Evidence map›Paper›PMID 41727338›Full record

ArticleNeuro-oncology advances

Ketogenic diet therapy for high-grade gliomas combined with standard treatment using an angiogenesis inhibitor: An exploratory pilot study on feasibility.

Takashi Sasayama, Kazuhiro Tanaka, Hiroaki Nagashima, Michiko Takahashi, Misa Yamanishi, Misaki Kuroda, Satoko Tabuchi, Keisuke Hagihara, Shunsuke Yamanishi, Yusuke Ikeuchi and 7 more

Abstract read
In one paragraph

Article in Neuro-oncology advances. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Takashi SasayamaDepartment of Neurosurgery, Kobe University Graduate School of Medicine, Kobe.ORCID https://orcid.org/0000-0002-5593-9045
Kazuhiro TanakaDepartment of Neurosurgery, Kobe University Graduate School of Medicine, Kobe.
Hiroaki NagashimaDepartment of Neurosurgery, Kobe University Graduate School of Medicine, Kobe.
Michiko TakahashiDepartment of Nutrition, Kobe University Hospital, Kobe.
Misa YamanishiDepartment of Nutrition, Kobe University Hospital, Kobe.
Misaki KurodaDepartment of Nutrition, Kobe University Hospital, Kobe.
Satoko TabuchiDepartment of Nutrition, Kobe University Hospital, Kobe.
Keisuke HagiharaResearch Institute for Microbial Diseases (RIMD), Osaka -University, Suita.ORCID https://orcid.org/0000-0002-6179-0195
Shunsuke YamanishiDepartment of Neurosurgery, Kobe University Graduate School of Medicine, Kobe.
Yusuke IkeuchiDepartment of Neurosurgery, Kobe University Graduate School of Medicine, Kobe.
Yuichi FujitaDepartment of Neurosurgery, Kobe University Graduate School of Medicine, Kobe.
Hirohumi IwahashiDepartment of Neurosurgery, Kobe University Graduate School of Medicine, Kobe.
Sayaka HottaDepartment of Respiratory Medicine and Clinical Immunology, Osaka University Graduate School of Medicine, Suita.
Michiko MatsunagaGraduate School of Education, Kyoto University, Kyoto.ORCID https://orcid.org/0000-0002-0316-3839
Shoji SanadaClinical and Translational Research Center, Kobe University Hospital, Kobe.
Yoshihiro MuragakiDepartment of Medical Device Engineering, Kobe University Graduate School of Medicine, Kobe (Y.M.).
Masamitsu NishiharaDepartment of Neurosurgery, Nishi-Kobe Medical Center, Kobe.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Altered tumor metabolism has renewed interest in ketogenic strategies, despite limited clinical evidence in glioma. Whereas the ketogenic diet (KD) alone elevates intratumoral amino acids, bevacizumab (BEV) co-administration suppresses these metabolites and curtails tumor growth, pointing to a synergistic therapeutic potential. Methods: We conducted a clinical pilot study to evaluate the combination of KD and standard therapy, combining BEV, in patients with malignant glioma. A standardized modified ketogenic diet (mKD) regimen was implemented: carbohydrate intake was restricted to 10 g/day in the first week, 20 g/day in the following 2 months, and ≤30 g/day thereafter. MCT oil was administered at ≥50 mL/day, and ketone formula supplements were provided as needed. The primary endpoint was to assess safety and feasibility. Results: 10 patients were enrolled. The duration of mKD ranged from 63 to 1,954 days, with a median of 185 days. All patients showed a rapid increase in serum ketone levels and achieved therapeutically adequate glucose-ketone index values. All participants met the predefined safety criteria, and no severe adverse events were reported. One patient discontinued the diet owing to moderate abdominal pain. The objective response rate was 50%, and notably, one patient remained on mKD for more than 5 years without tumor recurrence. The median progression-free survival from mKD initiation was 9.5 months, and the median overall survival was 31 months. Conclusions: The combination of mKD and standard therapy with BEV was safe and feasible in patients with malignant glioma. Larger clinical trials are needed to determine its anti-tumor efficacy and clinical benefit.

Indexed as

angiogenesis inhibitorfeasibilityketogenic dietmalignant gliomasafety

Identifiers

PMID41727338
PMCPMC12924638

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.