Department of Dermatology, College of Medicine, Hanyang University, Hanyang University Guri Hospital, Guri-Si, Korea.
Hanyang Institute of Bioscience and Biotechnology, Hanyang University, Seoul, Korea.
J Eur Acad Dermatol Venereol. 2024 Aug;38(8):1514-1521. doi: 10.1111/jdv.19802. Epub 2024 Feb 15.
Frontal fibrosing alopecia (FFA) is a scarring alopecia with fronto-temporo-parietal hairline recession. Although no proven treatment for FFA exists, dutasteride has been suggested as a potential treatment option. We aimed to evaluate the therapeutic response of oral dutasteride in FFA patients. The identification and selection of studies were conducted according to the Preferred Reporting Items for Systematic Reviews and Meta-analysis 2020 criteria. To assess the risk of bias for each study, we used the Cochrane's risk of bias in non-randomized studies of interventions (ROBINS-I) assessment tool. A random effects model meta-analysis was performed. Estimated proportion of stabilization for eligible studies was calculated to evaluate the effectiveness of dutasteride for treating FFA. Among patients who achieved stabilization, subgroup analysis was conducted on those showing improvement. Seven studies including 366 patients who received oral dutasteride were identified. The estimated proportion of patients who experienced stabilization of FFA with oral dutasteride was 0.628 (95% CI: 0.398-0.859). In subgroup analyses of patients who experienced improvement, the estimated proportion of improvement was 0.356 (95% CI: 0.163-0.549). In this systematic review and meta-analysis, oral dutasteride revealed to be a good treatment option for disease stabilization or improvement in patients with FFA.
额部纤维性脱发(FFA)是一种瘢痕性脱发,伴有额颞顶部发际线后退。虽然目前尚无针对 FFA 的有效治疗方法,但已有人提出使用度他雄胺作为潜在的治疗选择。我们旨在评估口服度他雄胺治疗 FFA 患者的疗效。研究的识别和选择是根据系统评价和荟萃分析的首选报告项目 2020 标准进行的。为了评估每项研究的偏倚风险,我们使用了 Cochrane 非随机干预研究偏倚风险(ROBINS-I)评估工具。进行了随机效应模型荟萃分析。计算了合格研究中稳定的估计比例,以评估度他雄胺治疗 FFA 的疗效。在达到稳定的患者中进行了亚组分析,以评估那些显示改善的患者。确定了 7 项包括 366 名接受口服度他雄胺治疗的患者的研究。口服度他雄胺治疗 FFA 稳定的患者估计比例为 0.628(95%CI:0.398-0.859)。在改善的患者亚组分析中,估计改善的比例为 0.356(95%CI:0.163-0.549)。在这项系统评价和荟萃分析中,口服度他雄胺显示出是 FFA 患者疾病稳定或改善的良好治疗选择。