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一项基于上市后监测试验的光化性角化病干预措施的系统评价和荟萃分析。

A Systematic Review and Meta-Analysis of Interventions for Actinic Keratosis from Post-Marketing Surveillance Trials.

作者信息

Steeb Theresa, Wessely Anja, Harlaß Matthias, Heppt Franz, Koch Elias A T, Leiter Ulrike, Garbe Claus, Schöffski Oliver, Berking Carola, Heppt Markus V

机构信息

Department of Dermatology, Universitätsklinikum Erlangen, Friedrich-Alexander-University Erlangen-Nürnberg (FAU), 91054 Erlangen, Germany.

Comprehensive Cancer Center Erlangen-European Metropolitan Area of Nuremberg (CCC ER-EMN), 91054 Erlangen, Germany.

出版信息

J Clin Med. 2020 Jul 15;9(7):2253. doi: 10.3390/jcm9072253.

Abstract

Multiple interventions are available for the treatment of actinic keratosis (AK) showing high efficacy in pivotal trials. However, data from post-marketing surveillance studies have received little attention until now. Here, we systematically investigate interventions for AK from post-marketing surveillance trials as a proxy for real-world efficacy and tolerability. A systematic literature search was conducted in Medline, Embase, and CENTRAL. Pertinent trial registers were hand-searched until 25 March 2020. Results were pooled using a random-effects model to calculate pooled proportions and relative risks (RR) or were described qualitatively. Eleven records with a total sample size of = 4109 were included. Three of the studies had an active-controlled design, while seven were single-armed. Participant complete clearance ranged from 23.1% for diclofenac sodium 3% gel to 88.9% for ingenol mebutate 0.05% gel. The lesion-specific clearance rate for photodynamic therapy (PDT) was 74% (95% confidence interval (CI) 56-87%). The recurrence rate was significantly higher for diclofenac sodium 3% in comparison to imiquimod 5% cream (RR 1.10, 95% CI 1.02-1.1.8) and ranged from 10.6% for ingenol mebutate 0.015% gel to 23.5% for PDT. Few patients discontinued the trials due to adverse events. The results from the majority of the post-marketing surveillance studies deviated from those of pivotal trials.

摘要

有多种干预措施可用于治疗光化性角化病(AK),在关键试验中显示出高效性。然而,迄今为止,上市后监测研究的数据很少受到关注。在此,我们系统地研究了上市后监测试验中针对AK的干预措施,以此作为实际疗效和耐受性的替代指标。在Medline、Embase和CENTRAL中进行了系统的文献检索。对相关试验注册库进行了手工检索,直至2020年3月25日。使用随机效应模型汇总结果以计算汇总比例和相对风险(RR),或进行定性描述。纳入了11项记录,总样本量n = 4109。其中三项研究采用活性对照设计,七项为单臂研究。参与者的完全清除率范围为:3%双氯芬酸钠凝胶为23.1%,0.05%鬼臼毒素酯凝胶为88.9%。光动力疗法(PDT)的病灶特异性清除率为74%(95%置信区间(CI)56 - 87%)。与5%咪喹莫特乳膏相比,3%双氯芬酸钠的复发率显著更高(RR 1.10,95% CI 1.02 - 1.18),复发率范围为:0.015%鬼臼毒素酯凝胶为10.6%,PDT为23.5%。很少有患者因不良事件而中断试验。大多数上市后监测研究的结果与关键试验的结果不同。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1190/7408895/6b07a20c1dc3/jcm-09-02253-g001.jpg

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