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Long-term Follow up of Diclofenac Sodium 3 in 2.5 Hyaluronic Acid Gel for Actinic Keratosis: One-year Evaluation

机译:2.5%透明质酸凝胶中的3%双氯芬酸钠对光化性角化病的长期随访:一年评估

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摘要

>Objective: To evaluate the long-term effects of treatment with diclofenac sodium 3% in 2.5% hyaluronic acid gel on clinically diagnosed actinic keratosis lesions in well-defined skin areas. >Design: A one-year extension of a Phase 4, single-arm, multicenter, open-label study was conducted. Patients in the original study received diclofenac sodium 3% gel twice daily for 90 days. The extension study consisted of a single evaluation approximately one year post-treatment. >Setting: Five US centers. >Participants: Patients who had completed the initial treatment phase with no further treatment for actinic keratosis in the designated treatment blocks. >Measurements: The primary endpoint was the proportion of patients achieving 75-percent clearance of actinic keratosis lesions at one-year follow up based on percent change from baseline in target lesion number score or cumulative lesion number score. Secondary endpoints were the proportion of patients achieving 100-percent actinic keratosis lesion clearance and change in investigator’s global improvement index scores. >Results: Eighty-one percent of patients reported no additional treatment for actinic keratosis lesions for one year after completing treatment with diclofenac sodium 3% gel. The proportion of patients with 75-percent clearance after one year was 91 percent (95% CI, 84–99%) for target lesions and 70 percent (95% CI, 57–83%) for cumulative lesions. The proportion of patients with 100-percent clearance at one year was 79 percent (95% CI, 67–90%) for target lesions and 30 percent (95% CI, 17–43%) for cumulative lesions. Investigator’s global improvement index severity scores showed that the majority (96%) of patients improved from baseline after one year. >Conclusion: The efficacy of a single, 90-day course of diclofenac sodium 3% gel persisted in the majority of patients at one year. (J Clin Aesthetic Dermatol. 2009;2(7):20–25.)
机译:>目的:评估在定义明确的皮肤区域中用3%的双氯芬酸钠在2.5%的透明质酸凝胶中治疗对光化性角化病病变的长期效果。 >设计:对第4期单臂,多中心,开放标签的研究进行了为期一年的延期。原始研究的患者每天两次接受90%的双氯芬酸钠3%凝胶治疗。扩展研究由治疗后约一年的单项评估组成。 >设置:五个美国中心。 >参与者:在指定的治疗区域内完成了初始治疗阶段且未进一步治疗光化性角化病的患者。 >测量结果:主要终点是根据目标病灶数得分或累积病灶数得分相对于基线的变化百分比,在一年的随访中获得光化性角化病病变清除率达到75%的患者比例。次要终点是达到100%的光化性角化病病变清除率和研究者的整体改善指数得分变化的患者比例。 >结果:在完成3%双氯芬酸钠凝胶治疗后的一年中,有81%的患者报告没有进一步治疗光化性角化病。一年后清除率为75%的患者比例为目标病变为91%(95%CI,84–99%),累积病变为70%(95%CI,57–83%)。一年内清除率为100%的患者比例为目标病变为79%(95%CI,67-90%),累积病变为30%(95%CI,17-43%)。研究人员的全球改善指数严重程度评分显示,大多数(96%)患者在一年后从基线开始改善。 >结论:大多数患者在一年后仍坚持90天疗程的双氯芬酸钠3%凝胶治疗。 (《临床美容皮肤病杂志》 2009年; 2(7):20–25。)

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