Puig Lluís, Izu Belloso Rosa, Rivera-Díaz Raquel, Mollet Sánchez Jordi, Rodríguez Fernández-Freire Lourdes, Sahuquillo-Torralba Antonio, Ruiz-Villaverde Ricardo
Dermatology Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain.
Dermatology Department, Hospital Universitario Basurto, Bilbao, Spain.
Dermatology. 2024;240(5-6):778-792. doi: 10.1159/000540019. Epub 2024 Jul 17.
Generalized pustular psoriasis (GPP) is a chronic, rare, and potentially life-threatening skin condition characterized by flares comprising widespread sterile pustules and systemic inflammation. Both the rarity and heterogeneity of the disease have made GPP classification and standardization of clinical criteria challenging. Before the approval of spesolimab (IL-36R antibody) in 2022, there were no approved treatments in the USA or Europe for GPP flares. Treatment for GPP has amounted to off-label use of medicines approved to treat plaque psoriasis. Our aim was to describe the sociodemographics, clinical characteristics, and treatment patterns of patients with GPP in Spain.
Non-interventional, descriptive, multi-center, retrospective chart review of patients diagnosed with GPP in Spain.
56 patients (50% women) were included, with a mean (standard deviation, SD) age at diagnosis of 53.7 (20.5) and a mean (SD) time of follow-up of 3.7 (3.1) years. In 80% of patients, GPP diagnosis was associated with a flare and 67.3% had known risk factors for GPP (such as previous diagnosis or family history of plaque psoriasis, comorbidities, smoking or stress). Hypertension and plaque psoriasis were the most frequent comorbidities (44.6% each). The number of GPP flares per patient-year was 0.55 with (range 0-4) a mean (SD) body surface area involvement of 21.3% (19.1). The most frequent manifestations of GPP flares were pustules (88.5%), erythema (76.9%), and scaling (76.9%). Additionally, 65.4% of patients had plaque psoriasis, 53.8% had unspecified skin lesions, and 30.8% experienced pain. The treatments used for GPP flares were off-label conventional systemic drugs (75%), mostly corticosteroids, cyclosporine, and acitretin. In the periods between flares, off-label biologics were used in 56.5% of patients. During the study period, 9 patients (16.1%) had at least one complication and 5 of them required hospitalization.
This is the first multicenter study in Spanish GPP patients. Most patients were in their fifties, with personal or family history of plaque psoriasis, stress, smoking and a wide range of comorbidities and complications. Even though the number of flares per patient/year was 0.55, there was variability between patients. Both off-label conventional systemics and off-label biologics were used for flare management without a clear treatment pattern.
泛发性脓疱型银屑病(GPP)是一种慢性、罕见且可能危及生命的皮肤病,其特征为发作时出现广泛的无菌性脓疱和全身炎症。该疾病的罕见性和异质性使得GPP的分类和临床标准的标准化具有挑战性。在2022年司库奇尤单抗(IL-36R抗体)获批之前,美国和欧洲均没有获批用于治疗GPP发作的药物。GPP的治疗相当于对已获批用于治疗斑块状银屑病的药物进行超说明书用药。我们的目的是描述西班牙GPP患者的社会人口统计学特征、临床特征和治疗模式。
对西班牙诊断为GPP的患者进行非干预性、描述性、多中心回顾性病历审查。
纳入56例患者(50%为女性),诊断时的平均(标准差,SD)年龄为53.7(20.5)岁,平均(SD)随访时间为3.7(3.1)年。80%的患者GPP诊断与发作相关,67.3%的患者有已知的GPP危险因素(如既往斑块状银屑病诊断或家族史、合并症、吸烟或压力)。高血压和斑块状银屑病是最常见的合并症(各占44.6%)。每位患者每年的GPP发作次数为0.55次(范围0 - 4次),平均(SD)体表面积受累为21.3%(19.1)。GPP发作最常见的表现为脓疱(88.5%)、红斑(76.9%)和脱屑(76.9%)。此外,65.4%的患者有斑块状银屑病,53.8%有未明确的皮肤病变,30.8%经历疼痛。用于治疗GPP发作的是超说明书使用的传统全身性药物(75%),主要是皮质类固醇、环孢素和阿维A。在发作间期,56.5%的患者使用超说明书的生物制剂。在研究期间,9例患者(16.1%)至少有1种并发症,其中5例需要住院治疗。
这是第一项针对西班牙GPP患者的多中心研究。大多数患者为五十多岁,有斑块状银屑病的个人或家族史、压力、吸烟以及多种合并症和并发症。尽管每位患者每年的发作次数为0.55次,但患者之间存在差异。超说明书使用的传统全身性药物和超说明书使用的生物制剂均用于发作管理,且没有明确的治疗模式。