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

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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.

In: DERMATOLOGY THER, Vol. 13, No. 8, 08.2023, p. 1773-1787.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Smith, SD, Stratigos, A, Augustin, M, Carrascosa, JM, Grond, S, Riedl, E, Xu, W, Patel, H & Lebwohl, M 2023, 'Integrated Safety Analysis on Skin Cancers among Patients with Psoriasis Receiving Ixekizumab in Clinical Trials', DERMATOLOGY THER, vol. 13, no. 8, pp. 1773-1787. https://doi.org/10.1007/s13555-023-00966-4

APA

Smith, S. D., Stratigos, A., Augustin, M., Carrascosa, J. M., Grond, S., Riedl, E., Xu, W., Patel, H., & Lebwohl, M. (2023). Integrated Safety Analysis on Skin Cancers among Patients with Psoriasis Receiving Ixekizumab in Clinical Trials. DERMATOLOGY THER, 13(8), 1773-1787. https://doi.org/10.1007/s13555-023-00966-4

Vancouver

Bibtex

@article{475ea614f4f748a1bc111d127e9bdf1a,
title = "Integrated Safety Analysis on Skin Cancers among Patients with Psoriasis Receiving Ixekizumab in Clinical Trials",
abstract = "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.",
author = "Smith, {Saxon D} and Alexandros Stratigos and Matthias Augustin and Carrascosa, {Jose Manuel} and Susanne Grond and Elisabeth Riedl and Wen Xu and Himanshu Patel and Mark Lebwohl",
note = "{\textcopyright} 2023. The Author(s).",
year = "2023",
month = aug,
doi = "10.1007/s13555-023-00966-4",
language = "English",
volume = "13",
pages = "1773--1787",
journal = "DERMATOLOGY THER",
issn = "2193-8210",
publisher = "Springer",
number = "8",

}

RIS

TY - JOUR

T1 - Integrated Safety Analysis on Skin Cancers among Patients with Psoriasis Receiving Ixekizumab in Clinical Trials

AU - Smith, Saxon D

AU - Stratigos, Alexandros

AU - Augustin, Matthias

AU - Carrascosa, Jose Manuel

AU - Grond, Susanne

AU - Riedl, Elisabeth

AU - Xu, Wen

AU - Patel, Himanshu

AU - Lebwohl, Mark

N1 - © 2023. The Author(s).

PY - 2023/8

Y1 - 2023/8

N2 - 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.

AB - 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.

U2 - 10.1007/s13555-023-00966-4

DO - 10.1007/s13555-023-00966-4

M3 - SCORING: Journal article

C2 - 37351831

VL - 13

SP - 1773

EP - 1787

JO - DERMATOLOGY THER

JF - DERMATOLOGY THER

SN - 2193-8210

IS - 8

ER -