Comparison of thermal damage calculated using magnetic resonance thermometry, with magnetic resonance imaging post-treatment and histology, after interstitial microwave thermal therapy of rabbit brain
Md. Sherar et al., Comparison of thermal damage calculated using magnetic resonance thermometry, with magnetic resonance imaging post-treatment and histology, after interstitial microwave thermal therapy of rabbit brain, PHYS MED BI, 45(12), 2000, pp. 3563-3576
Clinical application of high-temperature thermal therapy as a treatment for
solid tumours requires an accurate and close to real-time method for asses
sing tissue damage. Imaging methods that detect structural changes during h
eating may underestimate the extent of thermal damage. This is due to the o
ccurrence of delayed damage manifested at tissue locations exposed to tempe
ratures lower than those required to cause immediate structural changes. An
alternative approach is to measure temperature and then calculate the expe
cted damage based on the temperature history at each tissue location. Magne
tic resonance (MR) imaging methods now allow temperature maps of the target
and surrounding tissues to he generated in almost real-time. The aim of th
is work was to evaluate whether thermal damage zones calculated on the basi
s of MR thermometry maps measured during heating correspond to actual tissu
e damage as measured after treatment by histological methods and MR imaging
.
Four male rabbits were treated with high-temperature thermal therapy delive
red in the brain by a single microwave antenna operating at 915 MHz. MR sca
nning was performed before, during and after treatment in a 1.5 T whole-bod
y scanner. Temperature maps were produced using the proton resonance freque
ncy (PRF) shift method of MR thermometry. In addition, conventional T-1-wei
ghtcd and T-2-weighted spin-echo images were acquired after treatment. Ther
mal damage zones corresponding to cell death, microvascular blood flow stas
is and protein coagulation were calculated using an Arrhenius analysis of t
he MR temperature/time course data. The calculated zones were compared with
the lesions seen on histopathological examination of the brains which were
removed within 6-8 h of treatment.
The results showed that calculated damage zones based on MR thermometry agr
eed well with areas of damage as assessed using histology after heating was
completed. The data suggest that real-time calculations of final expected
thermal damage based on an Arrhenius analysis of MR temperature data may pr
ovide a useful method of real-time monitoring of thermal therapy when combi
ned with conventional T-2-weighted images taken after treatment.