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From the Wires
New Publications Show Noninvasive Magnetic Resonance-Guided Focused Ultrasound to be a Potentially Safe, Effective Pain-Relieving Treatment for Bone Metastases
Pivotal Study Now Being Conducted at Nine Sites in North America
By: PR Newswire
Dec. 2, 2008 08:01 AM
TIRAT CARMEL, "The increasing longevity of the population along with the rise in cancer
incidence during the last decade and ever-improving treatment outcomes for
primary cancers contributes to the growing number of patients living with
metastatic bone disease," said Of the 25 patients included in Dr. Liberman's efficacy analysis, 72% (18/25) experienced significant pain relief, with 36% (9/25) reporting no pain at three months. More than half of the patients (52%) reported substantial pain relief at the follow-up visit three days after their treatment. A majority of the patients also decreased their opioid and non-opioid analgesic intake following treatment. No device-related adverse events were reported. In subgroup analysis, researchers from Mount Sinai Hospital in InSightec is currently enrolling patients into a FDA approved Phase 3
pivotal study to confirm these earlier results. InSightec expects to enroll
148 subjects with bone metastases who are not candidates to radiation
treatments into the study at centers throughout the U.S. and around the
world. Participating sites include Brigham & Women's Hospital in (Due to the length of this URL, it may be necessary to copy and paste this hyperlink into your Internet browser's URL address field. Remove the space if one exists.) InSightec is also conducting a similar study outside Bone pain is the most common source of pain in patients suffering from metastatic cancer. Almost all patients with metastatic prostate cancer have skeletal metastases and 90% of patients with progressive breast cancer develop these painful and debilitating lesions. Current pain treatments consist of systemic therapy (analgesics, chemotherapy, hormonal therapy and bisphosphonates) and local treatments (radiation, surgery and more recently, Radio Frequency Ablation (RFA)). During the ExAblate(R) treatment, the physician uses the Magnetic Resonance Imaging (MRI) with registered CT images to visualize the patient's anatomy and then aims focused ultrasound waves at the tumor to relieve the pain. The MRI allows the physician to monitor and continuously adjust the treatment in real time. The patient is consciously sedated to alleviate pain and minimize motion. Due to the high acoustic absorption and low thermal conductivity of the bone cortex, it is possible to use a low level of energy and still achieve a localized heating effect that will relieve the pain while minimizing damage to adjacent tissue. The ExAblate(R) system will be on display at the GE Healthcare booth
(number #5529 South Hall) at the Radiological Society of About ExAblate(R) ExAblate(R) is currently used commercially as a treatment for symptomatic
uterine fibroids. The system received its European CE Mark in uterine
fibroids in 2002 and the U.S. Food and Drug Administration approved the
system as a treatment for symptomatic uterine fibroids in 2004. Over 4,500
symptomatic women have been treated with the ExAblate to date with 92%
reporting symptom relief up to 36-months after treatment. The ExAblate system
received the European CE Mark certification for pain palliation of bone
metastases in About InSightec InSightec Ltd. is a privately held company owned by Elbit Imaging,
General Electric, MediTech Advisors, LLC and employees. It was founded in
1999 to develop the breakthrough MR guided Focused Ultrasound technology and
transform it into the next generation operating room. Headquartered near
For media inquiries:
Lazar Partners, Ltd.
Tel: +1-212-867-1762
Email: hhovey@lazarpartners.com
SOURCE InSightec Ltd
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