Pilot Study for Palliation of Pain in Bone Metastases by MR-HIFU

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Philips Healthcare
ClinicalTrials.gov Identifier:
NCT01117246
First received: May 3, 2010
Last updated: February 17, 2012
Last verified: February 2012
  Purpose

This study is to confirm the safety and technical of MRI guided High Intensity Focused Ultrasound (HIFU) for Palliation for Pain of Skeletal Metastases.

MRI guided high intensity focused ultrasound uses ultrasound to heat and thermally ablate tissue. The MRI system identifies the ultrasound path and monitors heat rise in the tissue. The goal of the study is to show treatment safety and effectiveness. MR-guided HIFU will be performed in patients who pass inclusion/exclusion criteria.


Condition Intervention Phase
Secondary Malignant Neoplasm of Bone
Device: High Intensity Focused Ultrasound
Phase 1
Phase 2

Study Type: Interventional
Study Design: Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Supportive Care
Official Title: Pilot Study for the Treatment of Bone Metastases by High Intensity Focused Ultrasound Guided by MRI to Perform Pain Palliation

Resource links provided by NLM:


Further study details as provided by Philips Healthcare:

Primary Outcome Measures:
  • Technical efficacy by medication and pain score [ Time Frame: 0, 2, 7, 14, 30, 90 days ] [ Designated as safety issue: No ]
    Technical efficacy of HIFU for treatment of bone metastasis as assessed by a change in the medication and pain scores

  • Safety of treatment [ Time Frame: 0-90 days ] [ Designated as safety issue: Yes ]
    Safety of HIFU for treatment of the bone metastasis as determined by adverse event reporting

  • Safety determined by intended lesions [ Time Frame: 0-90 days ] [ Designated as safety issue: Yes ]
    Safety of HIFU for treatment of the bone metastasis as determined by formation of intended lesions.


Secondary Outcome Measures:
  • Treatment size [ Time Frame: 0-90 days ] [ Designated as safety issue: No ]
    MR-HIFU treatment size measurements

  • X-Ray treatment size measurements [ Time Frame: 0-90 days ] [ Designated as safety issue: No ]
    X-Ray treatment size measurements

  • Length of Hospital Stay [ Time Frame: 0-90 days ] [ Designated as safety issue: No ]
    Length of Hospital Stay

  • Quality of Life [ Time Frame: 0, 7, 14, 30, 90 days ] [ Designated as safety issue: No ]
    Quality of Life Questionnaire scores


Enrollment: 2
Study Start Date: May 2010
Study Completion Date: October 2011
Primary Completion Date: July 2011 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
Experimental: Treated bone metastasis
Patients with bone metastasis causing pain.
Device: High Intensity Focused Ultrasound
HIFU is the use of focused ultrasound energy to penetrate through soft tissue and causes localized high temperatures (55°C to 70°C) for a few seconds within the target producing well defined regions of protein and nerve denaturation, irreversible cell damage, and coagulative necrosis.
Other Names:
  • • HIFU
  • • Ablation
  • • High Intensity Focused Ultrasound

Detailed Description:

Bone is the third most common site of metastases spread after the liver and the lungs, with a great incidence in breast, prostate, lung, kidney and thyroid cancers. For example, 90% of patients dying from breast cancer and most of patients with advanced prostate cancer suffer from bone metastases, which are frequently responsible of chronic pain and lead to an increase in morbidity and mortality with pathological fractures, compression syndrome and hypercalcemia..Moreover, the increasing longevity of patients with cancer resulting from the improvement of the effectiveness of the treatments leads to a higher incidence and prevalence of metastating bone lesions.

Palliative treatment with management of pain and improvement of quality of life remains the first goal of therapy. Current treatments options include systemic drug therapy (chemotherapy, hormonal therapy, analgesics and bi-phosphonates), local invasive treatment (surgery), local mini-invasive treatment with interventional radiological techniques (cimentoplasty, cryotherapy and radiofrequency ablation) and radiation therapy.

External-beam radiation therapy remains the current standard of care for patients with bone metastases in first intention. However, up to 20-30 % of patients treated do not experience pain relief and recurrence of pain appear in 27 % after treatment. Moreover radiation treatment is limited due to accumulation of dose. Since few years, cryotherapy and percutaneous radiofrequency ablation have shown good results in management of pain with bone metastases, however these techniques are still invasive.

In MRI-guided High Intensity Focused Ultrasound (HIFU), the ultrasound generated by the transducer is focused into a small focal tissue volume at specific target locations. During treatment, the beam of focused ultrasound energy penetrates through soft tissue and causes localized temperatures elevation up 55-70°C for a few seconds within the target producing well defined regions of irreversible protein denaturation, cell damage, and coagulative necrosis. A single exposure of focused ultrasound energy is called a "sonication." Multiple sonications are necessary to ablate the targeted tissue. Tight focusing is designed to limit the ablation to the targeted location.

Applying HIFU energy to a patient's lesion requires treatment planning, targeting of the ultrasound (US) beam to desired locations and monitoring of the energy delivery. In some applications this can be performed using diagnostic ultrasound imaging in combination with the HIFU. While diagnostic US provides some anatomical details and helps with procedure planning and treatment targeting, it does not provide 3D planning, means of measuring the temperature increase generated by HIFU, or metrics for quantifying the energy/dose delivered to the treatment zone. Currently, only MR imaging can provide a validated non-invasive temperature measurement and thermal dose quantification in the treated tissue. Furthermore, these real-time MR temperature measurements can be used to control the HIFU system to deliver optimal temperatures to the target locations. The Philips MR-guided focused ultrasound system will provide real-time tissue temperature mapping in multiple planes and control of the temperature delivering dose to the target location. Recent advances in MR temperature mapping make it possible to achieve temperature accuracy of 1°C in stationary soft tissues.

  Eligibility

Ages Eligible for Study:   18 Years to 80 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Men and women aged > 18 years
  • Covered by social security insurance
  • Patient able to give consent and able to attend
  • study visit
  • Weight < 140kg
  • Patient with bone metastases
  • Pain localized on bone metastases to be treated with NRS (0-10 scale) pain score 4 irrespective of medication
  • Targeted tumor accessible for MR-HIFU treatment
  • The maximum size of the bone metastases smaller than 8cm in diameter
  • Targeted tumor visible by non contrast MRI
  • Interface between bone and skin deeper than 10 mm
  • Able to communicate sensation during treatment
  • Treatment day must be planned at least 2 weeks after any treatment of the primary tumor, chemotherapy or RT treatment of a bone targeted for HIFU

Exclusion Criteria:

  • Person subject to a judicial safeguard order, subject participating in another research study including an exclusion period which has not expired at the time of screening
  • Patient enrolled in another clinical study related to bone metastases or pain relief treatment
  • Pregnant or nursing woman
  • Need of surgical stabilization or site at risk of
  • fracture
  • More than one painful lesion per treatment
  • Patients who are not able to tolerate required stationary position during treatment
  • HIFU targeted tumor in contact with hollow viscera
  • Targeted tumor less than 1 cm to nerve bundles, bladder and bowel
  • Targeted tumor located in skull, spine (excepted sacrum) or sternum.
  • MRI or contrast agent contraindicated
  • Severe Cardiovascular, neurological, renal or hematological chronic disease
  • Active infection
  • Scar in the beam path
  • Orthopedic implant at the site of treatment
  • Previous surgery at the site of treatment Patient history, MRI exam
  • Primary musculoskeletal malignancies, lymphoma, or leukemia
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01117246

Locations
France
Hôpital St. André
Bordeaux, France
Sponsors and Collaborators
Philips Healthcare
Investigators
Principal Investigator: Hervé Trillaud, Professor Hôpital St. André, Service de Radiologie
  More Information

Publications:
Responsible Party: Philips Healthcare
ClinicalTrials.gov Identifier: NCT01117246     History of Changes
Other Study ID Numbers: 998771A, 2010-A00353-36
Study First Received: May 3, 2010
Last Updated: February 17, 2012
Health Authority: France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)

Keywords provided by Philips Healthcare:
bone metastasis
pain palliation

Additional relevant MeSH terms:
Neoplasm Metastasis
Neoplasms
Bone Neoplasms
Neoplasms, Second Primary
Bone Marrow Diseases
Neoplastic Processes
Pathologic Processes
Neoplasms by Site
Bone Diseases
Musculoskeletal Diseases
Hematologic Diseases

ClinicalTrials.gov processed this record on October 19, 2014