Psoriasis vulgaris in patients with a recent history of neoplasia: safety of interleukin-23 inhibitors. A multicentre retrospective study

医学 银屑病 恶性肿瘤 内科学 癌症 人口 观察研究 入射(几何) 回顾性队列研究 耐受性 肿瘤科 皮肤病科 不利影响 环境卫生 光学 物理
作者
Francesca Satolli,Silvia Gerosa,Martina Burlando,Emanuele Cozzani,Claudia Lasagni,Marco Manfredini,Alessandra Narcisi,Angelo Valerio Marzano,Carlo Giovanni Carrera,Matteo Megna,Anna Elisabetta Cagni,Maria Esposito,Maria Concetta Fargnoli,Vito Di Lernia,Francesca Peccerillo,Marco Romanelli,Emanuele Trovato,Paolo Amerio,Andrea Carugno,Alexandra Maria Giovanna Brunasso
出处
期刊:Clinical and Experimental Dermatology [Oxford University Press]
标识
DOI:10.1093/ced/llaf184
摘要

Abstract Background The management of psoriasis in patients with a history of cancer remains debated, especially for the limited literature available. Given the lack of large, well-designed studies focused on this patient group, real-world clinical experiences and expert insights serve as crucial resources for guiding informed treatment decisions. This issue particularly regards the newest anti-interleukin (IL) drugs available, such as those targeting IL-23. Objectives To analyse a real-world population of patients with psoriasis undergoing biologic treatment with anti-IL-23 drugs who also have a concurrent cancer diagnosis. Methods A retrospective, observational, multicentre study was conducted, enrolling adult patients with moderate-to-severe plaque psoriasis and a personal history of malignancy. The patients were undergoing any anti-IL-23 treatment approved for psoriasis (guselkumab, risankizumab or tildrakizumab). Results In total, 198 patients were enrolled. Among these, 67 (33.8%) had a history of malignancy within the past 5 years, whereas 131 (66.2%) had been diagnosed with cancer prior to that time. During the period of the study, six patients (3.0%) experienced progression or recurrence of their existing neoplasia. Moreover, six (3.0%) were diagnosed with a new neoplasia during the study period, discontinuing biologic treatment in only two cases. A subanalysis investigating the relationship between comorbidities and the incidence of neoplastic progression or recurrence during therapy, as well as the development of a new neoplasia, did not show any statistically significant associations. Similarly, significant associations between previous treatments and increased risk of cancer recurrence, progression or development were not found. Conclusions Our real-life experience is the largest study investigating the use of anti-IL-23 agents and the risk of cancer recurrence, progression and development in patients with a history of cancer. This study confirms their safety also in this cohort of patients.

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