Copenhagen, Denmark
Onsite/Online

ESTRO 2022

Session Item

Monday
May 09
16:45 - 17:45
Auditorium 12
Dosimetry & treatment planning
James Iddenden, United Kingdom;
Liselotte ten Asbroek-Zwolsman, The Netherlands
3500
Proffered Papers
RTT
17:25 - 17:35
Dosimetry & toxicity comparison between CBCT-Guided and MR-Guided Prostate Ultra-hypofractionated RT
Vickie Kong, Canada
OC-0952

Abstract

Dosimetry & toxicity comparison between CBCT-Guided and MR-Guided Prostate Ultra-hypofractionated RT
Authors:

Vickie Kong1, Jerusha Padayachee1, Jennifer Dang1, Winnie Li1, Victor Malkov1, Jeff Winter1, Inmaculada Navarro1, Alejandro Berlin1, Joelle Helou1, Srinivas Raman1, Peter Chung1

1Princess Margaret Cancer Centre, Radiation Medicine Program, Toronto, Canada

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Purpose or Objective

Ultra-hypofractionated (³6Gy/fraction) radiotherapy for localized prostate cancer has been delivered at our institution with either online CBCT-guided 3 degrees of freedom (3DOF) translational correction or online MR-guided adaptation. Herein, we compared the daily dosimetry and acute toxicity between these two systems.

Material and Methods

Fifty patients recruited to a Phase 2 trial evaluating the efficacy of External Beam Radiation Therapy (EBRT) plus High Dose Rate Brachytherapy intraprostatic boost (1500cGy/1) were included in this analysis. Hydrogel spacer was inserted at the discretion of physicians. An EBRT reference plan was generated to deliver 3000cGy/5 to the CTV (Prostate ± Seminal Vesicles) with a margin of 5mm using VMAT for 25 patients treated with CBCT-3DOF. The remainder were planned with IMRT and MR-guided adapt-to-shape (AtS). Daily EBRT delivered dose to CTV, bladder and rectum was computed using the daily CBCT or MR images. Deviation of >10% from reference dose was considered clinically significant. Acute toxicity was prospectively recorded using Common Terminology Criteria for Adverse Events (ver 4.0).

Results

Delivered dose per fraction to 95% of CTV was acceptable for all 250 fractions, with a median of 660cGy (Range: 649–680cGy). Hydrogel spacer was present in 17 patients in the CBCT-3DOF and 15 patients in the MRL cohort. VMAT with CBCT-3DOF was associated with lower daily rectal D50% but higher D1cm3 compared to IMRT using MR-AtS, especially in the presence of hydrogel spacer (Table 1). The use of MR-AtS resulted in more fractions delivering a significantly lower rectal D20% and D1cm3 than the reference dose, when compared to CBCT-3DOF (56 vs 26 for D20%, 51 vs 2 for D1cm3; Figure 1). In contrary, difference between reference and delivered dose to 5cm3 of bladder was significant in <15 fractions by either systems. Median follow up was 26 months for CBCT-3DOF and 25 months for MR-AtS. The cumulative incidence of G2+ urinary/gastrointestinal toxicity by 6 months was 8%/8% for the CBCT-3DOF cohort and 20%/0% for the MR-AtS.

Conclusion

Significant deviation from the reference plan dose for rectum was observed with both systems due to large range of anatomical changes exhibited between planning and treatment sessions. MR-guided adaptation was able to deliver a lower than reference plan dose to the rectum in the high dose region more frequently than CBCT-guided 3DOF, and these patients experienced a lower incidence of G2+ GI acute toxicity. Follow up is ongoing and will assess the clinical efficacy of these two treatment delivery systems.