Glucocorticoid withdrawal and glucocorticoid-induced adrenal insufficiency: Study protocol of the ra...
Glucocorticoid withdrawal and glucocorticoid-induced adrenal insufficiency: Study protocol of the randomized controlled «TOASST" (Taper Or Abrupt Steroid STop) multicenter trial
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Author / Creator
Komminoth, Mathis , Donath, Marc Y , Hepprich, Matthias , Schuetz, Philipp , Blum, Claudine A , Mueller, Beat , Reny, Jean-Luc , Gosselin, Pauline , Breville, Gautier , Brändle, Michael , Henzen, Christoph , Leuppi, Jörg D , Kistler, Andreas D , Thurnheer, Robert , Beuschlein, Felix , Rudofsky, Gottfried , Aeberli, Daniel , Villiger, Peter M , Böhm, Stephan , Chifu, Irina , Fassnacht, Martin , Meyer, Gesine , Bojunga, Jörg , Cattaneo, Marco , Sluka, Constantin , Schneider, Helga , Rutishauser, Jonas , TOASST» study group and for the «TOASST» study group
Publisher
United States: Public Library of Science
Journal title
Language
English
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Publisher
United States: Public Library of Science
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Scope and Contents
Contents
Despite the widespread use of glucocorticoids in inflammatory and autoimmune disorders, there is uncertainty about the safe cessation of long-term systemic treatment, as data from prospective trials are largely missing. Due to potential disease relapse or glucocorticoid-induced hypocortisolism, the drug is often tapered to sub-physiological doses rather than stopped when the underlying disease is clinically stable, increasing the cumulative drug exposure. Conversely, the duration of exposure to glucocorticoids should be minimized to lower the risk of side effects.
We designed a multicenter, randomized, triple-blinded, placebo-controlled trial to test the clinical noninferiority of abrupt glucocorticoid stop compared to tapering after ≥28 treatment days with ≥420 mg cumulative and ≥7.5 mg mean daily prednisone-equivalent dose. 573 adult patients treated systemically for various disorders will be included after their underlying disease has been stabilized. Prednisone in tapering doses or matching placebo is administered over 4 weeks. A 250 mg ACTH-test, the result of which will be revealed a posteriori, is performed at study inclusion; all patients are instructed on glucocorticoid stress cover dosing. Follow-up is for 6 months. The composite primary outcome measure is time to hospitalization, death, initiation of unplanned systemic glucocorticoid therapy, or adrenal crisis. Secondary outcomes include the individual components of the primary outcome, cumulative glucocorticoid doses, signs and symptoms of hypocortisolism, and the performance of the ACTH test in predicting the clinical outcome. Cox proportional hazard, linear, and logistic regression models will be used for statistical analysis.
This trial aims to demonstrate the clinical noninferiority and safety of abrupt treatment cessation after ≥28 days of systemic glucocorticoid therapy in patients with stabilized underlying disease.
ClinicalTrials.gov Identifier: NCT03153527; EUDRA-CT: 2020-005601-48 https://clinicaltrials.gov/ct2/show/NCT03153527?term=NCT03153527&draw=2&rank=1....
Alternative Titles
Full title
Glucocorticoid withdrawal and glucocorticoid-induced adrenal insufficiency: Study protocol of the randomized controlled «TOASST" (Taper Or Abrupt Steroid STop) multicenter trial
Authors, Artists and Contributors
Author / Creator
Donath, Marc Y
Hepprich, Matthias
Schuetz, Philipp
Blum, Claudine A
Mueller, Beat
Reny, Jean-Luc
Gosselin, Pauline
Breville, Gautier
Brändle, Michael
Henzen, Christoph
Leuppi, Jörg D
Kistler, Andreas D
Thurnheer, Robert
Beuschlein, Felix
Rudofsky, Gottfried
Aeberli, Daniel
Villiger, Peter M
Böhm, Stephan
Chifu, Irina
Fassnacht, Martin
Meyer, Gesine
Bojunga, Jörg
Cattaneo, Marco
Sluka, Constantin
Schneider, Helga
Rutishauser, Jonas
TOASST» study group
for the «TOASST» study group
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Primary Identifiers
Record Identifier
TN_cdi_plos_journals_2796098047
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_2796098047
Other Identifiers
ISSN
1932-6203
E-ISSN
1932-6203
DOI
10.1371/journal.pone.0281585