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
Hauptverfasser: Dirix, Piet, Vandecaveye, Vincent, De Keyzer, Frederik, Stroobants, Sigrid, Hermans, Robert, Nuyts, Sandra
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container_issue 7
container_start_page 1020
container_title The Journal of nuclear medicine (1978)
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creator Dirix, Piet
Vandecaveye, Vincent
De Keyzer, Frederik
Stroobants, Sigrid
Hermans, Robert
Nuyts, Sandra
description 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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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]</description><identifier>ISSN: 0161-5505</identifier><identifier>EISSN: 1535-5667</identifier><identifier>CODEN: JNMEAQ</identifier><language>eng</language><publisher>New York: Society of Nuclear Medicine</publisher><subject>Clinical outcomes ; Head &amp; neck cancer ; Hypoxia ; NMR ; Nuclear magnetic resonance ; Patients ; Radiation therapy ; Tumors</subject><ispartof>The Journal of nuclear medicine (1978), 2009-07, Vol.50 (7), p.1020</ispartof><rights>Copyright Society of Nuclear Medicine Jul 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids></links><search><creatorcontrib>Dirix, Piet</creatorcontrib><creatorcontrib>Vandecaveye, Vincent</creatorcontrib><creatorcontrib>De Keyzer, Frederik</creatorcontrib><creatorcontrib>Stroobants, Sigrid</creatorcontrib><creatorcontrib>Hermans, Robert</creatorcontrib><creatorcontrib>Nuyts, Sandra</creatorcontrib><title>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</title><title>The Journal of nuclear medicine (1978)</title><description>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. 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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]</abstract><cop>New York</cop><pub>Society of Nuclear Medicine</pub></addata></record>
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subjects Clinical outcomes
Head & neck cancer
Hypoxia
NMR
Nuclear magnetic resonance
Patients
Radiation therapy
Tumors
title 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
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