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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
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.
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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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