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Study Comparing the Safety and Effectiveness of Magnetic Resonance Guided Focused Ultrasound (MRgFUS) and External Beam Radiation (EBRT) for Treatment of Metastatic Bone Tumors and Multiple Myeloma

Primary Purpose

Bone Cancer, Bone Metastases, Pain

Status
Completed
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
Exablate treatment
Radiation
Sponsored by
InSightec
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bone Cancer focused on measuring Bone cancer, Bone Metastases, pain palliation, metastasis, breast cancer, lung cancer, prostate cancer, cancer related pain, tumors

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Men and women age 18 years and older.
  2. Able and willing to give consent and to attend all study visits
  3. Patients with bone metastasis or primary bone lesion identifiable by imaging techniques.
  4. Worst NRS Pain Score of ≥ 4 from the tumor to be treated.
  5. Targeted tumor(s) are accessible to both ExAblate and EBRT (ExAblate accessible lesions are located in ribs, extremities (excluding joints), pelvis, shoulders and in the posterior aspects of the following spinal vertebra: Lumbar vertebra (L3 - L5), Sacral vertebra (S1 - S5), please see ExAblate "Information for Prescribers".
  6. Targeted tumor(s) area is smaller than 100cm2.
  7. Tumor(s) clearly visible by non-contrast MRI.
  8. No radiation therapy to the treated lesion during one month prior to enrollment.
  9. Radiation therapy is not contraindicated
  10. Bisphosphonate, chemo or hormone therapy intake should remain stable throughout follow up duration.

Exclusion Criteria:

  1. Patients who either

    • Need pre-treatment surgical stabilization of the affected bony structure OR
    • prior surgical stabilization of tumor site
  2. Targeted tumor is in a vertebra body or in the posterior aspects of the cervical part of the vertebral column.
  3. Targeted tumor is in the skull.
  4. Patients on anti-coagulation therapy or with an underlying uncontrolled bleeding disorder.
  5. Patients with life expectancy < 6-Months.
  6. Patients with unstable cardiac status including:

    • Unstable angina pectoris on medication.
    • Patients with documented myocardial infarction within last 40 days to protocol entry.
    • Congestive heart failure NYHA Class IV
  7. Severe hypertension (diastolic BP > 100 on medication).
  8. Patients with standard contraindications for MR imaging such as non-MRI compatible implanted ferromagnetic objects/devices.
  9. Known intolerance or allergies to MRI contrast agent (e.g. Gadolinium or Magnevist)
  10. KPS score of below 60
  11. Severe cerebro-vascular disease (multiple CVA or CVA within 6 months)
  12. Individuals who are not able or willing to tolerate the required prolonged stationary position during treatment (approximately 2 hrs.)
  13. Target tumor is less then 1cm from spinal cord, skin, or hollow viscera.

Sites / Locations

  • Taipei Medical University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Exablate treatment

Radiation

Arm Description

Exablate 2000

External Beam Radiation

Outcomes

Primary Outcome Measures

Safety of treatment
Incidence and severity of adverse events associated with the ExAblate MRgFUS bone system used in the palliation of pain due to metastatic bone tumors or multiple myeloma to that of EBRT
NRS score
Effect of treatment with MRgFUS ExAblate Bone System (BS) of painful bone tumors or multiple myeloma

Secondary Outcome Measures

Pain Medication dose and quantity
Decrease in analgesics/opiate
Quality of Life score
Improved quality of life (measured by questionnaires)

Full Information

First Posted
March 18, 2010
Last Updated
March 11, 2019
Sponsor
InSightec
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1. Study Identification

Unique Protocol Identification Number
NCT01091883
Brief Title
Study Comparing the Safety and Effectiveness of Magnetic Resonance Guided Focused Ultrasound (MRgFUS) and External Beam Radiation (EBRT) for Treatment of Metastatic Bone Tumors and Multiple Myeloma
Official Title
Phase IIIA Study Comparing the Safety and Effectiveness of MR Guided Focused Ultrasound and External Beam Radiation for Treatment of Metastatic Bone Tumors and Multiple Myeloma
Study Type
Interventional

2. Study Status

Record Verification Date
March 2019
Overall Recruitment Status
Completed
Study Start Date
May 2010 (undefined)
Primary Completion Date
January 2019 (Actual)
Study Completion Date
March 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
InSightec

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The goal of this study is to collect comparative data on safety and efficacy of MR Guided Focused Ultrasound and External Beam Radiation for treatment of metastatic bone tumors or multiple myeloma.
Detailed Description
Bone is the third most common organ involved by metastatic disease behind lung and liver [6]. In breast cancer, bone is the second most common site of metastatic spread, and 90% of patients dying of breast cancer have bone metastasis. Breast and prostate cancer metastasize to bone most frequently, which reflects the high incidence of both these tumors, as well as their prolonged clinical courses. Post-cancer survival has increased with improvement in early detection and treatments. As a consequence, the number of patients developing metastatic bone disease during their lifetime has also increased. Current treatments for patients with bone metastases are primarily palliative and include localized therapies (radiation and surgery), systemic therapies (chemotherapy, hormonal therapy, radiopharmaceutical, and bisphosphonates although the primary goal of the use of these therapies are often to address the disease itself), and analgesics (opioids and non-steroidal anti-inflammatory drugs). Recently, radiofrequency ablation has been tested as a treatment option for bone metastases [8]. Currently, an off label use of Cryoablation techniques are being tested as another alternative for bone Mets palliation. The main goals of these treatments are improvement of quality of life and functional level. These goals can be further described: Pain relief Preservation and restoration of function Local tumor control Skeletal stabilization Treatment with external beam radiation therapy (EBRT) is the standard of care for patients with localized bone pain, and results in the palliation of pain for many of these patients. Twenty to 30% of patients treated with radiation therapy do not experience pain relief [9-13]. Re-treatment rates are generally reported in the range of 10-25%. Many patients with relapsed pain or poor response to initial radiation may be lost to follow up or may not be referred back to oncologists for consideration of re-radiation. In addition to relapse and re-treatment, there is an increased risk of pathologic fracture in the peri-radiation period. The fracture rate reported in radiation studies is generally in the range of 1% to 8%. The hyperemic response weakens the adjacent bone and increases the risk of spontaneous fracture. Furthermore, patients who have recurrent pain at a site previously irradiated may not be eligible for further radiation therapy secondary to limitations in normal tissue tolerance. Hesitation on the part of physicians to use a larger dose may be related to increased long-term toxicity. Larger radiation dose produces a greater risk of complications such as fibrosis of normal soft tissue, which can cause a decrement in the quality of life in cases of life expectancy longer than 6 months. There may also be a greater incidence of acute side effects of nausea and vomiting if the treatment field includes the stomach. The percent of patients experiencing vomiting following EBRT ranges from about 5% to 30%. A palliative treatment for painful bone metastases that is non-invasive, without long-term toxicity and having minimal complications would be a useful tool for treating physicians and also a beneficial option for patients suffering from painful bone metastases. Results of preliminary studies indicate that ExAblate treatment of painful bone metastases may be a beneficial treatment option [14, 15]. The ExAblate system is a non-invasive thermal ablation device used in the coagulation of various types of soft tissue. The ExAblate system has the potential to achieve the first three of the four previously mentioned goals in the treatment of bone tumors; namely pain relief, preservation and restoration of functional levels and local tumor control [11]. This study will compare the safety and effectiveness of MR Guided Focused Ultrasound and External Beam Radiation for treatment of metastatic bone tumors or multiple myeloma.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bone Cancer, Bone Metastases, Pain
Keywords
Bone cancer, Bone Metastases, pain palliation, metastasis, breast cancer, lung cancer, prostate cancer, cancer related pain, tumors

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Exablate treatment
Arm Type
Experimental
Arm Description
Exablate 2000
Arm Title
Radiation
Arm Type
Active Comparator
Arm Description
External Beam Radiation
Intervention Type
Device
Intervention Name(s)
Exablate treatment
Intervention Description
MR Guided Focused Ultrasound
Intervention Type
Radiation
Intervention Name(s)
Radiation
Intervention Description
External Beam Radiation
Primary Outcome Measure Information:
Title
Safety of treatment
Description
Incidence and severity of adverse events associated with the ExAblate MRgFUS bone system used in the palliation of pain due to metastatic bone tumors or multiple myeloma to that of EBRT
Time Frame
6 months
Title
NRS score
Description
Effect of treatment with MRgFUS ExAblate Bone System (BS) of painful bone tumors or multiple myeloma
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Pain Medication dose and quantity
Description
Decrease in analgesics/opiate
Time Frame
6 months
Title
Quality of Life score
Description
Improved quality of life (measured by questionnaires)
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Men and women age 18 years and older. Able and willing to give consent and to attend all study visits Patients with bone metastasis or primary bone lesion identifiable by imaging techniques. Worst NRS Pain Score of ≥ 4 from the tumor to be treated. Targeted tumor(s) are accessible to both ExAblate and EBRT (ExAblate accessible lesions are located in ribs, extremities (excluding joints), pelvis, shoulders and in the posterior aspects of the following spinal vertebra: Lumbar vertebra (L3 - L5), Sacral vertebra (S1 - S5), please see ExAblate "Information for Prescribers". Targeted tumor(s) area is smaller than 100cm2. Tumor(s) clearly visible by non-contrast MRI. No radiation therapy to the treated lesion during one month prior to enrollment. Radiation therapy is not contraindicated Bisphosphonate, chemo or hormone therapy intake should remain stable throughout follow up duration. Exclusion Criteria: Patients who either Need pre-treatment surgical stabilization of the affected bony structure OR prior surgical stabilization of tumor site Targeted tumor is in a vertebra body or in the posterior aspects of the cervical part of the vertebral column. Targeted tumor is in the skull. Patients on anti-coagulation therapy or with an underlying uncontrolled bleeding disorder. Patients with life expectancy < 6-Months. Patients with unstable cardiac status including: Unstable angina pectoris on medication. Patients with documented myocardial infarction within last 40 days to protocol entry. Congestive heart failure NYHA Class IV Severe hypertension (diastolic BP > 100 on medication). Patients with standard contraindications for MR imaging such as non-MRI compatible implanted ferromagnetic objects/devices. Known intolerance or allergies to MRI contrast agent (e.g. Gadolinium or Magnevist) KPS score of below 60 Severe cerebro-vascular disease (multiple CVA or CVA within 6 months) Individuals who are not able or willing to tolerate the required prolonged stationary position during treatment (approximately 2 hrs.) Target tumor is less then 1cm from spinal cord, skin, or hollow viscera.
Facility Information:
Facility Name
Taipei Medical University Hospital
City
Taipei city
State/Province
Taipei
ZIP/Postal Code
11031
Country
Taiwan

12. IPD Sharing Statement

Citations:
PubMed Identifier
30519467
Citation
Bertrand AS, Iannessi A, Natale R, Beaumont H, Patriti S, Xiong-Ying J, Baudin G, Thyss A. Focused ultrasound for the treatment of bone metastases: effectiveness and feasibility. J Ther Ultrasound. 2018 Nov 30;6:8. doi: 10.1186/s40349-018-0117-3. eCollection 2018.
Results Reference
derived
Links:
URL
http://www.insightec.com
Description
Sponsor's Website

Learn more about this trial

Study Comparing the Safety and Effectiveness of Magnetic Resonance Guided Focused Ultrasound (MRgFUS) and External Beam Radiation (EBRT) for Treatment of Metastatic Bone Tumors and Multiple Myeloma

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