Long-Term Corticosteroid-Sparing Immunosuppression for Cardiac Sarcoidosis.
Adalimumab
/ therapeutic use
Anti-Inflammatory Agents
/ therapeutic use
Arrhythmias, Cardiac
/ physiopathology
Cardiomyopathies
/ diagnostic imaging
Deprescriptions
Drug Therapy, Combination
Electrocardiography
Female
Fluorodeoxyglucose F18
Glucocorticoids
/ administration & dosage
Humans
Immunosuppressive Agents
/ therapeutic use
Maintenance Chemotherapy
Male
Methotrexate
/ therapeutic use
Middle Aged
Positron-Emission Tomography
Prednisone
/ administration & dosage
Radiopharmaceuticals
Recurrence
Retrospective Studies
Sarcoidosis
/ diagnostic imaging
Treatment Outcome
immunosuppression
sarcoidosis
ventricular arrhythmia
Journal
Journal of the American Heart Association
ISSN: 2047-9980
Titre abrégé: J Am Heart Assoc
Pays: England
ID NLM: 101580524
Informations de publication
Date de publication:
17 09 2019
17 09 2019
Historique:
entrez:
21
9
2019
pubmed:
21
9
2019
medline:
15
9
2020
Statut:
ppublish
Résumé
Background Long-term corticosteroid therapy is the standard of care for treatment of cardiac sarcoidosis (CS). The efficacy of long-term corticosteroid-sparing immunosuppression in CS is unknown. The goal of this study was to assess the efficacy of methotrexate with or without adalimumab for long-term disease suppression in CS, and to assess recurrence and adverse event rates after immunosuppression discontinuation. Methods and Results Retrospective chart review identified treatment-naive CS patients at a single academic medical center who received corticosteroid-sparing maintenance therapy. Demographics, cardiac uptake of 18-fluorodeoxyglucose, and adverse cardiac events were compared before and during treatment and between those with persistent or interrupted immunosuppression. Twenty-eight CS patients were followed for a mean 4.1 (SD 1.5) years. Twenty-five patients received 4 to 8 weeks of high-dose prednisone (>30 mg/day), followed by taper and maintenance therapy with methotrexate±low-dose prednisone (low-dose prednisone, <10 mg/day). Adalimumab was added in 19 patients with persistently active CS or in those with intolerance to methotrexate. Methotrexate±low-dose prednisone resulted in initial reduction (88%) or elimination (60%) of 18-fluorodeoxyglucose uptake, and patients receiving adalimumab-containing regimens experienced improved (84%) or resolved (63%) 18-fluorodeoxyglucose uptake. Radiologic relapse occurred in 8 of 9 patients after immunosuppression cessation, 4 patients on methotrexate-containing regimens, and in no patients on adalimumab-containing regimens. Conclusions Corticosteroid-sparing regimens containing methotrexate with or without adalimumab is an effective maintenance therapy in patients after an initial response is confirmed. Disease recurrence in patients on and off immunosuppression support need for ongoing radiologic surveillance regardless of immunosuppression regimen.
Identifiants
pubmed: 31538835
doi: 10.1161/JAHA.118.010952
pmc: PMC6818011
doi:
Substances chimiques
Anti-Inflammatory Agents
0
Glucocorticoids
0
Immunosuppressive Agents
0
Radiopharmaceuticals
0
Fluorodeoxyglucose F18
0Z5B2CJX4D
Adalimumab
FYS6T7F842
Prednisone
VB0R961HZT
Methotrexate
YL5FZ2Y5U1
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
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