Abstract
Purpose
To evaluate the therapeutic effect and safety of mycophenolate mofetil (MMF) on chronic uveitis in Korean patients.
Methods
This study included 25 patients with chronic uveitis who used MMF and were followed up more than 6 months in 2 referral centers from 2010 to 2014. The medical records were analyzed retrospectively. The therapeutic effect was assessed based on control of inflammation, corticosteroid sparing effects, and discontinuation of MMF, and the safety was assessed based on side effects. Control of inflammation was defined as no active inflammation observed on at least 2 consecutive visits 28 days apart or more.
Results
The 25 patients consisted of 18 males and 7 females. The mean age of the patients was 47.52 years. The etiology of uveitis was as follows: Behcet's disease in 15 patients (60%), Vogt-Koyanagi-Harada disease in 4 (16%), sympathetic ophthalmia in 2 (8%), systemic lupus erythematosus in 1 (4%), and idiopathic uveitis in 3 (12%). Anatomic classification was anterior uveitis in 20% and posterior uveitis or panuveitis in 80% of patients. Complete control of inflammation was achieved in 44% and 50% of patients within 6 months and 1 year, respectively. Systemic corticosteroid dosage was reduced to 10 mg of prednisone or less while maintaining sustained control of inflammation in 36% and 45% of patients for 6 months and 1 year, respectively. MMF was discontinued in 3 patients (12%) due to side effects and in 2 patients (8%) due to lack of effectiveness.
REFERENCES
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Table 1.
Table 2.
Characteristics | N (%) |
---|---|
Previous corticosteroid treatment | 22 (88) |
Previous immunosuppressive and other treatment | |
Azathioprine | 6 (24) |
Cyclosporine A | 17 (68) |
Methotrexate | 7 (28) |
Colchicine | 6 (24) |
Reason for starting MMF treatment | |
Inability to taper prednisolone to <10 mg daily | 11 (44) |
Recurrences of uveitis under previous immunosuppressive therapy | 6 (24) |
First immunosuppressive therapy for active uveitis | 1 (4) |
Intolerability to previous immunosuppressive therapy | 7 (28) |
Disease activity when MMF started* | |
On high-dose corticosteroid taper for active disease | 7 (28) |
Active despite 10 mg prednisolone daily or other immunosuppressive treatment | 16 (64) |
Inactive disease | 2 (8) |
Table 3.
Outcomes | Anterior uveitis | Posterior/panuveitis | Total |
---|---|---|---|
Patients at 6 months | 5 | 20 | 25 |
Controlled inflammation – no activity at 6 m | 4 (80%) | 7 (35%) | 11 (44%)* |
Controlled inflammation – no activity or slight active at 6 m | 4 (80%) | 14 (70%) | 18 (72%) |
Controlled inflammation and steroid sparing – ≤10 mg at 6 m | 2 (40%) | 7 (35%) | 9 (36%) |
Controlled inflammation and steroid sparing – ≤5 mg at 6 m | 2 (40%) | 4 (20%) | 6 (24%) |
Controlled inflammation and steroid sparing – 0 mg at 6 m | 1 (20%) | 1 (5%) | 2 (8%) |
Patients at 12 months | 4 | 16 | 20 |
Controlled inflammation – no activity at 12 m | 3 (75%) | 7 (43.8%) | 10 (50%)* |
Controlled inflammation – no activity or slight active at 12 m | 3 (75%) | 8 (50%) | 11 (55%) |
Controlled inflammation and steroid sparing – ≤10 mg at 12 m | 2 (50%) | 7 (43.8%) | 9 (45%) |
Controlled inflammation and steroid sparing – ≤5 mg at 12 m | 2 (50%) | 4 (25%) | 6 (30%) |
Controlled inflammation and steroid sparing – 0 mg at 12 m | 2 (50%) | 1 (6.3%) | 3 (15%) |
Table 4.
Reasons | No. of patients | Duration of MMF treatment (months) |
---|---|---|
Remission | 1 (4%) | 41.0 |
Discontinuation for side effects | 3 (12%)* | |
Gastrointestinal upset | 2 (8%) | 29.0 |
Anemia | 1 (4%) | 15.0 |
Ineffectiveness | 2 (8%) | 24.5 |
Pregnancy | 1 (4%) | 24.0 |
Voluntarily | 3 (12%) | 31.7 |
Total | 10 (40%) |