Efficacy And Safety Of Low-Dose Methotrexate In Generalized And Recalcitrant Lichen Planus: A Retrospective Study At A Tertiary Care Center.

IF 2.5 4区 医学 Q2 DERMATOLOGY Dermatology practical & conceptual Pub Date : 2024-10-30 DOI:10.5826/dpc.1404a220
Ananta Khurana, Savitha Sharath, Kabir Sardana
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Abstract

Introduction: Methotrexate (MTX) acts by suppressing multiple immune pathways involved in the pathogenesis of lichen planus (LP). Trials assessing the efficacy and relapse rates of methotrexate in LP are lacking.

Objectives: Our objective was to analyze the efficacy and safety of low-dose methotrexate in generalized and recalcitrant LP patients retrospectively and to assess the relapse rates in patients after stopping MTX therapy.

Methods: We analyzed clinical and therapeutic details of LP patients treated with low-dose MTX at our center. The cumulative dose and duration of MTX was calculated, and the time to achieve disease control was noted. We analyzed duration of remission and time after which recurrences were seen post-treatment.

Results: Records of 42 generalized and recalcitrant LP patients treated with MTX were analyzed. The starting dose of MTX was 7.5 mg (n=7) or 10 mg (n= 35) once weekly, increased to 10/15 mg weekly in patients with inadequate response. Ten patients were lost to follow-up. Complete resolution was achieved in 30/32 (93%) patients within a mean duration of 14.76 weeks (4-32 weeks), and the cumulative dose of MTX to achieve remission was 153.58 mg (50-375 mg). Only minor side effects were noted in 12/32 (37.5%) patients, and none required treatment discontinuation. The mean duration of remission was 29.43 months (5-60 months).

Conclusion: MTX demonstrated high efficacy and a good safety profile in extensive cutaneous LP and may be a safer alternative to steroids for this condition.

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低剂量甲氨蝶呤治疗广泛性和顽固性扁平苔藓的疗效和安全性:一项三级保健中心的回顾性研究。
简介:甲氨蝶呤(MTX)通过抑制参与扁平苔藓(LP)发病的多种免疫途径起作用。目前缺乏评估甲氨蝶呤治疗LP的疗效和复发率的试验。目的:回顾性分析低剂量甲氨蝶呤治疗广泛性和顽固性LP患者的疗效和安全性,并评估患者停止MTX治疗后的复发率。方法:分析我院低剂量甲氨蝶呤治疗LP患者的临床及治疗细节。计算甲氨蝶呤的累积剂量和持续时间,并记录实现疾病控制的时间。我们分析了缓解的持续时间和治疗后复发的时间。结果:对42例全身性顽固性LP患者的MTX治疗记录进行分析。MTX的起始剂量为7.5 mg (n=7)或10 mg (n= 35),每周一次,在反应不足的患者中增加到10/15 mg。10例患者失访。30/32(93%)患者在平均持续时间14.76周(4-32周)内完全缓解,MTX达到缓解的累积剂量为153.58 mg (50-375 mg)。在12/32(37.5%)的患者中,只有轻微的副作用,没有人需要停止治疗。平均缓解期为29.43个月(5 ~ 60个月)。结论:甲氨蝶呤在广泛的皮肤LP中表现出高效率和良好的安全性,可能是一种更安全的替代类固醇治疗这种疾病。
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