Cargando…

Radiation dose escalation based on FDG-PET driven dose painting by numbers in oropharyngeal squamous cell carcinoma: a dosimetric comparison between TomoTherapy-HA and RapidArc

PURPOSE: Validation of dose escalation through FDG-PET dose painting (DP) for oropharyngeal squamous cell carcinoma (SCC) requires randomized clinical trials with large sample size, potentially involving different treatment planning and delivery systems. As a first step of a joint clinical study of...

Descripción completa

Detalles Bibliográficos
Autores principales: Differding, Sarah, Sterpin, Edmond, Hermand, Nicolas, Vanstraelen, Bianca, Nuyts, Sandra, de Patoul, Nathalie, Denis, Jean-Marc, Lee, John Aldo, Grégoire, Vincent
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5364636/
https://www.ncbi.nlm.nih.gov/pubmed/28335778
http://dx.doi.org/10.1186/s13014-017-0793-0
Descripción
Sumario:PURPOSE: Validation of dose escalation through FDG-PET dose painting (DP) for oropharyngeal squamous cell carcinoma (SCC) requires randomized clinical trials with large sample size, potentially involving different treatment planning and delivery systems. As a first step of a joint clinical study of DP, a planning comparison was performed between Tomotherapy HiArt® (HT) and Varian RapidArc® (RA). METHODS: The planning study was conducted on five patients with oropharyngeal SCC. Elective and therapeutic CTVs were delineated based on anatomic information, and the respective PTVs (CTVs + 4 mm) were prescribed a dose of 56 (PTV(56)) and 70 Gy (PTV(70)). A gradient-based method was used to delineate automatically the external contours of the FDG-PET volume (GTV(PET)). Variation of the FDG uptake within the GTV(PET) was linearly converted into a prescription between 70 and 86 Gy. A dilation of the voxel-by-voxel prescription of 2.5 mm was applied to account for geometric errors in dose delivery (PTV(PET)). The study was divided in two planning phases aiming at maximizing target coverage (phase I) and lowering doses to OAR (phase II). A Quality-Volume Histogram (QVH) assessed conformity with the DP prescription inside the PTV(PET). RESULTS: In phase I, for both HT and RA, all plans achieved comparable target coverage for PTV(56) and PTV(70), respecting the planning objectives. A median value of 99.9 and 97.2% of all voxels in the PTV(PET) received at least 95% of the prescribed dose for RA and HT, respectively. A median value of 0.0% and 3.7% of the voxels in the PTV(PET) received 105% or more of prescribed dose for RA and HT, respectively. In phase II, no significant differences were found in OAR sparing. Median treatment times were 13.7 min for HT and 5 min for RA. CONCLUSIONS: Both HT and RA can generate similar dose distributions for FDG-PET based dose escalation and dose painting in oropharyngeal SCC patients. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13014-017-0793-0) contains supplementary material, which is available to authorized users.