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Feasibility of ExAblate MRI Guided High Intensity Focused Ultrasound Tx of Soft Tissue Tumors

28 de abril de 2018 actualizado por: Pejman Ghanouni

A Feasibility Study to Evaluate the Safety and Effectiveness of ExAblate Magnetic Resonance Imaging Guided High Intensity Focused Ultrasound Treatment of Soft Tissue Tumors of the Extremities

The goal of this project is to evaluate the safety and preliminary efficacy of ExAblate magnetic resonance-guided high-intensity focused ultrasound (MRgHIFU) surgery in the treatment of soft tissue tumors of the extremities.

Descripción general del estudio

Descripción detallada

Given that the incidence of cancer increases with age, the number of elderly patients diagnosed and treated for soft tissue sarcomas (STS) will increase. The dilemma is that surgeons and medical oncologists may be hesitant to treat elderly patients in a comparably intensive manner as is used in the treatment of younger patients; factors such as decreased performance status, significant comorbidities, and disease natural history may erode enthusiasm for aggressive STS resection. To this end, a less invasive way of treating soft tissue tumors would be helpful in younger patients to minimize morbidity and in the elderly to provide less aggressive treatment options. The InSightec ExAblate 2000 magnetic resonance-guided high-intensity focused ultrasound (MRgHIFU) system is a non-invasive thermal ablation device fully integrated with an MR imaging system and used for the ablation of soft tissue (5-10). The ExAblate combines a focused ultrasound surgery (FUS) delivery system and a conventional diagnostic 1.5 T or 3 T MRI scanner. It provides a real-time therapy planning algorithm, thermal dosimetry, and closed-loop therapy control.

Tipo de estudio

Intervencionista

Inscripción (Actual)

5

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

    • California
      • Stanford, California, Estados Unidos, 94305
        • Stanford University School of Medicine

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

10 años y mayores (Niño, Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

INCLUSION CRITERIA

  • ≥ 10 years of age.
  • Benign or malignant soft tissue tumors of the extremities, flanks, pelvis, or shoulders requiring surgical intervention.
  • Tumor must not have been treated previously with radiation.
  • Targeted tumor(s) are accessible to the ExAblate device
  • Targeted volume within the tumor is located deeper than 1 cm from the skin
  • Targeted tumor is clearly visible by non-contrast magnetic resonance imaging (MRI)
  • Karnofsky Performance Status > 60
  • Normal platelet count and coagulation profile
  • Glomerular filtration rate > 60 mL/min
  • Able to safely undergo MRI exam and receive mild sedation for the treatment.
  • Able to tolerate being in the MRI scanner for the duration of the study.
  • Able and willing to give consent (or consent + assent where applicable), and able to attend all study visits.

EXCLUSION CRITERIA

  • Previous radiation treatment to the tumor.
  • Currently receiving dialysis.
  • Acute medical condition (eg, pneumonia, sepsis) expected to hinder completion of the study
  • Unstable cardiac status including:

    • Unstable angina pectoris on medication
    • Patients with documented myocardial infarction within six months of protocol entry
    • Congestive heart failure requiring medication (other than diuretic)
    • Patients on anti-arrhythmic drugs
  • Severe hypertension (diastolic BP > 100 on medication)
  • Contraindication for MR imaging such as implanted metallic devices that are not MRI-safe, size limitations, etc
  • Severe hematologic, neurologic, or other uncontrolled disease
  • Known intolerance or allergy to medications used for sedation (midazolam), analgesia (fentanyl), and local and regional anesthesia (lidocaine, bupivacaine, and ropivacaine)
  • Known intolerance or allergy to MR contrast agent (gadolinium chelates) including advanced kidney disease
  • Pregnant and nursing
  • Karnofsky Performance Score < 60
  • Severe cerebrovascular disease [cardiovascular accident (CVA) within 6 months]
  • Not able or not willing to tolerate the required prolonged stationary position during treatment (up to 5 hrs of total table time)
  • Target volume in tumor is less than 1 cm from neurovascular bundles, major blood vessels, bowel, or bladder.
  • Targeted tumors:

    • NOT visible by non-contrast MRI, OR
    • NOT accessible to ExAblate device
  • Not a candidate for either regional anesthesia or mild sedation
  • Not be participating in another trial testing other investigational agents or devices

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: N / A
  • Modelo Intervencionista: Asignación de un solo grupo
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: MRgHIFU
The InSightec ExAblate 2000 magnetic resonance-guided high-intensity focused ultrasound (MRgHIFU) system is a non-invasive device that is fully integrated with an MR imaging system and used for the ablation of soft tissue. The treatment process begins with the physician acquiring a set of MR images, identifying 1+ target volume(s) of fibroid tissue to be ablated, and drawing the treatment contours. The therapy planning software computes the type and number of sonications required to treat the defined volume while minimizing total treatment time. MR images taken during the sonication provide a diagnostic quality image of the target tissue and a quantitative, real-time temperature map overlay to confirm the therapeutic effect of the treatment. The transducer is then automatically moved to the succeeding treatment point and the process is repeated until the entire volume has been treated. About 100 individual sonications can be delivered over a 3-hour period to complete a treatment.
The InSightec ExAblate 2000 magnetic resonance-guided high-intensity focused ultrasound (MRgHIFU) system is a non-invasive thermal ablation device fully integrated with an MR imaging system and used for the ablation of soft tissue
Otros nombres:
  • ExAblate Magnetic Resonance Imaging Guided High Intensity Focused Ultrasound
325 mg PO for deep venous thrombosis (DVT) prophylaxis initiated 2 hours prior to magnetic resonance-guided high-intensity focused ultrasound (MRgHIFU) treatment
Otros nombres:
  • Ecotrina
40 mg by subcutaneous (SC) administration, for deep venous thrombosis (DVT) prophylaxis initiated 2 hours prior to magnetic resonance-guided high-intensity focused ultrasound (MRgHIFU) treatment
Otros nombres:
  • Lovenox

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Overall Safety - Incidence of Any Device-related Adverse Events
Periodo de tiempo: 1 week
Safety determined by evaluating for the incidence of any device-related adverse events. Patients will be assessed for pain and limb function, and by clinical examination before and after treatment to collect adverse events related to the treatment. Safety is reported as the total incidence of device-related adverse events.
1 week

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Adverse Event Severity
Periodo de tiempo: 6 months

Safety is further assessed by an evaluation of severity for the treatment-related adverse events, reported as the number of adverse events for each of the Common Terminology Criteria for Adverse Events (CTCAE) v4.0 grades.

CTCAE Severity:

  1. mild
  2. moderate
  3. severe
  4. life-threatening
  5. fatal
6 months
Percent Successful Tumor Ablation
Periodo de tiempo: Up to 1 week
In the resected tumor specimen, the volume of the ablated area will be determined by obtaining a digital photograph of each pathology slice. The region of interest corresponding to the ablated area will be traced, and the ablated area will be calculated for each slice and summed. Accuracy is assessed as the percent ablated volume relative to pre-treatment tumor volume.
Up to 1 week

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Investigadores

  • Investigador principal: Pejman Ghanouni, MD, PhD, Stanford University
  • Investigador principal: Raffi Avedian, MD, Stanford University

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio

1 de mayo de 2014

Finalización primaria (Actual)

24 de marzo de 2015

Finalización del estudio (Actual)

24 de marzo de 2015

Fechas de registro del estudio

Enviado por primera vez

15 de octubre de 2013

Primero enviado que cumplió con los criterios de control de calidad

15 de octubre de 2013

Publicado por primera vez (Estimar)

17 de octubre de 2013

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

23 de mayo de 2018

Última actualización enviada que cumplió con los criterios de control de calidad

28 de abril de 2018

Última verificación

1 de abril de 2018

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

Ensayos clínicos sobre MRgHIFU

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