Stereotactic Radiotherapy of Prostate Cancer With Reduction of Safety Margins

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

About this trial

The study aims to reduce the PTV (Planning Target Volume) safety margins to 1-2 mm in stereotactic prostate radiotherapy for low- and medium-risk prostate cancers while maintaining a dose of 36.25 Gy in 5 fractions per day. By reducing the hems, the investigators expect a reduction of acute and late toxicity on the organs at risk, dominantly the urethra, bladder, penile bulb, and rectum, and an improvement in the quality of life.

Eligibility criteria

Qualifiers

histologically verified, localized prostate cancer without regional lymphadenopathy or distant metastases

low or intermediate risk - favorable risk

low risk: no staging required

intermediate risk- favorable risk: CT abdomen and pelvis

Disqualifiers

a histological type other than acinar adenocarcinoma

the presence of local lymphadenopathy or distant metastases

a dominant lesion in the periphery that is in contact with the capsule or grows through it

PSA over 15

Trial design

Treatments tested in this trial

  • Stereotactic radiotherapy

Treatment groups

100 Participants
are divided into 1 treatment group

Sponsors and collaborators