Department of Dermatology, St George Hospital, University of New South Wales Faculty of Medicine, Sydney, NSW, Australia.
2nd Dermatology Department, Aristotle University Faculty of Medicine, Papageorgiou General Hospital, Thessaloniki, Greece.
Br J Dermatol. 2021 Oct;185(4):745-755. doi: 10.1111/bjd.20431. Epub 2021 Jun 15.
Bruton tyrosine kinase (BTK) inhibition targets B-cell and other non-T-cell immune cells implicated in the pathophysiology of pemphigus, an autoimmune disease driven by anti-desmoglein autoantibodies. Rilzabrutinib is a new reversible, covalent BTK inhibitor demonstrating preclinical efficacy as monotherapy in canine pemphigus foliaceus.
To evaluate the efficacy and safety of oral rilzabrutinib in patients with pemphigus vulgaris in a multicentre, proof-of-concept, phase II trial.
Patients with Pemphigus Disease Area Index severity scores 8-45 received 12 weeks of oral rilzabrutinib 400-600 mg twice daily and 12 weeks of follow-up. Patients initially received between 0 and ≤ 0·5 mg kg prednisone-equivalent corticosteroid (CS; i.e. 'low dose'), tapered after control of disease activity (CDA; no new lesions, existing lesions healing). The primary endpoints were CDA within 4 weeks on zero-to-low-dose CS and safety.
In total, 27 patients with pemphigus vulgaris were included: nine newly diagnosed (33%) and 18 relapsing (67%); 11 had moderate disease (41%) and 16 moderate to severe (59%). The primary endpoint, CDA, was achieved in 14 patients (52%, 95% confidence interval 32-71): 11 using low-dose CS and three using no CS. Over 12 weeks of treatment, mean CS doses reduced from 20·0 to 11·8 mg per day for newly diagnosed patients and from 10·3 to 7·8 mg per day for relapsing patients. Six patients (22%) achieved complete response by week 24, including four (15%) by week 12. Treatment-related adverse events were mostly mild (grade 1 or 2); one patient experienced grade 3 cellulitis.
Rilzabrutinib alone, or with much lower CS doses than usual, was safe, with rapid clinical activity in pemphigus vulgaris. These data suggest that BTK inhibition may be a promising treatment strategy and support further investigation of rilzabrutinib for the treatment of pemphigus.
布鲁顿酪氨酸激酶(BTK)抑制剂可靶向参与天疱疮病理生理学的 B 细胞和其他非 T 细胞免疫细胞,天疱疮是一种由抗桥粒芯糖蛋白自身抗体驱动的自身免疫性疾病。利扎鲁单抗是一种新型可逆、共价 BTK 抑制剂,在犬类落叶型天疱疮的临床前研究中显示出单药治疗的疗效。
在一项多中心、概念验证、II 期试验中,评估口服利扎鲁单抗治疗寻常型天疱疮患者的疗效和安全性。
Pemphigus Disease Area Index 严重程度评分为 8-45 的患者接受为期 12 周的口服利扎鲁单抗 400-600mg 每日两次治疗和 12 周的随访。患者最初接受 0-≤0.5mg·kg 泼尼松等效皮质类固醇(CS;即“低剂量”)治疗,在疾病活动控制后(无新皮损,现有皮损愈合)逐渐减量。主要终点是在 0-低剂量 CS 治疗的 4 周内达到疾病控制和安全性。
共有 27 例寻常型天疱疮患者入组:初诊 9 例(33%),复发 18 例(67%);11 例为中度疾病(41%),16 例为中重度疾病(59%)。主要终点,即疾病控制,在 14 例患者(52%,95%置信区间 32-71%)中达到:11 例患者使用低剂量 CS,3 例患者未使用 CS。在 12 周的治疗过程中,新发患者的 CS 剂量从 20.0mg 减少到 11.8mg/天,复发患者的 CS 剂量从 10.3mg 减少到 7.8mg/天。6 例患者(22%)在 24 周时达到完全缓解,其中 4 例(15%)在 12 周时达到完全缓解。治疗相关不良事件大多为轻度(1 级或 2 级);1 例患者发生 3 级蜂窝织炎。
利扎鲁单抗单独使用,或与通常低得多的 CS 剂量联合使用,是安全的,在寻常型天疱疮中具有快速的临床疗效。这些数据表明 BTK 抑制可能是一种有前途的治疗策略,并支持进一步研究利扎鲁单抗治疗天疱疮。