Photodynamic therapy (PDT) has been studied and applied to various disease
processes. The potential of PDT for selective destruction of target tissues
is especially appealing in cardiovascular disease, in which other existing
interventional tools are somewhat nonselective and carry substantial risk
of damage to the normal arterial wall. Enthusiasm for photoangioplasty (PDT
of vascular de novo atherosclerotic and, potentially, restenotic lesions)
is fueled by more effective second-generation photosensitizers and technolo
gical advances in endovascular light delivery. This excitement revolves aro
und at least 4 significant attributes of light-activated therapy: the putat
ive selectivity and safety of photoangioplasty, the potential for atraumati
c and effective debulking of atheromatous plaque through a biological mecha
nism, the postulated capability to reduce or inhibit restenosis, and the po
tential to treat long segments of abnormal vessel by simply using fibers wi
th longer light-emitting regions. The available nonclinical data, coupled w
ith the observations of a new phase I trial in human peripheral atheroscler
osis, suggest a promising future for photoangioplasty in the treatment of p
rimary atherosclerosis and prevention of restenosis.