapy myocarditis myositis

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
11 Oct 2022
Historique:
received: 26 08 2022
revised: 30 09 2022
accepted: 03 10 2022
entrez: 27 10 2022
pubmed: 28 10 2022
medline: 28 10 2022
Statut: epublish

Résumé

There are differences in recommendations for the management of immune-related adverse events (irAEs) associated with immune checkpoint inhibitors (ICIs). To assess the real-world management of irAEs, three surveys regarding ICI-induced hepatitis (IIH), renal irAEs, and myositis were developed and sent to experts in each area. Fifty-six surveys were completed (17 IIH, 20 renal irAEs, and 19 myositis). All experts agreed on performing imaging in every suspected case of severe IIH. Sixty-five percent agreed on performing a liver biopsy in patients not responding to corticosteroids. The most common indication for corticosteroid use (59%) was for severe IIH not improving after discontinuation of ICIs. Additionally, 60% of the experts agreed on performing a biopsy for stage 2/3 acute kidney injury (AKI), and 70% recommended imaging for any stage of AKI. Thirty-five percent favored corticosteroids in AKI patients with creatinine levels 2-3-fold above baseline. For myositis, 58% would recommend a muscle biopsy in a patient with weakness and creatine kinase levels of 5000 U/L; 47% would also opt for an endomyocardial biopsy when the troponin levels are increased. Fifty-eight percent recommended oral corticosteroids for myositis, and 37% recommended additional therapy, mainly immunoglobulins. These results show substantial differences in expert practice patterns for the management of severe liver, kidney, and muscular irAEs.

Identifiants

pubmed: 36294298
pii: jcm11205977
doi: 10.3390/jcm11205977
pmc: PMC9604376
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Instituto de Salud Carlos III
ID : PI17/00257
Organisme : Instituto de Salud Carlos III
ID : PI21/01292
Organisme : Instituto de Salud Carlos III
ID : RD16/0009/0030
Organisme : RICORS
ID : RD21/0005/0016
Organisme : CSUR
ID : Enfermedades glomerulares complejas

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Auteurs

Mar Riveiro-Barciela (M)

Liver Unit, Internal Medicine Department, Vall d'Hebron University Hospital, Vall d'Hebron Barcelona Hospital Campus, 08035 Barcelona, Spain.
Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Instituto de Salud Carlos III, 28029 Madrid, Spain.
Department of Medicine, Autonomous Univeristy of Barcelona (AUB), 08035 Barcelona, Spain.

Maria Jose Soler (MJ)

Department of Medicine, Autonomous Univeristy of Barcelona (AUB), 08035 Barcelona, Spain.
Department of Nephrology, Vall d´Hebron University Hospital, Vall d'Hebron Barcelona Hospital Campus, 08035 Barcelona, Spain.

Ana Barreira-Diaz (A)

Liver Unit, Internal Medicine Department, Vall d'Hebron University Hospital, Vall d'Hebron Barcelona Hospital Campus, 08035 Barcelona, Spain.
Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Instituto de Salud Carlos III, 28029 Madrid, Spain.
Department of Medicine, Autonomous Univeristy of Barcelona (AUB), 08035 Barcelona, Spain.

Sheila Bermejo (S)

Department of Medicine, Autonomous Univeristy of Barcelona (AUB), 08035 Barcelona, Spain.
Department of Nephrology, Vall d´Hebron University Hospital, Vall d'Hebron Barcelona Hospital Campus, 08035 Barcelona, Spain.

Sebastian Bruera (S)

Section of Immunology, Allergy and Rheumatology, Baylor College of Medicine, Houston, TX 77030, USA.

Maria E Suarez-Almazor (ME)

Department of Health Services Research and Section of Rheumatology and Clinical Immunology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.

Classifications MeSH