The Clinical Impact of Time-restricted Eating on Cancer: A Systematic Review

Author:

Stringer Eleah J123ORCID,Cloke Rob W G14,Van der Meer Lindsay123,Murphy Rachel A56,Macpherson Nicol A78,Lum Julian J910

Affiliation:

1. Nursing and Allied Health Research and KT Department, BC Cancer , Vancouver, BC V5Z 1G1, Canada

2. Department of Oncology Nutrition, BC Cancer , Victoria, BC V8R 6V5, Canada

3. Food, Nutrition and Health, Faculty of Land and Food Systems, University of British Columbia , Vancouver, BC V6T 1Z4, Canada

4. Department of Microbiology and Immunology, University of British Columbia , Vancouver, BC V6T 1Z4, Canada

5. School of Population and Public Health, University of British Columbia , Vancouver, BC V6T 1Z3, Canada

6. Department of Cancer Control Research, BC Cancer Research Institute , Vancouver, BC V5Z 1L3, Canada

7. Department of Medical Oncology, BC Cancer – Victoria , Victoria, BC V8R 6V5, Canada

8. Department of Medical Oncology, Faculty of Medicine, University of British Columbia , Vancouver, BC V5Z 1M9, Canada

9. Trev and Joyce Deeley Research Centre, BC Cancer – Victoria , Victoria, BC V8R 6V5, Canada

10. Department of Biochemistry and Microbiology, University of Victoria , Victoria, BC V8W 2Y2, Canada

Abstract

Abstract Context In the face of the growing global burden of cancer, there is increasing interest in dietary interventions to mitigate its impacts. Pre-clinical evidence suggests that time-restricted eating (TRE), a type of intermittent fasting, induces metabolic effects and alterations in the gut microbiome that may impede carcinogenesis. Research on TRE in cancer has progressed to human studies, but the evidence has yet to be synthesized. Objective The objective of this study was to systematically evaluate the clinical and/or metabolomic effects of TRE compared with ad libitum eating or alternative diets in people with cancer. Data Sources Ovid MEDLINE, Ovid Embase, CINAHL, Ovid Cochrane Central Register of Control Trials (CENTRAL), Web of Science Core Collection (ESCI, CPCI-SSH, CPCI-S), and SCOPUS were searched up to January 4, 2023, using the core concepts of “intermittent fasting” and “cancer.” Original study designs, protocols, and clinical trial registries were included. Data Extraction After evaluating 13 900 results, 24 entries were included, consisting of 8 full articles, 2 abstracts, 1 published protocol and 13 trial registries. All data were extracted, compared, and critically analyzed. Data Analysis There was heterogeneity in the patient population (eg, in tumor sites), TRE regimens (eg, degree of restriction, duration), and clinical end points. A high rate (67–98%) of TRE adherence was observed, alongside improvements in quality of life. Four articles assessed cancer markers and found a reduction in tumor marker carcinoembryonic antigen, reduced rates of recurrence, and a sustained major molecular response, following TRE. Five articles demonstrated modified cancer risk factors, including beneficial effects on body mass index, adiposity, glucoregulation, and inflammation in as short a period as 8 weeks. None of the completed studies assessed the effect of TRE on the microbiome, but analysis of the microbiome is a planned outcome in 2 clinical trials. Conclusions Preliminary findings suggest that TRE is feasible and acceptable by people with cancer, may have oncological benefits, and improves quality of life. Registration PROSPERO registration No. CRD42023386885.

Funder

Michael Smith Health Research

BC Cancer Foundation

Canadian Institutes of Health Research

Terry Fox Research Institute

Lotte and John Hecht Memorial Foundation

Publisher

Oxford University Press (OUP)

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