Stender I M, Bech-Thomsen N, Poulsen T, Wulf H C
Department of Dermatology, Bispebjerg Hospital, University of Copenhagen, Denmark.
Photochem Photobiol. 1997 Oct;66(4):493-6. doi: 10.1111/j.1751-1097.1997.tb03178.x.
Photodynamic therapy (PDT) with topical application of delta-aminolevulinic acid (ALA) followed by irradiation with visible light (ALA-PDT) is a relatively new and promising experimental treatment of superficial premalignant and malignant skin neoplasms. The purpose of this study was to determine whether ALA-PDT can prevent photocarcinogenesis in hairless mice exposed to solar UV. A total of 140 mice was divided into seven groups of 20 mice each. Group 1: solar-UV exposure. Group 2: solar UV and a cream base+visible light once a week. Group 3: solar UV and ALA-PDT once a week. Group 4: solar UV and ALA-PDT once every second week. Group 5: solar UV and ALA-PDT every fourth week. Group 6: ALA-PDT once a week. Group 7: no treatment. The time to first and to second tumor > or = 1 mm was registered. Predefined endpoints, such as one tumor > or = 4 mm or an area of small confluent tumors on the back of the mice were criteria for withdrawal from the experiment. The time to first and to second tumor was significantly longer in the ALA-PDT-treated mice than in mice only exposed to solar UV and solar-UV/cream base-visible light (P < 0.005). However, we observed an increased death and accident rate in the ALA-PDT-treated groups compared to the groups not treated with ALA-PDT (chi-square test, P = 0.0250). Significantly more ALA-PDT-treated mice were withdrawn because of a tumor > or = 4 mm (P = 0.0005). The UV unexposed mice developed no tumors. Repetitive treatments with ALA-PDT delay photoinduced carcinogenesis in mice.
局部应用δ-氨基乙酰丙酸(ALA)后再用可见光照射进行光动力疗法(PDT)(ALA-PDT)是一种相对新颖且有前景的浅表癌前和恶性皮肤肿瘤实验性治疗方法。本研究的目的是确定ALA-PDT能否预防暴露于太阳紫外线的无毛小鼠发生光致癌作用。总共140只小鼠被分为7组,每组20只。第1组:暴露于太阳紫外线。第2组:太阳紫外线照射且每周一次涂抹乳膏基质并照射可见光。第3组:太阳紫外线照射且每周一次进行ALA-PDT。第4组:太阳紫外线照射且每两周一次进行ALA-PDT。第5组:太阳紫外线照射且每四周一次进行ALA-PDT。第6组:每周一次进行ALA-PDT。第7组:不进行治疗。记录首次出现直径≥1mm肿瘤和第二次出现直径≥1mm肿瘤的时间。预先设定的终点,例如出现一个直径≥4mm的肿瘤或小鼠背部出现小的融合性肿瘤区域,是停止实验的标准。ALA-PDT治疗的小鼠首次和第二次出现肿瘤的时间明显长于仅暴露于太阳紫外线以及暴露于太阳紫外线/乳膏基质-可见光的小鼠(P<0.005)。然而,我们观察到与未用ALA-PDT治疗的组相比,ALA-PDT治疗组的死亡和意外发生率有所增加(卡方检验,P = 0.0250)。由于出现直径≥4mm的肿瘤,ALA-PDT治疗的小鼠中因该原因退出实验的明显更多(P = 0.0005)。未暴露于紫外线的小鼠未发生肿瘤。重复进行ALA-PDT治疗可延缓小鼠光诱导的致癌作用进程。