[MR-guided laser-induced thermo-ablation of liver tumors: clinical experiences and therapy control concepts]. / MRT-gestützte laserinduzierte Thermoablation bei Lebertumoren--Klinische Aspekte und Konzept eines Uberwachungssystems.

Minimally-invasive, laser-induced interstitial thermotherapy (LITT) of solid tumors represents a valid alternative to surgical procedures such as tumor resections. Within the framework of a palliative study on 16 patients, a total of 25 metastases in the liver were treated in an open MR system (0.5 T). The intraoperative scanner design allows patient-based navigation, decisive for a safe applicator positioning, as well as temperature monitoring and direct inspection of the therapy result, without need for patient transfer or repositioning. Although the MR thermometry applied in the open scanner assisted LITT monitoring, the current accuracy of temperature data was not sufficient to serve automatic irradiation control. Therefore, an experimental monitoring and control system was developed in a closed MR scanner (1.5 T) featuring a calibrated MR thermometry. The system provides also an interface to the laser system, allowing the automatic off/on switching of the laser power according to preoperatively defined control criteria. The basic functionality of the automatic laser control was successfully demonstrated with laser ablation experiments of liver samples using irradiation parameters close to typical clinical values.

Simulations of thermal tissue coagulation and their value for the planning and monitoring of laser-induced interstitial thermotherapy (LITT).

MRI information is widely used for the monitoring of thermal therapies, such as laser-induced interstitial thermotherapy (LITT). However, a detailed knowledge about the relationship between time/temperature exposure and resulting tissue thermal damage is needed to estimate the lesion extent. The aims of this work were to model the thermal response of laser-irradiated tissue and to assess the value of Monte Carlo simulation (MCS) for tumor therapy planning and monitoring. MCS yielded true 3D distributions of laser-induced temperature and thermal damage. These results were compared with 2D MR thermometry data from in vitro experiments performed on animal liver tissue over an ordinary range of laser powers (10-25 W) and irradiation times (5-25 min). Clinical reference data were available from MR-guided liver LITT procedures. MCS correctly predicted the shape of temperature and damage distributions. The quantitative agreement between simulated and measured lesion diameters was within 10% and 15% for the in vitro and in vivo cases, respectively. The simulated 53 degrees C isotherm best estimated the boundary of the final thermal damage (6% variance). This study shows that MCS of interstitial laser coagulation provides unique information that can be of use in the empirical correlation of temperature with thermal damage, and can assist greatly in thermal treatment planning and monitoring.

Effects of laser-induced thermotherapy (LITT) on proliferation and apoptosis of glioma cells in rat brain transplantation tumors.

BACKGROUND AND OBJECTIVES: Laser-induced thermotherapy (LITT) is an approach to the treatment of brain tumors especially in poorly accessible regions. Its clinical applicability with tumor cell destruction has been shown in several studies. However, no data are known about specific effects on tumors cells due to LITT in the time course of the lesion. STUDY DESIGN/MATERIALS AND METHODS: LITT was performed in adult Lewis rats with implanted glioma cells in the brain using a standard exposure of 3 W for 30 seconds. Before and following LITT, neoplastic lesions were monitored by MRI. Proliferation of implanted cells and gliosis were assessed by several histological techniques and immunohistochemistry. Apoptosis was detected by TUNEL staining. RESULTS: Our experiments show a destruction of neoplastic cells by LITT but surviving tumor cells at the margin of the lesion. Apoptosis was detected following LITT restricted to residual neoplastic cells. Marginal survival of tumor cells lead to a secondary outgrowth into the necrotic lesion adjacent to sprouting capillaries. CONCLUSIONS: LITT is a suitable technique for the treatment of brain neoplasms. However, further investigations are necessary to prevent tumor recurrences after LITT.