Tada Yayoi, Sugiura Yukako, Kamishima Manami, Takahashi Shoya, Tanaka Yoshihito, Masuda Junya, Yamanaka Keiichi
Department of Dermatology, Teikyo University, Tokyo, Japan.
Medical Affairs Division, Johnson & Johnson, Tokyo, Japan.
J Dermatol. 2025 Jun;52(6):967-982. doi: 10.1111/1346-8138.17710. Epub 2025 Mar 29.
Guselkumab is a monoclonal antibody that binds to the p19 subunit of interleukin-23 and inhibits its downstream signaling. The safety profile of guselkumab and its superior efficacy over placebo and adalimumab for the treatment of patients with moderate-to-severe psoriasis were reported in phase 3 studies conducted within and outside Japan. To assess the real-world safety and effectiveness of guselkumab in Japanese patients with psoriasis, we conducted a multicenter, single-arm, prospective, post-marketing surveillance study. Guselkumab was administered by subcutaneous injection at a dose of 100 mg at weeks 0 and 4, then every following 8 weeks. The patient observation period was 52 weeks after the initial guselkumab dose or until treatment withdrawal. The safety analysis set consisted of 416 patients, including 310 patients with vulgaris (PsV); and the effectiveness analysis set consisted of 251 patients, including 236 patients with PsV or psoriatic arthritis (PsA). There were more men (71.3%, 221/310) than women among the PsV group. The median age among those with PsV was 58 years, the median disease duration was 11.50 years, 50.0% (155/310) had comorbidity, and 41.3% (128/310) had previously been treated with biologic agents. During the observation period, 8.4% (35/416) of patients experienced 49 adverse drug reactions, 2.9% (12/416) experienced 13 serious adverse drug reactions, and 3.4% (14/416) experienced 16 adverse events leading to treatment discontinuation. In the effectiveness analysis set of 236 patients with PsV or PsA, the Psoriasis Area and Severity Index (PASI) 75, 90, and 100 response rates at week 52 were 69.9%, 54.5%, and 32.5%, respectively. Bio-naïve patients consistently had higher PASI 75 and 90 response rates than bio-experienced patients. This post-marketing surveillance study demonstrated that guselkumab was well-tolerated and effective in a real-world setting in Japanese patients with psoriasis.
古塞库单抗是一种单克隆抗体,可与白细胞介素-23的p19亚基结合并抑制其下游信号传导。在日本国内外进行的3期研究中报告了古塞库单抗的安全性概况及其在治疗中重度银屑病患者方面优于安慰剂和阿达木单抗的疗效。为了评估古塞库单抗在日本银屑病患者中的实际安全性和有效性,我们开展了一项多中心、单臂、前瞻性上市后监测研究。古塞库单抗通过皮下注射给药,在第0周和第4周时剂量为100mg,之后每8周注射一次。患者观察期为首次注射古塞库单抗后的52周或直至停药。安全性分析集包括416例患者,其中包括310例寻常型银屑病(PsV)患者;有效性分析集包括251例患者,其中包括236例PsV或银屑病关节炎(PsA)患者。PsV组中男性(71.3%,221/310)多于女性。PsV患者的中位年龄为58岁,中位病程为11.50年,50.0%(155/310)有合并症,41.3%(128/310)曾接受过生物制剂治疗。在观察期内,8.4%(35/416)的患者发生了49例药物不良反应,2.9%(12/416)的患者发生了13例严重药物不良反应,3.4%(14/416)的患者发生了16例导致停药的不良事件。在236例PsV或PsA患者的有效性分析集中,第52周时银屑病面积和严重程度指数(PASI)改善75%、90%和100%的缓解率分别为69.9%、54.5%和32.5%。初治患者的PASI改善75%和90%的缓解率始终高于经治患者。这项上市后监测研究表明,在日本银屑病患者的实际临床环境中,古塞库单抗耐受性良好且有效。