Methotrexate and Prednisolone compared to placebo and prednisolone in the treatment of Erythema Nodosum Leprosum - an international multicentre, double-blind randomised controlled clinical trial - MaPs in ENL
de Barros, B.; Sultana, F.; Maximus, N.; Pai, V. V.; Wakade, A.; Bhame, B.; Acharya, B.; Hamza, A.; Getachew, A.; Alinda, M. D.; Listiawan, M. Y.; Nigusse, S. D.; Hagge, D. A.; Napit, I.; Shah, M.; Darlong, J.; Nicholls, P.; Bernd, B.; Lambert, S. M.; Lockwood, D. N. J.; Walker, S. L.
Show abstract
Background Erythema nodosum leprosum (ENL) is a severe inflammatory complication of leprosy that often requires prolonged corticosteroid therapy which is associated with adverse effects. Methotrexate is an affordable immunomodulatory agent with limited evidence for its use in ENL treatment. We evaluated whether weekly oral methotrexate in additional to prednisolone reduces the need for additional prednisolone in adults with severe ENL. Methods and Findings We performed an international, multicentre, double-blind, randomised, placebo-controlled trial conducted at five leprosy referral centres in Ethiopia, India, Indonesia, and Nepal. Adults aged 18-60 years with severe ENL were randomised to receive oral methotrexate and prednisolone, or matching placebo and prednisolone. All participants received an identical prednisolone regime over 20 weeks and were followed for 60 weeks. The primary outcome was time to first ENL flare requiring additional prednisolone, assessed over 24 and 48 weeks. Between January 2023 and June 2024, 231 individuals were screened and 137 were randomised (68 methotrexate and prednisolone; 69 placebo and prednisolone). By 24 weeks, 85/137 (62.0%) participants experienced an ENL flare requiring additional prednisolone; the adjusted hazard ratio (HR) for methotrexate versus placebo was 0.98 (95% CI 0.62-1.54). By 48 weeks, 102/137 (74.5%) experienced an ENL flare; adjusted HR 0.95 (95% CI 0.62-1.43). Secondary outcomes were similar: methotrexate did not reduce ENL severity at first flare, flare frequency, or severity of subsequent flares. Health-related quality of life improved substantially in both groups with no evidence of a differential treatment effect. Methotrexate was generally well tolerated. The trial was registered at ClinicalTrials.gov (NCT03775460). Conclusions Oral methotrexate added to prednisolone did not reduce the requirement for additional prednisolone or delay ENL flares compared to placebo and prednisolone, and our study does not support the use of methotrexate for severe ENL.
Matching journals
The top 10 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- UVESCREEN1: A randomised feasibility study of imaging-based uveitis screening for children with juvenile idiopathic arthritis- Study Protocol 93%
- A low molecular weight dextran sulphate, ILB(R), for the treatment of amyotrophic lateral sclerosis (ALS): an open-label, single-arm, single-centre, phase II trial 93%
- Hydroxychloroquine and Tocilizumab Therapy in COVID-19 Patients - An Observational Study 92%
Similar papers in this journal
- Safety of Hydroxychloroquine among Outpatient Clinical Trial Participants for COVID-19 92%
- Cost-effectiveness of remdesivir and dexamethasone for COVID-19 treatment in South Africa 91%
- Safety and Efficacy of Dupilumab for the Treatment of Hospitalized Patients with Moderate to Severe COVID 19: A Phase IIa Trial 91%
Similar papers in this journal
- Validation of patient-reported outcome measures for dactylitis, psoriatic skin and nail disease, and uveitis in patients with psoriatic arthritis in routine care 92%
- Risk-stratified monitoring for sulfasalazine toxicity: prognostic model development and validation. 92%
- Beneficial effects of colchicine for moderate to severe COVID-19: an interim analysis of a randomized, double-blinded, placebo controlled clinical trial 91%
Similar papers in this journal
- CATALYST trial protocol: A multicentre, open-label, phase II, multi-arm trial for an early and accelerated evaluation of the potential treatments for COVID-19 in hospitalised adults 93%
- The DEXACELL Trial; a protocol for a pragmatic, multicentre, double-blind, placebo-controlled, randomised, parallel group, phase 3 superiority trial to assess the effectiveness and cost-effectiveness of DEXAmethasone as an adjunctive therapy for the management of CELLulitis in adults presenting to urgent secondary care in the UK 92%
- Folic Acid And Methotrexate Use And Their Association With COVID-19 Diagnosis And Mortality: An Analysis From The UK Biobank 92%
Similar papers in this journal
- Early treatment with nitazoxanide prevents worsening of mild and moderate COVID-19 and subsequent hospitalization 91%
- Characterizing Long COVID in an International Cohort: 7 Months of Symptoms and Their Impact 91%
- The angiotensin type 2 receptor agonist C21 restores respiratory function in COVID19 - a double-blind, randomized, placebo-controlled Phase 2 trial 91%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.