Clinical implementation of real time motion management for prostate SBRT: A radiation therapist’s perspective

•Monitoring intrafaction motion during external beam prostate SBRT.•Correlation of acute toxicity to intrafraction motion.•Demonstration of a new and efficient SBRT clinical workflow.•RTT led process. The adoption of hypo-fractionated stereotactic body radiotherapy (SBRT) for treating prostate cance...

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Veröffentlicht in:Technical innovations & patient support in radiation oncology 2024-09, Vol.31, p.100267, Article 100267
Hauptverfasser: Mitchell, Joanne, McLaren, Duncan B., Burns Pollock, Donna, Wright, Joella, Killean, Angus, Trainer, Michael, Adamson, Susan, McKernan, Laura, Nailon, William H.
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Sprache:eng
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Zusammenfassung:•Monitoring intrafaction motion during external beam prostate SBRT.•Correlation of acute toxicity to intrafraction motion.•Demonstration of a new and efficient SBRT clinical workflow.•RTT led process. The adoption of hypo-fractionated stereotactic body radiotherapy (SBRT) for treating prostate cancer has led to an increase in specialised techniques for monitoring prostate motion. The aim of this study was to comprehensively review a radiation therapist (RTT) led treatment process in which two such systems were utilised, and present initial findings on their use within a SBRT prostate clinical trial. 18 patients were investigated, nine were fitted with the Micropos RayPilotTM (RP) system (Micropos Medical, Gothenburg, SE) and nine were fitted with the Micropos Raypilot Hypocath TM (HC) system. 36.25 Gray (Gy) was delivered in 5 fractions over 7 days with daily pre- and post-treatment cone beam computed tomography (CBCT) images acquired. Acute toxicity was reported on completion of treatment at six- and 12-weeks post-treatment, using the Radiation Therapy Oncology Group (RTOG) grading system and vertical (Vrt), longitudinal (Lng) and lateral (Lat) transmitter displacements recorded. A significant difference was found in the Lat displacement between devices (P=0.003). A more consistent bladder volume was reported in the HC group (68.03 cc to 483.7 cc RP, 196.11 cc to 313.85 cc HC). No significant difference was observed in mean dose to the bladder, rectum and bladder dose maximum between the groups. Comparison of the rectal dose maximum between the groups reported a significant result (P=0.09). Comparing displacements with toxicity endpoints identified two significant correlations: Grade 2 Genitourinary (GU) at 6 weeks, P=0.029; and no toxicity, Gastrointestinal (GI) at 12 weeks P=0.013. Both the directly implanted RP device and the urinary catheter-based HC device are capable of real time motion monitoring. Here, the HC system was advantageous in the SBRT prostate workflow.
ISSN:2405-6324
2405-6324
DOI:10.1016/j.tipsro.2024.100267