The objectives of this study were to measure by in-vivo techniques the radi
ation doses received by the anorectum during pelvic radiotherapy and compar
e these with doses predicted by a GE TARGET(TM) treatment planning system.
Nine patients with cancers of the prostate. bladder, cervix or uterus were
planned with computed tomography (CT) using the TARGET system. A Scanditron
ix rectal probe containing five n-type photon-detecting diodes was placed i
n the anorectum during the planning CT scans. The probe position was standa
rdized with the five diodes at 2 cm intervals from the anal verge. The prob
e diodes were calibrated for 10 MV photons. Doses were measured for each di
ode for two consecutive fractions in the first four patients and for five c
onsecutive fractions in the remaining five. Thermoluminescent dosimeters we
re used initially to verify diode doses. The TARGET and diode measured dose
s were compared.
In all patients diodes situated in the target volume were within 7% of pred
icted doses. This improved to 2.5% after measurement on five fractions. At
the edges of the target volume, wide variability existed between measured a
nd predicted doses (measured dose range -68% to +68% of predicted dose). Ou
tside the target volume, considerable doses (up to 0.3 Gy per fraction) wer
e measured in the anal canal. which were not predicted by TARGET.
We conclude that TARGET planned doses are accurate within the confines of t
he target volume. The greatest variability was seen at the edges of the tar
get volume, where dose can vary by 50% across a 1 cm distance in the anteri
or-posterior plane. TARGET does not account for scattered dose beyond the f
ield edges and therefore underestimates the dose received by the anal canal
.