Frontiers in Oncology (Sep 2021)

Dosimetric Impact of Inter-Fraction Anatomical Changes in Carbon Ion Boost Treatment for High-Risk Prostate Cancer (AIRC IG 14300)

  • Stefania Russo,
  • Rosalinda Ricotti,
  • Silvia Molinelli,
  • Filippo Patti,
  • Filippo Patti,
  • Amelia Barcellini,
  • Edoardo Mastella,
  • Andrea Pella,
  • Chiara Paganelli,
  • Giulia Marvaso,
  • Giulia Marvaso,
  • Matteo Pepa,
  • Stefania Comi,
  • Mattia Zaffaroni,
  • Barbara Avuzzi,
  • Tommaso Giandini,
  • Emanuele Pignoli,
  • Riccardo Valdagni,
  • Riccardo Valdagni,
  • Guido Baroni,
  • Guido Baroni,
  • Federica Cattani,
  • Mario Ciocca,
  • Barbara Alicja Jereczek-Fossa,
  • Barbara Alicja Jereczek-Fossa,
  • Ester Orlandi,
  • Roberto Orecchia,
  • Barbara Vischioni

DOI
https://doi.org/10.3389/fonc.2021.740661
Journal volume & issue
Vol. 11

Abstract

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Rectum and bladder volumes play an important role in the dose distribution reproducibility in prostate cancer adenocarcinoma (PCa) radiotherapy, especially for particle therapy, where density variation can strongly affect the dose distribution. We investigated the reliability and reproducibility of our image-guided radiotherapy (IGRT) and treatment planning protocol for carbon ion radiotherapy (CIRT) within the phase II mixed beam study (AIRC IG 14300) for the treatment of high-risk PCa. In order to calculate the daily dose distribution, a set of synthetic computed tomography (sCT) images was generated from the cone beam computed tomography (CBCT) images acquired in each treatment session. Planning target volume (PTV) together with rectum and bladder volume variation was evaluated with sCT dose-volume histogram (DVH) metric deviations from the planning values. The correlations between the bladder and rectum volumes, and the corresponding DVH metrics, were also assessed. No significant difference in the bladder, rectum, and PTV median volumes between the planning computed tomography (pCT) and the sCT was found. In addition, no significant difference was assessed when comparing the average DVHs and median DVH metrics between pCT and sCT. Dose deviations determined by bladder and rectum filling variations demonstrated that dose distributions were reproducible in terms of both target coverage and organs at risk (OARs) sparing.

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