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在资源有限的目标人群中,一项关于低剂量沙利度胺治疗严重结节性红斑麻风的真实世界研究强调了其在机制上的合理性。

A real-world study of low-dose thalidomide in severe erythema nodosum leprosum highlighting its mechanistic rationale in a resource-constrained target population.

机构信息

Department of Dermatology, Venereology and Leprosy, Atal Bihari Vajpayee Institute of Medical Sciences and Dr. Ram Manohar Lohia Hospital, New Delhi, India.

Department of Pathology, Atal Bihari Vajpayee Institute of Medical Sciences and Dr. Ram Manohar Lohia Hospital, New Delhi, India.

出版信息

Int J Dermatol. 2023 Jan;62(1):48-55. doi: 10.1111/ijd.16315. Epub 2022 Aug 4.

Abstract

BACKGROUND

Corticosteroids remain the main therapy in erythema nodosum leprosum (ENL), and long-term usage in chronic or recurrent ENL is a cause of significant morbidity and mortality. Thalidomide exerts dramatic effect in controlling ENL and helps reduce the dose of steroids, but the cost is a hindrance to its usage.

METHODS

Patients of ENL (steroid naïve and steroid-dependent) were recruited over a 1-year period. An escalating dose of low-dose thalidomide with a reducing dose of prednisolone was titrated depending on the control of disease activity. The primary aim was to reduce the dose of steroids to the lowest effective dose, and the secondary aim was to stop.

RESULTS

Sixteen patients of ENL were studied (mean duration of ENL 22.1 months, 15 severe ENL), and a majority (11/16, 68%) were on steroids with a mean duration of 11.27 months. All patients had steroid-related side effects (cushingoid habitus 81.8%, weight gain 54.5%, diabetes mellitus 9%, hyperlipidemia 18.18%, cataract 18.1%, osteoporosis 36.3%, striae 36.3%, acneiform eruptions 18.1%, and myopathy 9%). Steroids could be tapered in a majority of patients (n = 9) within 3 months (mean 2.44 months) with a low dose of thalidomide (25-150 mg/day, mean 78.3 mg) achieving a significant reduction in prednisolone dose (33.16 mg at baseline; 4.28 mg at 3 months, P < 0.05). Steroids could be stopped in 92% of patients by 3.03 months, and both drugs could be stopped in 80% of cases by 5.83 months.

CONCLUSION

The rapid and effective control of ENL with low-dose thalidomide in our series is comparable to the historical efficacy of high-dose thalidomide regimens, making it an affordable therapy in resource-constrained settings and an excellent steroid-sparing agent. The rapid onset of disease control is likely attributable to its action via neutrophils.

摘要

背景

皮质类固醇仍然是结节性红斑麻风(ENL)的主要治疗方法,在慢性或复发性 ENL 中长期使用是导致显著发病率和死亡率的原因。沙利度胺在控制 ENL 方面具有显著效果,并有助于减少皮质类固醇的剂量,但成本是其使用的一个障碍。

方法

在一年的时间内,招募了 ENL 患者(皮质类固醇初治和依赖患者)。根据疾病活动的控制情况,逐渐滴定低剂量沙利度胺和逐渐减少泼尼松龙的剂量。主要目的是将皮质类固醇的剂量降至最低有效剂量,次要目的是停药。

结果

研究了 16 例 ENL 患者(ENL 持续时间平均为 22.1 个月,15 例为严重 ENL),大多数患者(11/16,68%)正在使用皮质类固醇,平均使用时间为 11.27 个月。所有患者均有皮质类固醇相关副作用(库欣样体型 81.8%,体重增加 54.5%,糖尿病 9%,高脂血症 18.18%,白内障 18.1%,骨质疏松 36.3%,条纹 36.3%,痤疮样疹 18.1%,肌病 9%)。大多数患者(n=9)在 3 个月内(平均 2.44 个月)用低剂量沙利度胺(25-150mg/天,平均 78.3mg)逐渐减少皮质类固醇剂量,可使皮质类固醇剂量显著减少(基线时为 33.16mg;3 个月时为 4.28mg,P<0.05)。92%的患者在 3.03 个月时可停用皮质类固醇,80%的患者在 5.83 个月时可停用两种药物。

结论

在我们的研究中,低剂量沙利度胺可快速有效控制 ENL,其疗效与高剂量沙利度胺方案相当,因此在资源有限的环境中是一种负担得起的治疗方法,也是一种极好的皮质类固醇节约剂。疾病控制的快速起效可能归因于其对中性粒细胞的作用。

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