Utilization Trends and Impact of Secukinumab Treatment on Clinical Outcomes in Biologic-Naive Patients with Psoriasis in a US Real-World Setting

被引:5
|
作者
Strober, Bruce [1 ,2 ]
Patil, Dhaval [3 ]
McLean, Robert R. [4 ]
Moore-Clingenpeel, Melissa [4 ]
Guo, Ning [4 ]
Levi, Eugenia [3 ]
Lebwohl, Mark [5 ]
机构
[1] Yale Univ, New Haven, CT USA
[2] Cent Connecticut Dermatol Res, 1 Willowbrook Rd,Suite 2, Cromwell, CT 06416 USA
[3] Novartis Pharmaceut, E Hanover, NJ USA
[4] CorEvitas LLC, Waltham, MA USA
[5] Icahn Sch Med Mt Sinai, New York, NY 10029 USA
关键词
Effectiveness; Psoriasis; Registry; Secukinumab; PLAQUE PSORIASIS; NATIONAL PSORIASIS; MODERATE; EFFICACY; GUIDELINES; SEVERITY; SAFETY; CARE;
D O I
10.1007/s13555-022-00740-y
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Introduction Real-world evidence has demonstrated the effectiveness of secukinumab in the treatment of psoriasis; however, limited data are available on patient profiles of US secukinumab initiators over time and clinical outcomes in biologic-naive patients. This study describes clinical characteristics of secukinumab initiators by year, and the clinical outcomes in patients after 6- and/or 12-month follow-up visits, stratified by prior biologic use. Methods This observational study included patients enrolled in the CorEvitas (formerly Corrona) Psoriasis Registry. Analyses were conducted in two patient cohorts: (1) all secukinumab initiators, stratified by year, and (2) those who initiated and maintained secukinumab through a 6- and/or 12-month follow-up visit. For all secukinumab initiators, patient characteristics at initiation were described per calendar year; in initiators with follow-up visits, mean (SD) differences in percentage affected body surface area (BSA), five-point Investigator's Global Assessment (IGA), and Psoriasis Area and Severity Index (PASI) scores between baseline and follow-up visits were calculated. Analyses were conducted separately for biologic-naive and biologic-experienced patients. Results Between 2015 and 2020, the proportion of secukinumab initiators in the registry who were biologic-naive increased each year from 12.5% to 49.7%. Overall, 1518 patients initiated secukinumab at or after enrollment; 980 (64.6%) were biologic experienced, and 538 (35.4%) were biologic naive. At 6 months, biologic-experienced and biologic-naive patients reported mean (SD) decreases in BSA (-9.3 [14.5] versus -11.7 [16.6]), IGA (-1.4 [1.3] versus -1.7 [1.4]), and PASI (-5.2 [6.6] versus -6.7 [7.8]). The proportion of patients with an IGA score of clear/almost clear (0/1) increased over fivefold, irrespective of biologic experience. At 12 months, similar improvements were seen. Conclusions The proportion of biologic-naive secukinumab initiators increased over time. Biologic-naive patients demonstrated similar improvements in clinical outcomes compared with biologic-experienced patients, suggesting that secukinumab may be considered as a first-line therapy for psoriasis.
引用
收藏
页码:1351 / 1365
页数:15
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