Reduced Dose Methotrexate and Mycophenolate Mofetil in Noninfectious Uveitis: A Sub-Analysis from the First-Line Antimetabolites as Steroid Sparing Therapy (FAST) Trial

被引:0
|
作者
Sura, Amol A. [1 ,2 ]
Sun, Yuwei [1 ]
Reddy, Amit K. [1 ,2 ]
Rathinam, S. R. [3 ]
Gonzales, John A. [1 ,2 ]
Thundikandy, Radhika [3 ]
Vedhanayaki, Rajesh [3 ]
Kanakath, Anuradha [4 ]
Murugan, Bala [5 ]
Doan, Thuy A. [1 ,2 ]
Lim, Lyndell L. [6 ]
Suhler, Eric B. [7 ,8 ]
Al-Dhibi, Hassan A. [9 ]
Acharya, Nisha R. [1 ,2 ,10 ]
机构
[1] Univ Calif San Francisco, Francis I Proctor Fdn, San Francisco, CA USA
[2] Univ Calif San Francisco, Dept Ophthalmol, San Francisco, CA USA
[3] Aravind Eye Hosp & Postgrad Inst Ophthalmol, Uvea Serv, Madurai, India
[4] Aravind Eye Hosp & Postgrad Inst Ophthalmol, Uvea Serv, Coimbatore, India
[5] Aravind Eye Hosp & Postgrad Inst Ophthalmol, Uvea Serv, Pondicherry, India
[6] Royal Victorian Eye & Ear Hosp, Ctr Eye Res Australia, East Melbourne, Australia
[7] Oregon Hlth & Sci Univ, Casey Eye Inst, OHSU PSU Sch Publ Hlth, Portland, OR USA
[8] Portland Vet Affairs Hlth Care Syst, Portland, OR USA
[9] King Khalid Eye Specialist Hosp, Div Vitreoretinal Surg & Uveitis, Riyadh, Saudi Arabia
[10] Univ Calif San Francisco, 490 Illinois St,2nd Floor, San Francisco, CA 94158 USA
关键词
Antimetabolite; dosing; methotrexate; mycophenolate mofetil; uveitis; VOGT-KOYANAGI-HARADA; RHEUMATOID-ARTHRITIS; PSORIASIS; TOLERABILITY; MULTICENTER; SUBANALYSIS; MODERATE; DISEASE;
D O I
10.1080/09273948.2023.2165949
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
PurposeSome patients taking methotrexate (MTX) or mycophenolate mofetil (MMF) experience intolerable side effects at full doses. We evaluated whether dose reduction affected treatment outcomes in uveitis patients.MethodsSubanalysis of the First-line Antimetabolites as Steroid-sparing Treatment (FAST) uveitis trial. Patients were randomized to receive MTX (25 mg weekly) or MMF (3 g daily). A pre-specified dose reduction protocol could be employed for intolerable side effects. Primary analysis was performed at 6 months.Results43/194 patients (22%) required dose reduction. 88/151 patients (58%) on maximum doses and 32/43 patients (74%) on reduced doses were deemed treatment successes at 6 months. The odds ratio point estimate (1.60, 95% CI 0.72-3.74) favored dose-reduction but this was not significant. Following reduction, adverse events improved at the subsequent study visit (79 events reduced to 63 events).ConclusionDose reduction of antimetabolites was not associated with worse outcomes in this subanalysis of a uveitis trial.
引用
收藏
页码:955 / 960
页数:6
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