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NCT Number: NCT06331013

CyberKnife Ultra-hypofractionated SBRT for Localized PROStatE cancEr

This is a prospective observational study. The study will proceed with the enrollment of 60 patients in 2 years. he aim of the present study is to evaluate effectiveness of ultra-hypofractionated (UH) CyberKnife Stereotactic Body Radiation Therapy treatment on the whole prostate gland plus Simultaneous integrated boost (SIB) to the dominant intraprostatic lesions (DIL(s) in intermediate-unfavourable to high-risk Prostate Cancer (PCa) patients.

Recruiting

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Key information

Age range

18 year–80 year

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

European Institute of Oncology

Milan, Italy

Location status: Recruiting

Location contact

Barbara Alicja Jereczek

CONTACT

About this study

The patient to be enrolled in the prospective observational phase will be screened at first visit; prescription of Prostate Specific Antigen (PSA) and testosterone analysis, uroflowmetry and multiparametric Magnetic Resonance Imaging (mpMRI) are mandatory if not already done.

Additional staging imaging (computed tomography (CT) and/or bone scan) will be required according to National Comprehensive Cancer Network (NCCN) category risk group.

Subsequently, for the eligible patient, the enrollment phase involves eco-guided transrectal insertion of 3-4 gold fiducials in the prostate gland.

CT with full bladder and empty rectum will be done after 7-10 days from fiducials insertion; CyberKnife-Stereotactic Body Radiation Therapy (SBRT) treatment will start after 5-7 days from the simulation CT. A total of 36.25 Gy to the prostate gland will be executed in 5 alternate days. For each treatment delivery, the patient is required to be prepared in roughly the same bladder and rectum filling condition of the simulation day. Finally, in the last treatment day QoL and both clinician- and patient-reported genitourinary (GU) and gastrointestinal (GI) acute toxicity assessment is required.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age > 18 and < 80 years
  • Histologically confirmed adenocarcinoma of the prostate
  • Low, Intermediate and high-risk category according to NCCN version 02.2021
  • Clinically node negative and no distant metastasis
  • Eastern Cooperative Oncology Group (ECOG) Performance Status <2
  • Good urinary flow (peak flow >10 mL/s) or IPSS < 15
  • Prostate volume < 100 cc
  • Available mpMRI of the prostate
  • Less than 3 DILs at mpMRI (if >2 DILs, only DILs with higher Prostate Imaging - Reporting and Data System (PIRADS) will be included and only PI-RADS >2)
  • Written informed consent for treatment and research purpose

Exclusion criteria

  • platelets count < 75000
  • urethral stricture
  • Previous pelvic RT
  • Concomitant inflammatory bowel disease or other serious systemic comorbidities
  • Previous prostatectomy
  • Presence of hip prosthesis

Treatment and study plan

CyberKnife ultra-hypofractionated SBRT

Radiation

CyberKnife ultra-hypofractionated SBRT for localized Prostate cancer with dose-escalation to the dominant intraprostatic lesion

Primary outcomes

  1. Number of Participants with Acute GU and GI toxicities (RTOG)

    Time frame: 3 months

    Evaluation of acute genitourinary and gastrointestinal toxicity using Radiation Toxicity Grading (RTOG) distinguishing between lower toxicities (G1 and G2) and worse toxicities (G3 and G4)

  2. Number of Participants with Late GU and GI toxicities (RTOG)

    Time frame: 24 months

    Evaluation of late genitourinary and gastrointestinal toxicity using Radiation Toxicity Grading (RTOG) distinguishing between lower toxicities (G1 and G2) and worse toxicities (G3 and G4)

  3. Evaluation of patient-reported toxicity

    Time frame: 24 months

    Evaluation of patient-reported toxicity using International Prostatic Symptoms Score IPSS

  4. Evaluation of patient-reported quality of life

    Time frame: 24 months

    Evaluation of patient-reported toxicity using International Index of Erectile Function Questionnaire

Study contacts

Contact information is provided by the study sponsor or research team.

Barbara Alicja Jereczek, MD

CONTACT

[email protected]

+39 0257489037

Sponsors and collaborators

Lead sponsor

European Institute of Oncology

Other

Registry information

Official study title

CyberKnife Ultra-hypofractionated SBRT for Localized PROStatE cancEr With Dose-escalation to the Dominant Intraprostatic Lesion: is the Juice Worth the Squeeze? The PRO-SPEED Trial

Acronym: PRO-SPEED

Important dates

Study start
2023
Primary completion
2025
Study completion
2029
First posted
Mar 26, 2024
Registry last updated
Aug 28, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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