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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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 & 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. [PUBLICATION ABSTRACT]</description><subject>Clinical outcomes</subject><subject>Head & neck cancer</subject><subject>Hypoxia</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Patients</subject><subject>Radiation therapy</subject><subject>Tumors</subject><issn>0161-5505</issn><issn>1535-5667</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNqNkMtKw1AURYMoWB__cHDcQNKaGJ0mje1AKbHorOWQnCS33tyT3gdS_9Y_MbUOHDrasFksNvvEG4XRNPKjOL479UZBGId-FAXRuXdhzDYIgjhJkpH3lbEhWKJQVqgGhIICK8G2JY39HmrWMCesAFUFz1S-w8vOYcfOQEpSQoq6FIo7fIBXlI6AayioJ7RUQe5UaQUrlLDosDn4P4RtYW1cD2Gyzv08e4TlbDX-W0nHmjthWIkKP1nSkchEXTsz2Pw3Ek178D8Vi_HPsGyvsBMlpKysRmP9mWpRlUfkyjurURq6_s1L7yafrdK532veOTJ2s2Wnh5FmMwnvJ9Pb6fDbv6Bv5YpxFg</recordid><startdate>20090701</startdate><enddate>20090701</enddate><creator>Dirix, Piet</creator><creator>Vandecaveye, Vincent</creator><creator>De Keyzer, Frederik</creator><creator>Stroobants, Sigrid</creator><creator>Hermans, Robert</creator><creator>Nuyts, Sandra</creator><general>Society of Nuclear Medicine</general><scope>3V.</scope><scope>4T-</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>M7Z</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>S0X</scope></search><sort><creationdate>20090701</creationdate><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><author>Dirix, Piet ; 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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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