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Dual-Energy CT in Patients Treated with Anti-Angiogenic Agents for Non-Small Cell Lung Cancer: New Method of Monitoring Tumor Response?

OBJECTIVE: To evaluate tumor responses in patients treated with anti-angiogenic agents for non-small cell lung cancer (NSCLC) by assessing intratumoral changes using a dual-energy CT (DECT) (based on Choi's criteria) and to compare it to traditional Response Evaluation Criteria in Solid Tumors...

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Autores principales: Kim, Yoo Na, Lee, Ho Yun, Lee, Kyung Soo, Seo, Joon Beom, Chung, Myung Jin, Ahn, Myung-Ju, Park, Keunchil, Kim, Tae Sung, Yi, Chin A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Radiology 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3484290/
https://www.ncbi.nlm.nih.gov/pubmed/23118568
http://dx.doi.org/10.3348/kjr.2012.13.6.702
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author Kim, Yoo Na
Lee, Ho Yun
Lee, Kyung Soo
Seo, Joon Beom
Chung, Myung Jin
Ahn, Myung-Ju
Park, Keunchil
Kim, Tae Sung
Yi, Chin A
author_facet Kim, Yoo Na
Lee, Ho Yun
Lee, Kyung Soo
Seo, Joon Beom
Chung, Myung Jin
Ahn, Myung-Ju
Park, Keunchil
Kim, Tae Sung
Yi, Chin A
author_sort Kim, Yoo Na
collection PubMed
description OBJECTIVE: To evaluate tumor responses in patients treated with anti-angiogenic agents for non-small cell lung cancer (NSCLC) by assessing intratumoral changes using a dual-energy CT (DECT) (based on Choi's criteria) and to compare it to traditional Response Evaluation Criteria in Solid Tumors (RECIST) criteria. MATERIALS AND METHODS: Ten NSCLC patients treated with bevacizumab underwent DECT. Tumor responses to anti-angiogenic therapy were assessed and compared with the baseline CT results using both RECIST (size changes only) and Choi's criteria (reflecting net tumor enhancement). Kappa statistics was used to evaluate agreements between tumor responses assessed by RECIST and Choi's criteria. RESULTS: The weighted κ value for the comparison of tumor responses between the RECIST and Choi's criteria was 0.72. Of 31 target lesions (21 solid nodules, 8 lymph nodes, and two ground-glass opacity nodules [GGNs]), five lesions (16%) showed discordant responses between RECIST and Choi's criteria. Iodine-enhanced images allowed for a distinction between tumor enhancement and hemorrhagic response (detected in 14% [4 of 29, excluding GGNs] of target lesions on virtual nonenhanced images). CONCLUSION: DECT may serve as a useful tool for response evaluation after anti-angiogenic treatment in NSCLC patients by providing information on the net enhancement of target lesions without obtaining non-enhanced images.
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spelling pubmed-34842902012-11-02 Dual-Energy CT in Patients Treated with Anti-Angiogenic Agents for Non-Small Cell Lung Cancer: New Method of Monitoring Tumor Response? Kim, Yoo Na Lee, Ho Yun Lee, Kyung Soo Seo, Joon Beom Chung, Myung Jin Ahn, Myung-Ju Park, Keunchil Kim, Tae Sung Yi, Chin A Korean J Radiol Original Article OBJECTIVE: To evaluate tumor responses in patients treated with anti-angiogenic agents for non-small cell lung cancer (NSCLC) by assessing intratumoral changes using a dual-energy CT (DECT) (based on Choi's criteria) and to compare it to traditional Response Evaluation Criteria in Solid Tumors (RECIST) criteria. MATERIALS AND METHODS: Ten NSCLC patients treated with bevacizumab underwent DECT. Tumor responses to anti-angiogenic therapy were assessed and compared with the baseline CT results using both RECIST (size changes only) and Choi's criteria (reflecting net tumor enhancement). Kappa statistics was used to evaluate agreements between tumor responses assessed by RECIST and Choi's criteria. RESULTS: The weighted κ value for the comparison of tumor responses between the RECIST and Choi's criteria was 0.72. Of 31 target lesions (21 solid nodules, 8 lymph nodes, and two ground-glass opacity nodules [GGNs]), five lesions (16%) showed discordant responses between RECIST and Choi's criteria. Iodine-enhanced images allowed for a distinction between tumor enhancement and hemorrhagic response (detected in 14% [4 of 29, excluding GGNs] of target lesions on virtual nonenhanced images). CONCLUSION: DECT may serve as a useful tool for response evaluation after anti-angiogenic treatment in NSCLC patients by providing information on the net enhancement of target lesions without obtaining non-enhanced images. The Korean Society of Radiology 2012 2012-10-12 /pmc/articles/PMC3484290/ /pubmed/23118568 http://dx.doi.org/10.3348/kjr.2012.13.6.702 Text en Copyright © 2012 The Korean Society of Radiology 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, Yoo Na
Lee, Ho Yun
Lee, Kyung Soo
Seo, Joon Beom
Chung, Myung Jin
Ahn, Myung-Ju
Park, Keunchil
Kim, Tae Sung
Yi, Chin A
Dual-Energy CT in Patients Treated with Anti-Angiogenic Agents for Non-Small Cell Lung Cancer: New Method of Monitoring Tumor Response?
title Dual-Energy CT in Patients Treated with Anti-Angiogenic Agents for Non-Small Cell Lung Cancer: New Method of Monitoring Tumor Response?
title_full Dual-Energy CT in Patients Treated with Anti-Angiogenic Agents for Non-Small Cell Lung Cancer: New Method of Monitoring Tumor Response?
title_fullStr Dual-Energy CT in Patients Treated with Anti-Angiogenic Agents for Non-Small Cell Lung Cancer: New Method of Monitoring Tumor Response?
title_full_unstemmed Dual-Energy CT in Patients Treated with Anti-Angiogenic Agents for Non-Small Cell Lung Cancer: New Method of Monitoring Tumor Response?
title_short Dual-Energy CT in Patients Treated with Anti-Angiogenic Agents for Non-Small Cell Lung Cancer: New Method of Monitoring Tumor Response?
title_sort dual-energy ct in patients treated with anti-angiogenic agents for non-small cell lung cancer: new method of monitoring tumor response?
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3484290/
https://www.ncbi.nlm.nih.gov/pubmed/23118568
http://dx.doi.org/10.3348/kjr.2012.13.6.702
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