Stein Gold Linda, Bagel Jerry, Lebwohl Mark, Lin Tina, Martin Gina, Pillai Radhakrishnan
J Drugs Dermatol. 2018 Dec 1;17(12):1290-1296.
Background: A unique fixed combination halobetasol propionate 0.01% and tazarotene 0.045% (HP/TAZ) lotion has been shown to be effective in psoriasis using Investigator Global Assessment (IGA) tools to assess erythema, plaque elevation, and scaling. However, these do not consider changes in Body Surface Area (BSA). The IGAxBSA composite tool is a simple, effective, validated alternative for measuring improvement in psoriasis severity. It correlates well with the Psoriasis Area and Severity Index (PASI) and demonstrates sensitivity to changes from baseline in patients with both mild and moderately severe disease. Objective: To further define the role of a fixed combination halobetasol propionate 0.01% and tazarotene 0.045% (HP/TAZ) lotion in moderate-to-severe plaque psoriasis using the IGAxBSA composite tool. Methods: Post hoc analysis of 212 patients with moderate-to-severe plaque psoriasis randomized (2:2:2:1) to HP/TAZ lotion, HP, TAZ, or vehicle once-daily for 8 weeks, with a 4-week posttreatment follow-up. Efficacy assessments using the validated IGAxBSA composite tool. Results: HP/TAZ lotion demonstrated statistically significant superiority at week 8 (versus TAZ and vehicle) and week 12 (versus HP, TAZ, and vehicle). By week 8, HP/TAZ lotion achieved a 63.5% reduction in mean IGAxBSA composite score (P<0.001 versus TAZ and vehicle), that was sustained four weeks posttreatment (P<0.001 versus TAZ and vehicle and P=0.003 versus HP). A 25% and 50% improvement in IGAxBSA was achieved within 1.9 and 4.6 weeks, respectively, and 47.5% of patients achieved IGAxBSA-75 by week 8. Limitations: This post hoc analysis was limited to patients with moderate-to-severe plaque psoriasis with IGA ≥3 and BSA involvement (3%-12%). Conclusions: HP/TAZ lotion was associated with significant and rapid reductions in disease severity as assessed by the IGAxBSA composite tool. The addition of tazarotene affords sustained benefits posttreatment. J Drugs Dermatol. 2018;17(12):1290-1296.
一种独特的固定复方制剂,即0.01%丙酸氯倍他索与0.045%他扎罗汀(HP/TAZ)洗剂,已被证明在治疗银屑病方面有效,该研究使用研究者整体评估(IGA)工具来评估红斑、斑块隆起和脱屑情况。然而,这些评估未考虑体表面积(BSA)的变化。IGAxBSA综合工具是一种简单、有效的、经过验证的用于衡量银屑病严重程度改善情况的替代方法。它与银屑病面积和严重程度指数(PASI)相关性良好,并对轻度和中度严重疾病患者相对于基线的变化具有敏感性。目的:使用IGAxBSA综合工具进一步明确0.01%丙酸氯倍他索与0.045%他扎罗汀(HP/TAZ)固定复方洗剂在中度至重度斑块状银屑病中的作用。方法:对212例中度至重度斑块状银屑病患者进行事后分析,这些患者被随机(2:2:2:1)分为接受HP/TAZ洗剂、HP、TAZ或赋形剂治疗,每日一次,共8周,并在治疗后进行4周随访。使用经过验证的IGAxBSA综合工具进行疗效评估。结果:HP/TAZ洗剂在第8周(与TAZ和赋形剂相比)和第12周(与HP、TAZ和赋形剂相比)显示出统计学上的显著优势。到第8周时,HP/TAZ洗剂使平均IGAxBSA综合评分降低了63.5%(与TAZ和赋形剂相比,P<0.001),且在治疗后4周仍保持这一水平(与TAZ和赋形剂相比,P<0.001;与HP相比,P=0.003)。IGAxBSA分别在1.9周和4.6周内实现了25%和50%的改善,到第8周时,47.5%的患者实现了IGAxBSA - 75改善。局限性:该事后分析仅限于中度至重度斑块状银屑病、IGA≥3且有BSA受累(3% - 12%)的患者。结论:根据IGAxBSA综合工具评估,HP/TAZ洗剂可使疾病严重程度显著且迅速降低。添加他扎罗汀可在治疗后带来持续益处。《皮肤药物学杂志》。2018年;17(12):1290 - 1296。