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[Cancer Research 65, 5872-5880, July 1, 2005]
© 2005 American Association for Cancer Research


Experimental Therapeutics, Molecular Targets, and Chemical Biology

Noninvasive Magnetic Resonance Thermography of Recurrent Rectal Carcinoma in a 1.5 Tesla Hybrid System

Johanna Gellermann1, Waldemar Wlodarczyk1, Bert Hildebrandt2, Hildegard Ganter1, Anett Nicolau2, Beate Rau3, Wolfgang Tilly1, Horst Fähling1, Jacek Nadobny1, Roland Felix1 and Peter Wust1

1 Clinic for Radiation Medicine, 2 Clinic for Medicine, Hematology, and Medical Oncology, and 3 Clinic for Surgery and Surgical Oncology, Charité Medical School, Berlin, Germany

Requests for reprints: Peter Wust, Clinic for Radiation Medicine, Charité Medical School, Campus Virchow Klinikum, Augustenburger Platz 1, D-13353 Berlin, Germany. Phone: 49-450-557202; Fax: 49-450-557979; E-mail: peter.wust{at}charite.de.

To implement noninvasive thermometry, we installed a hybrid system consisting of a radiofrequency multiantenna applicator (SIGMA-Eye) for deep hyperthermia (BSD-2000/3D) integrated into the gantry of a 1.5 Tesla magnetic resonance (MR) tomograph Symphony. This system can record MR data during radiofrequency heating and is suitable for application and evaluation of methods for MR thermography.

In 15 patients with preirradiated pelvic rectal recurrences, we acquired phase data sets (25 slices) every 10 to 15 minutes over the treatment time (60-90 minutes) using gradient echo sequences (echo time = 20 ms), transformed the phase differences to MR temperatures, and fused the color-coded MR-temperature distributions with anatomic T1-weighted MR data sets. We could generate one complete series of MR data sets per patient with satisfactory quality for further analysis. In fat, muscle, water bolus, prostate, bladder, and tumor, we delineated regions of interest (ROI), used the fat ROI for drift correction by transforming these regions to a phase shift zero, and evaluated the MR-temperature frequency distributions. Mean MR temperatures (TMR), maximum TMR, full width half maximum (FWHM), and other descriptors of tumors and normal tissues were noninvasively derived and their dependencies outlined. In 8 of 15 patients, direct temperature measurements in reference points were available. We correlated the tumor MR temperatures with direct measurements, clinical response, and tumor features (volume and location), and found reasonable trends and correlations. Therefore, the mean TMR of the tumor might be useful as a variable to evaluate the quality and effectivity of heat treatments, and consequently as optimization variable.

Feasibility of noninvasive MR thermography for regional hyperthermia has been shown and should be further investigated.




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Copyright © 2005 by the American Association for Cancer Research.