Real time three-dimensional heat-induced echo-strain imaging for monitoring high-intensity acoustic ablation produced by conformal interstitial and external directional ultrasound therapy applicators

1. A system for thermal treatment or ablation of tissue comprising:

an ultrasonic thermal ablation probe including one or more ultrasonic transducers;

an ultrasonic three-dimensional imaging probe configured to capture at least one image from radio frequency image data obtained before the radio frequency image data is processed;

a control system for multi-axis control of the imaging probe's position; and

an ultrasonic feedback mechanism configured to measure ultrasound echo strain to estimate heat-induced structural changes of an area surrounding the ultrasonic thermal ablation probe, from the at least one image,

wherein the ultrasonic thermal ablation probe comprises one of:

an interstitial ablator configured to be inserted into tissue, a natural cavity or a vessel to emit high intensity ultrasound energy to deposit thermal dose, or

an external applicator configured to emit a directional high intensity ultrasound energy to deposit thermal dose via surface contact with tissue,

wherein control variables of the control system include at least one of a temperature profile or an actual thermal dose profile of a particular location, the temperature profile generated based on the heat-induced structural changes estimated by the ultrasonic feedback mechanism, which control variables are indicative of a level of tissue ablation, and

wherein the control system receives the estimated heat-induced structural changes from the ultrasonic feedback mechanism and adjusts power levels of the ultrasonic thermal ablation probe based on the estimated heat-induced structural changes.

2. The system of claim 1 , wherein the ultrasonic thermal ablation probe is a high-intensity focused ultrasound probe.

3. The system of claim 1 , wherein the ultrasonic thermal ablation probe is the interstitial ablator, and the interstitial ablator comprises a needle applicator or a catheter applicator, the needle applicator or catheter applicator having one or more ultrasonic transducers.

4. The system of claim 3 , wherein the one or more ultrasonic transducers of the needle applicator or the catheter applicator are semi-cylinder transducers having a 180-degree insonification angle.

5. The system of claim 3 , wherein the one or more ultrasonic transducers of the needle applicator or the catheter applicator are multiple directional angles or omni-directional 360-degree transducers.

6. The system of claim 3 , wherein the one or more ultrasonic transducers operate at a same frequency or at different frequencies.

7. The system of claim 3 , wherein the needle applicator or the catheter applicator has an ablation zone of 5 cc to 50 cc in an insonation period of 1-5 minutes.

8. The system of claim 1 , wherein the ultrasonic thermal ablation probe is the external applicator, and the external applicator comprises at least two piezoelectric elements.

9. The system of claim 8 , wherein the external applicator creates a rectangular or ellipsoidal ablation zone.

10. The system of claim 8 , wherein the external applicator focuses at depths ranging from 3 mm to 50 mm beneath a point of contact of the external applicator and a tissue surface, with lateral zones at a focal depth from 2 mm 2 to 120 mm 2 .

11. A method for real time control of thermal treatment of a tissue region comprising:

placing an ultrasonic thermal ablation probe in relation to the tissue region to be treated, the ultrasonic thermal ablation probe comprising one of an interstitial ablator or an external applicator;

placing an ultrasonic three-dimensional imaging probe in relation to the tissue region to be treated and the ultrasonic thermal ablation probe;

emitting sonic energy from the ultrasonic thermal ablation probe directed at the tissue region;

monitoring, with the ultrasonic three-dimensional imaging probe, the tissue region, wherein monitoring includes capturing at least one image from radio frequency image data obtained before the radio frequency image data is processed;

measuring ultrasonic echo strain information regarding the tissue region from the at least one image;

generating a temperature map for the tissue region based upon changes in the ultrasonic echo strain information for the tissue region, where the changes in the ultrasonic echo strain information are due to increasing thermal dose;

determining a level of tissue ablation for a particular portion of the tissue region based upon at least one of the temperature map or thermal dose profiles associated with the particular portion of the tissue region; and

controlling power delivered by the ultrasonic thermal ablation probe based upon the ultrasonic echo strain information, which is indicative of the determined level of tissue ablation.

12. The method of claim 11 , wherein

when the ultrasonic thermal ablation probe is the interstitial ablator, placing the ultrasonic thermal ablation probe in relation to the tissue region to be treated comprises inserting the interstitial ablator into a tissue, a natural cavity or a vessel in the tissue region, and

when the ultrasonic thermal ablation probe is the external applicator, placing the ultrasonic thermal ablation probe in relation to the tissue region to be treated comprises contacting a surface of a tissue in the tissue region with the external applicator.

13. The method of claim 11 , further comprising:

comparing the actual thermal dose profiles to a planned thermal dose profile; and

controlling of the power delivered by the ultrasonic thermal ablation probe is determined by the comparison of the actual thermal dose profiles to the planned thermal dose profile.

14. The method of claim 12 , wherein the controlling comprises independently controlling intensity of a plurality of ultrasonic transducer elements provided on the ultrasonic thermal ablation probe.

15. The method of claim 11 , wherein the monitoring comprises the use of a heat-induced strain algorithm.

16. The method of claim 15 , wherein determining the level of tissue ablation comprises parallel implementation of the heat-induced strain algorithm.

17. The method of claim 16 , wherein the parallel implementation of the heat-induced strain algorithm comprises:

dividing each line of radio frequency image data of an image captured by the ultrasonic three-dimensional imaging probe into pixels, the image having n lines of radio frequency image data and m pixels, and

performing separate parallel computations by running n blocks with m threads in each block.

18. The method of claim 17 , wherein subsequent images captured by the ultrasonic three-dimensional imaging probe are compared using the parallel implementation of the heat-induced strain algorithm by aligning a number p of images, and performing separate parallel computations by running m blocks with (n×p) threads in each block.