Morton Colin A
Department of Dermatology, Stirling Community Hospital, Stirling, UK -
G Ital Dermatol Venereol. 2018 Dec;153(6):783-792. doi: 10.23736/S0392-0488.18.05896-0. Epub 2018 Feb 7.
Photodynamic therapy (PDT), using topically administered photosensitizing agents, is widely approved as a treatment for certain nonmelanoma skin cancers. As a tissue-sparing non-surgical modality, there is great potential for PDT to enhance the choice of therapies available to treat, and potentially prevent, skin cancer. Treatment-specific guidelines have assessed the evidence for various photosensitizing agents and light sources, dosimetry, and evaluate reported adverse effects. Discomfort is frequently experienced during treatment but no analgesia was required in most pivotal lesion-directed studies. Durability of response has been assessed with studies of PDT for basal cell carcinomas (BCC) extending to 5 years and beyond, 2 years for Bowen's disease and up to 1 year for actinic keratoses (AK). Disease-specific guidelines consider the place for topical PDT in routine clinical practice recognizing that PDT is typically office/clinic-based and usually initiated by specialists. Where updated guidelines are awaited, national and international consensus publications offer recommendations, including on the use of daylight to activate the photosensitizer for treating AK. Reviewed studies indicate equivalent efficacy of daylight PDT, but greatly reduced pain compared with conventional PDT. Guidelines and consensus publications also consider the place of PDT in treating skin lesions arising in organ transplant recipients and in the potential for PDT to delay/prevent the development of nonmelanoma skin cancers. There is now a substantial evidence-base to support the use of topical PDT in routine clinical practice with daylight PDT indicated for AK, providing suitable outside climate, whilst conventional PDT remains suitable for AK, Bowen's Disease, superficial and certain thin nodular BCC.
光动力疗法(PDT)通过局部应用光敏剂,已被广泛批准用于治疗某些非黑色素瘤皮肤癌。作为一种保留组织的非手术治疗方式,PDT在增加治疗选择以及潜在预防皮肤癌方面具有巨大潜力。针对特定治疗的指南评估了各种光敏剂、光源、剂量测定的证据,并对报告的不良反应进行了评估。治疗过程中常出现不适,但在大多数关键的病灶定向研究中无需镇痛。对基底细胞癌(BCC)进行的PDT研究评估了反应的持久性,长达5年及以上;对鲍恩病的研究为2年;对光化性角化病(AK)的研究为1年。特定疾病指南考虑了局部PDT在常规临床实践中的地位,认识到PDT通常在门诊/诊所进行,且通常由专科医生启动。在等待更新指南的情况下,国家和国际共识出版物提供了建议,包括使用日光激活光敏剂治疗AK。综述研究表明日光PDT疗效相当,但与传统PDT相比疼痛大大减轻。指南和共识出版物还考虑了PDT在治疗器官移植受者皮肤病变中的地位,以及PDT在延迟/预防非黑色素瘤皮肤癌发生方面的潜力。现在有大量证据支持在常规临床实践中使用局部PDT,日光PDT适用于AK(需有适宜的室外气候),而传统PDT仍适用于AK、鲍恩病、浅表性和某些薄结节性BCC。