Adaptive IMRTAdaptive biological image-guided IMRT with anatomic and functional imaging in pharyngo-laryngeal tumors: Impact on target volume delineation and dose distribution using helical tomotherapy
Section snippets
Patient selection
Ten consecutive patients (mean age 57 years; range 45–80 years) with a stage III–IV (1997 AJCC Classification) HN were prospectively enrolled in this study between January 2004 and 2005. From these 10 patients, 7 had hypopharyngeal tumors, 2 had laryngeal tumors and one had an oropharyngeal tumor. Details about the patients’ characteristics are shown in Table 1. All patients were treated by radical concomitant chemo-radiation (forward planning linac-based IMRT with a prophylactic dose of 50 Gy
Comparison between imaging modalities for the primary tumor GTVs delineation before and during treatment (Table 2 and Fig. 1)
The individual patient GTVs before and during treatment for the different imaging modalities are presented in Appendix A. As explained in the Materials and methods section, the first 2 patients did not get any MRI examinations. Thus, this first comparison will only involve the 8 patients who underwent all imaging examinations. On all imaging modalities, the mean primary tumor GTVs significantly decreased during the treatment course (ANOVA, p < 0.001), with a relative tumor reduction at 45 Gy
Discussion
The objectives of the present proof of concept study were to assess the potential value of adaptive multi-modality image-guided IMRT for the treatment of patients with pharyngo-laryngeal squamous cell carcinoma, and in this framework, to determine the optimal imaging modality to use. In summary, in a series of 10 patients with locally advanced pharyngo-laryngeal tumors, the study demonstrated (1) that the re-assessment of the target volumes during treatment with anatomical or functional imaging
Acknowledgements
Xavier Geets was a research fellow of the Belgian national fund for scientific research (FNRS, Fonds National de la Recherche Scientifique, convention # 7.4538.02). This research program was supported by grants from the European Community (BIOCARE research program #LSHC-CT-2004-505785), the Belgian Federation against Cancer (convention #SCIE 2003-23FR) and the Fonds J. Maisin of the Université Catholique de Louvain. This project also benefited from a collaboration with Tomotherapy Inc.
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