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      Long‐Term Corticosteroid‐Sparing Immunosuppression for Cardiac Sarcoidosis

      research-article
      , MD 1 , , MD 1 , , MD 1 , , MD 5 , , MD 3 , , MD 1 , , MD 1 , , MD 1 , , MD, MS 1 , , MD 1 , , MD 1 , , MD 1 , , MD 1 , , MD 1 , , MD 3 , , MD, PhD 4 , , MD 2 , , , MD, PhD 1 ,
      Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
      John Wiley and Sons Inc.
      immunosuppression, sarcoidosis, ventricular arrhythmia, Arrhythmias, Cardiomyopathy, Inflammatory Heart Disease, Nuclear Cardiology and PET

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          Abstract

          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.

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          Most cited references60

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          Cardiac sarcoidosis: epidemiology, characteristics, and outcome over 25 years in a nationwide study.

          This study was designed to assess the epidemiology, characteristics, and outcome of cardiac sarcoidosis (CS) in Finland.
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            Prognostic determinants of long-term survival in Japanese patients with cardiac sarcoidosis treated with prednisone.

            Cardiac involvement is an important prognostic factor in sarcoidosis, but reliable indicators of mortality risk in cardiac sarcoidosis are unstudied in a large number of patients. To determine the significant predictors of mortality and to assess the efficacy of corticosteroids, we analyzed clinical findings, treatment, and prognosis in 95 Japanese patients with cardiac sarcoidosis. Twenty of these 95 patients had cardiac sarcoidosis proven by autopsy; none of these patients had received corticosteroids. We assessed 12 clinical variables as possible predictors of mortality by Cox proportional hazards model in 75 steroid-treated patients. During the mean follow-up of 68 months, 29 patients (73%) died of congestive heart failure and 11 (27%) experienced sudden death. Kaplan-Meier survival curves showed 5-year survival rates of 75% in the steroid-treated patients and of 89% in patients with a left ventricular ejection fraction > or = 50%, whereas there was only 10% 5-year survival rate in autopsy subjects. There was no significant difference in survival curves of patients treated with a high initial dose (> 30 mg) and a low initial dose (> or = 30 mg) of prednisone. Multivariate analysis identified New York Heart Association functional class (hazard ratio 7.72 per class I increase, p = 0.0008), left ventricular end-diastolic diameter (hazard ratio 2.60/10 mm increase, p = 0.02), and sustained ventricular tachycardia (hazard ratio 7.20, p = 0.03) as independent predictors of mortality. In conclusion, the severity of heart failure was one of the most significant independent predictors of mortality for cardiac sarcoidosis. Starting corticosteroids before the occurrence of systolic dysfunction resulted in an excellent clinical outcome. A high initial dose of prednisone may not be essential for treatment of cardiac sarcoidosis.
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              Infliximab therapy in patients with chronic sarcoidosis and pulmonary involvement.

              Evidence suggests that tumor necrosis factor (TNF)-alpha plays an important role in the pathophysiology of sarcoidosis. To assess the efficacy of infliximab in sarcoidosis. A phase 2, multicenter, randomized, double-blind, placebo-controlled study was conducted in 138 patients with chronic pulmonary sarcoidosis. Patients were randomized to receive intravenous infusions of infliximab (3 or 5 mg/kg) or placebo at Weeks 0, 2, 6, 12, 18, and 24 and were followed through Week 52. The primary endpoint was the change from baseline to Week 24 in percent of predicted FVC. Major secondary efficacy parameters included Saint George's Respiratory Questionnaire, 6-min walk distance, Borg's CR10 dyspnea score, and the proportion of Lupus Pernio Physician's Global Assessment responders for patients with facial skin involvement. Patients in the combined infliximab groups (3 and 5 mg/kg) had a mean increase of 2.5% from baseline to Week 24 in the percent of predicted FVC, compared with no change in placebo-treated patients (p = 0.038). No significant differences between the treatment groups were observed for any of the major secondary endpoints at Week 24. Results of post hoc exploratory analyses suggested that patients with more severe disease tended to benefit more from infliximab treatment. Infliximab therapy resulted in a statistically significant improvement in % predicted FVC at Week 24. The clinical importance of this finding is not clear. The results of this Phase 2 clinical study support further evaluation of anti-TNF-alpha therapy in severe, chronic, symptomatic sarcoidosis.
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                Author and article information

                Contributors
                vasanth.vedantham@ucsf.edu
                julie.zikherman@ucsf.edu
                Journal
                J Am Heart Assoc
                J Am Heart Assoc
                10.1002/(ISSN)2047-9980
                JAH3
                ahaoa
                Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease
                John Wiley and Sons Inc. (Hoboken )
                2047-9980
                17 September 2019
                06 September 2019
                : 8
                : 18 ( doiID: 10.1002/jah3.v8.18 )
                : e010952
                Affiliations
                [ 1 ] Division of Cardiology Department of Medicine University of California, San Francisco San Francisco CA
                [ 2 ] Division of Rheumatology Department of Medicine University of California, San Francisco San Francisco CA
                [ 3 ] Division of Pulmonary and Critical Care Department of Medicine University of California, San Francisco San Francisco CA
                [ 4 ] Division of Nuclear Medicine Department of Radiology University of California, San Francisco San Francisco CA
                [ 5 ] Department of Medicine Massachusetts General Hospital Boston MA
                Author notes
                [*] [* ] Correspondence to: Vasanth Vedantham, MD, PhD, Cardiology Division, Department of Medicine, University of California, San Francisco, 555 Mission Bay Blvd South, SCVRB ‐ 352M, San Francisco, CA 94158. E‐mail: vasanth.vedantham@ 123456ucsf.edu and Julie Zikherman, MD, Department of Medicine, Rheumatology Division, University of California, San Francisco, 513 Parnassus Avenue, HSW‐ 1201A, San Francisco, CA 94143. E‐mail: julie.zikherman@ 123456ucsf.edu
                Article
                JAH34389
                10.1161/JAHA.118.010952
                6818011
                31538835
                f386c6b9-dca6-49b0-a6a7-10bbb1864514
                © 2019 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.

                History
                : 24 September 2018
                : 03 July 2019
                Page count
                Figures: 3, Tables: 4, Pages: 11, Words: 8773
                Categories
                Original Research
                Original Research
                Arrhythmia and Electrophysiology
                Custom metadata
                2.0
                jah34389
                17 September 2019
                Converter:WILEY_ML3GV2_TO_NLMPMC version:5.7.0 mode:remove_FC converted:23.10.2019

                Cardiovascular Medicine
                immunosuppression,sarcoidosis,ventricular arrhythmia,arrhythmias,cardiomyopathy,inflammatory heart disease,nuclear cardiology and pet

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