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J Ther Ultrasound. 2014 Oct 10;2:16. doi: 10.1186/2050-5736-2-16. eCollection 2014.

Feasibility of volumetric MRI-guided high intensity focused ultrasound (MR-HIFU) for painful bone metastases.

Journal of therapeutic ultrasound

Merel Huisman, Mie K Lam, Lambertus W Bartels, Robbert J Nijenhuis, Chrit T Moonen, Floor M Knuttel, Helena M Verkooijen, Marco van Vulpen, Maurice A van den Bosch

Affiliations

  1. Department of Radiology, University Medical Center Utrecht, Heidelberglaan 100, 3508 GA Utrecht, The Netherlands.
  2. Image Sciences Institute, University Medical Center Utrecht, 3508 GA Utrecht, The Netherlands.
  3. Department of Radiation Oncology, University Medical Center Utrecht, 3508 GA Utrecht, The Netherlands.

PMID: 25309743 PMCID: PMC4193684 DOI: 10.1186/2050-5736-2-16

Abstract

BACKGROUND: Magnetic resonance-guided high intensity focused ultrasound (MR-HIFU) has recently emerged as an effective treatment option for painful bone metastases. We describe here the first experience with volumetric MR-HIFU for palliative treatment of painful bone metastases and evaluate the technique on three levels: technical feasibility, safety, and initial effectiveness.

METHODS: In this observational cohort study, 11 consecutive patients (7 male and 4 female; median age, 60 years; age range, 53-86 years) underwent 13 treatments for 12 bone metastases. All patients exhibited persistent metastatic bone pain refractory to the standard of care. Patients were asked to rate their worst pain on an 11-point pain scale before treatment, 3 days after treatment, and 1 month after treatment. Complications were monitored. All data were prospectively recorded in the context of routine clinical care. Response was defined as a ≥2-point decrease in pain at the treated site without increase in analgesic intake. Baseline pain scores were compared to pain scores at 3 days and 1 month using the Wilcoxon signed-rank test. For reporting, the STROBE guidelines were followed.

RESULTS: No treatment-related major adverse events were observed. At 3 days after volumetric MR-HIFU ablation, pain scores decreased significantly (p = 0.045) and response was observed in a 6/11 (55%) patients. At 1-month follow-up, which was available for nine patients, pain scores decreased significantly compared to baseline (p = 0.028) and 6/9 patients obtained pain response (overall response rate 67% (95% confidence interval (CI) 35%-88%)).

CONCLUSIONS: This is the first study reporting on the volumetric MR-HIFU ablation for painful bone metastases. No major treatment-related adverse events were observed during follow-up. The results of our study showed that volumetric MR-HIFU ablation for painful bone metastases is technically feasible and can induce pain relief in patients with metastatic bone pain refractory to the standard of care. Future research should be aimed at standardization of the treatment procedures and treatment of larger numbers of patients to assess treatment effectiveness and comparison to the standard of care.

Keywords: Bone metastases; Feasibility; Focused ultrasound; Magnetic resonance imaging; Oncology; Palliative treatment

References

  1. Radiother Oncol. 2002 Sep;64(3):275-80 - PubMed
  2. Eur Radiol. 2012 Feb;22(2):411-7 - PubMed
  3. Pain. 1997 Jan;69(1-2):1-18 - PubMed
  4. Int J Radiat Oncol Biol Phys. 1984 Jun;10(6):787-800 - PubMed
  5. Radiology. 2014 Feb;270(2):589-600 - PubMed
  6. N Engl J Med. 2013 Aug 15;369(7):640-8 - PubMed
  7. Cancer Imaging. 2011 Oct 03;11:S161-6 - PubMed
  8. Int J Radiat Oncol Biol Phys. 2012 Sep 1;84(1):8-14 - PubMed
  9. Radiology. 2011 Apr;259(1):39-56 - PubMed
  10. J Ther Ultrasound. 2014 Feb 27;2:2 - PubMed
  11. Pain. 2001 Nov;94(2):149-158 - PubMed
  12. J Magn Reson Imaging. 2008 Feb;27(2):376-90 - PubMed
  13. Lancet. 2009 Sep 26;374(9695):1105-12 - PubMed
  14. Radiology. 2008 Oct;249(1):355-63 - PubMed
  15. Clin Oncol (R Coll Radiol). 2012 Mar;24(2):112-24 - PubMed
  16. Eur J Clin Invest. 2008 Apr;38(4):268-75 - PubMed
  17. Eur Radiol. 2007 Sep;17(9):2401-10 - PubMed
  18. Lancet Oncol. 2014 Feb;15(2):164-71 - PubMed
  19. Radiother Oncol. 1999 Aug;52(2):101-9 - PubMed
  20. Int J Radiat Oncol Biol Phys. 2011 Mar 15;79(4):965-76 - PubMed
  21. Neurosurgery. 2010 Feb;66(2):323-32; discussion 332 - PubMed
  22. Radiographics. 1996 Jan;16(1):185-95 - PubMed
  23. Med Phys. 2009 Aug;36(8):3521-35 - PubMed
  24. J Natl Cancer Inst. 2014 Apr 23;106(5): - PubMed
  25. Magn Reson Med. 1995 Dec;34(6):814-23 - PubMed
  26. Radiother Oncol. 2014 Jan;110(1):61-70 - PubMed
  27. Int J Radiat Oncol Biol Phys. 2012 Apr 1;82(5):1730-7 - PubMed
  28. Ann Surg Oncol. 2009 Jan;16(1):140-6 - PubMed
  29. Med Phys. 2013 Aug;40(8):080901 - PubMed
  30. Ann Oncol. 2007 Jan;18(1):163-167 - PubMed
  31. Cardiovasc Intervent Radiol. 2013 Oct;36(5):1190-203 - PubMed
  32. Invest Radiol. 2013 Jun;48(6):351-8 - PubMed
  33. Neuroimaging Clin N Am. 2001 Nov;11(4):737-47, xi - PubMed
  34. Magn Reson Med. 1998 Sep;40(3):454-9 - PubMed
  35. Am J Obstet Gynecol. 2003 Jul;189(1):48-54 - PubMed
  36. Eur Radiol. 2013 Nov;23(11):3054-61 - PubMed
  37. Cancer J. 2002 May-Jun;8 Suppl 1:S100-12 - PubMed

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