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Dietary Flaxseed in Non-Small Cell Lung Cancer Patients Receiving Chemoradiation
Author(s) -
Abigail T. Berman,
J Turowski,
Rosemarie Mick,
Keith A. Cengel,
Nicole Farnese,
Lisa Basel-Brown,
Clementina Mesaros,
Ian A. Blair,
James Lawson,
Melpo ChristofidouSolomidou,
James Lee,
Ramesh Rengan
Publication year - 2013
Publication title -
journal of pulmonary and respiratory medicine
Language(s) - English
Resource type - Journals
ISSN - 2161-105X
DOI - 10.4172/2161-105x.1000154
Subject(s) - tolerability , medicine , discontinuation , lung cancer , gastroenterology , oxidative stress , pneumonitis , bioavailability , pharmacology , lung , adverse effect
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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