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Developing New Technology for Local Tumor Control:

Developing New Technology for Local Tumor Control:. A Bioengineering Approach. Andrew Wright MD Department of Surgery 1/25/02. Background. Greater than one half of patients with colorectal cancer will develop liver metastases at some point in their clinical course

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Developing New Technology for Local Tumor Control:

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  1. Developing New Technology for Local Tumor Control: A Bioengineering Approach Andrew Wright MD Department of Surgery 1/25/02

  2. Background • Greater than one half of patients with colorectal cancer will develop liver metastases at some point in their clinical course • Surgical resection of an isolated liver tumor offers a five-year survival between 25 and 38%, compared to a 0% five-year survival without resection

  3. Only 10–20% of patients with liver tumors will have disease amenable to surgical resection due to high surgical risk or unfavorable anatomy Background

  4. Radiofrequency Ablation • High-frequency (460 kHz) alternating current flows from electrical probe through tissue to ground Probe insertion Extension of prongs RF current application

  5. Cool-Tip probe (17-gauge needle) (Radionics) Radiofrequency Ablation 12-prong “Leveen” probe, 4 cm diameter (Radiotherapeutics) 9-prong “Starburst” probe, 5 cm diameter (Rita Medical)

  6. TemperatureChange Heat loss through blood flow Thermal Conductivityand heat constant Current Density * Electric Field Constant Radiofrequency Ablation • Bioheat Equation • Lesion  (Energy Applied x Local Tissue Factors) – Energy Lost

  7. Finite Element Modeling • Determine material and electrical properties of tissue and ablation system • Develop geometric model • Solve Bioheat equation

  8. Finite Element Modeling

  9. Bioengineering Approach • Define Problem • Determine Possible Solutions • Model • Test • Refine

  10. RF RF Define Problem • Local recurrence as high as 30% • Uneven or irregular heating • Heat sink vessels Several mm’s

  11. Define Problem • Local recurrence as high as 30% • Uneven or irregular heating • Heat sink vessels • Difficult to treat large or multiple tumors

  12. Define Problem • Local recurrence as high as 30% • Uneven or irregular heating • Heat sink vessels • Difficult to treat large or multiple tumors • Poor imaging and localization Ultrasound B-scan After RF Ablation Ultrasound B-scan Before RF Ablation

  13. TemperatureChange Heat loss through blood flow Thermal Conductivityand heat constant Current Density * Electric Field Constant Possible Approaches • Bioheat Equation • Lesion  (Energy Applied x Local Tissue Factors) – Energy Lost

  14. Potential Solution #1 • Bipolar RF Ablation • Increase current density between electrodes • Increase energy deposition • More uniform tissue heating

  15. Bipolar RF Ablation

  16. Bipolar RF Ablation • FEM predicts nearly double lesion volume with bipolar electrode

  17. Bipolar RF • In vivo porcine liver Monopolar Bipolar

  18. Bipolar RF • Monopolar 3.93  1.8 cm2 • Bipolar 12.2  3.0 cm2

  19. Bipolar RF

  20. Bipolar RF Monopolar, d=2.3 mm Bipolar asymmetric, d=1.8 mm Bipolar symmetric, d=1.0 mm

  21. Bipolar RF • Problems • Inability to control two electrodes independently • Difficult technical placement • Unable to treat multiple tumors

  22. Potential Solution #2 • Multiple Probe RF Ablation • Allows overlapping treatment of large solitary tumors • Allows simultaneous treatment of multiple tumors

  23. Bipolar Monopolar Multiple Probe RF Ablation • Disadvantage: electrical shielding between electrodes (Faraday cage)

  24. Block diagram of system Multiple Probe RF Ablation

  25. Bipolar Monopolar Alternating Monopolar Multiple Probe RF Ablation

  26. Multiple Probe RF Ablation • Prototype Multiple Probe Device • Computer controlled electromechanical switch

  27. Multiple Probe RF Ablation • Ex Vivo Testing

  28. Multiple Probe RF Ablation • In Vivo Testing

  29. Multiple Probe RF Ablation Single Probe Ablation Simultaneous Multiple Probe Ablation

  30. Multiple Probe RF Ablation • In Vivo Testing • Lesion Volume • Single 10.7 cm3 • Dual 17.3 cm3 (per lesion) • Time to Target Temperature • Single 2.7 minutes • Dual 3.4 minutes

  31. Multiple Probe RF Ablation • Change to electrical switch • Increase number of probes • Increase speed of switching • Decrease load on generator • Evaluate synergism of overlapping multiple probe RF ablations

  32. Potential Solution #3 • Bioheat Equation • Lesion  (Energy Applied x Local Tissue Factors) – Energy Lost • Tissue Impedance (resistivity)

  33. Tumor Resistivity • Electrical properties of normal liver and tumor (K12/TRb) measured in an in vivo rat liver model

  34. Tumor Resistivity • Finite Element Model Tumor diameter = 2 cm

  35. Tumor Resistivity • Current Density 500 kHz 100Hz

  36. Tumor Resistivity • Temperature 500 kHz 100Hz

  37. Gray circle represents tumor boundary Tumor Resistivity • Lesion Difference

  38. Tumor Resistivity • Human? • Colorectal metastasis to liver

  39. Alternative Solution • Microwave Ablation • Theoretical advantages over radiofrequency ablation • No ground pad • Not limited by tissue charring and impedance changes • Use of Multiple Probes

  40. Microwave Ablation • Larger zone of active heating 1-2 mm MW 1-2 cm MW

  41. Microwave Ablation RF MW

  42. Multiple Probe Ablation • Null Hypothesis • Because microwave and radiofrequency ablation are both heat based, there will be no difference in ablation size or lesion pathology between the two technologies

  43. Methods • Microwave Ablation • Vivant Medical prototype system • 10 minute ablation, 40 Watts • Radiofrequency Ablation • RITA Medical Systems Starburst • 10 minute ablation, 3cm deployment 100oC target temperature

  44. Microwave Ablation System • Vivant Medical • 13g, 15cm dipole antenna • 915MHz generator • Fiberoptic temperature monitor

  45. Radiofrequency Ablation System • RITA Medical • 14g, 15cm expandable array • 460 kHz generator • Integrated thermocouple

  46. Lesion Volume * * * p=.02

  47. Lesion Length * ▪ ▪ ◦ * ◦ * p<.001 ▪ p=.02 ◦ p<.001

  48. Lesion Diameter

  49. 48o Pathology RFA MW Immediate 4 weeks

  50. Laboratory Data • No significant difference in AST, ALT, LDH, Alkaline Phosphatase, WBC, or HCT * * p<0.001

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