Abstract

Outcome data on radiation therapy for prostate cancer in an elderly population are sparse. The CHHiP (Conventional or Hypofractionated High Dose Intensity Modulated Radiotherapy in Prostate Cancer) trial provides a large, prospectively collected, contemporary dataset in which to explore outcomes by age. CHHiP participants received 3 to 6months of androgen deprivation therapy and were randomly assigned (1:1:1) to receive 74Gy in 37 fractions (conventional fractionation), 60Gy in 20 fractions, or 57Gy in 19 fractions. Toxicity was assessed using clinician-reported outcome (CRO) and patient-reported outcome questionnaires. Participants were categorized as aged < 75years or ≥ 75years. Outcomes were compared by age group. Of 3216 patients, 491 (15%) were aged≥75years. There was no difference in biochemical or clinical failure rates between the groups aged < 75years and ≥ 75years for any of the fractionation schedules. In the group aged ≥ 75years, biochemical or clinical failure-free rates favored hypofractionation, and at 5years, they were 84.7% for 74Gy, 91% for 60Gy, and 87.7% for 57Gy. The incidence of CRO (grade 3) acute bowel toxicity was 2% in both age groups.The incidence of grade 3 acute bladder toxicity was 8% in patients aged<75years and 7% in those aged≥75years.The 5-year cumulative incidence of CRO grade≥2 late bowel side effects was similar in both age groups.However, in the group aged≥75years, there was a suggestion of a higher cumulative incidence of bowel bother (small or greater) with 60Gy compared with 74Gy and 57Gy. Patient-reported bladder bother was slightly higher in the group aged ≥ 75years than the group aged < 75years, and there was a suggestion of a lower cumulative incidence of bladder bother with 57Gy compared with 74Gy and 60Gy in patients aged ≥ 75years, which was not evident in those aged < 75years. Hypofractionated radiation therapy appears to be well tolerated and effective in men aged ≥ 75years. The 57-Gy schedule has potential advantages in that it may moderate long-term side effects without compromising treatment efficacy in this group.

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