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Clinical outcome and toxicity evaluation of simultaneous integrated boost pelvic IMRT/VMAT at different dose levels combined with androgen deprivation therapy in prostate cancer patients

OncoTargets and Therapy Oct 19, 2017

Daoud MA, et al. - This study was designed to determine whether dose escalation for ≥ 76–80 Gy had an advantage in terms of biochemical disease-free survival (BDFS), distant metastasis-free survival (DMFS), or overall survival outcomes over the dose levels from 70 to <76 Gy. The BDFS and DMFS did not differ significantly between patients treated with a dose of <76 and ≥76 Gy, including elective pelvic lymph nodes irradiation combined with androgen deprivation therapy (ADT).

Methods

  • A cohort of 24 patients classified with high- and intermediate-risk localized prostate cancer was studied.
  • ADT was administered to all patients, starting at 4–6 months before radiation therapy and continued for a total period of 12–24 months in high-risk patients.
  • In two phases, the treatment plan was provided.
  • The nodal planning target volume (PTV) and the prostate PTV in the first phase received 48.6 and 54 Gy, respectively, over 27 fractions.
  • Through intensity-modulated radiation therapy or volumetric modulated arc therapy with a simultaneous integrated boost technique, the treatment was applied.

Results

  • Findings revealed that more than half of the patients were in T3–T4 stage; 79.1% of the patients were in the high-risk category.
  • All patients received ADT.
  • Acute grade II gastrointestinal and genitourinary toxicities were observed in 41.7% and 62.5%, respectively.
  • For patients treated with dose levels <76 and ≥76 Gy, the rate of freedom from grade II rectal toxicity at 2 years was 89% and 83%, respectively.
  • The rate of BDFS at 2 years was 90% and 85% for doses <76 and ≥76 Gy, respectively.
  • At 2 years, the DMFS was 100% and 76% for dose levels <76 and ≥76 Gy, respectively.
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