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ALTERNATE DAY ULTRAHYPOFRACTIONATED OR DAILY MODERATELY HYPOFRACTIONATED POST OPERATIVE RADIOTHERAPY (AMPORA)

ALTERNATE DAY ULTRAHYPOFRACTIONATED OR DAILY MODERATELY HYPOFRACTIONATED POST OPERATIVE RADIOTHERAPY (AMPORA)

Recruiting
18 years and older
Male
Phase 2

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Overview

This is a multi-institution, randomized, non-inferiority Phase II trial comparing external beam radiotherapy delivered as 54 Gy in 20 fractions to prostate bed +/- 44 Gy in 20 fractions to pelvic lymph nodes delivered daily with external beam radiotherapy delivered as 30 Gy in 5 fractions to prostate bed +/- 25 Gy in 5 fractions to pelvic lymph nodes delivered on alternate days.

Eligibility

Inclusion Criteria:

  1. Age > 18 years
  2. Able to provide informed consent
  3. Histologic diagnosis of prostate adenocarcinoma
  4. ECOG performance status 0-1
  5. Previous radical prostatectomy > 6 months prior to radiotherapy start date
  6. Planned to receive post-operative radiation

Exclusion Criteria:

  1. Prior pelvic radiotherapy
  2. Contraindications to radiotherapy
  3. Mets confirmed as per (if scan has been done for clinical care)
  4. Participants with visible disease in the prostate bed or pelvic lymph nodes on imaging are not eligible for treatment on study.

Study details
    Post-Operative Prostate Cancer

NCT06409910

University Health Network, Toronto

15 October 2025

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