Features of Low-Dose-Rate (LDR) Brachytherapy
Low-Dose-Rate Brachytherapy (Low-Dose-Rate Brachytherapy) is widely used for low-risk prostate cancer. Microscopic iodine-125 isotope seeds are implanted into the prostate tissue as a radiation source. This isotope has a maximum X-ray energy of 35 keV and a half-life of 59 days. Due to these physical parameters, the therapeutic effect is protracted: continuous irradiation of the prostate occurs over several months following a single seed insertion procedure.
Imaging and the Seed Migration Problem
Surgical tissue trauma during implantation inevitably causes local bleeding and pronounced edema. Due to changes in organ geometry, uncontrolled migration of radioactive seeds frequently occurs.
The imaging protocol includes two important stages:
- Plain pelvic radiography — performed immediately after implantation for an initial assessment of the situation.
- Fused CT and MRI (Fused CT and MRI) — performed 28 days after source insertion.
It is precisely because of seed migration against the background of edema that the final radiation dose distribution must be determined based on delayed imaging results (after a few weeks), and categorically not from the initial position of the sources immediately after surgery.
Definition of Irradiation Volumes
Precise radiation therapy planning requires strict definition of Target Volumes (Target Volumes):
- Clinical target volume (Clinical target volume, CTV): Encompasses the visible tumor and accounts for its microscopic spread beyond what can be discerned using modern diagnostic imaging methods.
- Planning target volume (Planning target volume, PTV): Formed by further geometric expansion of the CTV. This expansion is necessary to compensate for set-up errors (set-up errors) related to equipment geometry variability and beam alignment, as well as to account for physiological tumor movement during the irradiation fraction (intrafraction tumour movement).
The goal of treatment optimization is to reduce toxicity to healthy tissues and increase the dose to the tumor itself by reducing the safety margin (safety margin). This is achievable only with advanced imaging methods that ensure high accuracy in volume definition and allow tracking of tumor movement directly during radiation delivery.
Computed Tomography Simulation
To date, Computed Tomography Simulation (Computed Tomography Simulation) has almost completely replaced traditional treatment simulators in radiological practice. The main disadvantage of traditional simulators was that they were based on simple kilovoltage X-ray images. Under such conditions, the treatment area was determined exclusively by bony anatomical landmarks, as the technology did not provide soft-tissue definition (no soft-tissue definition). CT simulation completely solved this problem.
Alternative Techniques: MRI-Guided and Non-Imaging Methods
Imaging approaches and source selection can differ radically for other localizations:
- Magnetic Resonance–Guided Brachytherapy for cervical cancer (Magnetic Resonance–Guided Brachytherapy): Sagittal MRI projection is used for clear visualization of the urinary bladder (with a catheter), tumor, and applicators. Unlike prostate LDR therapy, high-dose-rate (HDR) iridium-based therapy is used here. The system includes an intrauterine tube (Intrauterine tube), a vaginal ring (Vaginal ring), and interstitial catheters (Interstitial catheters) inserted at the tumor periphery for adequate dose coverage.
- Clinical Volume Definition - Non-Imaging Based (Clinical Volume Definition - Non-Imaging Based): Used in palliative treatment or for visually identifiable formations where extreme precision is not critical. For example, in skin cancer, the visible tumor border is simply outlined with a marker with the addition of a margin (margin) for microscopic spread. For deep structures, treatment field boundaries are formed using anatomical landmarks.
Briefly: answers to topical questions
What are the main differences between low-dose-rate (LDR) and high-dose-rate (HDR) brachytherapy in the treatment of prostate cancer?
The main differences lie in the technique, duration of exposure, and indications for treatment.
| Characteristic | Low-dose-rate brachytherapy (Low-Dose-Rate Brachytherapy) | High-dose-rate brachytherapy (high-dose-rate brachytherapy) |
|---|---|---|
| Implantation type | Permanent (implantable seeds) | Temporary (catheter placement) |
| Radiation source | Iodine-125 | Radionuclides are removed after the session |
| Irradiation time | Over several months | Limited to the duration of the irradiation session |
| Indications | Low-risk cancer | Stages T1–T3, Gleason score up to 10 |
To memorize volumes: CTV is the tumor itself + occult cells. PTV is set-up errors + periodic movements.
Class and exam questions
Why is final dosimetry in prostate brachytherapy performed only after 28 days?
Due to needle insertion trauma, prostate edema and hemorrhage occur. This causes displacement (migration) of the implanted seeds. The final dose distribution can only be calculated after the edema subsides, based on fused CT and MRI data.
What does the planning target volume (PTV) account for, unlike the clinical target volume (CTV)?
PTV includes the CTV but is additionally expanded to compensate for patient set-up errors (due to equipment geometry) and tumor displacement directly during the irradiation session.
What is the main disadvantage of traditional X-ray simulators compared to CT simulation?
Traditional simulators operated in the kilovoltage range and showed only bony structures, failing to differentiate soft tissues for precise tumor targeting.
What else to study on this topic
- Assessment of image fusion quality (Fused CT and MRI) during planning in planning
- Isotope physics: comparison of iodine-125 (LDR) and iridium (HDR)
- Applicator placement technique in cervical cancer brachytherapy
- Methods for compensating respiratory and physiological tumor motion during irradiation
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