Effectiveness and safety of infliximab in cardiac Sarcoidosis.


Journal

International journal of cardiology
ISSN: 1874-1754
Titre abrégé: Int J Cardiol
Pays: Netherlands
ID NLM: 8200291

Informations de publication

Date de publication:
01 05 2021
Historique:
received: 04 10 2020
revised: 17 01 2021
accepted: 08 02 2021
pubmed: 15 2 2021
medline: 29 5 2021
entrez: 14 2 2021
Statut: ppublish

Résumé

Immunosuppressive therapy in active cardiac sarcoidosis (CS) might prevent potential life-threatening complications. Infliximab (IFX) is a tumor necrosis factor alpha monoclonal antibody proven to be effective in refractory extracardiac sarcoidosis. It is sparsely used in CS, because of its association with worsening heart failure in prior studies. The goal of this study is to assess the effectiveness and safety of IFX in CS. A retrospective, single center cohort study was performed in sarcoidosis patients treated with IFX based on a cardiac indication between January 2016 and March 2019. Patients received IFX intravenously at a dose of 5 mg/kg at week 0, 2, and subsequently every 4 weeks. After every six months, treatment response was evaluated within the multidisciplinary team using FDG-PET/CT, transthoracic echocardiography, biomarkers and device interrogation reports. Responder analysis definitions were based on; dosage of immunosuppressive drugs, improvement in functional class, left ventricular ejection fraction (LVEF) and SUVmax. Twenty-two patients were included (mean age 51.0 SD10.0 years, male 68.2%) with a mean follow-up of 18.9 months (6 to 44 months) of whom 18 (82%) were classified as responders. Median SUVmax on FDG-PET/CT decreased from SUVmax 5.2 [3.7-8.4] to 2.3 [1.4-2.3], p = 0.015. The target-to-background ratio decreased from 3.2 [2.1-5.1] to 1.0 [0.7-2.4], p = 0.002. The median left ventricular (LV) ejection fraction increased from 45.0% [34.0-60.0] to 55.0% [41.0-60.0], p = 0.02. The majority of patients (73%) experienced no side effects and no patients had worsening of heart failure. In this pilot study, patients with refractory CS treated with infliximab, on top of standard of care, had a reduction in inflammation on FDG-PET/CT and an improvement in LV function, without serious adverse events.

Sections du résumé

BACKGROUND
Immunosuppressive therapy in active cardiac sarcoidosis (CS) might prevent potential life-threatening complications. Infliximab (IFX) is a tumor necrosis factor alpha monoclonal antibody proven to be effective in refractory extracardiac sarcoidosis. It is sparsely used in CS, because of its association with worsening heart failure in prior studies. The goal of this study is to assess the effectiveness and safety of IFX in CS.
METHODS AND RESULTS
A retrospective, single center cohort study was performed in sarcoidosis patients treated with IFX based on a cardiac indication between January 2016 and March 2019. Patients received IFX intravenously at a dose of 5 mg/kg at week 0, 2, and subsequently every 4 weeks. After every six months, treatment response was evaluated within the multidisciplinary team using FDG-PET/CT, transthoracic echocardiography, biomarkers and device interrogation reports. Responder analysis definitions were based on; dosage of immunosuppressive drugs, improvement in functional class, left ventricular ejection fraction (LVEF) and SUVmax. Twenty-two patients were included (mean age 51.0 SD10.0 years, male 68.2%) with a mean follow-up of 18.9 months (6 to 44 months) of whom 18 (82%) were classified as responders. Median SUVmax on FDG-PET/CT decreased from SUVmax 5.2 [3.7-8.4] to 2.3 [1.4-2.3], p = 0.015. The target-to-background ratio decreased from 3.2 [2.1-5.1] to 1.0 [0.7-2.4], p = 0.002. The median left ventricular (LV) ejection fraction increased from 45.0% [34.0-60.0] to 55.0% [41.0-60.0], p = 0.02. The majority of patients (73%) experienced no side effects and no patients had worsening of heart failure.
CONCLUSION
In this pilot study, patients with refractory CS treated with infliximab, on top of standard of care, had a reduction in inflammation on FDG-PET/CT and an improvement in LV function, without serious adverse events.

Identifiants

pubmed: 33582196
pii: S0167-5273(21)00275-8
doi: 10.1016/j.ijcard.2021.02.022
pii:
doi:

Substances chimiques

Fluorodeoxyglucose F18 0Z5B2CJX4D
Infliximab B72HH48FLU

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

179-185

Informations de copyright

Copyright © 2021 Elsevier B.V. All rights reserved.

Auteurs

A L M Bakker (ALM)

Department of Cardiology, St. Antonius Hospital, Nieuwegein, Utrecht, the Netherlands. Electronic address: almbakker@gmail.com.

H Mathijssen (H)

Department of Cardiology, St. Antonius Hospital, Nieuwegein, Utrecht, the Netherlands.

J Azzahhafi (J)

Department of Cardiology, St. Antonius Hospital, Nieuwegein, Utrecht, the Netherlands.

M J Swaans (MJ)

Department of Cardiology, St. Antonius Hospital, Nieuwegein, Utrecht, the Netherlands.

M Veltkamp (M)

Department of Pulmonology, St. Antonius Hospital, Nieuwegein, Utrecht, the Netherlands; Department of Pulmonology, Utrecht University Medical Center, Utrecht, the Netherlands.

R G M Keijsers (RGM)

Department of Nuclear Medicine, St. Antonius Hospital, Nieuwegein, Utrecht, the Netherlands.

F Akdim (F)

Department of Cardiology, St. Antonius Hospital, Nieuwegein, Utrecht, the Netherlands.

M C Post (MC)

Department of Cardiology, St. Antonius Hospital, Nieuwegein, Utrecht, the Netherlands; Department of Cardiology, Utrecht University Medical Center, Utrecht, the Netherlands.

J C Grutters (JC)

Department of Pulmonology, St. Antonius Hospital, Nieuwegein, Utrecht, the Netherlands; Department of Pulmonology, Utrecht University Medical Center, Utrecht, the Netherlands.

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