Quality rectal hydrogel placement allows for gel-enabled dose-escalated EBRT (GEDE-EBRT) without rectal interference
Jamie S K Takayesu1, Paul Heckman2, Eric Short2
1Department of Radiation Oncology, University of Michigan, Ann Arbor, MI, USA.
Summary
Rectal hydrogel (RH) placement improves radiation dose delivery for prostate cancer, enabling higher doses to target areas while protecting the rectum. This dosimetric study suggests RH can facilitate dose-escalation, potentially improving treatment outcomes.
Area of Science:
- Radiation Oncology
- Medical Physics
- Urologic Oncology
Background:
- Dose-escalation in prostate cancer radiation therapy improves outcomes but is limited by rectal toxicity.
- Rectal constraints often prevent optimal radiation delivery to the prostate and surrounding structures.
Purpose of the Study:
- To investigate if rectal hydrogel (RH) placement can improve radiation dose escalation and target coverage in prostate cancer.
- To assess the dosimetric impact of RH on planning target volumes (PTVs) and rectal dose metrics.
Main Methods:
- A dosimetric study comparing treatment plans with and without RH in patients with good-quality RH.
- Plans included prostate and seminal vesicle (PSV) target volumes and peripheral zone (PZ) boosts up to 112 Gy.
- Evaluated PTV coverage (D95%) and rectal dose-volume histogram parameters with and without RH.
Main Results:
- RH placement significantly improved PTV_boost D95% (median 98.5 Gy vs 75.53 Gy) and PTV_PSV D95% (71.87 Gy vs 71.04 Gy).
- All rectal dose metrics were improved with RH compared to non-RH plans.
- RH facilitated dose escalation up to 112 Gy (EQD2 160 Gy), achieving superior target coverage and rectal sparing.
Conclusions:
- High-quality RH placement allows for dose-escalation in prostate cancer radiotherapy, improving target coverage and rectal sparing.
- This dosimetric benefit suggests RH is a valuable tool for optimizing radiation delivery in prostate cancer.
- Prospective trials are warranted to evaluate the clinical efficacy and safety, including nonrectal toxicities, of RH-guided dose-escalation.


