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霉酚酸酯治疗弥漫性硬皮病皮肤病的长期疗效和耐受性

Long-term efficacy and tolerability of mycophenolate mofetil therapy in diffuse scleroderma skin disease.

作者信息

Boulos Daniel, Ngian Gene-Siew, Rajadurai Anton, Elford Kathleen, Stevens Wendy, Proudman Susanna, Owen Claire, Roddy Janet, Nikpour Mandana, Youssef Peter, Hill Catherine, Sahhar Joanne

机构信息

Department of Rheumatology, Monash Health, Melbourne, Victoria, Australia.

Department of Rheumatology, St Vincent's Health, Melbourne, Victoria, Australia.

出版信息

Int J Rheum Dis. 2017 Apr;20(4):481-488. doi: 10.1111/1756-185X.13035. Epub 2017 Mar 24.

Abstract

OBJECTIVES

To assess the long-term efficacy and tolerability of mycophenolate mofetil (MMF) in patients with diffuse cutaneous systemic sclerosis (dcSSc).

METHODS

Patients enrolled in the Australian Scleroderma Cohort study with dcSSc and baseline modified Rodnan skin score (mRSS) ≥ 12 who were treated for a minimum of 12 months with MMF for the primary indication of skin disease were included and their prospectively collected data retrieved. Change in mRSS, the proportion with a clinically significant improvement (reduction in mRSS ≥ 5 from baseline) and adverse effects due to therapy were determined.

RESULTS

Seventy-four participants treated with MMF were identified and of these, 42 met inclusion criteria. The mean age was 53 ± 12 years, with mean disease duration at MMF commencement of 4.8 ± 4.3 years. Twenty-one participants (50%) commenced MMF within 2 years of disease onset and the mean duration of therapy was 2.7 ± 1.7 years. The mean mRSS at baseline was 25.9 ± 9.2 with a reduction of 3.7 ± 7.1 (P = 0.07) after 1 year of therapy, 7.6 ± 8.3 after 2 years (P = 0.01) and 10.5 ± 10.3 after 5 years (P < 0.01). Response to treatment was not affected by disease duration at MMF commencement or baseline skin score. Eighteen participants (43%) demonstrated clinically significant improvement after 1 year, increasing to 92% after 4 years. Two participants (5%) ceased MMF due to adverse effects.

CONCLUSION

MMF was associated with a modest improvement in mRSS and was well tolerated in the treatment of dcSSc. Given the natural history of dcSSc where skin involvement can spontaneously improve, randomized, placebo-controlled studies are required to confirm whether improvement can be attributed to MMF therapy.

摘要

目的

评估霉酚酸酯(MMF)对弥漫性皮肤系统性硬化症(dcSSc)患者的长期疗效和耐受性。

方法

纳入澳大利亚硬皮病队列研究中患有dcSSc且基线改良Rodnan皮肤评分(mRSS)≥12、因皮肤病主要适应证接受MMF治疗至少12个月的患者,并检索其前瞻性收集的数据。确定mRSS的变化、临床显著改善(mRSS较基线降低≥5)的比例以及治疗引起的不良反应。

结果

确定了74名接受MMF治疗的参与者,其中42名符合纳入标准。平均年龄为53±12岁,开始使用MMF时的平均病程为4.8±4.3年。21名参与者(50%)在疾病发作2年内开始使用MMF,平均治疗时间为2.7±1.7年。基线时的平均mRSS为25.9±9.2,治疗1年后降低3.7±7.1(P = 0.07),2年后降低7.6±8.3(P = 0.01),5年后降低10.5±10.3(P < 0.01)。治疗反应不受开始使用MMF时的病程或基线皮肤评分影响。18名参与者(43%)在1年后表现出临床显著改善,4年后增至92%。两名参与者(5%)因不良反应停止使用MMF。

结论

MMF与mRSS的适度改善相关,在dcSSc治疗中耐受性良好。鉴于dcSSc的自然病程中皮肤受累可自发改善,需要进行随机、安慰剂对照研究以确认改善是否可归因于MMF治疗。

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