Clinical study reports that cycles of severe calorie restriction improve cancer immunity, a phenomenon often associated with a better prognosis.
Preclinical studies have shown that 'severe caloric restriction, achieved by cyclical episodes of fasting or using diets that mimic fasting (very low in carbohydrates and proteins), enhances the antitumor activity of chemotherapy, immunotherapy or endocrine therapies .(1)
These positive anti-cancer effects have been attributed to two major effects of fasting or fasting-mimicking diets:
1. a reduction in blood sugar, insulin and the growth factor IGF1, which reduces tumor growth and prevents the repair of damage inflicted on cancer cells by treatments and
2. an increase in antitumor immunity (infiltration of tumors by CD8+ T cells and a decrease in immunosuppressive T cells).
From lab to clinic
To see if these encouraging effects can be replicated in humans, clinical trials were conducted to assess the feasibility and antitumor activity of these fasting-mimicking diets in cancer patients who are treated with standard antitumor therapies.
In one of these trials, 101 patients who were being treated for various types of cancers agreed to adhere to cycles comprising 5 days of a very low calorie diet (600 calories the first day followed by 4 days at 300 calories), interspersed with a 3-week period of normal eating.(2)
The objective of this calorie restriction is to mimic fasting by drastically reducing the amount of calories ingested, but without cause malnutrition through plant intake (fruits, vegetables, nuts, tea) rich in vitamins, minerals and essential fats.
For example, a typical menu included a meal consisting of 300 g (75 kCal) of mixed vegetables (spinach, cabbage, zucchini, lettuce), a tablespoon of olive oil (108 kCal) and a piece of fruit (100 kCal ) like an orange, an apple, or a pear.
This type of intervention where the volunteers eat little, but do not completely fast, is much easier to accept and this is exactly what the study showed, with 99% of the patients who managed to follow a cycle of severe restriction. and 76% who have completed at least three cycles.
In addition, the weight losses that occur during the fasting period are canceled out by the return to normal food and therefore do not seem to be not pose a health hazard to the majority of patients.
Metabolic and Immune Effects
Practicing these cycles of severe calorie restriction had dramatic effects on metabolism, with decreases in blood sugar (19%), insulin (50%) and IGF-1 (30%) levels. .
From a therapeutic point of view, the best news, however, remains the strong modulation of anti-cancer immunity: transcriptomic analyzes have revealed that cycles of the diet mimicking fasting decrease immunosuppressive immune cells, with in parallel an improvement of several immune signatures (particularly intratumoral immune responses) which are known to be associated with a better clinical response in cancer patients.
According to the authors, the combined decrease in blood sugar, insulin and d IGF-1 caused by the drastic reduction in carbohydrate and protein intake profoundly alters the metabolism of cancer cells and immune cells. There is then an erosion of the immunosuppressive shield normally erected by tumors to protect themselves and grow unhindered, thus allowing immunity to carry out its work and destroy abnormal cells.
(1) Lee C et al. Fasting cycles retard growth of tumors and sensitize a range of cancer cell types to chemotherapy. Sci. Transl. Med. 2012; 4:124ra27. (2) Vernieri C et al. Fasting-mimicking diet is safe and reshapes metabolism and antitumor immunity in patients with cancer. Cancer Discov 2022; 12: 90-107.
Katrine Johns has been a reporter on the news desk since 2013. Before that she wrote about young adolescence and family dynamics for Styles and was the legal affairs correspondent for the Metro desk. Before joining The Gal Post, Katrine Johns worked as a staff writer at the Village Voice and a freelancer for Newsday, The Wall Street Journal, GQ and Mirabella. To get in touch, contact me through my email@example.com 1-800-268-7128