Dose Painting in Radiotherapy for Head and Neck Squamous Cell Carcinoma: Value of Repeated Functional Imaging with ^sup 18^F-FDG PET, ^sup 18^F-Fluoromisonidazole PET, Diffusion-Weighted MRI, and Dynamic Contrast-Enhanced MRI
The purpose of this work was to evaluate the potential of functional imaging with ^sup 18^F-FDG PET, ^sup 18^F-fluoromisonidazole PET, diffusion-weighted MRI, and dynamic contrast-enhanced MRI to provide an appropriate and reliable biologic target for dose painting in radiotherapy for head and neck...
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Veröffentlicht in: | The Journal of nuclear medicine (1978) 2009-07, Vol.50 (7), p.1020 |
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Zusammenfassung: | The purpose of this work was to evaluate the potential of functional imaging with ^sup 18^F-FDG PET, ^sup 18^F-fluoromisonidazole PET, diffusion-weighted MRI, and dynamic contrast-enhanced MRI to provide an appropriate and reliable biologic target for dose painting in radiotherapy for head and neck squamous cell carcinoma (HNSCC). Methods: Fifteen patients with locally advanced HNSCC, treated with concomitant chemoradiotherapy, were prospectively enrolled in a bioimaging protocol. Sequential PET (^sup 18^F-FDG and ^sup 18^F-fluoromisonidazole) and MRI (T1, T2, dynamic enhanced, and diffusion-weighted sequences) were performed before, during, and after radiotherapy. Results: Median follow-up was 30.7 mo (range, 6.3-56.3 mo); in 7 patients, disease recurred. Disease-free survival correlated negatively with the maximum tissue-to-blood ^sup 18^F-fluoromisonidazole ratio (T/B^sub max^) on the baseline ^sup 18^F-fluoromisonidazole scan (P = 0.04), with the size of the initial hypoxic volume (P = 0.04), and with T/B^sub max^ on the ^sup 18^F-fluoromisonidazole scan during treatment (P = 0.02). All locoregional recurrences were within the ^sup 18^F-FDG-avid regions on baseline ^sup 18^F-FDG PET; 3 recurrences mapped outside the hypoxic volume on baseline ^sup 18^F-fluoromisonidazole PET. Lesions (primary tumor and lymph nodes) where a locoregional recurrence developed during follow-up had significantly lower apparent diffusion coefficients on diffusion-weighted MRI during week 4 of radiotherapy (0.0013 vs. 0.0018 mm^sup 2^/s, P = 0.01) and at 3 wk after treatment (0.0014 vs. 0.0018 mm^sup 2^/s, P = 0.01) and a significantly higher initial slope on baseline dynamic enhanced MRI (26.2 vs. 17.5/s, P = 0.03) than did lesions that remained controlled. Conclusion: These results confirm the added value of ^sup 18^F-FDG PET and ^sup 18^F-fluoromisonidazole PET for radiotherapy planning of HNSCC and suggest the potential of diffusion-weighted and dynamic enhanced MRI for dose painting and early response assessment. [PUBLICATION ABSTRACT] |
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ISSN: | 0161-5505 1535-5667 |