Integrated Safety Analysis on Skin Cancers among Patients with Psoriasis Receiving Ixekizumab in Clinical Trials

Limited data exist on skin cancer risk in patients with psoriasis using biologics. Here, we report treatment-emergent adverse events (TEAEs) of skin cancer in patients treated with ixekizumab from psoriasis clinical trials. Integrated safety databases from 17 clinical trials of adults with moderate-...

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Detalles Bibliográficos
Autores: Smith, Saxon|||0000-0003-0995-4372, Stratigos, Alexandros, Augustin, Matthias|||0000-0002-4026-8728, Carrascosa, José Manuel|||0000-0003-4266-0771, Grond, Susanne, Riedl, Elisabeth, Xu, Wen, Patel, Himanshu, Lebwohl, Mark
Tipo de recurso: artículo
Fecha de publicación:2023
País:España
Institución:Universitat Autònoma de Barcelona
Repositorio:Dipòsit Digital de Documents de la UAB
Idioma:inglés
OAI Identifier:oai:ddd.uab.cat:313615
Acceso en línea:https://ddd.uab.cat/record/313615
https://dx.doi.org/urn:doi:10.1007/s13555-023-00966-4
Access Level:acceso abierto
Palabra clave:Ixekizumab
Long-term
Malignancy
Melanoma
Non-melanoma skin cancer
Psoriasis
Safety
Skin cancer
Skin neoplasm
Descripción
Sumario:Limited data exist on skin cancer risk in patients with psoriasis using biologics. Here, we report treatment-emergent adverse events (TEAEs) of skin cancer in patients treated with ixekizumab from psoriasis clinical trials. Integrated safety databases from 17 clinical trials of adults with moderate-to-severe psoriasis treated with ≥ 1 dose of ixekizumab for ≤ 5 years were used to analyze exposure-adjusted incidence rates (IRs) per 100 patient-years of exposure (PYE) and clinically characterize dermatologist-adjudicated skin cancer TEAEs. Of 6892 patients, 58 presented with ≥ 1 skin cancer TEAE (IR 0.3) with IRs remaining stable with longer ixekizumab exposure. Non-melanoma skin cancer (NMSC) was the most common event (IR 0.3) affecting 55 patients; of those, 44 had basal cell carcinoma (IR 0.2) and 16 had squamous cell carcinoma (IR 0.1). Two treatment-emergent melanoma events were identified; neither were classified as serious AEs. Incidence of skin neoplasms in patients with psoriasis treated with ixekizumab for ≤ 5 years was low, and among those events, NMSC was most common. Limitations included that longer exposure may be required to confirm risk of skin cancer and that the study exclusion criteria of several studies, which excluded patients with skin cancer events within 5 years prior to baseline, might limit interpretation of skin cancer risk in this cohort. These findings support the safety profile of ixekizumab for patients requiring long-term psoriasis control. The online version contains supplementary material available at 10.1007/s13555-023-00966-4.