Observational studyThe Journal of dermatology2025
Roflumilast for Oral Ulcers in Behçet's Disease and Recurrent Aphthous Stomatitis.
Observational study in The Journal of dermatology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed.
- How I Treat: Haploinsufficiency of A20.Journal of human immunity · 2026Review
- The "two flowers therapy": clinical efficacy and mechanisms of a total glucosides of paeony -colchicine dual-drugs for Behçet's disease derived from Chinese physicians' medication experience.Frontiers in immunology · 2026Observational
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors.
Funding
Abstract
Oral aphthous ulcer in Behçet's disease (BD) and recurrent aphthous stomatitis (RAS) is a cause of discomfort for many patients, especially in cases refractory to colchicine or azathioprine. Roflumilast, a phosphodiesterase-4 (PDE4) inhibitor, may be effective for treating refractory oral ulcers (OUs) in BD and RAS, especially in regions where apremilast is unavailable. In this study, we investigated the efficacy and safety profile of low-dose roflumilast for refractory OUs in BD and RAS. This single-center, single-arm, retrospective observational study included 46 patients screened from the outpatient department from May 2023 to Dec 2023. During the 12-week study period, the subjects received roflumilast at a dosage of 0.25 mg daily. For those experiencing adverse events (AEs) requiring adjustment, the dose was reduced to 0.125 mg. Objective clinical responses were evaluated as clinician-assessed treatment categories (complete remission, partial response, or non-response), based on the absence or presence of new OUs and symptom improvement. Subjective symptoms were evaluated through a patient-reported questionnaire, and AEs were monitored through the protocol. At week 12, 71.7% of patients showed a positive response to roflumilast, with 30.4% achieving complete remission. AEs were reported in 76.1% of the 46 subjects with follow-up visits, primarily gastrointestinal (71.7%) and neurological symptoms (17.4%). Among the cohort, 78.3% of patients tolerated roflumilast without discontinuation, including 15.2% with dose reduction, while 21.7% discontinued due to intolerable AEs. Roflumilast demonstrated rapid and sustained efficacy in reducing OUs in BD and RAS. Although AEs were frequent, they were generally tolerable and manageable. While the study has limitations, including its retrospective observational nature and small sample size, it suggests roflumilast as a potential treatment alternative for refractory OUs where apremilast is unavailable, deserving further research.
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