Gerber W, Arheilger B, Ha T A, Hermann J, Ockenfels H M
Department of Dermatology and Allergy, Klinikum Stadt Hanau, Leimenstrasse 20, 63450 Hanau, Germany.
Br J Dermatol. 2003 Dec;149(6):1250-8. doi: 10.1111/j.1365-2133.2003.05709.x.
Excimer laser-derived 308-nm ultraviolet (UV) B therapy is a new alternative for treating psoriasis by phototherapy. Some studies have been made showing the effectiveness of intralesional phototherapy technology in treating psoriasis. However, there has been no information available so far with regard to the cumulative dosage on a larger group of patients and on therapy optimized treatment strategies.
One hundred and twenty psoriatic patients were treated according to standard protocol to define the effectiveness. Our aim was to develop new parameters and determine whether effectiveness could be improved and whether treatment exposure, the cumulative UVB dose and adverse effects could be minimized.
Initially, the excimer laser's effectiveness in treating psoriasis was evaluated in an open prospective study according to standard protocol. This included 120 adult patients (67 female/53 male) with chronic plaque psoriasis and < 20% involved body surface. The initial dose was based on three multiples of a predetermined minimal erythema dose (MED). Patients were treated twice a week for the first 3 weeks, then once a week until clearance was achieved. The main parameters were the initial starting dose, psoriasis area and severity index (PASI), the number of treatments needed, the time in treatment and the cumulative dose needed to clear psoriatic plaques. Thereafter, 43 patients were treated as a second comparable group. Therapy began with a starter dose, defined as MED-I. MED-I was defined as a UVB 308-nm dose which provoked a visible increase in erythema after 24 h. In addition, the epidermal thickness of the plaques was measured on an individual basis by 20-MHz ultrasound and correlated to the MED-I.
Of the patients who met the standard protocol, 65.7% were at least 90% clear after a maximum of 10 treatments; an even greater number (85.3%) showed a > or = 90% improvement in PASI after 13 sessions, while 14.7% of patients had only a < or = 50% PASI improvement. The cumulative UVB dose was 11.25 +/- 4.21 J cm-2 and the average treatment time was 7.2 weeks. Patients treated individually with the MED-I starter dose showed nearly identical rates of clearance (83.7%), but were clear in 7.07 +/- 2.15 sessions with a cumulative dose of 6.25 +/- 4.02 J cm-2.
The majority of our patients benefited greatly from laser-derived 308-nm UVB therapy, which cleared skin lesions faster than conventional phototherapy. As this therapy targets only the involved skin, the thickness of the plaques and individual MED-I should determine the initial dose, thus increasing the effectiveness of the therapy. We propose that light therapy sparing uninvolved skin will become predominant in the future.
准分子激光产生的308纳米紫外线(UV)B疗法是一种通过光疗治疗银屑病的新方法。一些研究表明皮损内光疗技术治疗银屑病有效。然而,目前尚无关于更大规模患者群体的累积剂量以及优化治疗策略的相关信息。
按照标准方案对120例银屑病患者进行治疗以确定其有效性。我们的目的是制定新参数,并确定是否可以提高有效性,以及是否可以将治疗暴露、UVB累积剂量和不良反应降至最低。
最初,根据标准方案在一项开放性前瞻性研究中评估准分子激光治疗银屑病的有效性。这包括120例成年慢性斑块状银屑病患者(67例女性/53例男性),体表面积受累小于20%。初始剂量基于预定最小红斑量(MED)的三倍。患者在最初3周每周治疗两次,然后每周治疗一次直至皮损清除。主要参数包括初始起始剂量、银屑病面积和严重程度指数(PASI)、所需治疗次数、治疗时间以及清除银屑病斑块所需的累积剂量。此后,将43例患者作为第二个可比组进行治疗。治疗从起始剂量开始,定义为MED-I。MED-I定义为在24小时后引起可见红斑增加的308纳米UVB剂量。此外,通过20兆赫超声单独测量斑块的表皮厚度,并将其与MED-I相关联。
符合标准方案的患者中,65.7%在最多10次治疗后至少90%清除;更多患者(85.3%)在13次治疗后PASI改善≥90%,而14.7%的患者PASI改善≤50%。UVB累积剂量为11.25±4.21焦/平方厘米,平均治疗时间为7.2周。采用MED-I起始剂量单独治疗的患者清除率几乎相同(83.7%),但在7.07±2.15次治疗后清除,累积剂量为6.