Outcomes of prednisone-tapering regimens for cardiac sarcoidosis: A retrospective analysis demonstrating a benefit of infliximab.


Journal

Respiratory medicine
ISSN: 1532-3064
Titre abrégé: Respir Med
Pays: England
ID NLM: 8908438

Informations de publication

Date de publication:
11 2022
Historique:
received: 15 08 2022
revised: 22 09 2022
accepted: 26 09 2022
pubmed: 15 10 2022
medline: 26 10 2022
entrez: 14 10 2022
Statut: ppublish

Résumé

The optimal treatment strategy for cardiac sarcoidosis has not been standardized. We examined the effectiveness of three prednisone-tapering treatment regimens for cardiac sarcoidosis. We retrospectively reviewed prednisone-tapering treatment regimens for cardiac sarcoidosis that contained prednisone alone (P), prednisone plus methotrexate (P-M), and prednisone plus infliximab containing regimens (P-I). We defined the success of each regimen as the ability to lower the daily prednisone dose to 7.5 mg or less for 6 or more months without developing an adverse cardiac event. We also examined the lowest effective daily prednisone dose achieved without developing an adverse cardiac event. We identified 61 treatment regimens in 33 cardiac sarcoidosis patients that were analyzed. The success rate of prednisone-tapering regimens was significantly different P: 8/30, 27%; P-M: 3/23, 13%; P-I: 6/8, 75%., p = 0.04. The lowest effective daily prednisone dose for the regimens was also significantly different: P: 14.1 ± 10.1 mg; P-M: 16.9 ± 9.4 mg; infliximab: 7.8 ± 4.9 mg, (p = 0.03); by both measures the success was greatest with the P-I regimen. For the treatment of cardiac sarcoidosis, prednisone-tapering regimens containing infliximab are superior to those containing prednisone alone or prednisone plus methotrexate in terms of reaching 7.5 mg/day of prednisone for more than 6 months and achieving the lowest effective prednisone.

Sections du résumé

BACKGROUND
The optimal treatment strategy for cardiac sarcoidosis has not been standardized. We examined the effectiveness of three prednisone-tapering treatment regimens for cardiac sarcoidosis.
METHODS
We retrospectively reviewed prednisone-tapering treatment regimens for cardiac sarcoidosis that contained prednisone alone (P), prednisone plus methotrexate (P-M), and prednisone plus infliximab containing regimens (P-I). We defined the success of each regimen as the ability to lower the daily prednisone dose to 7.5 mg or less for 6 or more months without developing an adverse cardiac event. We also examined the lowest effective daily prednisone dose achieved without developing an adverse cardiac event.
RESULTS
We identified 61 treatment regimens in 33 cardiac sarcoidosis patients that were analyzed. The success rate of prednisone-tapering regimens was significantly different P: 8/30, 27%; P-M: 3/23, 13%; P-I: 6/8, 75%., p = 0.04. The lowest effective daily prednisone dose for the regimens was also significantly different: P: 14.1 ± 10.1 mg; P-M: 16.9 ± 9.4 mg; infliximab: 7.8 ± 4.9 mg, (p = 0.03); by both measures the success was greatest with the P-I regimen.
CONCLUSIONS
For the treatment of cardiac sarcoidosis, prednisone-tapering regimens containing infliximab are superior to those containing prednisone alone or prednisone plus methotrexate in terms of reaching 7.5 mg/day of prednisone for more than 6 months and achieving the lowest effective prednisone.

Identifiants

pubmed: 36240614
pii: S0954-6111(22)00269-4
doi: 10.1016/j.rmed.2022.107004
pii:
doi:

Substances chimiques

Prednisone VB0R961HZT
Infliximab B72HH48FLU
Methotrexate YL5FZ2Y5U1
Glucocorticoids 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

107004

Informations de copyright

Copyright © 2022 Elsevier Ltd. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of competing interest The authors declare the following financial interests/personal relationships which may be considered as potential competing interests:Marc A. Judson reports a relationship with Mallinckrodt LLC that includes: funding grants. Marc A. Judson reports a relationship with aTyr Pharma that includes: funding grants. Marc A. Judson reports a relationship with Star Therapeutics, Inc. that includes: funding grants. Marc A. Judson reports a relationship with Kinevant that includes: funding grants.

Auteurs

Marc A Judson (MA)

Albany Medical College, Albany, NY, USA. Electronic address: judsonm@mail.amc.edu.

Evan Adelstein (E)

Albany Medical College, Albany, NY, USA.

Kenneth M Fish (KM)

Albany Medical College, Albany, NY, USA.

Paul J Feustel (PJ)

Albany Medical College, Albany, NY, USA.

Recai Yucel (R)

Temple University, Philadelphia, PA, USA.

Sara Preston (S)

Louisiana State University Medical Center, Shreveport, LA, USA.

Rachel Vancavage (R)

Albany Medical College, Albany, NY, USA.

Amit Chopra (A)

Albany Medical College, Albany, NY, USA.

David A Steckman (DA)

Vassar Brothers Medical Center, Poughkeepsie, NY, USA.

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Classifications MeSH