Abstract

BackgroundIn comparison to the conventional whole-prostate dose escalation, an integrated boost to the macroscopic malignant lesion might potentially improve tumor control rates without increasing toxicity. Quality of life after radiotherapy (RT) with vs. without 18F-choline PET-CT detected simultaneous integrated boost (SIB) was prospectively evaluated in this study.MethodsWhole body image acquisition in supine patient position followed 1 h after injection of 178-355MBq 18F-choline. SIB was defined by a tumor-to-background uptake value ratio > 2 (GTVPET). A dose of 76Gy was prescribed to the prostate (PTVprostate) in 2Gy fractions, with or without SIB up to 80Gy. Patients treated with (n = 46) vs. without (n = 21) SIB were surveyed prospectively before (A), at the last day of RT (B) and a median time of two (C) and 19 month (D) after RT to compare QoL changes applying a validated questionnaire (EPIC - expanded prostate cancer index composite).ResultsWith a median cut-off standard uptake value (SUV) of 3, a median GTVPET of 4.0 cm3 and PTVboost (GTVPET with margins) of 17.3 cm3 was defined. No significant differences were found for patients treated with vs. without SIB regarding urinary and bowel QoL changes at times B, C and D (mean differences ≤3 points for all comparisons). Significantly decreasing acute urinary and bowel score changes (mean changes > 5 points in comparison to baseline level at time A) were found for patients with and without SIB. However, long-term urinary and bowel QoL (time D) did not differ relative to baseline levels - with mean urinary and bowel function score changes < 3 points in both groups (median changes = 0 points). Only sexual function scores decreased significantly (> 5 points) at time D.ConclusionsTreatment planning with 18F-choline PET-CT allows a dose escalation to a macroscopic intraprostatic lesion without significantly increasing toxicity.

Highlights

  • In comparison to the conventional whole-prostate dose escalation, an integrated boost to the macroscopic malignant lesion might potentially improve tumor control rates without increasing toxicity

  • Treatment was based on 18F-choline PET-CT for patients in focus of this study

  • We have identified an area of about 1 cm2 within the prostate with the lowest activity and defined the threshold for GTVPET after multiplying the SUVmax in this area by 2 [8]

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Summary

Introduction

In comparison to the conventional whole-prostate dose escalation, an integrated boost to the macroscopic malignant lesion might potentially improve tumor control rates without increasing toxicity. Quality of life after radiotherapy (RT) with vs without 18F-choline PET-CT detected simultaneous integrated boost (SIB) was prospectively evaluated in this study. Increasing doses for prostate cancer have been shown to be associated with improved biochemical control rates in several prospective randomized studies [1]. Local prostate cancer recurrence after primary radiotherapy (RT) usually originates in the location of the primary tumor. Cellini et al found the origin of all local recurrences within the initial tumor volume, supporting the rationale of a selective dose escalation only to the intraprostatic lesion [4]. Quality of life (QoL) changes were evaluated prospectively and compared to a patient group treated with the same concept in the same time interval - but without a SIB - to demonstrate an acceptable treatment tolerance and a rationale to continue this innovative strategy

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