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Integrated Safety Analysis on Skin Cancers among Patients with Psoriasis Receiving Ixekizumab in Clinical Trials
被引:4
|作者:
Smith, Saxon D.
[1
]
Stratigos, Alexandros
[2
]
Augustin, Matthias
[3
]
Carrascosa, Jose Manuel
[4
]
Grond, Susanne
[5
]
Riedl, Elisabeth
[6
]
Xu, Wen
[5
]
Patel, Himanshu
[5
]
Lebwohl, Mark
[7
]
机构:
[1] Australian Natl Univ, ANU Coll Hlth & Med, ANU Med Sch, Canberra, ACT, Australia
[2] Univ Athens, Andreas Sygros Hosp, Sch Med, Dept Dermatol, Athens, Greece
[3] Univ Med Ctr Hamburg Eppendorf, Inst Hlth Serv Res Dermatol & Nursing, Hamburg, Germany
[4] Univ Autonoma Barcelona, Hosp Univ Germans Trias I Pujol, Dept Dermatol, IGTP, Badalona, Spain
[5] Eli Lilly & Co, Indianapolis, IN USA
[6] Med Univ Vienna, Dept Dermatol, Vienna, Austria
[7] Mt Sinai Hosp, Dept Dermatol, New York, NY USA
关键词:
Ixekizumab;
Long-term;
Malignancy;
Melanoma;
Non-melanoma skin cancer;
Psoriasis;
Safety;
Skin cancer;
Skin neoplasm;
LONG-TERM SAFETY;
SEVERE PLAQUE PSORIASIS;
SQUAMOUS-CELL;
OPEN-LABEL;
MODERATE;
RISK;
INTERLEUKIN-17;
IL-17;
USTEKINUMAB;
ETANERCEPT;
D O I:
10.1007/s13555-023-00966-4
中图分类号:
R75 [皮肤病学与性病学];
学科分类号:
100206 ;
摘要:
IntroductionLimited 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.MethodsIntegrated safety databases from 17 clinical trials of adults with moderate-to-severe psoriasis treated with & GE; 1 dose of ixekizumab for & LE; 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.ResultsOf 6892 patients, 58 presented with & GE; 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.ConclusionsIncidence of skin neoplasms in patients with psoriasis treated with ixekizumab for & LE; 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.
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页码:1773 / 1787
页数:15
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