Immune checkpoint inhibitors-associated pericardial disease: a systematic review of case reports.

Cardiac tamponade Cardiotoxicity Immune checkpoint inhibitors Pericardial effusion Pericarditis Rechallenge

Journal

Cancer immunology, immunotherapy : CII
ISSN: 1432-0851
Titre abrégé: Cancer Immunol Immunother
Pays: Germany
ID NLM: 8605732

Informations de publication

Date de publication:
Oct 2021
Historique:
received: 29 12 2020
accepted: 07 04 2021
pubmed: 21 4 2021
medline: 30 9 2021
entrez: 20 4 2021
Statut: ppublish

Résumé

Treatment with immune checkpoint inhibitors (ICIs) can be complicated by cardiovascular toxicity, including pericardial disease. To date, no prospective studies specifically investigated the optimal treatment of ICI-associated pericardial disease, and the available evidence is based on case reports and series only. We performed a systematic review of case reports and series including 20 publications for a total of 28 cases of ICI-associated pericardial disease. In this review, pericardial disease was reversible in the majority of cases (75%), although 2 deaths were reported. The majority of cases were life-threatening (G4, 53.6%) or severe (G3, 21.4%), requiring pericardiocentesis. Higher rates of improvement were associated with administration of corticosteroids (86.7% vs 61.5%), presence of other immune-related adverse events (90.9% vs. 64.7%), and non-malignant effusions (86.7% vs 42.8%). ICIs were discontinued in the majority of cases and then restarted in 7 patients with no recurrence of pericardial disease. Based on these results, ICI-associated G3-G4 pericardial disease as well as G2 pericardial disease with moderate-severe effusion should be treated with ICIs discontinuation and high-dose steroids, also performing pericardiocentesis, pericardial drainage or pericardial window in case of cardiac tamponade. For G2 with small effusion or G1 pericardial disease, ICIs might be continued and colchicine or NSAIDs could be considered. For patients requiring ICIs discontinuation, a rechallenge with ICIs seems to be feasible after resolution or meaningful improvement of pericardial disease.

Identifiants

pubmed: 33877385
doi: 10.1007/s00262-021-02938-z
pii: 10.1007/s00262-021-02938-z
doi:

Substances chimiques

Immune Checkpoint Inhibitors 0

Types de publication

Case Reports Journal Article Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

3041-3053

Informations de copyright

© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

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Auteurs

Alessandro Inno (A)

Oncologia Medica, IRCCS Ospedale Sacro Cuore Don Calabria, Via don A. Sempreboni 5, 37024, Negrar di Valpolicella, Verona, Italy. alessandro.inno@sacrocuore.it.

Nicola Maurea (N)

Divisione di Cardiologia, IRCCS Fondazione G. Pascale, Napoli, Italy.

Giulio Metro (G)

Oncologia Medica, Ospedale Santa Maria della Misericordia, Azienda Ospedaliera Di Perugia, Perugia, Italy.

Andreina Carbone (A)

Divisione di Cardiologia, IRCCS Fondazione G. Pascale, Napoli, Italy.

Antonio Russo (A)

Oncologia Medica, Dipartimento di Discipline Chirurgiche, Oncologiche E Stomatologiche, Policlinico Universitario "A. Giaccone", Palermo, Italy.

Stefania Gori (S)

Oncologia Medica, IRCCS Ospedale Sacro Cuore Don Calabria, Via don A. Sempreboni 5, 37024, Negrar di Valpolicella, Verona, Italy.

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