Treatment outcomes of secukinumab in adult patients with moderate-to-severe plaque psoriasis in China: A real-world multicenter retrospective study

被引:3
作者
Ding, Yangfeng [1 ]
Li, Wei [2 ,3 ]
Guan, Xin [4 ]
Liu, Na [5 ]
Zhou, Ying [6 ]
Li, Gaojie [2 ,3 ]
Wang, Xiaohua [7 ]
Wang, Zhidong [8 ]
Xiao, Xiao [8 ]
Yang, Bin [9 ]
Lv, Chengzhi [6 ,10 ]
Zhang, Chunlei [4 ,11 ]
Shi, Yuling [1 ,12 ]
机构
[1] Tongji Univ, Sch Med, Shanghai Skin Dis Hosp, Dept Dermatol, Shanghai, Peoples R China
[2] Sichuan Univ, Dept Dermatol, West China Hosp, 37 Guoxue Alley, Chengdu, Peoples R China
[3] Sichuan Univ, West China Hosp, Rare Dis Ctr, 37 Guoxue Alley, Chengdu, Peoples R China
[4] Peking Univ Third Hosp, Beijing, Peoples R China
[5] Shanghai Sixth Peoples Hosp, Shanghai, Peoples R China
[6] Dalian Dermatol Hosp, Dalian, Peoples R China
[7] Southern Med Univ, Dermatol Hosp, Guangzhou, Peoples R China
[8] Beijing Novartis Pharma Co Ltd, Beijing, Peoples R China
[9] Southern Med Univ, Dermatol Hosp, 2 Lujing Rd, Guangzhou 510091, Peoples R China
[10] Dalian Dermatol Hosp, 788 Changjiang Rd Shahekou Dist, Dalian, Peoples R China
[11] Peking Univ Third Hosp, Huayuan North Rd 49, Beijing, Peoples R China
[12] Tongji Univ, Shanghai Skin Dis Hosp, Sch Med, Dept Dermatol, 1278 Baode St, Shanghai 200443, Peoples R China
来源
CTS-CLINICAL AND TRANSLATIONAL SCIENCE | 2023年 / 16卷 / 10期
关键词
QUALITY-OF-LIFE; SAFETY; INDEX; EFFICACY; AREA; VULGARIS; DECISION;
D O I
10.1111/cts.13583
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Secukinumab is effective in treating patients with moderate-to-severe plaque psoriasis. However, most studies assessing its effectiveness in routine clinical settings in China are mostly single-center studies with a limited sample size. The objective of this study was to assess secukinumab's efficacy, treatment patterns, and characteristics in patients with moderate-to-severe plaque psoriasis. This 24-week, multicenter (n = 5) retrospective study analyzed the data of Chinese adult patients with moderate-to-severe plaque psoriasis who initiated secukinumab treatment between May 2019 and March 2020. The Psoriasis Area and Severity Index (PASI), body surface area (BSA), Investigator's Global Assessment Modified 2011 (IGA mod 2011), and Dermatology Life Quality Index (DLQI) were assessed. Dermatologists documented the treatment dosage and modification reasons. Of the 244 secukinumab-naive patients, most were men (73.4%, 179/244) and weighed 60-90 kg (72.8%, 177/243). The mean (SD) age at secukinumab initiation was 38.1 (11.6) years, and the disease duration was 13.5 (7.9) years. Most patients (97.1%, 237/244) received secukinumab 300 mg. At weeks 4, 12, 16, and 24, the proportion of patients achieving PASI 75 = 75% reduction from baseline) was 40.0%, 92.1%, 88.4%, and 88.9%, respectively; PASI 90 was 15.0%, 73.7%, 81.4%, and 68.3%, respectively; and PASI 100 was 8.7%, 40.8%, 58.1%, and 41.3%, respectively. During the same periods, BSA and IGA mod 2011 showed similar improvement trends. An increasing proportion of patients achieved DLQI of 0-1 (21.6%, 65.7%, 75.0%, and 80.3%, respectively). Treatment modification was highest at week 12. The average interval between two administrations after week 4 was 62.95 days. Secukinumab was highly effective in improving the PASI, IGA, BSA, and DLQI in Chinese patients with moderate-to-severe plaque psoriasis throughout the first 24 weeks. The treatment pattern for Chinese patients differs from that in the clinical guidelines.
引用
收藏
页码:1803 / 1814
页数:12
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