PO69 - The prednisone-free regimens exploratory (PREDFREE) study - A real-world analysis of corticosteroid-tapering sarcoidosis treatment regimens with complete corticosteroid withdrawal
W. Ennis James (United States)1; Ogugua Ndili Obi (United States)2; Manuel Ribeiro Neto (United States)3; Nadera Sweiss (United States)4; Kerry Hena (United States)5; Dan Culver (United States)3; Recai Yucel (United States)6; Paul Feustel (United States)7; Sai Anoosh Parimi (United States)2; Derlis Fleitas Sosa (United States)1; Sanya Chandna (United States)3; Supritha Prasad (United States)4; Nathaniel Nelson (United States)5; Shravya Dharambhat (United States)2; Joseph Mazur (United States)1; Sooyeon Kwon (United States)7; Marc Judson (United States)7;
1 - medical university of South Carolina; 2 - East Carolina University; 3 - Cleveland Clinic; 4 - University of Illinois Chicago; 5 - New York University Langone Health; 6 - Temple University; 7 - Albany Medical College;
Keywords: Sarcoidosis; treatment; corticosteroids;
Select the theme: Controversies in Sarcoidosis Treatment
Type: Original Papers
Presentation: Poster Presentation

Introduction: There has been a recent paradigm shift in the treatment of sarcoidosis that emphasizes complete withdrawal of corticosteroid therapy. 

Objectives: We evaluated factors associated with successful discontinuation of corticosteroids in sarcoidosis patients treated at 6 US medical centers.

Materials and Methods: We analyzed two outcomes for corticosteroid-tapering regimens: A) Corticosteroid-free outcome: corticosteroids were successfully discontinued for at least 6 months; and B) Sarcoidosis exacerbation: Worsening sarcoidosis requiring increased doses of a sarcoidosis medication and/or addition of a sarcoidosis medication. All other potential outcomes of corticosteroid-tapering regimens were not analyzed.

Results: We analyzed 1049 corticosteroid-tapering regimens for the treatment of sarcoidosis in 686 patients. Most patients were black (57%) and female (56%). Mean (SD) number of organs involved with sarcoidosis was 2.5 (1.4). 421/1049 (40%) of the regimen outcomes were corticosteroid-free whereas 628/1049 (60%) were sarcoidosis exacerbations. In univariate analyses (Table 1), there was no difference in corticosteroid-free outcomes in terms of gender, Scadding stage, or patient age. Corticosteroid-free outcomes were less common in Blacks than Whites (37% vs 46%, p=006). Patients with corticosteroid-free outcomes had less organs involved than those with sarcoidosis exacerbations (2.47+1.4 vs 2.79 + 1.6, p<0.001). A corticosteroid-alone taper (without any other sarcoidosis medications) had less corticosteroid-free outcomes than regimens with >1 concomitant agent (33%,168/504 vs 46%,253/545, p <.001). Regimens with hydroxychloroquine, methotrexate, infliximab, all had a statistically higher percentage of corticosteroid-free outcomes than corticosteroid-alone regimens. In a multi-logistic regression analysis (Table 2), corticosteroid-free outcomes were less frequent in Blacks and corticosteroid-alone regimens. Corticosteroid-free outcomes were more common when lung or eye was the treated organ and in patients with longer disease duration.

Conclusions: Successful discontinuation of corticosteroids was less common in corticosteroid-alone tapering regimens than regimens containing at least one additional sarcoidosis medication. Blacks were less likely to have corticosteroids successfully discontinued than Whites.

Table 1. Differences in corticosteroid regimens based on specific factors: univariate analysesTable 2. Factors significantly associated with corticosteroid-free outcomes in multi-logistic regression analysis.