Daylight photodynamic therapy versus cryosurgery for the treatment and prophylaxis of actinic keratoses of the face - protocol of a multicenter, prospective, randomized, controlled, two-armed study.

Q2 Medicine BMC Dermatology Pub Date : 2017-10-25 DOI:10.1186/s12895-017-0064-7
E Kohl, M Koller, F Zeman, R-M Szeimies, W G Philipp-Dormston, W Prager, P A Gerber, S Karrer
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引用次数: 15

Abstract

Background: Photodynamic therapy with daylight (DL-PDT) is efficacious in treating actinic keratosis (AK), but the efficacy of field-directed, repetitive DL-PDT for the treatment and prophylaxis of AK in photodamaged facial skin has not yet been investigated.

Methods/design: In this multicenter, prospective, randomized, controlled, two-armed, observer-blinded trial, patients with a minimum of 5 mild-to-moderate AK lesions on photodamaged facial skin are randomly allocated to two treatment groups: DL-PDT with methyl aminolevulinate (MAL) and cryosurgery. In the DL-PDT group (experimental group), 5 treatments of the entire face are conducted over the course of 18 months. After preparation of the lesion and within 30 min after MAL application, patients expose themselves to daylight for 2 h. In the control group, lesion-directed cryosurgery is conducted at the first visit and, in the case of uncleared or new AK lesions, also at visits 2 to 5. The efficacy of the treatment is evaluated at visits 2 to 6 by documenting all existing and new AK lesions in the face. Cosmetic results and improvement of photoaging parameters are evaluated by means of a modified Dover scale. Primary outcome parameter is the cumulative number of AK lesions observed between visits 2 and 6. Secondary outcome parameters are complete clearance of AK, new AK lesions since the previous visit, cosmetic results independently evaluated by both patient and physician, patient-reported pain (visual analogue scale), patient and physician satisfaction scores with cosmetic results, and patient-reported quality of life (Dermatology Life Quality Index). Safety parameters are also documented (adverse events and serious adverse events).

Discussion: This clinical trial will assess the efficacy of repetitive DL-PDT in preventing AK and investigate possible rejuvenating effects of this treatment. (Trial registration: ClinicalTrials.gov Identifier: NCT02736760).

Trial registration: ClinicalTrials.gov Identifier: NCT02736760 . Study Code Daylight_01. EudraCT 2014-005121-13.

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日光光动力疗法与冷冻手术治疗和预防面部光化性角化病——一项多中心、前瞻性、随机、对照、双臂研究的方案。
背景:日光光动力疗法(DL-PDT)在治疗光化性角化病(AK)方面是有效的,但在光损伤的面部皮肤中,定向的、重复的DL-PDT治疗和预防AK的疗效尚未得到研究。方法/设计:在这项多中心、前瞻性、随机、对照、双臂、观察者盲法试验中,在光损伤的面部皮肤上至少有5个轻至中度AK病变的患者被随机分配到两个治疗组:氨基乙酰酸甲酯(MAL) DL-PDT和冷冻手术。DL-PDT组(实验组)在18个月的时间内进行5次全面部治疗。病变准备后,在MAL应用后30分钟内,患者将自己暴露在日光下2小时。在对照组中,在第一次就诊时进行病变定向冷冻手术,对于未清除或新的AK病变,也在第2至5次就诊时进行冷冻手术。在第2至6次就诊时,通过记录面部所有现有和新发AK病变来评估治疗效果。美容效果和光老化参数的改善通过改进的多佛量表进行评估。主要结果参数是在第2次和第6次就诊期间观察到的AK病变的累积数量。次要结局参数是AK的完全清除,自上次就诊以来新的AK病变,由患者和医生独立评估的美容结果,患者报告的疼痛(视觉模拟量表),患者和医生对美容结果的满意度评分,以及患者报告的生活质量(皮肤病生活质量指数)。安全参数也被记录(不良事件和严重不良事件)。讨论:这项临床试验将评估重复DL-PDT在预防AK中的功效,并研究这种治疗可能的恢复活力的作用。(试验注册:ClinicalTrials.gov标识符:NCT02736760)。试验注册:ClinicalTrials.gov标识符:NCT02736760。研究代码Daylight_01。EudraCT 2014-005121-13。
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来源期刊
BMC Dermatology
BMC Dermatology Medicine-Dermatology
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期刊介绍: BMC Dermatology is an open access journal publishing original peer-reviewed research articles in all aspects of the prevention, diagnosis and management of skin disorders, as well as related molecular genetics, pathophysiology, and epidemiology. BMC Dermatology (ISSN 1471-5945) is indexed/tracked/covered by PubMed, MEDLINE, CAS, EMBASE, Scopus and Google Scholar.
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