Rationale and design of the Diet Restriction and Exercise-induced Adaptations in Metastatic breast cancer (DREAM) study: a 2-arm, parallel-group, phase II, randomized control trial of a short-term, calorie-restricted, and ketogenic diet plus exercise during intravenous chemotherapy versus usual care.


Journal

BMC cancer
ISSN: 1471-2407
Titre abrégé: BMC Cancer
Pays: England
ID NLM: 100967800

Informations de publication

Date de publication:
10 Oct 2021
Historique:
received: 12 05 2021
accepted: 23 09 2021
entrez: 11 10 2021
pubmed: 12 10 2021
medline: 21 10 2021
Statut: epublish

Résumé

An underlying cause of solid tumor resistance to chemotherapy treatment is diminished tumor blood supply, which leads to a hypoxic microenvironment, dependence on anaerobic energy metabolism, and impaired delivery of intravenous treatments. Preclinical data suggest that dietary strategies of caloric restriction and low-carbohydrate intake can inhibit glycolysis, while acute exercise can transiently enhance blood flow to the tumor and reduce hypoxia. The Diet Restriction and Exercise-induced Adaptations in Metastatic Breast Cancer (DREAM) study will compare the effects of a short-term, 50% calorie-restricted and ketogenic diet combined with aerobic exercise performed during intravenous chemotherapy treatment to usual care on changes in tumor burden, treatment side effects, and quality of life. Fifty patients with measurable metastases and primary breast cancer starting a new line of intravenous chemotherapy will be randomly assigned to usual care or the combined diet and exercise intervention. Participants assigned to the intervention group will be provided with food consisting of 50% of measured calorie needs with 80% of calories from fat and ≤ 10% from carbohydrates for 48-72 h prior to each chemotherapy treatment and will perform 30-60 min of moderate-intensity cycle ergometer exercise during each chemotherapy infusion, for up to six treatment cycles. The diet and exercise durations will be adapted for each chemotherapy protocol. Tumor burden will be assessed by change in target lesion size using axial computed tomography (primary outcome) and magnetic resonance imaging (MRI)-derived apparent diffusion coefficient (secondary outcome) after up to six treatments. Tertiary outcomes will include quantitative MRI markers of treatment toxicity to the heart, thigh skeletal muscle, and liver, and patient-reported symptoms and quality of life. Exploratory outcome measures include progression-free and overall survival. The DREAM study will test a novel, short-term diet and exercise intervention that is targeted to mechanisms of tumor resistance to chemotherapy. A reduction in lesion size is likely to translate to improved cancer outcomes including disease progression and overall survival. Furthermore, a lifestyle intervention may empower patients with metastatic breast cancer by actively engaging them to play a key role in their treatment. ClinicalTrials.gov, NCT03795493 , registered 7 January, 2019.

Sections du résumé

BACKGROUND BACKGROUND
An underlying cause of solid tumor resistance to chemotherapy treatment is diminished tumor blood supply, which leads to a hypoxic microenvironment, dependence on anaerobic energy metabolism, and impaired delivery of intravenous treatments. Preclinical data suggest that dietary strategies of caloric restriction and low-carbohydrate intake can inhibit glycolysis, while acute exercise can transiently enhance blood flow to the tumor and reduce hypoxia. The Diet Restriction and Exercise-induced Adaptations in Metastatic Breast Cancer (DREAM) study will compare the effects of a short-term, 50% calorie-restricted and ketogenic diet combined with aerobic exercise performed during intravenous chemotherapy treatment to usual care on changes in tumor burden, treatment side effects, and quality of life.
METHODS METHODS
Fifty patients with measurable metastases and primary breast cancer starting a new line of intravenous chemotherapy will be randomly assigned to usual care or the combined diet and exercise intervention. Participants assigned to the intervention group will be provided with food consisting of 50% of measured calorie needs with 80% of calories from fat and ≤ 10% from carbohydrates for 48-72 h prior to each chemotherapy treatment and will perform 30-60 min of moderate-intensity cycle ergometer exercise during each chemotherapy infusion, for up to six treatment cycles. The diet and exercise durations will be adapted for each chemotherapy protocol. Tumor burden will be assessed by change in target lesion size using axial computed tomography (primary outcome) and magnetic resonance imaging (MRI)-derived apparent diffusion coefficient (secondary outcome) after up to six treatments. Tertiary outcomes will include quantitative MRI markers of treatment toxicity to the heart, thigh skeletal muscle, and liver, and patient-reported symptoms and quality of life. Exploratory outcome measures include progression-free and overall survival.
DISCUSSION CONCLUSIONS
The DREAM study will test a novel, short-term diet and exercise intervention that is targeted to mechanisms of tumor resistance to chemotherapy. A reduction in lesion size is likely to translate to improved cancer outcomes including disease progression and overall survival. Furthermore, a lifestyle intervention may empower patients with metastatic breast cancer by actively engaging them to play a key role in their treatment.
TRIAL REGISTRATION BACKGROUND
ClinicalTrials.gov, NCT03795493 , registered 7 January, 2019.

Identifiants

pubmed: 34629067
doi: 10.1186/s12885-021-08808-2
pii: 10.1186/s12885-021-08808-2
pmc: PMC8504029
doi:

Substances chimiques

Antineoplastic Agents 0
Dietary Carbohydrates 0
Dietary Fats 0

Banques de données

ClinicalTrials.gov
['NCT03795493']

Types de publication

Clinical Trial Protocol Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1093

Subventions

Organisme : Canadian Cancer Society
ID : 705816
Organisme : CIHR
ID : 160397
Pays : Canada

Informations de copyright

© 2021. The Author(s).

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Auteurs

Amy A Kirkham (AA)

Faculty of Kinesiology & Physical Education, University of Toronto, 422, 100 Devonshire Pl, Toronto, ON, M5S 2C9, Canada. amy.kirkham@utoronto.ca.

Karen King (K)

Cross Cancer Institute, Edmonton, AB, Canada.
University of Alberta, Edmonton, AB, Canada.

Anil A Joy (AA)

Cross Cancer Institute, Edmonton, AB, Canada.
University of Alberta, Edmonton, AB, Canada.

André B Pelletier (AB)

University of Alberta, Edmonton, AB, Canada.

John R Mackey (JR)

Cross Cancer Institute, Edmonton, AB, Canada.
University of Alberta, Edmonton, AB, Canada.

Kelvin Young (K)

Cross Cancer Institute, Edmonton, AB, Canada.
University of Alberta, Edmonton, AB, Canada.

Xiaofu Zhu (X)

Cross Cancer Institute, Edmonton, AB, Canada.
University of Alberta, Edmonton, AB, Canada.

Judith Meza-Junco (J)

Cross Cancer Institute, Edmonton, AB, Canada.
University of Alberta, Edmonton, AB, Canada.

Sanraj K Basi (SK)

Cross Cancer Institute, Edmonton, AB, Canada.
University of Alberta, Edmonton, AB, Canada.

Julie Price Hiller (JP)

Cross Cancer Institute, Edmonton, AB, Canada.
University of Alberta, Edmonton, AB, Canada.

Tina Brkin (T)

Cross Cancer Institute, Edmonton, AB, Canada.

Bonnie Michalowski (B)

Cross Cancer Institute, Edmonton, AB, Canada.

Edith Pituskin (E)

Cross Cancer Institute, Edmonton, AB, Canada.
University of Alberta, Edmonton, AB, Canada.

D Ian Paterson (DI)

University of Alberta, Edmonton, AB, Canada.

Kerry S Courneya (KS)

University of Alberta, Edmonton, AB, Canada.

Richard B Thompson (RB)

University of Alberta, Edmonton, AB, Canada.

Carla M Prado (CM)

University of Alberta, Edmonton, AB, Canada.

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