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Thermoacoustic Range Verification During Delivery of a Clinical Plan by a Synchrocyclotron: transition from research prototype to turnkey clinical device

Thermoacoustic Range Verification During Delivery of a Clinical Plan by a Synchrocyclotron: transition from research prototype to turnkey clinical device
同步回旋加速器交付临床计划期间的热声范围验证:从研究原型到交钥匙临床设备的过渡
批准号:
10600975
负责人:
SARAH Kathryn PATCH
金额:
$37.8万
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
未结题
起止时间:
2019-08-01 至 2025-03-31

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英文摘要
Particle therapy is a technique for treating solid tumors that is potentially more precise than x-ray radiation therapy. Charged particles enter the patient at relativistic speeds, depositing increasingly more dose as they come to rest inside the patient. X-ray photon beams deliver an exponentially decaying dose along the beam path, dosing healthy tissue before and after the tumor. Proton therapy causes less collateral damage, and when patient alignment is accurate, delivers less dose to healthy proximal tissue and spares distal tissue altogether. Today, patients are positioned by matching bony structures in daily x- ray images to planning CT volumes acquired days (or weeks) prior. Inter-fraction changes to soft tissue (weight loss, edema) are common and intra-fraction changes (digestion, respiration, etc.) are unavoidable. Range errors incorrectly dose healthy tissue and undertreat the tumor, limiting benefits of proton therapy. Therefore, the American Society for Therapeutic Radiation Oncology currently supports proton therapy for tumors near the base of the neck, spine, eye and in pediatric patients, and only in the context of research studies for most other tumor sites. Thermoacoustic range verification relies upon stress confinement and is suitable for compact synchrocyclotrons recently introduced by two manufacturers, IBA and Mevion. A prototype system has been validated for use with IBA systems and the same receive chain has been validated for Mevion. System design for a thermoacoustic range verification (tARV) device will be finalized and validated during Phase II. The tARV consists of a wireless ultrasound array around which six thermoacoustic receivers are packed. A compact (65mm x 55mm) data acquisition (DAQ) board provides 56-59 dB gain over the thermoacoustic frequency range of 10-100 kHz, samples at 500 ksps to minimize aliasing of high frequency noise, and stores data to a secure data card onboard. A compact gamma detector monitors beam intensity and provides a trigger to the DAQ. End-to-end validation requires software integration with the treatment planning system (TPS) software used in radiotherapy clinics. Furthermore, QA and clinically realistic test objects, called phantoms, are required. Thermoacoustics is a hybrid technique that combines aspects of ultrasound imaging and radiation therapy. Commercial phantoms designed for ultrasound imaging have not yet been vetted for radiation therapy. We will integrate software, quantify materials in ultrasound phantoms already produced by CIRS, Inc and add dosimetric capability to enable end-to-end validation in a clinical environment.
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Thermoacoustic Range Verification During Delivery of a Clinical Plan by a Synchrocyclotron: transition from research prototype to turnkey clinical device
  • 批准号:
    10481746
  • 项目类别:
  • 资助金额:
    $105.06万
  • 财政年份:
    2019
  • 负责人:
    SARAH Kathryn PATCH
  • 依托单位:
Testbed for Quantitative Thermoacoustic Tomography
  • 批准号:
    8017455
  • 项目类别:
  • 资助金额:
    $15.37万
  • 财政年份:
    2010
  • 负责人:
    SARAH Kathryn PATCH
  • 依托单位:
Testbed for Quantitative Thermoacoustic Tomography
  • 批准号:
    7798351
  • 项目类别:
  • 资助金额:
    $19.06万
  • 财政年份:
    2010
  • 负责人:
    SARAH Kathryn PATCH
  • 依托单位:
海外基金