Automated VMAT planning for postoperative adjuvant treatment of advanced gastric cancer

Postoperative/adjuvant radiotherapy of advanced gastric cancer involves a large planning target volume (PTV) with multi-concave shapes which presents a challenge for volumetric modulated arc therapy (VMAT) planning. This study investigates the advantages of automated VMAT planning for this site comp...

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Veröffentlicht in:Radiation oncology (London, England) England), 2018-04, Vol.13 (1), p.74-74, Article 74
Hauptverfasser: Sharfo, Abdul Wahab M, Stieler, Florian, Kupfer, Oskar, Heijmen, Ben J M, Dirkx, Maarten L P, Breedveld, Sebastiaan, Wenz, Frederik, Lohr, Frank, Boda-Heggemann, Judit, Buergy, Daniel
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Sprache:eng
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Zusammenfassung:Postoperative/adjuvant radiotherapy of advanced gastric cancer involves a large planning target volume (PTV) with multi-concave shapes which presents a challenge for volumetric modulated arc therapy (VMAT) planning. This study investigates the advantages of automated VMAT planning for this site compared to manual VMAT planning by expert planners. For 20 gastric cancer patients in the postoperative/adjuvant setting, dual-arc VMAT plans were generated using fully automated multi-criterial treatment planning (autoVMAT), and compared to manually generated VMAT plans (manVMAT). Both automated and manual plans were created to deliver a median dose of 45 Gy to the PTV using identical planning and segmentation parameters. Plans were evaluated by two expert radiation oncologists for clinical acceptability. AutoVMAT and manVMAT plans were also compared based on dose-volume histogram (DVH) and predicted normal tissue complication probability (NTCP) analysis. Both manVMAT and autoVMAT plans were considered clinically acceptable. Target coverage was similar (manVMAT: 96.6 ± 1.6%, autoVMAT: 97.4 ± 1.0%, p = 0.085). With autoVMAT, median kidney dose was reduced on average by > 25%; (for left kidney from 11.3 ± 2.1 Gy to 8.9 ± 3.5 Gy (p = 0.002); for right kidney from 9.2 ± 2.2 Gy to 6.1 ± 1.3 Gy (p 
ISSN:1748-717X
1748-717X
DOI:10.1186/s13014-018-1032-z