Long-Term Remission After Cessation of Interferon-α Treatment in Patients With Severe Uveitis Due to Behcet's Disease

被引:139
作者
Deuter, Christoph M. E. [1 ]
Zierhut, Manfred
Moehle, Antje
Vonthein, Reinhard [2 ]
Stuebiger, Nicole
Koetter, Ina
机构
[1] Univ Tubingen Hosp, Ctr Ophthalmol, D-72076 Tubingen, Germany
[2] Univ Lubeck, Univ Hosp Schleswig Holstein, Lubeck, Germany
来源
ARTHRITIS AND RHEUMATISM | 2010年 / 62卷 / 09期
关键词
REFRACTORY UVEITIS; VISUAL PROGNOSIS; EFFICACY; THERAPY; CYCLOSPORINE; SAFETY; AZATHIOPRINE; INFLIXIMAB; RECOMMENDATIONS; MANAGEMENT;
D O I
10.1002/art.27581
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. To retrospectively assess the development of visual acuity and the frequency and duration of relapse-free periods in patients who were treated with interferon-alpha (IFN alpha) for severe uveitis due to Behcet's disease (BD) and who completed a followup period of >= 2 years. Methods. IFN alfa-2a was administered at an initial dosage of 6 million IU per day, then tapered to a maintenance dosage of 3 million IU twice per week, and finally discontinued, if possible. In case of a relapse, IFN treatment was repeated. Visual acuity at the end of followup was compared with visual acuity when ocular disease was in remission. Results. Of 53 patients (96 eyes), 52 (98.1%) responded to IFN. In 47 patients (88.7%), IFN could be discontinued when the disease was in remission. Twenty of these 47 (42.6%) needed a second treatment course during a median followup of 6.0 years (range 2.0-12.6 years). Visual acuity improved or remained unchanged in 91 eyes (94.8%). Ocular disease was still in remission in 50% of the patients 45.9 months after cessation of the first IFN course. The relapse rate tended to be lower in women than in men. The BD activity score decreased significantly during followup, but long-term remission of nonocular BD manifestations was not achieved. However, since local treatments were sufficient, no systemic treatment was administered. Conclusion. Our findings indicate that IFN alpha induces long-lasting remission in patients with severe ocular BD, resulting in a notable improvement in visual prognosis.
引用
收藏
页码:2796 / 2805
页数:10
相关论文
共 34 条
  • [21] Systematic review of ethnic variation in the phenotype of Behcet's disease
    Lewis, K. A.
    Graham, E. M.
    Stanford, M. R.
    [J]. SCANDINAVIAN JOURNAL OF RHEUMATOLOGY, 2007, 36 (01) : 1 - 6
  • [22] MAMO JG, 1970, ARCH OPHTHALMOL-CHIC, V84, P451
  • [23] Ohno S, 2004, J RHEUMATOL, V31, P1362
  • [24] RENAL HISTOPATHOLOGIC ALTERATIONS IN PATIENTS TREATED WITH CYCLOSPORINE FOR UVEITIS
    PALESTINE, AG
    AUSTIN, HA
    BALOW, JE
    ANTONOVYCH, TT
    SABNIS, SG
    PREUSS, HG
    NUSSENBLATT, RB
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1986, 314 (20) : 1293 - 1298
  • [25] PIVETTIPEZZI P, 1985, ANN OPHTHALMOL, V17, P327
  • [26] SAKAMOTO M, 1995, OPHTHALMOLOGY, V102, P317
  • [27] SILMAN AJ, 1990, LANCET, V335, P1078
  • [28] Behcet's disease:: uveitis-therapy with interferon α2a -: prospective clinical study in 33 patients
    Stübiger, N
    Kötter, I
    Deuter, C
    Zierhut, M
    [J]. KLINISCHE MONATSBLATTER FUR AUGENHEILKUNDE, 2001, 218 (12) : 768 - 773
  • [29] Stuebiger N, 2000, BRIT J OPHTHALMOL, V84, P1437
  • [30] BEHCETS-SYNDROME - TREATMENT WITH RECOMBINANT LEUKOCYTE ALPHA-INTERFERON
    TSAMBAOS, D
    EICHELBERG, D
    GOOS, M
    [J]. ARCHIVES OF DERMATOLOGICAL RESEARCH, 1986, 278 (04) : 335 - 336