Outcomes of Uveitic Macular Edema in the First-line Antimetabolites as Steroid-Sparing Treatment Uveitis Trial.
Antimetabolite
Clinical trial
Immunosuppression
Macular edema
Methotrexate
Mycophenolate mofetil
OCT
Uveitis
Journal
Ophthalmology
ISSN: 1549-4713
Titre abrégé: Ophthalmology
Pays: United States
ID NLM: 7802443
Informations de publication
Date de publication:
06 2022
06 2022
Historique:
received:
14
12
2021
revised:
31
01
2022
accepted:
02
02
2022
pubmed:
11
2
2022
medline:
25
5
2022
entrez:
10
2
2022
Statut:
ppublish
Résumé
To evaluate the outcomes of uveitic macular edema at 6 and 12 months in patients treated with methotrexate or mycophenolate mofetil. Subanalysis of a block-randomized, observer-masked, multicenter clinical trial. Patients were enrolled in the First-line Antimetabolites as Steroid-sparing Treatment (FAST) Uveitis Trial between August 2013 and August 2017. Patients were randomized to oral methotrexate 25 mg weekly or mycophenolate mofetil 1.5 g twice daily for 12 months, along with a corticosteroid taper. In addition to standardized clinical examination, all patients underwent spectral-domain OCT imaging at each visit. At the 6-month primary end point, patients who achieved treatment success continued the same treatment for a subsequent 6 months, and treatment failures switched to the other treatment group. Prespecified 6-month primary outcome and 12-month outcomes of central subfield thickness and visual acuity. Of 216 patients in the FAST Trial, 42 eyes (30 patients) in the methotrexate group and 55 eyes (41 patients) in the mycophenolate group had uveitic macular edema. Baseline median central subfield thickness was 359 μm and 342 μm in the methotrexate and mycophenolate groups, respectively. At 12 months, for those who stayed on the same treatment, macular thickness decreased from baseline by 30.5 μm (interquartile range [IQR], -132.3 to 4.0) and 54 μm (IQR, -95.5 to -4.5) in the methotrexate and mycophenolate groups, respectively (P = 0.73). In patients who switched treatment at 6 months, macular thickness decreased from baseline by 12.5 μm (IQR, -32.3 to -0.5) and 50 μm (IQR, -181.0 to -10.0) in the methotrexate and mycophenolate groups, respectively (P = 0.34). At 12 months, 7 of 19 eyes (37%) on methotrexate had resolution of macular edema compared with 15 of 25 eyes (60%) on mycophenolate (P = 0.10). For those who switched treatments, 8 of 17 eyes (47%) on methotrexate and 6 of 11 eyes (55%) on mycophenolate had resolution of macular edema (P = 0.92). Treatment with methotrexate or mycophenolate mofetil for uveitic macular edema results in similar improvements in macular thickness at 6 and 12 months. At 12 months, approximately half of eyes in each antimetabolite group still had persistent macular edema.
Identifiants
pubmed: 35143800
pii: S0161-6420(22)00091-4
doi: 10.1016/j.ophtha.2022.02.002
pii:
doi:
Substances chimiques
Antimetabolites
0
Enzyme Inhibitors
0
Immunosuppressive Agents
0
Steroids
0
Mycophenolic Acid
HU9DX48N0T
Methotrexate
YL5FZ2Y5U1
Types de publication
Journal Article
Multicenter Study
Randomized Controlled Trial
Research Support, Non-U.S. Gov't
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
661-667Subventions
Organisme : NEI NIH HHS
ID : U10 EY021125
Pays : United States
Informations de copyright
Copyright © 2022 American Academy of Ophthalmology. Published by Elsevier Inc. All rights reserved.