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Planning and delivery of intensity modulated bolus electron conformal therapy.
Hilliard, Elizabeth N; Carver, Robert L; Chambers, Erin L; Kavanaugh, James A; Erhart, Kevin J; McGuffey, Andrew S; Hogstrom, Kenneth R.
Afiliação
  • Hilliard EN; Department of Physics and Astronomy, Louisiana State University, Baton Rouge, Louisiana, USA.
  • Carver RL; Department of Physics and Astronomy, Louisiana State University, Baton Rouge, Louisiana, USA.
  • Chambers EL; Mary Bird Perkins Cancer Center, Baton Rouge, Louisiana, USA.
  • Kavanaugh JA; Department of Physics and Astronomy, Louisiana State University, Baton Rouge, Louisiana, USA.
  • Erhart KJ; Department of Radiation Oncology, Washington University School of Medicine, Saint Louis, Missouri, USA.
  • McGuffey AS; .decimal, LLC, Sanford, Florida, USA.
  • Hogstrom KR; Department of Physics and Astronomy, Louisiana State University, Baton Rouge, Louisiana, USA.
J Appl Clin Med Phys ; 22(10): 8-21, 2021 Oct.
Article em En | MEDLINE | ID: mdl-34558774
ABSTRACT

PURPOSE:

Bolus electron conformal therapy (BECT) is a clinically useful, well-documented, and available technology. The addition of intensity modulation (IM) to BECT reduces volumes of high dose and dose spread in the planning target volume (PTV). This paper demonstrates new techniques for a process that should be suitable for planning and delivering IM-BECT using passive radiotherapy intensity modulation for electrons (PRIME) devices.

METHODS:

The IM-BECT planning and delivery process is an addition to the BECT process that includes intensity modulator design, fabrication, and quality assurance. The intensity modulator (PRIME device) is a hexagonal matrix of small island blocks (tungsten pins of varying diameter) placed inside the patient beam-defining collimator (cutout). Its design process determines a desirable intensity-modulated electron beam during the planning process, then determines the island block configuration to deliver that intensity distribution (segmentation). The intensity modulator is fabricated and quality assurance performed at the factory (.decimal, LLC, Sanford, FL). Clinical quality assurance consists of measuring a fluence distribution in a plane perpendicular to the beam in a water or water-equivalent phantom. This IM-BECT process is described and demonstrated for two sites, postmastectomy chest wall and temple. Dose plans, intensity distributions, fabricated intensity modulators, and quality assurance results are presented.

RESULTS:

IM-BECT plans showed improved D90-10 over BECT plans, 6.4% versus 7.3% and 8.4% versus 11.0% for the postmastectomy chest wall and temple, respectively. Their intensity modulators utilized 61 (single diameter) and 246 (five diameters) tungsten pins, respectively. Dose comparisons for clinical quality assurance showed that for doses greater than 10%, measured agreed with calculated dose within 3% or 0.3 cm distance-to-agreement (DTA) for 99.9% and 100% of points, respectively.

CONCLUSION:

These results demonstrated the feasibility of translating IM-BECT to the clinic using the techniques presented for treatment planning, intensity modulator design and fabrication, and quality assurance processes.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Radioterapia Conformacional Limite: Female / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Radioterapia Conformacional Limite: Female / Humans Idioma: En Ano de publicação: 2021 Tipo de documento: Article