H. Oikawa et al., SPECTROSCOPIC IMAGING OF THE WATER RESONANCE WITH SHORT REPETITION TIME TO STUDY TUMOR RESPONSE TO HYPEROXIA, Magnetic resonance in medicine, 38(1), 1997, pp. 27-32
A variety of treatments that modulate tumor oxygen tension are used cl
inically to improve the outcome of radiotherapy, High resolution, noni
nvasive measurements of the effects of these treatments would greatly
facilitate the development of improved therapies and could guide treat
ment of cancer patients, Previous work demonstrated that magnetic reso
nance (MR) gradient echo imaging of the water proton resonance detects
changes in T-2 and T-1 in tumors during hyperoxia that may reflect i
ncreased tumor oxygenation, This report describes the use of high reso
lution MR spectroscopic imaging with short repetition time (TR = 0.2 s
) to improve the accuracy with which changes in T-2 and T-1 are measu
red, Mammary adenocarcinomas grown in the hind limbs of rats were stud
ied, Carbogen inhalation was used to induce hyperoxia, A single 2-mm s
lice through the center of tumors and underlying muscle was imaged at
4.7 Tesla with in-plane resolution of approximately 1,2 mm and frequen
cy resolution of 5.8 Hz, The peak integral increased by an average of
6% in tumors during carbogen inhalation suggesting a decrease in T-1 (
n = 8, P < 0.001), Peak height increased by an average of 15% in tumor
s during carbogen inhalation (n = 8, P < 0.001), The large difference
between increases in peak height and peak integral demonstrates that t
he width of the water resonance decreased, Assuming a Lorentzian lines
hape, an average increase of 12% in T-2 was observed in tumors, In mu
scle, peak integral and peak height increased slightly (about 1.2% and
3%, respectively; P < 0.02) during carbogen inhalation but no signifi
cant change in T-2 was observed, Spectroscopic imaging detects change
s in the water proton resonance in tumors during hyperoxia accurately
and reproducibly with high signal-to-noise ratio and allows clear sepa
ration of T-1 and T-2 effects, Increases in T-1* may be due to decrea
sed deoxyhemoglobin in tumor blood vessels (i,e,, the BOLD effect) and
may provide a clinically useful index of increases in tumor oxygenati
on.