|Efficacy and Safety of Ustekinumab in Chinese Patients With Moderate to Severe Plaque-type Psoriasis: Results From a Phase 3 Clinical Trial (LOTUS)|
|Zhu, Xuejun1; Zheng, Min2; Song, Michael3; Shen, Yaung-Kaung4; Chan, Daphne3; Szapary, Philippe O.3; Wang, Baoxi5; LOTUS Investigators|
|刊名||JOURNAL OF DRUGS IN DERMATOLOGY|
|WOS标题词||Science & Technology|
|关键词[WOS]||PLACEBO-CONTROLLED TRIAL ; TO-SEVERE PSORIASIS ; INTERLEUKIN-12/23 MONOCLONAL-ANTIBODY ; LATENT TUBERCULOSIS INFECTION ; DOUBLE-BLIND TRIAL ; HAN POPULATION ; FOLLOW-UP ; THERAPY ; POLYMORPHISMS ; MULTICENTER|
Background: Available biologic agents for the treatment of psoriasis in China are limited.
Objectives: The LOTUS study is a phase 3, double-blind, placebo-controlled study that evaluated the efficacy and safety of ustekinumab in Chinese patients with moderate to severe plaque-type psoriasis.
Patients and Methods: Patients (n=322) were randomized to receive ustekinumab 45 mg or placebo at weeks 0 and 4, with placebo crossover to ustekinumab at week 12; all patients were followed up to week 36. The primary end point was the proportion of patients achieving at least a 75% improvement in the Psoriasis Area and Severity Index (PASI 75) at week 12. Other end points at week 12 included the proportion of patients with a Physician′s Global Assessment (PGA) score of 0 or 1 and the change in Dermatology Life Quality Index (DLQI) score from baseline.
Results: At week 12, 82.5% of ustekinumab-treated patients achieved PASI 75 responses compared with 11.1% of placebo-treated patients (P<.001). Clinical responses were maintained through week 28, with maximum responses observed at week 24. Significant improvements in PGA and DLQI were observed at week 12 and were generally maintained through week 28. At week 12, adverse events rates were similar between groups (45 mg: 42.5% vs placebo: 38.5%), and serious adverse events were reported in 0.6% of patients in each group. Through week 36, no cases of active tuberculosis, serious infections, malignancies, or major adverse cardiovascular events were reported.
Conclusions: Consistent with results previously reported in global phase 3 studies, ustekinumab was highly effective and generally well tolerated in Chinese patients with moderate to severe psoriasis through 36 weeks. J Drugs Dermatol. 2013;12(2):166-174.
|作者单位||1.Peking Univ, Hosp 1, Dept Dermatol & Venerol, Beijing 100871, Peoples R China|
2.Zhejiang Univ, Sch Med, Affiliated Hosp 2, Dept Dermatol & Venerol, Hangzhou 310003, Zhejiang, Peoples R China
3.Janssen Res & Dev LLC, Dept Immunol, Spring House, PA USA
4.Janssen Res & Dev LLC, Dept Biostat, Spring House, PA USA
5.Chinese Acad Med Sci, Inst Dermatol, Nanjing, Jiangsu, Peoples R China
|Zhu, Xuejun,Zheng, Min,Song, Michael,et al. Efficacy and Safety of Ustekinumab in Chinese Patients With Moderate to Severe Plaque-type Psoriasis: Results From a Phase 3 Clinical Trial (LOTUS)[J]. JOURNAL OF DRUGS IN DERMATOLOGY,2013,12(2):166-174.|
|APA||Zhu, Xuejun.,Zheng, Min.,Song, Michael.,Shen, Yaung-Kaung.,Chan, Daphne.,...&LOTUS Investigators.(2013).Efficacy and Safety of Ustekinumab in Chinese Patients With Moderate to Severe Plaque-type Psoriasis: Results From a Phase 3 Clinical Trial (LOTUS).JOURNAL OF DRUGS IN DERMATOLOGY,12(2),166-174.|
|MLA||Zhu, Xuejun,et al."Efficacy and Safety of Ustekinumab in Chinese Patients With Moderate to Severe Plaque-type Psoriasis: Results From a Phase 3 Clinical Trial (LOTUS)".JOURNAL OF DRUGS IN DERMATOLOGY 12.2(2013):166-174.|