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Original Research |
1 All authors: Department of Radiology, University Imaging-Guided Therapy Center, 3848 FAU Blvd., Ste. 200, Boca Raton, FL 33431.
OBJECTIVE. The purpose of this study was to assess the degree of leiomyoma ablation and shrinkage after MRI-guided focused ultrasound treatment performed according to U.S. Food and Drug Administration protocols for commercial trials.
MATERIALS AND METHODS. A total of 147 symptomatic leiomyomas in 80 women (average age, 46 years; range, 34–55 years) were managed with MRI-guided focused ultrasound. The average volume of treated fibroids was 175 ± 201 (SD) cm3. Before treatment, T2-weighted MR images in three planes were obtained to measure leiomyoma volume. Immediately after treatment, T1-weighted contrast-enhanced fat-suppressed MR images in three planes were used to measure nonperfused volume ratio. Similar images obtained 6 months after treatment were used to determine leiomyoma shrinkage. Qualitative and quantitative relations between fibroid volume, nonperfused volume ratio at treatment, and 6-month shrinkage were measured.
RESULTS. The average nonperfused volume ratio was 55% ± 25% immediately after treatment. Six months after treatment, the average volume of treated fibroids had decreased to 112 ± 141 cm3 (n = 81) (p < 0.0001) with an average volume reduction of 31% ± 28%. A linear regression model showed highly significant correlation between posttreatment nonperfused volume ratio and shrinkage at 6 months (p < 0.0001).
CONCLUSION. MRI-guided focused ultrasound therapy for leiomyoma can result in nonperfused volume ratio and shrinkage that exceed those in previous clinical trials because the treatment guidelines have been relaxed to allow a greater amount of tissue ablation. The results suggest that a larger nonperfused volume ratio can be achieved, resulting in greater shrinkage and improved relief of symptoms.
Keywords: ablation fibroid leiomyoma MRI-guided focused ultrasound
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