Photodynamic therapy of cancer: An update

Patrizia Agostinis(Catholic University of America), Kristian Berg(Oslo University Hospital), Keith A. Cengel(RTOG Foundation), Thomas H. Foster(University of Rochester), Albert W. Girotti(Medical College of Wisconsin), Sandra O. Gollnick(Roswell Park Comprehensive Cancer Center), Stephen M. Hahn(University of Pennsylvania), Michael R. Hamblin(Harvard University), Asta Juzeniene(Oslo University Hospital), David Kessel(Wayne State University), Mladen Korbelik(BC Cancer Agency), Johan Moan(Oslo University Hospital), Paweł Mróz(Harvard University), Dominika Nowis(Medical University of Warsaw), Jacques Piette(University of Liège), Brian C. Wilson(Ontario Institute for Cancer Research), Jakub Gołąb(Medical University of Warsaw)
CA A Cancer Journal for Clinicians
May 26, 2011
Cited by 5,087Open Access
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Abstract

Photodynamic therapy (PDT) is a clinically approved, minimally invasive therapeutic procedure that can exert a selective cytotoxic activity toward malignant cells. The procedure involves administration of a photosensitizing agent followed by irradiation at a wavelength corresponding to an absorbance band of the sensitizer. In the presence of oxygen, a series of events lead to direct tumor cell death, damage to the microvasculature, and induction of a local inflammatory reaction. Clinical studies revealed that PDT can be curative, particularly in early stage tumors. It can prolong survival in patients with inoperable cancers and significantly improve quality of life. Minimal normal tissue toxicity, negligible systemic effects, greatly reduced long-term morbidity, lack of intrinsic or acquired resistance mechanisms, and excellent cosmetic as well as organ function-sparing effects of this treatment make it a valuable therapeutic option for combination treatments. With a number of recent technological improvements, PDT has the potential to become integrated into the mainstream of cancer treatment.


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