Ketogenic diets as an adjuvant therapy for glioblastoma (KEATING): a randomized, mixed methods, feasibility study.


Journal

Journal of neuro-oncology
ISSN: 1573-7373
Titre abrégé: J Neurooncol
Pays: United States
ID NLM: 8309335

Informations de publication

Date de publication:
Mar 2020
Historique:
received: 09 12 2019
accepted: 30 01 2020
pubmed: 10 2 2020
medline: 21 11 2020
entrez: 10 2 2020
Statut: ppublish

Résumé

We conducted a feasibility study to investigate the use of ketogenic diets (KDs) as an adjuvant therapy for patients with glioblastoma (GBM), investigating (i) trial feasibility; (ii) potential impacts of the trial on patients' quality of life and health; (iii) patients' perspectives of their decision-making when invited to participate in the trial and (iv) recommending improvements to optimize future phase III trials. A single-center, prospective, randomized, pilot study (KEATING), with an embedded qualitative design. Twelve newly diagnosed patients with GBM were randomized 1:1 to modified ketogenic diet (MKD) or medium chain triglyceride ketogenic diet (MCTKD). Primary outcome was retention at three months. Semi-structured interviews were conducted with a purposive sample of patients and caregivers (n = 15). Descriptive statistics were used for quantitative outcomes and qualitative data were analyzed thematically aided by NVivo. KEATING achieved recruitment targets, but the recruitment rate was low (28.6%). Retention was poor; only four of 12 patients completed the three-month diet (MCTKD n = 3; MKD n = 1). Participants' decisions were intuitive and emotional; caregivers supported diet implementation and influenced the patients' decision to participate. Those who declined made a deliberative and considered decision factoring diet burden and quality of life. A three-month diet was undesirable to patients who declined and withdrew. Recruitment to a KD trial for patients with GBM is possible. A six-week intervention period is proposed for a phase III trial. The role of caregivers should not be underestimated. Future trials should optimize and adequately support the decision-making of patients.

Identifiants

pubmed: 32036576
doi: 10.1007/s11060-020-03417-8
pii: 10.1007/s11060-020-03417-8
pmc: PMC7076054
doi:

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

213-227

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Auteurs

Kirsty J Martin-McGill (KJ)

Institute of Translational Medicine, University of Liverpool, Brownlow Hill, Liverpool, L69 3BX, UK. Kirsty.martin@liverpool.ac.uk.
Department of Clinical Sciences and Nutrition, University of Chester, Chester, UK. Kirsty.martin@liverpool.ac.uk.

Anthony G Marson (AG)

Institute of Translational Medicine, University of Liverpool, Brownlow Hill, Liverpool, L69 3BX, UK.
The Walton Centre NHS Foundation Trust, Lower Lane, Liverpool, L9 7LJ, UK.

Catrin Tudur Smith (C)

Department of Biostatistics, University of Liverpool, Brownlow Hill, Liverpool, L69 3BX, UK.

Bridget Young (B)

Department of Health Services Research, University of Liverpool, Brownlow Hill, Liverpool, L69 3BX, UK.

Samantha J Mills (SJ)

The Walton Centre NHS Foundation Trust, Lower Lane, Liverpool, L9 7LJ, UK.

M Gemma Cherry (MG)

Department of Psychological Sciences, University of Liverpool, Brownlow Hill, Liverpool, L69 3BX, UK.
Clinical Health Psychology Service, Royal Liverpool University Hospital, Liverpool, L7 8XP, UK.

Michael D Jenkinson (MD)

Institute of Translational Medicine, University of Liverpool, Brownlow Hill, Liverpool, L69 3BX, UK.
The Walton Centre NHS Foundation Trust, Lower Lane, Liverpool, L9 7LJ, UK.

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