Fania Luca, Giovanardi Giulia, Samela Tonia, Caposiena Dante, Chiricozzi Andrea, Antonelli Flaminia, Saraceni Pierluigi, Elia Fulvia, Garcovich Simone, Ciccone Davide, Cannizzaro Maria Vittoria, Miraglia Emanuele, Iacovino Chiara, Giustini Sandra, Skroza Nevena, Mambrin Alessandra, Potenza Concetta, Bianchi Luca, Peris Ketty, Abeni Damiano
Clinical Epidemiology Unit and Dermatology Department, Istituto Dermopatico dell'Immacolata, IDI-IRCCS, 00167 Rome, Italy.
Department of Dermatology, Università Cattolica del Sacro Cuore, Fondazione Policlinico Universitario A Gemelli IRCCS, 00168 Rome, Italy.
J Clin Med. 2022 Jul 12;11(14):4037. doi: 10.3390/jcm11144037.
Adalimumab is the only biologic agent approved for the treatment of moderate-to-severe hidradenitis suppurativa (HS) patients (i.e., with Hurley II or III), which is recommended in two different maintenance doses (i.e., 40 mg weekly or 80 mg every two weeks). We conducted a prospective multicentric study to measure outcomes related to the severity of disease and quality of life (QoL) of patients affected by moderate-to-severe HS, treated with adalimumab at a maintenance dosing of 40 mg or 80 mg. Assessments were performed at baseline (T0) and after 32 weeks of treatment (T32). We enrolled 85 moderate-to-severe HS Italian patients, 43 men (50.6%) and 42 women, aged between 16 and 62 years (median 31 years, interquartile range 24.4-43.8). Statistically significant improvements were observed for clinical status (with a mean reduction of 7.1 points for the International Hidradenitis Suppurativa Severity Score System (IHS4)), pain levels (3.1 mean decrease in VAS), and QoL (3.4 mean improvement in DLQI score). Patients with no comorbidities, and those with higher levels of perceived pain showed significantly greater improvement in QoL than their counterpart from T0 to T32. As for the proportion of patients who at follow-up reached the minimal clinical important difference (MCID) in QoL, significantly higher proportions of success were observed for age (patients in the 29-39 category), pain (patients with higher reported pain), and Hurley stage III. While both treatment regimen groups (i.e., 40 vs. 80 mg) improved significantly, no statistical differences were observed when comparing the two treatment dosages.
阿达木单抗是唯一被批准用于治疗中度至重度化脓性汗腺炎(HS)患者(即Hurley II或III级)的生物制剂,推荐使用两种不同的维持剂量(即每周40毫克或每两周80毫克)。我们进行了一项前瞻性多中心研究,以测量中度至重度HS患者在接受40毫克或80毫克维持剂量阿达木单抗治疗后与疾病严重程度和生活质量(QoL)相关的结果。在基线(T0)和治疗32周后(T32)进行评估。我们招募了85名中度至重度HS的意大利患者,其中43名男性(50.6%)和42名女性,年龄在16至62岁之间(中位数31岁,四分位间距24.4 - 43.8)。观察到临床状况(国际化脓性汗腺炎严重程度评分系统(IHS4)平均降低7.1分)、疼痛水平(视觉模拟评分平均降低3.1分)和生活质量(皮肤病生活质量指数(DLQI)评分平均提高3.4分)有统计学意义的改善。无合并症的患者以及疼痛感知水平较高的患者从T0到T32的生活质量改善明显大于其对应患者。至于在随访中达到生活质量最小临床重要差异(MCID)的患者比例,在年龄(29 - 39岁类别患者)、疼痛(报告疼痛较高的患者)和Hurley III期观察到显著更高的成功比例。虽然两个治疗方案组(即40毫克与80毫克)均有显著改善,但比较两种治疗剂量时未观察到统计学差异。