Real-World Effectiveness of Dupilumab in Atopic Dermatitis Patients: Analysis of an Electronic Medical Records Dataset

被引:7
作者
Eichenfield, Lawrence F. [1 ,2 ]
Armstrong, April [3 ]
Guttman-Yassky, Emma [4 ]
Lio, Peter A. [5 ]
Chen, Chi-Chang
Hines, Dionne M.
McGuiness, Catherine B.
Ganguli, Sohini [6 ]
Delevry, Dimittri [7 ]
Sierka, Debra [6 ]
Mallya, Usha G. [6 ]
机构
[1] Univ Calif San Diego, Sch Med, Dept Dermatol, 3020 Childrens Way,Mail Code 5092, San Diego, CA 92123 USA
[2] Univ Calif San Diego, Sch Med, Dept Pediat, 3020 Childrens Way,Mail Code 5092, San Diego, CA 92123 USA
[3] Univ Southern Calif, Dept Dermatol, Keck Sch Med, Los Angeles, CA 90007 USA
[4] Mt Sinai Hlth Syst, New York, NY USA
[5] Northwestern Univ, Chicago, IL 60611 USA
[6] Sanofi, Cambridge, MA USA
[7] Regeneron Pharmaceut Inc, 777 Old Saw Mill River Rd, Tarrytown, NY 10591 USA
关键词
Atopic dermatitis; Dupilumab; Real-world effectiveness; Itch; Body surface area affected; Investigator global assessment; ADULT PATIENTS; MODERATE; PLACEBO; SAFETY; EFFICACY; IMPROVES; TRIALS;
D O I
10.1007/s13555-022-00731-z
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Introduction While the efficacy of dupilumab for the treatment of adults with moderate-to-severe atopic dermatitis (AD) has been demonstrated in several clinical trials, patients in such trials may not necessarily reflect the real-world clinical practice setting. This study evaluated the real-world effectiveness of dupilumab in adults with moderate-to-severe AD based on physician global assessment, percent body surface area affected, and patient-reported itch. Methods From Modernizing Medicine's Electronic Medical Assistant dermatology-specific electronic medical records, adults (>= 18 years) were identified with a diagnosis of AD and >= 1 dupilumab prescription (index event) between 1 April 2017 and 31 January 2019. Three cohorts were identified based on 3-month pre-index (1) Investigator Global Assessment (IGA) score >= 3, (2) an itch severity numerical rating scale (NRS) score >= 3, and (3) body surface area (BSA) affected >= 10%. Changes from pre-index on the outcome within each cohort were evaluated at 4 months post-index. Patients were also stratified for evaluation of outcomes by baseline demographic (sex, age) and prior AD treatments (topical therapy only or no treatment, any systemic therapy). Results More than 70% of the 435 AD patients with baseline IGA score >= 3 improved to an IGA score of <= 2 at month 4 post-dupilumab initiation, including 42.8% who achieved IGA 0/1 (clear/minimal). Among 112 patients with a pre-index itch severity NRS >= 3, scores were reduced from mean (SD) 7.0 (2.4) pre-index to 2.8 (2.8) at month 4 (p < 0.0001); 70.5% of patients had a reduction >= 3 points. In the BSA cohort (n = 387), affected BSA was significantly reduced from a pre-index mean (SD) of 39.3% (26.1%) to 16.3% (21.2%) at month 4 (p < 0.0001). Significant improvements in IGA, itch NRS, and BSA were observed regardless of demographic (age and sex) or clinical characteristics such as treatment history (all p < 0.0001 compared with pre-index). Conclusions Consistent with outcomes observed in clinical trials, patients treated with dupilumab in real-world clinical settings achieved clinically meaningful improvements in severity and extent of AD and severity of itch comparable to those reported in clinical trials at a similar time point.
引用
收藏
页码:1337 / 1350
页数:14
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