Photodynamic therapy (PDT) is a treatment modality using a photosensitising
drug and light to kill cells. The clinical use of PDT requires the presenc
e of a photosensitising agent, oxygen and light of a specific wavelength wh
ich matches the absorption characteristics of the photosensitiser. When the
photosensitiser is activated by the appropriate wavelength of light, it in
teracts with molecular oxygen to form a toxic, short-lived species known as
singlet oxygen, which is thought to mediate cellular death. The appeal of
PDT in oncology is that the photosensitiser tends to be retained in tumour
tissues for a longer period of time as compared with normal tissues resulti
ng in a large therapeutic index. This potential for minimal normal tissue t
oxicity has prompted an interest in studying PDT as a cancer treatment. Fur
thermore, the use of PDT is not precluded by prior radiotherapy, chemothera
py or surgery. The development of PDT has been hampered by the limitations
of the older photosensitisers, namely limited depth of tissue penetration,
and extended skin phototoxicity which limits the number of applications dur
ing a course of treatment. However, newer photosensitisers are being develo
ped which allow greater depth of tissue penetration and have minimal skin p
hototoxicity allowing for multiple fractionated treatments. With such advan
cements, PDT has great potential to become an integral part of cancer treat
ment in the future.