Long-Term Corticosteroid-Sparing Immunosuppression for Cardiac Sarcoidosis.


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
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

e010952

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Auteurs

David G Rosenthal (DG)

Division of Cardiology Department of Medicine University of California, San Francisco San Francisco CA.

Purvi Parwani (P)

Division of Cardiology Department of Medicine University of California, San Francisco San Francisco CA.

Tyler O Murray (TO)

Division of Cardiology Department of Medicine University of California, San Francisco San Francisco CA.

Bradley J Petek (BJ)

Department of Medicine Massachusetts General Hospital Boston MA.

Bryan S Benn (BS)

Division of Pulmonary and Critical Care Department of Medicine University of California, San Francisco San Francisco CA.

Teresa De Marco (T)

Division of Cardiology Department of Medicine University of California, San Francisco San Francisco CA.

Edward P Gerstenfeld (EP)

Division of Cardiology Department of Medicine University of California, San Francisco San Francisco CA.

Munir Janmohamed (M)

Division of Cardiology Department of Medicine University of California, San Francisco San Francisco CA.

Liviu Klein (L)

Division of Cardiology Department of Medicine University of California, San Francisco San Francisco CA.

Byron K Lee (BK)

Division of Cardiology Department of Medicine University of California, San Francisco San Francisco CA.

Joshua D Moss (JD)

Division of Cardiology Department of Medicine University of California, San Francisco San Francisco CA.

Melvin M Scheinman (MM)

Division of Cardiology Department of Medicine University of California, San Francisco San Francisco CA.

Henry H Hsia (HH)

Division of Cardiology Department of Medicine University of California, San Francisco San Francisco CA.

Van Selby (V)

Division of Cardiology Department of Medicine University of California, San Francisco San Francisco CA.

Laura L Koth (LL)

Division of Pulmonary and Critical Care Department of Medicine University of California, San Francisco San Francisco CA.

Miguel H Pampaloni (MH)

Division of Nuclear Medicine Department of Radiology University of California, San Francisco San Francisco CA.

Julie Zikherman (J)

Division of Rheumatology Department of Medicine University of California, San Francisco San Francisco CA.

Vasanth Vedantham (V)

Division of Cardiology Department of Medicine University of California, San Francisco San Francisco CA.

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Classifications MeSH