Journal List > J Korean Ophthalmol Soc > v.57(2) > 1010508

Ahn, Kim, and Lee: Mycophenolate Mofetil for Chronic Uveitis in Koreans

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.

Conclusions

MMF was effective and side effects were uncommon when managing chronic uveitis in Korean patients.

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Figure 1.
Visual acuity before and after treatment of MMF at 6 months (A) and 12 months (B). All data points located below the bi-secting line represent an improvement or maintenance in visual acuity. VA = visual acuity; MMF = mycophenolate mofetil.
jkos-57-283f1.tif
Figure 2.
Kaplan-Meier curve: probability of MMF discontinuation due to ineffectiveness and side effects. The vertical ticks: mark censored patients. MMF = mycophenolate mofetil.
jkos-57-283f2.tif
Table 1.
Characteristics of patients trreated with mycophenolate mofetil for chronic uveitis
Patient characteristics N (%) or period time
No. of patients 25
Gender (female, %) 7 (28)
Mean age (years) 47.52 (22-74)
Bilateral uveitis (%) 19 (76)
Uveitis type
Anterior uveitis (%) 5 (19.2)
Post/panuveitis (%) 20 (76.9)
Etiology of uveitis
Behcet disease (%) 15 (60)
VKH disease (%) 4 (16)
Sympathetic ophthalmia (%) 2 (8)
SLE (%) 1 (4)
Idiopathic uveitis (%) 3 (12)
Mean duration of uveitis (months) 66.5 (6-150)

Values are presented as mean ± SD unless otherwise indicated.

VKH = Vogt-Koyanagi-Harada; SLE = systemic lupus erythematosus.

Table 2.
Patient characteristics at the time of starting mycophenolate mofetil
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)

MMF = mycophenolate mofetil.

* Active/inactive disease was defined according to the Standardization of Uveitis Nomenclature criteria.10

Table 3.
Control of ocular inflammation with mycophenolate mofetil in chronic uveitis patients within 6 months and 1 year
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%)

m = months.

* Complete control of inflammation sustained over consecutive visits spanning at least 28 days was achieved in 44% and 50% of patients within 6 months and 1 year respectively.

Table 4.
Reasons for stopping mycophenolate mofetil among patients with chronic uveitis
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%)

MMF = mycophenolate mofetil.

* Treatment limiting side effects were observed in 12% of patients and typically were reversible.

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