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Dietary Flaxseed in Non-Small Cell Lung Cancer Patients Receiving Chemoradiation
PURPOSE: The standard of care in Locally-Advanced Non-Small Cell Lung Cancer (LA-NSCLC) is chemotherapy and radiation; however, Radiation-Induced Lung Injury (RILI), which may be prevented by the anti-inflammatory and anti-oxidant properties of Flaxseed (FS), impedes its maximum benefit. MATERIALS A...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3932620/ https://www.ncbi.nlm.nih.gov/pubmed/24575360 http://dx.doi.org/10.4172/2161-105X.1000154 |
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author | Berman, Abigail T Turowski, Jason Mick, Rosemarie Cengel, Keith Farnese, Nicole Basel-Brown, Lisa Mesaros, Clementina Blair, Ian Lawson, James Christofidou-Solomidou, Melpo Lee, James Rengan, Ramesh |
author_facet | Berman, Abigail T Turowski, Jason Mick, Rosemarie Cengel, Keith Farnese, Nicole Basel-Brown, Lisa Mesaros, Clementina Blair, Ian Lawson, James Christofidou-Solomidou, Melpo Lee, James Rengan, Ramesh |
author_sort | Berman, Abigail T |
collection | PubMed |
description | PURPOSE: The standard of care in Locally-Advanced Non-Small Cell Lung Cancer (LA-NSCLC) is chemotherapy and radiation; however, Radiation-Induced Lung Injury (RILI), which may be prevented by the anti-inflammatory and anti-oxidant properties of Flaxseed (FS), impedes its maximum benefit. MATERIALS AND METHODS: Patients with LA-NSCLC requiring definitive RT were randomized to one FS or control muffin daily from start to 2 weeks after RT. Blood and urine were collected to quantify plasma FS metabolites, Enterodione (ED) and Enterolactone (EL), and urinary oxidative stress biomarkers, 8, 12-iso-iPF2a-VI (isoprostane) and 8-oxo-7,8-dihydro-2′deoxyguanosine (8-oxo-dGuo). Tolerability was defined as consuming ≥ 75% of the intended muffins and no ≥ grade 3 gastrointestinal toxicities. RESULTS: Fourteen patients (control,7; FS,7) were enrolled. The tolerability rates were 42.9 versus 71.4% (p=0.59) for FS and control, respectively. Mean percentages of intended number of muffins consumed were 37% versus 73% (p=0.12). ED and EL increased at onset of FS and decreased with discontinuation, confirming bioavailability. Isoprostane and 8-oxo-dGuo were detectable. There was a trend towards decreased rates of pneumonitis in FS. CONCLUSIONS: This is the first study to report FS bioavailability and quantify oxidative stress markers in NSCLC patients. FS in the administered muffin formulation did not meet tolerability criteria. Given the promising mechanism of FS as a radioprotectant, further investigations should focus on the optimal method for administration of FS. |
format | Online Article Text |
id | pubmed-3932620 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
record_format | MEDLINE/PubMed |
spelling | pubmed-39326202014-02-24 Dietary Flaxseed in Non-Small Cell Lung Cancer Patients Receiving Chemoradiation Berman, Abigail T Turowski, Jason Mick, Rosemarie Cengel, Keith Farnese, Nicole Basel-Brown, Lisa Mesaros, Clementina Blair, Ian Lawson, James Christofidou-Solomidou, Melpo Lee, James Rengan, Ramesh J Pulm Respir Med Article PURPOSE: The standard of care in Locally-Advanced Non-Small Cell Lung Cancer (LA-NSCLC) is chemotherapy and radiation; however, Radiation-Induced Lung Injury (RILI), which may be prevented by the anti-inflammatory and anti-oxidant properties of Flaxseed (FS), impedes its maximum benefit. MATERIALS AND METHODS: Patients with LA-NSCLC requiring definitive RT were randomized to one FS or control muffin daily from start to 2 weeks after RT. Blood and urine were collected to quantify plasma FS metabolites, Enterodione (ED) and Enterolactone (EL), and urinary oxidative stress biomarkers, 8, 12-iso-iPF2a-VI (isoprostane) and 8-oxo-7,8-dihydro-2′deoxyguanosine (8-oxo-dGuo). Tolerability was defined as consuming ≥ 75% of the intended muffins and no ≥ grade 3 gastrointestinal toxicities. RESULTS: Fourteen patients (control,7; FS,7) were enrolled. The tolerability rates were 42.9 versus 71.4% (p=0.59) for FS and control, respectively. Mean percentages of intended number of muffins consumed were 37% versus 73% (p=0.12). ED and EL increased at onset of FS and decreased with discontinuation, confirming bioavailability. Isoprostane and 8-oxo-dGuo were detectable. There was a trend towards decreased rates of pneumonitis in FS. CONCLUSIONS: This is the first study to report FS bioavailability and quantify oxidative stress markers in NSCLC patients. FS in the administered muffin formulation did not meet tolerability criteria. Given the promising mechanism of FS as a radioprotectant, further investigations should focus on the optimal method for administration of FS. 2013-08-30 /pmc/articles/PMC3932620/ /pubmed/24575360 http://dx.doi.org/10.4172/2161-105X.1000154 Text en Copyright: © 2013 Berman Abigail T, et al. http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Article Berman, Abigail T Turowski, Jason Mick, Rosemarie Cengel, Keith Farnese, Nicole Basel-Brown, Lisa Mesaros, Clementina Blair, Ian Lawson, James Christofidou-Solomidou, Melpo Lee, James Rengan, Ramesh Dietary Flaxseed in Non-Small Cell Lung Cancer Patients Receiving Chemoradiation |
title | Dietary Flaxseed in Non-Small Cell Lung Cancer Patients Receiving Chemoradiation |
title_full | Dietary Flaxseed in Non-Small Cell Lung Cancer Patients Receiving Chemoradiation |
title_fullStr | Dietary Flaxseed in Non-Small Cell Lung Cancer Patients Receiving Chemoradiation |
title_full_unstemmed | Dietary Flaxseed in Non-Small Cell Lung Cancer Patients Receiving Chemoradiation |
title_short | Dietary Flaxseed in Non-Small Cell Lung Cancer Patients Receiving Chemoradiation |
title_sort | dietary flaxseed in non-small cell lung cancer patients receiving chemoradiation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3932620/ https://www.ncbi.nlm.nih.gov/pubmed/24575360 http://dx.doi.org/10.4172/2161-105X.1000154 |
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