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Prostate permanent implant brachytherapy with BARC I-125 Ocu-Prosta seeds
Siddanna R Palled1, Sathiyan Saminathan1, Tanvir Pasha1
1Departments of Radiation Physics and Radiation Oncology, Kidwai Memorial Institute of Oncology, Bengaluru, Karnataka, India.
Journal of Cancer Research and Therapeutics
|June 14, 2021
Summary
This study establishes a standard operating procedure for permanent prostate brachytherapy using Iodine-125 seeds. The technique, utilizing ultrasound guidance and specialized planning systems, demonstrates a viable method for prostate cancer treatment.
Area of Science:
- Oncology
- Radiation Oncology
- Medical Physics
Background:
- Permanent prostate brachytherapy is a low-dose-rate treatment for localized prostate cancer.
- Iodine-125 (I-125) seeds are commonly used radioactive sources for this procedure.
- Establishing standardized protocols is crucial for safe and effective brachytherapy delivery.
Purpose of the Study:
- To implement and establish a standard operating procedure (SOP) for permanent prostate brachytherapy.
- To evaluate the use of BARC I-125 Ocu-Prosta seeds for this technique.
- To assess the feasibility of transrectal ultrasound (US)-guided implantation with intraoperative planning.
Main Methods:
- Transrectal ultrasound (US)-guided implantation using the Best Sonalis US Imaging System.
- Pre-implant dosimetry and intraoperative planning with the Best NOMOS Treatment Planning system.
- Implantation of BARC I-125 Ocu-Pro radioactive seeds using a Mick Applicator.
Main Results:
- Quality assurance tests were completed for the US system.
- A boost dose of 110 Gy was prescribed to a prostate volume of 34.71 cc.
- Approximately 48 seeds (0.35 mCi each) were implanted, with seed counts verified post-procedure.
Conclusions:
- Low-dose-rate permanent brachytherapy offers a one-time procedure with excellent outcomes and low morbidity.
- BARC supplies I-125 seeds suitable for Mick applicator implantation.
- While staff radiation exposure is a consideration, it can be minimized with good practice; this pilot study validates the SOP and implant system.

