Our purpose was to develop temperature-sensitive MR sequences and image-pro
cessing techniques to assess their potential of monitoring interstitial las
er therapy (ILT) in brain tumors (n = 3) and liver tumors (n = 7). ILT last
ed 2 to 26 minutes, whereas images from T1-weighted fast-spin-echo (FSE) or
spoiled gradient-recalled (SPGR) sequences were acquired within 5 to 13 se
conds. Pixel subtraction and visualization of T1-weighted images or optical
now computation was done within less than 110 msec, Alternating phase-mapp
ing of real and imaginary components of SPGR sequences was performed within
220 msec. Pixel subtraction of T1-weighted images identified thermal chang
es in liver and brain tumors but could not evaluate the temperature values
as chemical shift-based imaging, which was, however, more affected by susce
ptibility effects and motion, Optical now computation displayed the predict
ed course of thermal changes and revealed that the rate of heat deposition
can be anisotropic, which may be related to heterogeneous tumor structure a
nd/or vascularization.