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Secondary Malignant Neoplasm of BonePhase 1/2NCT01117246

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

A Phase 1/2 study testing High Intensity Focused Ultrasound in people with Secondary Malignant Neoplasm of Bone, run by Philips Healthcare at 1 site in France.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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. Read more about this study

Who is it for?
Ages 18 to 80 years
Conditions the study is for
Secondary Malignant Neoplasm of Bone
What is being tested?
High Intensity Focused Ultrasound
Type of treatment
Medical device
Could I receive a placebo?
No, everyone receives an active treatment
How many people
2 participants
Where
1 siteFrance
Study dates
May 2010to Oct 2011
Phase
Phase 1/2
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • 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
Show all 13Show fewer
  • 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

Who cannot join

  • 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
Show all 17Show fewer
  • 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

Trial locations and contacts

1 site in 1 country.

France1 site
  • Hôpital St. André

    Bordeaux

Other trials in France

About this study

Official title: Pilot Study for the Treatment of Bone Metastases by High Intensity Focused Ultrasound Guided by MRI to Perform Pain Palliation

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.

Read the 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.

Being tested
High Intensity Focused Ultrasound
Keywords
bone metastasis, pain palliation

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • High Intensity Focused UltrasoundDevice

    Also called • HIFU, • Ablation, • 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.

Study groups in NCT01117246
Study groupRoleWhat they receive
Treated bone metastasisExperimentalPatients with bone metastasis causing pain.
Receives: Device: High Intensity Focused Ultrasound

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Technical efficacy by medication and pain score

    Technical efficacy of HIFU for treatment of bone metastasis as assessed by a change in the medication and pain scores

    Measured: 0, 2, 7, 14, 30, 90 days

  2. Safety of treatment

    Safety of HIFU for treatment of the bone metastasis as determined by adverse event reporting

    Measured: 0-90 days

  3. Safety determined by intended lesions

    Safety of HIFU for treatment of the bone metastasis as determined by formation of intended lesions.

    Measured: 0-90 days

Secondary outcomes (4)
  1. Treatment size

    MR-HIFU treatment size measurements

    Measured: 0-90 days

  2. X-Ray treatment size measurements

    X-Ray treatment size measurements

    Measured: 0-90 days

  3. Length of Hospital Stay

    Length of Hospital Stay

    Measured: 0-90 days

  4. Quality of Life

    Quality of Life Questionnaire scores

    Measured: 0, 7, 14, 30, 90 days

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted5 May 2010 (estimated)
  2. Study startMay 2010
  3. Primary completionJul 2011
  4. Study completionOct 2011

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 1/2
Primary purpose
Supportive care
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
2 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01117246
Sponsor's protocol ID
998771A
Other IDs
2010-A00353-36
Status last verified
Feb 2012
First submitted
3 May 2010
Last updated
20 Feb 2012
Results posted
No
Data monitoring committee
Yes

Publications

  • Chow E, Wu JS, Hoskin P, Coia LR, Bentzen SM, Blitzer PH. International consensus on palliative radiotherapy endpoints for future clinical trials in bone metastases. Radiother Oncol. 2002 Sep;64(3):275-80. doi: 10.1016/s0167-8140(02)00170-6.

    PubMed 12242115

Questions about this trial

What is this clinical trial studying?

A Phase 1/2 study testing High Intensity Focused Ultrasound in people with Secondary Malignant Neoplasm of Bone, run by Philips Healthcare at 1 site in France.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 13 inclusion and 17 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 20 Feb 2012. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in France. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this combined phase mean?

Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Technical efficacy by medication and pain score (time frame: 0, 2, 7, 14, 30, 90 days). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT01117246, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Feb 2012.

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