MR guided Focused Ultrasound Surgery MRgFUS for Uterine Fibroids
Transcription
MR guided Focused Ultrasound Surgery MRgFUS for Uterine Fibroids
Focused Ultrasound (FUS) MR guided Focused Ultrasound Surgery MRgFUS for Uterine Fibroids •The ExAblate 2000 system is a device that can target and ablate tissue without requiring surgical incision Abdullah BJJ, Department of Biomedical Imaging, University of Malaya, Kuala Lumpur, Malaysia How Focused Ultrasound Works • • • A sound wave is a mechanical disturbance that induces oscillatory motion in particles of a medium. Diagnostic ultrasound produces internal organ pictures by exposing the body to high-frequency sound waves. Ultrasound therapy uses lower frequencies with significantly higher intensities. How Focused Ultrasound Works (con’t) •Similar to how a magnifying glass focuses light energy, ultrasound can be focused on a specific point Treated spot Tumor Transducer Energy pass zone Ultrasound Effect on Tissue • • • Focused Ultrasound Transducer When ultrasound waves propagate in tissue, the energy is absorbed and converted to molecule movement that generates heat • A phased array transducer electronically adjusts the focal location The highest temperature increase is at the focus, since this is where the sound waves converge and have the highest energy density In the beam pass zone the energy density is low hence the temperature increase is low ls igna RF S Multi-element phased array transducer Tissue heating 40 50 60 70 80 1 Ultrasound Effect on Tissue • Thermal simulations show the shape of the focus Thermal Therapy When tissue is heated and exceeds a certain thermal dose threshold, tissue ablation occurs • Thermal dose of 100% tissue ablation*: • At 43oC – 240 minutes • Or at 54oC – 3 second • Or at 57oC – 1 second Parallel to beam path Total ablation Perpendicular to beam path *Sapareto SA, Dewey WC. Thermal dose determination in cancer therapy Physiology of Thermal Therapy •Coagulated regions seen in macro pathology image MRgFUS treated liver (pig) •Histology analysis shows a sharp demarcation between treated and non treated regions Uterine fibroids • Most common tumors on women over the age of 30 • High prevalence • Most common indication for hysterectomy • Hysterectomy annual costs in US in excess of $2 billion • (Zhao, 1999) • Lost productivity due to menorrhagia $1692/woman/year • (Cote 2002) 0.1 mm 2 MRgFUS Two technologies combined: • Focused ultrasound beam to ablate the specific tissue • MR imaging and thermal mapping system for visualization of patient anatomy and feedback on tissue temperature during the treatment MRI MR Imaging Anatomy • Magnetic Resonance Imaging (MRI) is a method used to visualize the inside of living organisms. • MRI uses non-ionizing, radio frequency signals to acquire images. MRI is best suited for soft (noncalcified) tissues. • Medical MRI relies on the relaxation properties of excited hydrogen nuclei in water and fat. Ribs Nerves Uterus Fibroid Breast Tumor Bladder Pubic bone T1W+C breast MR image T2W pelvic MR image MR Thermometry MR Guidance •Provides real-time feedback during treatment, showing regions that have met thermal dose requirements •Visualization of treatment plan before energy is delivered, identifies: Bowel Nerves Surgical clips 6 sec 12 sec 18 sec Parallel to beam path + + + 24 sec + Perpendicular to beam path + + + + Temperature graph sonicating cooling Scar 3 Patient Table Patient Table (con’t) • The table consists of front end electronics, and a cradle with the FUS transducer Transducer • The phased array transducer is housed in a sealed water bath • The transducer is connected to a robotic positioner cradle Electronics storage Robotic positioner • The patient table docks to the GE MR scanner Power cable Treatment Evaluation • Pre-treatment screening NPV ratio is the Non Perfused Volume (immediately post treatment) divided by the Total Fibroid Volume. • High NPV ratio was found to be related to: • SSS (Symptoms Severity Score, from the QOL questionnaire) improvement. • Low number of alternative treatments (in follow up). • Fibroids shrinkage (in follow up). 30% 90% Purpose • Identification of fibroids • Type, number and size • Position of organs, bowel and nerves • Accessibility of fibroids • Scars on abdominal wall Pre-treatment screening Procedure for screening MRI • T2WI in 2 planes (anatomy + pathology) • T1WI in one plane with and without contrast (for viability) • Use screening pad • Feet in first • Patient bladder should be empty Exclude patients that • • • • • • • Are younger than 18 yrs Are post menopausal Are pregnant or seek for future pregnancies Have serious health complications Have contraindications to MRI Uterine size is more than 24 weeks Have massive abdominal scarring in the pass zone (e.g. from laparotomy) • Have been previously treated with Uterine Artery Embolization (UAE) 4 MR Screening (1) • Perform MRI screening prior to the treatment to check the accessibility, viability and texture of the fibroid(s). • Use the images to check the size and number of fibroid(s) • MR screening can also reveal other uterine disorders that cannot be treated with MRgFUS, such as adenomyosis. MR Screening (2) • Screening procedure: • Position patient prone. Perform 2 plane T2w imaging (for anatomy and pathological conditions) and T1w imaging with and without contrast agent (to identify fibroid’s viability) Recommendation: •Screen the patient with empty bladder. •Use the ExAblate table, with the 4cm screening pad. Alternatively, use the 1cm screening pad on the MR table. Accessibility (1) Bowels should not be present in the beam path, as it may contain of air or energy absorbing particles. Accessibility (2) Refrain from other obstacles on the beam path, as: No No •IUD • Surgical clips • • No access • Surgical scars Yes Full access • Limited access Accessibility (3) • 12 cm from the skin is the maximal effective focal distance of the system. • Exclude patient with a significant deeper fibroid portion. Viability 12 cm Non-enhancing Partly enhancing Enhancing Non-enhancing on T1W with contrast are not viable, thus the treatment will have no additional benefit 5 Texture Viability Non-enhancing Partly enhancing Enhancing Non-enhancing on T1W with contrast are not viable, thus the treatment will have no additional benefit Dark Bright Bright fibroids on T2w images (relative to the uterus wall) are less susceptible to the treatment Size and number Adenomyosis • both adenomyosis and leiomyomas commonly coexist; concomitant adenomyosis • in hysterectomy specimens of women with leiomyomas ranges from 15 to 57% Don’t treat patients with 5 or more symptomsrelated fibroids •Total fibroid load should be less than 500 cc per treatment Adenomyosis Efficiency of treating adenomyosis has not yet been proven in clinical trials; there is anecdotal evidence. Treatment Cycle Sonication Cooling Sonication MR Scans Fetch Images Monitor sonication Compute Dose Review Results Adenomyosis during menstruation 6 Treatment Evaluation Accumulated Dose Coronal planning image with accumulated dose overlay • • • • Treated region (Non-Perfused Volume, NPV) Coronal image of posttreatment MRI with contrast There were no life-threatening adverse events in either group. Overall, the number of significant clinical complications and adverse events was lower in women in the MRgFUS group compared to women undergoing hysterectomy. MRgFUS was associated with significantly faster recovery, including resumption of usual activities. Women undergoing MRgFUS had steady improvement in all parameters throughout the 6-month follow-up period, despite the fact that they continued to have myomatous uteri and menstruation, which at baseline had given them significant symptomatology. • • • • • the non-perfused volume (NPV) ratio in 287 Japanese patients divided into two equal groups according to the chronological treatment time to estimate the learning curve effect. The NPV ratio increased chronologically, from 39.3% to 54.0% (P < 0.001), indicating increasing effectiveness of the treatment with experience. The mean NPV ratios for the entire patient population were over double that of previous clinical trials (46.6% vs. 21.9%; P < 0.001). No serious complications were reported The learning process and accumulation of data on MRgFUS enable the optimization of treatments in order to safely achieve large NPV ratios and sustained clinical benefit. Result(s): Fifty-four pregnancies in 51 women have occurred after MRgFUS treatment of uterine leiomyomas. The mean time to conception was 8 months after treatment. Live births occurred in 41% of pregnancies, with a 28% spontaneous abortion rate, an 11% rate of elective pregnancy termination, and 11 (20%) ongoing pregnancies beyond 20 gestational weeks. The mean birth weight was 3.3 kg, and the vaginal delivery rate was 64%. Conclusion(s): Preliminary pregnancy experience after MRgFUS is encouraging, with a high rate of delivered and ongoing pregnancies. 7 • • • • • • • • Result(s): Fifty-four pregnancies in 51 women have occurred after MRgFUS treatment of uterine leiomyomas. The mean time to conception was 8 months after treatment. Live births occurred in 41% of pregnancies 28% spontaneous abortion rate 11% rate of elective pregnancy termination 20% ongoing pregnancies beyond 20 gestational weeks. The mean birth weight was 3.3 kg, and the vaginal delivery rate was 64%. Conclusion(s): Preliminary pregnancy experience after MRgFUS is encouraging, with a high rate of delivered and ongoing pregnancies. Fertility and Sterility Vol. 93, No. 1, January 2010 1 8