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Comparing docosahexaenoic acid (DHA) concomitant with neoadjuvant chemotherapy versus neoadjuvant chemotherapy alone in the treatment of breast cancer (DHA WIN): protocol of a double-blind, phase II, randomised controlled trial

INTRODUCTION: Neoadjuvant chemotherapy for breast cancer treatment is prescribed to facilitate surgery and provide confirmation of drug-sensitive disease, and the achievement of pathological complete response (pCR) predicts improved long-term outcomes. Docosahexaenoic acid (DHA) has been shown to re...

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Autores principales: Newell, Marnie, Mackey, John R, Bigras, Gilbert, Alvarez-Camacho, Mirey, Goruk, Susan, Ghosh, Sunita, Schmidt, Alison, Miede, Deborah, Chisotti, Ann, Postovit, Lynne, Baker, Kristi, Mazurak, Vera, Courneya, Kerry, Berendt, Richard, Dong, Wei-Feng, Wood, George, Basi, Sanraj K, Joy, Anil Abraham, King, Karen, Meza-Junco, Judith, Zhu, Xiaofu, Field, Catherine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6756327/
https://www.ncbi.nlm.nih.gov/pubmed/31530611
http://dx.doi.org/10.1136/bmjopen-2019-030502
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author Newell, Marnie
Mackey, John R
Bigras, Gilbert
Alvarez-Camacho, Mirey
Goruk, Susan
Ghosh, Sunita
Schmidt, Alison
Miede, Deborah
Chisotti, Ann
Postovit, Lynne
Baker, Kristi
Mazurak, Vera
Courneya, Kerry
Berendt, Richard
Dong, Wei-Feng
Wood, George
Basi, Sanraj K
Joy, Anil Abraham
King, Karen
Meza-Junco, Judith
Zhu, Xiaofu
Field, Catherine
author_facet Newell, Marnie
Mackey, John R
Bigras, Gilbert
Alvarez-Camacho, Mirey
Goruk, Susan
Ghosh, Sunita
Schmidt, Alison
Miede, Deborah
Chisotti, Ann
Postovit, Lynne
Baker, Kristi
Mazurak, Vera
Courneya, Kerry
Berendt, Richard
Dong, Wei-Feng
Wood, George
Basi, Sanraj K
Joy, Anil Abraham
King, Karen
Meza-Junco, Judith
Zhu, Xiaofu
Field, Catherine
author_sort Newell, Marnie
collection PubMed
description INTRODUCTION: Neoadjuvant chemotherapy for breast cancer treatment is prescribed to facilitate surgery and provide confirmation of drug-sensitive disease, and the achievement of pathological complete response (pCR) predicts improved long-term outcomes. Docosahexaenoic acid (DHA) has been shown to reduce tumour growth in preclinical models when combined with chemotherapy and is known to beneficially modulate systemic immune function. The purpose of this trial is to investigate the benefit of DHA supplementation in combination with neoadjuvant chemotherapy in patients with breast cancer. METHODS AND ANALYSIS: This is a double-blind, phase II, randomised controlled trial of 52 women prescribed neoadjuvant chemotherapy to test if DHA supplementation enhances chemotherapy efficacy. The DHA supplementation group will take 4.4 g/day DHA orally, and the placebo group will take an equal fat supplement of vegetable oil. The primary outcome will be change in Ki67 labelling index from prechemotherapy core needle biopsy to definitive surgical specimen. The secondary endpoints include assessment of (1) DHA plasma phospholipid content; (2) systemic immune cell types, plasma cytokines and inflammatory markers; (3) tumour markers for apoptosis and tumour infiltrating lymphocytes; (4) rate of pCR in breast and in axillary nodes; (5) frequency of grade 3 and 4 chemotherapy-associated toxicities; and (6) patient-perceived quality of life. The trial has 81% power to detect a significant between-group difference in Ki67 index with a two-sided t-test of less than 0.0497, and accounts for 10% dropout rate. ETHICS AND DISSEMINATION: This study has full approval from the Health Research Ethics Board of Alberta - Cancer Committee (Protocol #: HREBA.CC-18-0381). We expect to present the findings of this study to the scientific community in peer-reviewed journals and at conferences. The results of this study will provide evidence for supplementing with DHA during neoadjuvant chemotherapy treatment for breast cancer. TRIAL REGISTRATION NUMBER: NCT03831178
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spelling pubmed-67563272019-10-07 Comparing docosahexaenoic acid (DHA) concomitant with neoadjuvant chemotherapy versus neoadjuvant chemotherapy alone in the treatment of breast cancer (DHA WIN): protocol of a double-blind, phase II, randomised controlled trial Newell, Marnie Mackey, John R Bigras, Gilbert Alvarez-Camacho, Mirey Goruk, Susan Ghosh, Sunita Schmidt, Alison Miede, Deborah Chisotti, Ann Postovit, Lynne Baker, Kristi Mazurak, Vera Courneya, Kerry Berendt, Richard Dong, Wei-Feng Wood, George Basi, Sanraj K Joy, Anil Abraham King, Karen Meza-Junco, Judith Zhu, Xiaofu Field, Catherine BMJ Open Oncology INTRODUCTION: Neoadjuvant chemotherapy for breast cancer treatment is prescribed to facilitate surgery and provide confirmation of drug-sensitive disease, and the achievement of pathological complete response (pCR) predicts improved long-term outcomes. Docosahexaenoic acid (DHA) has been shown to reduce tumour growth in preclinical models when combined with chemotherapy and is known to beneficially modulate systemic immune function. The purpose of this trial is to investigate the benefit of DHA supplementation in combination with neoadjuvant chemotherapy in patients with breast cancer. METHODS AND ANALYSIS: This is a double-blind, phase II, randomised controlled trial of 52 women prescribed neoadjuvant chemotherapy to test if DHA supplementation enhances chemotherapy efficacy. The DHA supplementation group will take 4.4 g/day DHA orally, and the placebo group will take an equal fat supplement of vegetable oil. The primary outcome will be change in Ki67 labelling index from prechemotherapy core needle biopsy to definitive surgical specimen. The secondary endpoints include assessment of (1) DHA plasma phospholipid content; (2) systemic immune cell types, plasma cytokines and inflammatory markers; (3) tumour markers for apoptosis and tumour infiltrating lymphocytes; (4) rate of pCR in breast and in axillary nodes; (5) frequency of grade 3 and 4 chemotherapy-associated toxicities; and (6) patient-perceived quality of life. The trial has 81% power to detect a significant between-group difference in Ki67 index with a two-sided t-test of less than 0.0497, and accounts for 10% dropout rate. ETHICS AND DISSEMINATION: This study has full approval from the Health Research Ethics Board of Alberta - Cancer Committee (Protocol #: HREBA.CC-18-0381). We expect to present the findings of this study to the scientific community in peer-reviewed journals and at conferences. The results of this study will provide evidence for supplementing with DHA during neoadjuvant chemotherapy treatment for breast cancer. TRIAL REGISTRATION NUMBER: NCT03831178 BMJ Publishing Group 2019-09-17 /pmc/articles/PMC6756327/ /pubmed/31530611 http://dx.doi.org/10.1136/bmjopen-2019-030502 Text en © Author(s) (or their employer(s)) 2019. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.
spellingShingle Oncology
Newell, Marnie
Mackey, John R
Bigras, Gilbert
Alvarez-Camacho, Mirey
Goruk, Susan
Ghosh, Sunita
Schmidt, Alison
Miede, Deborah
Chisotti, Ann
Postovit, Lynne
Baker, Kristi
Mazurak, Vera
Courneya, Kerry
Berendt, Richard
Dong, Wei-Feng
Wood, George
Basi, Sanraj K
Joy, Anil Abraham
King, Karen
Meza-Junco, Judith
Zhu, Xiaofu
Field, Catherine
Comparing docosahexaenoic acid (DHA) concomitant with neoadjuvant chemotherapy versus neoadjuvant chemotherapy alone in the treatment of breast cancer (DHA WIN): protocol of a double-blind, phase II, randomised controlled trial
title Comparing docosahexaenoic acid (DHA) concomitant with neoadjuvant chemotherapy versus neoadjuvant chemotherapy alone in the treatment of breast cancer (DHA WIN): protocol of a double-blind, phase II, randomised controlled trial
title_full Comparing docosahexaenoic acid (DHA) concomitant with neoadjuvant chemotherapy versus neoadjuvant chemotherapy alone in the treatment of breast cancer (DHA WIN): protocol of a double-blind, phase II, randomised controlled trial
title_fullStr Comparing docosahexaenoic acid (DHA) concomitant with neoadjuvant chemotherapy versus neoadjuvant chemotherapy alone in the treatment of breast cancer (DHA WIN): protocol of a double-blind, phase II, randomised controlled trial
title_full_unstemmed Comparing docosahexaenoic acid (DHA) concomitant with neoadjuvant chemotherapy versus neoadjuvant chemotherapy alone in the treatment of breast cancer (DHA WIN): protocol of a double-blind, phase II, randomised controlled trial
title_short Comparing docosahexaenoic acid (DHA) concomitant with neoadjuvant chemotherapy versus neoadjuvant chemotherapy alone in the treatment of breast cancer (DHA WIN): protocol of a double-blind, phase II, randomised controlled trial
title_sort comparing docosahexaenoic acid (dha) concomitant with neoadjuvant chemotherapy versus neoadjuvant chemotherapy alone in the treatment of breast cancer (dha win): protocol of a double-blind, phase ii, randomised controlled trial
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6756327/
https://www.ncbi.nlm.nih.gov/pubmed/31530611
http://dx.doi.org/10.1136/bmjopen-2019-030502
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