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Effect of modern, high-quality prostate intensity-modulated radiation therapy on outcome: Evidence from a community radiation oncology program.
Kao, Johnny; Zucker, Amanda; Timmins, Jonathan; Taramangalam, Shankar; Pettit, Jeffrey; Woodall, Aaron J; Loizides, Edward; Wong, Andrew T.
Afiliação
  • Kao J; Department of Radiation Oncology, Good Samaritan Hospital Medical Center, West Islip, NY 11795, USA.
  • Zucker A; Department of Radiation Oncology, Good Samaritan Hospital Medical Center, West Islip, NY 11795, USA.
  • Timmins J; Department of Radiation Oncology, Good Samaritan Hospital Medical Center, West Islip, NY 11795, USA.
  • Taramangalam S; Department of Radiation Oncology, Good Samaritan Hospital Medical Center, West Islip, NY 11795, USA.
  • Pettit J; Department of Radiation Oncology, Good Samaritan Hospital Medical Center, West Islip, NY 11795, USA.
  • Woodall AJ; Division of Urology, Good Samaritan Hospital Medical Center, West Islip, NY 11795, USA.
  • Loizides E; Division of Urology, Good Samaritan Hospital Medical Center, West Islip, NY 11795, USA.
  • Wong AT; Department of Radiation Oncology, Good Samaritan Hospital Medical Center, West Islip, NY 11795, USA.
Mol Clin Oncol ; 7(2): 252-258, 2017 Aug.
Article em En | MEDLINE | ID: mdl-28781797
ABSTRACT
Radiation technique for prostate cancer has continuously evolved over the past several decades. The aim of the present study was to describe the effects of implementing modern prostate intensity-modulated radiation therapy (M-IMRT) on dosimetry and outcome. Between January 2010 and April 2012, 48 consecutive patients were treated with conventional prostate IMRT (C-IMRT) to a dose of 81 Gy. Between May 2012 and April 2015, 50 consecutive patients were treated with M-IMRT to the entire prostate to a dose of 75.6-79.2 Gy, while using prostate magnetic resonance imaging fusion, dose-volume constraints prioritizing normal tissue avoidance above planning target volume coverage, and boosting any dominant intraprostatic masses to 79.2-81 Gy. Rectal Dmax, V75, V60, V65 and V50, bladder Dmax, V75, V70 and V65, and acute and late toxicities were compared between the C-IMRT and M-IMRT groups. The median follow-up for the C-IMRT and M-IMRT groups was 61 vs. 26 months, respectively (P<0.001). M-IMRT resulted in a significant reduction in median rectal Dmax, rectal V75, rectal V70, rectal V65, bladder Dmax, bladder V75, bladder V70 and bladder V65 (P<0.01 for all). There was no significant difference in rectal V50. The 2-year rate of late grade ≥2 rectal bleeding was 13% with C-IMRT vs. 3% with M-IMRT (P=0.03). The 2-year rate of late grade ≥2 genitourinary toxicity was 11% for C-IMRT vs. 5% for M-IMRT (P=0.21). There were no significant differences in acute toxicity, biochemical control or overall survival. Therefore, compared with C-IMRT, M-IMRT was associated with reduced rectal toxicity without compromising disease control.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Mol Clin Oncol Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Mol Clin Oncol Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos