Malignancy rates through 5 years of follow-up in patients with moderate-to-severe psoriasis treated with guselkumab: Pooled results from the VOYAGE 1 and VOYAGE 2 trials

被引:13
作者
Blauvelt, Andrew [9 ,10 ]
Lebwohl, Mark [1 ]
Langley, Richard G. [2 ]
Rowland, Katelyn [3 ]
Yang, Ya-Wen [4 ]
Chan, Daphne [3 ]
Miller, Megan [5 ]
You, Yin [5 ]
Yu, Jenny [5 ]
Thaci, Diamant [6 ]
Foley, Peter [7 ]
Papp, Kim A. [8 ]
机构
[1] Oregon Med Res Ctr, Portland, OR USA
[2] Icahn Sch Med Mt Sinai, Dept Dermatol, New York, NY USA
[3] Dalhousie Univ, Div Clin Dermatol & Cutaneous Sci, Halifax, NS, Canada
[4] Janssen Sci Affairs LLC, Dept Immunol, Horsham, PA USA
[5] Janssen Pharmaceut Co Johnson & Johnson, Immunol Global Med Affairs, Horsham, PA USA
[6] Janssen Res & Dev LLC, Spring House, PA USA
[7] Univ Lubeck, Comprehens Ctr Inflammatory Med, Lubeck, Germany
[8] Univ Melbourne, St Vincents Hosp Melbourne, Dept Med, Carlton, Vic, Australia
[9] Alliance Clin Trials & Prob Med Res, Waterloo, ON, Canada
[10] Oregon Med Res Ctr, 9495 SW Locust St, Suite G, Portland, OR 97223 USA
关键词
guselkumab; malignancy; nonmelanoma skin cancer; psoriasis; safety; tumor; SKIN-CANCER; LONGITUDINAL ASSESSMENT; RISK; IL-23; SAFETY; USTEKINUMAB; POPULATION; COHORT;
D O I
10.1016/j.jaad.2023.03.035
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Malignancy risk surveillance among patients receiving long-term immunomodulatory psoriasis treatments remains an important safety objective.Objective: To report malignancy rates in patients with moderate-to-severe psoriasis treated with guselkumab for up to 5 years versus general and psoriasis patient populations.Methods: Cumulative rates of malignancies/100 patient-years (PY) were evaluated in 1721 guselkumab-treated patients from VOYAGE 1 and 2. Malignancy rates (excluding nonmelanoma skin cancer [NMSC]) were compared with rates in the Psoriasis Longitudinal Assessment and Registry. Standardized incidence ratios comparing malignancy rates (excluding NMSC and cervical cancer in situ) between guselkumab-treated patients and the general US population using Surveillance, Epidemiology, and End Results data were calculated, adjusting for age, sex, and race.Results: Of 1721 guselkumab-treated patients ([7100 PY), 24 had NMSC (0.34/100PY; basal:squamous cell carcinoma ratio, 2.2:1), and 32 had malignancies excluding NMSC (0.45/100PY). For comparison, the malignancy rate excluding NMSC was 0.68/100PY in the Psoriasis Longitudinal Assessment and Registry. Malignancy rates (excluding NMSC/cervical cancer in situ) in guselkumab-treated patients were consistent with those expected in the general US population (standardized incidence ratio = 0.93).Limitations: Inherent imprecision in determining malignancy rates. Conclusions: In patients treated with guselkumab for up to 5 years, malignancy rates were low and generally consistent with rates in general and psoriasis patient populations. ( J Am Acad Dermatol 2023
引用
收藏
页码:274 / 282
页数:9
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