Safety Surveillance for Ustekinumab and Other Psoriasis Treatments From the Psoriasis Longitudinal Assessment and Registry (PSOLAR)

被引:4
作者
Papp, Kim [1 ]
Gottlieb, Alice B. [2 ]
Naldi, Luigi [3 ]
Pariser, David [4 ,5 ]
Ho, Vincent [6 ]
Goyal, Kavitha [7 ]
Fakharzadeh, Steven [7 ]
Chevrier, Marc [8 ]
Calabro, Stephen [7 ]
Langholff, Wayne [8 ]
Krueger, Gerald [9 ]
机构
[1] Prob Research, Waterloo, ON, Canada
[2] Tufts Med Ctr, Boston, MA USA
[3] Azienda Ospeda Papa Giovanni XXIII, Ctr Studi Grp Italiano Studi Epidemiol Dermatol G, Bergamo, Italy
[4] Eastern Virginia Med Sch, Norfolk, VA 23501 USA
[5] Virginia Clin Res Inc, Norfolk, VA USA
[6] Univ British Columbia, Vancouver, BC V5Z 1M9, Canada
[7] LLC, Janssen Sci Affairs, Horsham, PA USA
[8] LLC, Janssen Res & Dev, Horsham, PA USA
[9] Univ Utah, Hlth Sci Ctr, Salt Lake City, UT USA
关键词
LONG-TERM SAFETY; INTERLEUKIN-12/23; MONOCLONAL-ANTIBODY; DISEASE-BASED REGISTRY; DOUBLE-BLIND; CARDIOVASCULAR EVENTS; PLAQUE PSORIASIS; EFFICACY; MODERATE; THERAPY; MULTICENTER;
D O I
暂无
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: Safety surveillance is needed for biologic therapies for psoriasis. Objective: To assess the risk of adverse events of special interest (AEoSIs) with ustekinumab and other psoriasis treatments in a real-world setting using 2014 Psoriasis Longitudinal Assessment and Registry (PSOLAR) data. AEoSIs included malignancy (excluding nonmelanoma skin cancer), major adverse cardiovascular events (MACE), serious infection, and all-cause mortality. Methods: Cumulative rates of AEoSIs/100 patient-years (PY) are reported for ustekinumab, infliximab, other biologics (mostly adalimumab/etanercept), and non-biologics based on pre-specified analyses using attribution rules biased against ustekinumab. Risk factors for AEoSIs, including treatments, were determined using multivariate statistical analysis. Results: A total of 12,093 patients (40,388 PY) were enrolled in PSOLAR. Overall incidence rates were 0.68/100PY for malignancy, 0.33/100PY for MACE, 1.60/100PY for serious infection, and 0.46/100PY for mortality. Unadjusted rates of serious infection for infliximab (2.91/100PY) and other biologics (1.91/100PY) were numerically higher compared with ustekinumab (0.93/100PY). Exposure to the combined group of biologics other than ustekinumab was significantly associated with serious infection (hazard ratio=1.96, P<.001). None of the biologics was associated with increased risk of malignancy, MACE, or mortality. Limitations: Observational data have inherent biases. Conclusion: Analysis of 2014 PSOLAR data identified no increased risk of malignancy, MACE, serious infection, or mortality with ustekinumab.
引用
收藏
页码:58 / 66
页数:9
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