AI Article Synopsis

  • The study aims to explore the link between prostate trauma during brachytherapy and the resulting acute urinary toxicity experienced by patients.
  • Researchers tracked needle repositioning and manipulations near the urethra, alongside other metrics, to analyze their relationship with urinary complications.
  • Findings indicate that increased periurethral needle manipulations correlate significantly with higher urinary toxicity, suggesting that minimizing these manipulations may help reduce side effects.

Article Abstract

Purpose: To determine if there is an association between the degree of prostate trauma during prostate brachytherapy and development of acute urinary toxicity.

Methods And Materials: In a consecutive prospective cohort of permanent (125)I prostate brachytherapy patients, the number of times each needle was repositioned was tracked, and the dosimetry plans were used to determine the number of times needles within 1 cm of the urethra were manipulated. Additionally, prostate volume, total number of needles, number of needles/prostate volume, and the number of periurethral needle manipulations/prostate volume were determined. The need for catheterization beyond 24 hours and the Radiation Therapy Oncology Group (RTOG) urinary toxicity score at 4 weeks were recorded. The independent samples t test was used to search for a correlation between these parameters and the recorded toxicity scores.

Results: Twenty-eight consecutive implant patients were evaluated in the study. Median (range) values were as follows: prostate volume 35 cc ( range, 15-51 cc), number of needles per patient 32 (range, 21-41), number of needle manipulations per patient 94.5 ( range, 55-147), and number of periurethral needle manipulations 42 (range, 17-65). The only significant association between urinary toxicity and these variables was for the number of periurethral needle manipulations (p = 0.025).

Conclusions: These data provide evidence that needle prostate trauma during brachytherapy contributes to acute urinary toxicity.

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Source
http://dx.doi.org/10.1016/j.ijrobp.2004.01.041DOI Listing

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