Prostate Cancer Patients Treated With Alternative Radiation Oncology Strategies

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexMale
Age18+
SponsorUniversity Hospital Heidelberg

About this trial

As the most common male carcinoma, prostate cancer is a major tumor entity in oncology. In addition to definitive radiotherapy, surgical procedure is considered to be an oncologically equivalent therapeutic alternative for non-metastatic malignancies in the primary setting. However, a subsequent radiotherapy of the prostate bed is often necessary, which takes place as an "adjuvant" treatment immediately after surgery or in the course of a repeated increase in PSA and usually extends over several weeks. For the primary situation (without previous surgery), several randomized phase III clinical trials have shown that it is possible to shorten radiotherapy by increasing the single dose (called hypofractionation). In the context of two prospective Phase II studies, which were carried out in Heidelberg, it has since been shown that hypofractionation with both photons and protons is safe and feasible even in the postoperative situation.

The current, prospective and randomized PAROS study is now intended to demonstrate a multicentric phase III study as an improvement in the quality of life caused by rectum toxicity (primary endpoint) by the use of protons. The oncological non-inferiority of hypofractionated radiotherapy after surgery is a secondary endpoint.

Eligibility criteria

Qualifiers

histology-proven prostate cancer with Gleason Score and PSA-value;

indication for prostate bed irradiation (adjuvant/ salvage) after prostatectomy;

Karnofsky-Index ≥ 70%

age ≥ 18 years

Disqualifiers

androgen deprivation therapy

lymphatic spread

macroscopic tumor/ R2

stage IV (M1)

Trial design

Treatments tested in this trial

  • Hypofractionated radiotherapy with photons
  • Hypofractionated radiotherapy with protons
  • Normofractionated radiotherapy with photons

Treatment groups

897 Participants
are divided into 3 treatment groups

Sponsors and collaborators