The glucocorticoid toxicity index: Measuring change in glucocorticoid toxicity over time.

ANCA-associated vasculitis Aggregate improvement score Asthma Behçet's disease Bone mineral density Bullous pemphigoid Cumulative worsening score Giant cell arteritis Glucocorticoid myopathy Glucocorticoid toxicity index Idiopathic inflammatory myopathies IgG4-related disease Kawasaki's disease Lupus nephritis Minimum clinically important difference Myasthenia gravis Pemphigus vulgaris Polymyalgia rheumatica Sarcoidosis Systemic lupus erythematosus

Journal

Seminars in arthritis and rheumatism
ISSN: 1532-866X
Titre abrégé: Semin Arthritis Rheum
Pays: United States
ID NLM: 1306053

Informations de publication

Date de publication:
08 2022
Historique:
received: 09 11 2021
revised: 10 04 2022
accepted: 13 04 2022
pubmed: 30 4 2022
medline: 8 7 2022
entrez: 29 4 2022
Statut: ppublish

Résumé

Glucocorticoids (GCs) have been the cornerstone of treating dozens of inflammatory conditions for more than seven decades. GC toxicity is ubiquitous in both clinical trials and clinical practice, and toxicities associated with GC use are central to the experience of most patients being treated for immune-mediated conditions. These conditions span the full range of medical specialties, including rheumatology, nephrology, gastroenterology, neurology, pulmonology, ophthalmology, and others. One of the goals of novel therapies for inflammatory disease must be to diminish the effects of GC toxicity in clinically important ways, thereby differentiating these new treatments from existing approaches. Despite the importance of glucocorticoids in the treatment of inflammatory disease for more than 70 years, no reliable means of calculating the degree to which GC toxicity has worsened or improved over the course of treatment has been available. The Glucocorticoid Toxicity Index (GTI), developed by an international group of subspecialty physician experts as a clinician-facing clinical trials outcome measure, is a standardized, validated measure of the phenomenon known as GC toxicity. The purpose of the instrument is to measure change in GC toxicity between two points in time: for example, between the baseline visit and the time of the primary efficacy outcome assessment. The instrument is designed to quantify both worsening and improvement in GC toxicity. The GTI has been validated in both real-world experiences and clinical trials, including a phase 3, label-enabling trial in ANCA associated vasculitis. This article reviews the history and rationale for the development of the GTI, describes key data from validation studies, considers the minimum clinically important difference, and provides instructions for use of the instrument.

Identifiants

pubmed: 35486995
pii: S0049-0172(22)00061-0
doi: 10.1016/j.semarthrit.2022.152010
pii:
doi:

Substances chimiques

Glucocorticoids 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

152010

Commentaires et corrections

Type : ErratumIn

Informations de copyright

Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved.

Auteurs

John H Stone (JH)

Harvard Medical School, Massachusetts General Hospital, Boston, MA, United States. Electronic address: jhstone@mgh.harvard.edu.

P Jane McDowell (PJ)

Harvard Medical School, Massachusetts General Hospital, Boston, MA, United States.

David R W Jayne (DRW)

Harvard Medical School, Massachusetts General Hospital, Boston, MA, United States.

Peter A Merkel (PA)

Harvard Medical School, Massachusetts General Hospital, Boston, MA, United States.

Joanna Robson (J)

Harvard Medical School, Massachusetts General Hospital, Boston, MA, United States.

Naomi J Patel (NJ)

Harvard Medical School, Massachusetts General Hospital, Boston, MA, United States.

Yuqing Zhang (Y)

Harvard Medical School, Massachusetts General Hospital, Boston, MA, United States.

Huibin Yue (H)

Harvard Medical School, Massachusetts General Hospital, Boston, MA, United States.

Pirow Bekker (P)

Harvard Medical School, Massachusetts General Hospital, Boston, MA, United States.

Liam G Heaney (LG)

Harvard Medical School, Massachusetts General Hospital, Boston, MA, United States.

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Classifications MeSH