Although photodynamic therapy (PDT) was first used in the treatment of
skin diseases, phase-III-clinical trials were primarily conducted for
the treatment of bladder cancer, endobronchial and oesophageal carcin
oma. In dermatology PDT has most extensively been used for the treatme
nt of malignant cutaneous lesions. Up to now those patients have been
treated systemically with first-generation photosensitizers. However,
prolonged skin photosensitivity is a major disadvantage of this form o
f therapy. Topical PDT utilizing a variety of sensitizers bypass this
unwanted effect. Of strong interest is 5-aminolevulinic acid (ALA), fi
rst introduced in the topical PDT of skin disorders in 1990 by Kennedy
and co-workers. ALA serves as a pro-drug, i.e. the active photosensit
izing compound is protoporphyrin IX which is synthesized in vivo after
exogenous application of ALA. In several oncologic and non-oncologic
skin conditions including non-melanoma skin cancer, premalignant condi
tions like actinic keratoses and in psoriasis, topical ALA-PDT showed
it's effectiveness. Besides ALA, new sensitizers like benzoporphyrines
and porphycenes may play a role in topical PDT. However, at the momen
t, there is still a need for comparative studies and standardized ther
apeutic protocols to define the place of topical PDT in Dermatology.