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

INTRODUCTION: 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. METHODS: Integrated safety databases from 17 clinical trials o...

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Autores principales: Smith, Saxon D., Stratigos, Alexandros, Augustin, Matthias, Carrascosa, Jose Manuel, Grond, Susanne, Riedl, Elisabeth, Xu, Wen, Patel, Himanshu, Lebwohl, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Healthcare 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10366039/
https://www.ncbi.nlm.nih.gov/pubmed/37351831
http://dx.doi.org/10.1007/s13555-023-00966-4
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author Smith, Saxon D.
Stratigos, Alexandros
Augustin, Matthias
Carrascosa, Jose Manuel
Grond, Susanne
Riedl, Elisabeth
Xu, Wen
Patel, Himanshu
Lebwohl, Mark
author_facet Smith, Saxon D.
Stratigos, Alexandros
Augustin, Matthias
Carrascosa, Jose Manuel
Grond, Susanne
Riedl, Elisabeth
Xu, Wen
Patel, Himanshu
Lebwohl, Mark
author_sort Smith, Saxon D.
collection PubMed
description INTRODUCTION: 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. METHODS: 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. RESULTS: 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. CONCLUSIONS: 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s13555-023-00966-4.
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spelling pubmed-103660392023-07-26 Integrated Safety Analysis on Skin Cancers among Patients with Psoriasis Receiving Ixekizumab in Clinical Trials Smith, Saxon D. Stratigos, Alexandros Augustin, Matthias Carrascosa, Jose Manuel Grond, Susanne Riedl, Elisabeth Xu, Wen Patel, Himanshu Lebwohl, Mark Dermatol Ther (Heidelb) Original Research INTRODUCTION: 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. METHODS: 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. RESULTS: 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. CONCLUSIONS: 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. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s13555-023-00966-4. Springer Healthcare 2023-06-23 /pmc/articles/PMC10366039/ /pubmed/37351831 http://dx.doi.org/10.1007/s13555-023-00966-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by-nc/4.0/Open Access This article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Original Research
Smith, Saxon D.
Stratigos, Alexandros
Augustin, Matthias
Carrascosa, Jose Manuel
Grond, Susanne
Riedl, Elisabeth
Xu, Wen
Patel, Himanshu
Lebwohl, Mark
Integrated Safety Analysis on Skin Cancers among Patients with Psoriasis Receiving Ixekizumab in Clinical Trials
title Integrated Safety Analysis on Skin Cancers among Patients with Psoriasis Receiving Ixekizumab in Clinical Trials
title_full Integrated Safety Analysis on Skin Cancers among Patients with Psoriasis Receiving Ixekizumab in Clinical Trials
title_fullStr Integrated Safety Analysis on Skin Cancers among Patients with Psoriasis Receiving Ixekizumab in Clinical Trials
title_full_unstemmed Integrated Safety Analysis on Skin Cancers among Patients with Psoriasis Receiving Ixekizumab in Clinical Trials
title_short Integrated Safety Analysis on Skin Cancers among Patients with Psoriasis Receiving Ixekizumab in Clinical Trials
title_sort integrated safety analysis on skin cancers among patients with psoriasis receiving ixekizumab in clinical trials
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10366039/
https://www.ncbi.nlm.nih.gov/pubmed/37351831
http://dx.doi.org/10.1007/s13555-023-00966-4
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