Golda Nicholas, Benham Shahrad M, Koo John
Keck School of Medicine of the University of Southern California, Los Angeles, CA, USA.
J Drugs Dermatol. 2006 Jan;5(1):63-5.
Recently, the biologics have emerged as a new class of drugs for systemic therapy of psoriasis with efalizumab (Raptiva) being one of the most recently FDA-approved agents. We report a case of a 34-year-old Caucasian male who experienced psoriasis rebound during a 7-week lapse in treatment with subcutaneous efalizumab 0.8 mg/kg/week, which he had been using for 4 weeks up to that point. The patient then restarted efalizumab, but his psoriasis continued to worsen causing him to be admitted for Goeckerman day care. He rebounded again 4 weeks following his ultimate discontinuation of efaluzimab despite intensive therapy with the Goeckerman regimen. This case is reported to highlight the recent findings that psoriasis rebound, defined as psoriasis area and severity index (PASI) of 125% or greater or morphology change, has been associated with both the use and the discontinuation of efalizumab.
最近,生物制剂已成为一类用于银屑病全身治疗的新型药物,依法利珠单抗( Raptiva )是美国食品药品监督管理局(FDA)最近批准的药物之一。我们报告了一例34岁的白人男性病例,该患者在皮下注射依法利珠单抗0.8mg/kg/周治疗4周后,停药7周期间出现银屑病反弹。之后患者重新开始使用依法利珠单抗,但银屑病仍持续恶化,导致其因戈克曼日间护理入院。尽管采用戈克曼疗法进行了强化治疗,但在其最终停用依法利珠单抗4周后再次出现反弹。报告该病例是为了突出最近的研究发现,即银屑病反弹(定义为银屑病面积和严重程度指数(PASI)达到或超过125%或形态改变)与依法利珠单抗的使用和停用均有关联。