Purpose : To study the biologic and clinical effects of ionizing radiation
on blood vessels.
Materials and Methods : Data extracted from experimental and clinical repor
ts and articles.
Results : Radiation-induced demise of endothelial cells is due to apoptosis
. These cells are considered to be very radiosensitive. In vivo, however, t
he basal membrane might play a protective role. Early effects are character
ized by swelling and shloughing of endothelial cells. Late effects are due
to endothelial and smooth muscular cell proliferation. The underlying biolo
gic mechanisms are little known. One hypothesis is the production of PDGF (
platelet derived growth factor) and FGF (fibroblast growth factor) by endot
helial cells. Perivascular fibrosis might occur because of the TGF-beta pro
duction by endothelial cells and/or macrophages. Occurrence of late complic
ations is probably multifactorial. Individual susceptibility to harmful eff
ects of ionizing radiation, other vascular risk factors, and non optimal us
e of radiation treatment might contribute to the occurrence of late vascula
r complications. Modern radiotherapy using new techniques as the intensity
modulation radiation therapy (IMRT) and the reduction of radiation doses an
d size of radiation fields should permit a dramatic reduction of vascular c
omplications in cancer patients.
Conclusions : Ionizing radiation treatments can lead to serious late vascul
ar complications. A better understanding of the underlying biologic process
es and newer radiation techniques might lead to fewer late complications in
the very near future.