Feasibility and Safety of a Combined Metabolic Strategy in Glioblastoma Multiforme: A Prospective Case Series

Author:

Phillips M. C. L.1ORCID,Leyden J.2,McManus E. J.1,Lowyim D. G.13,Ziad F.4,Moon B. G.5,Haji Mohd Yasin N. A. B.6,Tan A.7,Thotathil Z.6,Jameson M. B.37

Affiliation:

1. Department of Neurology, Waikato Hospital, Hamilton, New Zealand

2. Calvary Adelaide Hospital, Adelaide, Australia

3. Waikato Clinical Campus, University of Auckland, Hamilton, New Zealand

4. Department of Pathology, Waikato Hospital, Hamilton, New Zealand

5. Department of Radiology, Waikato Hospital, Hamilton, New Zealand

6. Department of Radiation Oncology, Waikato Hospital, Hamilton, New Zealand

7. Department of Oncology, Waikato Hospital, Hamilton, New Zealand

Abstract

Background. Glioblastoma multiforme (GBM) may be susceptible to metabolic strategies such as fasting and ketogenic diets, which lower blood glucose and elevate ketones. Combining these two strategies may be an ideal approach for sustaining a potentially therapeutic glucose ketone index (GKI). In this prospective case series, we observed whether a combined metabolic strategy was feasible, safe, and capable of sustaining a GKI <6 in patients with GBM. Methods. We provided recommendations and guidelines to 10 GBM patients at various stages of tumour progression and treatment that enabled them to complete a 5–7-day fast every 1–2 months combined with a modified ketogenic diet during the intervening weeks. Patients monitored their blood glucose and ketone levels and body weight. Adverse effects were assessed. Results. Patients completed a mean of 161 ± 74 days of the combined metabolic strategy, with 34 ± 18 (21%) days of prolonged fasting (mean fast duration: 6.0 ± 1.4 days) and 127 ± 59 (79%) days on the ketogenic diet. The mean GKI for all 10 patients was 3.22 (1.28 during the fasts, 5.10 during the ketogenic diet). Body weight decreased by 8.4 ± 6.9 kg (11.2% decrease in baseline weight). The most common adverse effects attributed to the fasts and ketogenic diet were fatigue, irritability, and feeling lightheaded. The metabolic strategy did not interfere with standard oncological treatments. Conclusion. This is the first study to observe the feasibility and safety of repeated, prolonged fasting combined with a modified ketogenic diet in patients with GBM. Using minimal support, patients maintained the combined metabolic strategy for 5–6 months while sustaining a potentially therapeutic mean GKI of 3.22. Weight loss was considerable. Adverse effects attributed to the metabolic strategy were mild, and it did not interfere with standard oncological treatments. Study Registration: This study is registered on the Australia New Zealand Clinical Trials Registry, number ACTRN12620001310954. The study was registered on 4 December 2020.

Publisher

Hindawi Limited

Subject

Oncology

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