Skip to main content
OpenTrials
Recruiting

NCT Number: NCT05715502

Focal Salvage Brachytherapy Study (FocaSaBra)

The aim of this prospective phase II study is to evaluate the toxicity of salvage partial (focal) prostate brachytherapy in patients after prior radiotherapy (standard teleradiotherapy with / without brachytherapy, hypofractionated, self-reactive HDR / LDR brachytherapy) with local recurrence on the part of the prostate gland.

Recruiting

Interested in participating?

Request Info

Key information

Age range

18 year and older

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

Primary location

About this study

Prostate cancer is the second most common cancer among men in Poland. Currently, a large number of diagnosed patients undergo radical radiotherapy. Despite the high effectiveness of treatment, some patients experience failures in the form of regional and / or distant metastases, most often in the form of isolated local recurrence. In patients with suspected local recurrence, we can decide on emergency treatment after PET, pelvic MRI with an assessment of the prostate gland, and after excluding metastases. The oncological(NCCN ) and urological (EUA) recommendations allow salvage surgical treatment, observation, palliative pharmacological castration, or treatment using salvage brachytherapy.

Salvage surgical treatment is associated with a 30-65% chance of cure in the top cancer centers in the world, and the risk of significant toxicity ranges from 17 to 48%.

Treatment with brachytherapy, due to the intra-tissue nature and the short therapeutic range of radiation, can deliver a high dose to the treated area despite prior radiotherapy treatment and exhaustion of tolerance doses in critical organs, e.g., rectum and/or bladder. Treatment of the entire prostate gland gives a chance of disease-free survival for five years in approximately 65% of patients, according to the prospective study RTOG 0526. However, emergency treatment in this study was associated with a 14% risk of significant post-treatment toxicity requiring medical intervention. There are some reports in the literature on brachytherapy involving cancer in the part of the prostate gland (focal brachytherapy), but they are only retrospective. They show significant treatment efficacy and lower toxicity.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Histopathologically confirmed by biopsy (fusion mapping biopsy preferred) recurrence of prostate cancer after prior radical radiotherapy (brachytherapy, external beam radiotherapy alone or with brachytherapy boost, stereotaxic radiotherapy)
  • Localized tumor lesion assessed by MRI or in the case of MR contraindications with TRUS and CT
  • Exclusion of distant metastases using CT, MR, or PET imaging
  • PSA doubling time over six months
  • PSA value <10 ng / ml
  • No anti-androgen treatment in the year prior
  • Dysuria on the IPSS (International Prostate Symptom Score) ≤ 20 points
  • General condition according to the WHO scale ≤ 2
  • Signing informed consent to participate in the study

Exclusion criteria

  • PSA value> 10ng / ml
  • General condition according to the WHO scale> 2
  • Dysuria on the IPSS scale> 20 points
  • PSA doubling time <6 months
  • Inability to discontinue anticoagulants.
  • An active urinary tract infection.
  • Contraindications to general anesthesia
  • Active inflammatory bowel diseases.
  • Second active cancer or treatment with completion less than 3 years earlier, except for low-stage skin cancer
  • Estimated Survival <5 years

Treatment and study plan

Brachytherapy

Radiation

Radiation: focal low dose rate or high dose rate brachytherapy for the lesion with appropriate margin, defined in magnetic resonance or positron emission tomography All recruited participants will be treated with interstitial brachytherapy for local recurrence of prostate cancer. The low dose rate of brachytherapy is used with a total dose of 145 Gy in the clinical target volume for participants after hypofractionated radiotherapy, a high dose rate brachytherapy as monotherapy or boost with external beam radiotherapy The high dose rate brachytherapy with two fractions of 13 Gy in the clinical target volume with a 3 to 14 days break is used after primary low dose rate brachytherapy or external beam radiotherapy alone.

Primary outcomes

  1. Assessment of the change in the urological toxicity in points with the International Prostate Symptoms Scale

    Time frame: change from baseline to 24 months of follow-up

    Assessment of the change in the urological toxicity in points with the International Prostate Symptoms Scale - IPSS within 0-35 points

  2. Assessment of the change in the erectile function in points with the International Index of Erectile Function 5 (IIEF-5) (0-25 points)

    Time frame: change from baseline to 24 months of follow-up

    Assessment of the change in the erectile function in points with the International Index of Erectile Function 5 (IIEF-5): scale 0-25 points

  3. Assessment of the change in the quality of life in points with EORTC C30 and PR25 protocols. (0-100 points)

    Time frame: change from baseline to 24 months of follow-up

    Assessment of the change in the quality of life in points with EORTC C30 and PR25 protocols, scale: 0-100 points

Secondary outcomes

  1. Assessment of the adverse events in the percentage of grades with the CTCAE v4.0

    Time frame: 24 months after treatment

    Assessment of the adverse events in the percentage of grades with the CTCAE v4.0 scale: 0-5 grades

Study contacts

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

Ewa Tańska, PhD, MSc.

CONTACT

[email protected]

+618850767

Wojciech Burchardt, PhD, MD

CONTACT

[email protected]

+48505149659

Sponsors and collaborators

Lead sponsor

The Greater Poland Cancer Centre

Other

Registry information

Official study title

Assessment of the Toxicity of Focal Salvage Brachytherapy of Recurrent Prostate Cancer After Prior Radiotherapy - the Prospective Focal Salvage Brachytherapy Study (FocaSaBra)

Acronym: FocaSaBra

Important dates

Study start
2022
Primary completion
2025
Study completion
2028
First posted
Feb 8, 2023
Registry last updated
Apr 30, 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.

Published trials that share one or more normalized conditions with this study.