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Prediction of response by FDG PET early during concurrent chemoradiotherapy for locally advanced non-small cell lung cancer

PURPOSE: To evaluate the predictive value of the early response of (18)F-flurodeoxyglucose positron emission tomography (FDG PET) during concurrent chemoradiotherapy (CCRT) for locally advanced non-small cell lung cancer (NSCLC). MATERIALS AND METHODS: FDG PET was performed before and during CCRT fo...

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Autores principales: Kim, Suzy, Oh, So Won, Kim, Jin Soo, Kim, Ki Hwan, Kim, Yu Kyeong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Radiation Oncology 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4282997/
https://www.ncbi.nlm.nih.gov/pubmed/25568851
http://dx.doi.org/10.3857/roj.2014.32.4.231
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author Kim, Suzy
Oh, So Won
Kim, Jin Soo
Kim, Ki Hwan
Kim, Yu Kyeong
author_facet Kim, Suzy
Oh, So Won
Kim, Jin Soo
Kim, Ki Hwan
Kim, Yu Kyeong
author_sort Kim, Suzy
collection PubMed
description PURPOSE: To evaluate the predictive value of the early response of (18)F-flurodeoxyglucose positron emission tomography (FDG PET) during concurrent chemoradiotherapy (CCRT) for locally advanced non-small cell lung cancer (NSCLC). MATERIALS AND METHODS: FDG PET was performed before and during CCRT for 13 NSCLC patients. Maximum standardized uptake value (SUV(max)), mean standardized uptake value (SUV(mean)), metabolic tumor volume (MTV), and total lesion glycolysis (TLG) were measured and the changes were calculated. These early metabolic changes were compared with the standard tumor response by computed tomograms (CT) one month after CCRT. RESULTS: One month after the completion of CCRT, 9 patients had partial response (PR) of tumor and 4 patients had stable disease. The percent changes of SUV(max) (%ΔSUV(max)) were larger in responder group than in non-responder group (55.7% ± 15.6% vs. 23.1% ± 19.0%, p = 0.01). The percent changes of SUV(mean) (%ΔSUV(mean)) were also larger in responder group than in non-responder group (54.4% ± 15.9% vs. 22.3% ± 23.0%, p = 0.01). The percent changes of MTV (%ΔMTV) or TLG (%ΔTLG) had no correlation with the tumor response after treatment. All the 7 patients (100%) with %ΔSUV(max) ≥ 50% had PR, but only 2 out of 6 patients (33%) with %ΔSUV(max) < 50% had PR after CCRT (p = 0.009). Likewise, all the 6 patients (100%) with %ΔSUV(mean) ≥ 50% had PR, but only 3 out of 7 patients (43%) with %ΔSUV(mean) < 50% had PR after CCRT (p = 0.026). CONCLUSION: The degree of metabolic changes measured by PET-CT during CCRT was predictive for NSCLC tumor response after CCRT.
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spelling pubmed-42829972015-01-07 Prediction of response by FDG PET early during concurrent chemoradiotherapy for locally advanced non-small cell lung cancer Kim, Suzy Oh, So Won Kim, Jin Soo Kim, Ki Hwan Kim, Yu Kyeong Radiat Oncol J Original Article PURPOSE: To evaluate the predictive value of the early response of (18)F-flurodeoxyglucose positron emission tomography (FDG PET) during concurrent chemoradiotherapy (CCRT) for locally advanced non-small cell lung cancer (NSCLC). MATERIALS AND METHODS: FDG PET was performed before and during CCRT for 13 NSCLC patients. Maximum standardized uptake value (SUV(max)), mean standardized uptake value (SUV(mean)), metabolic tumor volume (MTV), and total lesion glycolysis (TLG) were measured and the changes were calculated. These early metabolic changes were compared with the standard tumor response by computed tomograms (CT) one month after CCRT. RESULTS: One month after the completion of CCRT, 9 patients had partial response (PR) of tumor and 4 patients had stable disease. The percent changes of SUV(max) (%ΔSUV(max)) were larger in responder group than in non-responder group (55.7% ± 15.6% vs. 23.1% ± 19.0%, p = 0.01). The percent changes of SUV(mean) (%ΔSUV(mean)) were also larger in responder group than in non-responder group (54.4% ± 15.9% vs. 22.3% ± 23.0%, p = 0.01). The percent changes of MTV (%ΔMTV) or TLG (%ΔTLG) had no correlation with the tumor response after treatment. All the 7 patients (100%) with %ΔSUV(max) ≥ 50% had PR, but only 2 out of 6 patients (33%) with %ΔSUV(max) < 50% had PR after CCRT (p = 0.009). Likewise, all the 6 patients (100%) with %ΔSUV(mean) ≥ 50% had PR, but only 3 out of 7 patients (43%) with %ΔSUV(mean) < 50% had PR after CCRT (p = 0.026). CONCLUSION: The degree of metabolic changes measured by PET-CT during CCRT was predictive for NSCLC tumor response after CCRT. The Korean Society for Radiation Oncology 2014-12 2014-12-30 /pmc/articles/PMC4282997/ /pubmed/25568851 http://dx.doi.org/10.3857/roj.2014.32.4.231 Text en Copyright © 2014. The Korean Society for Radiation Oncology http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kim, Suzy
Oh, So Won
Kim, Jin Soo
Kim, Ki Hwan
Kim, Yu Kyeong
Prediction of response by FDG PET early during concurrent chemoradiotherapy for locally advanced non-small cell lung cancer
title Prediction of response by FDG PET early during concurrent chemoradiotherapy for locally advanced non-small cell lung cancer
title_full Prediction of response by FDG PET early during concurrent chemoradiotherapy for locally advanced non-small cell lung cancer
title_fullStr Prediction of response by FDG PET early during concurrent chemoradiotherapy for locally advanced non-small cell lung cancer
title_full_unstemmed Prediction of response by FDG PET early during concurrent chemoradiotherapy for locally advanced non-small cell lung cancer
title_short Prediction of response by FDG PET early during concurrent chemoradiotherapy for locally advanced non-small cell lung cancer
title_sort prediction of response by fdg pet early during concurrent chemoradiotherapy for locally advanced non-small cell lung cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4282997/
https://www.ncbi.nlm.nih.gov/pubmed/25568851
http://dx.doi.org/10.3857/roj.2014.32.4.231
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