Evidence map›Paper›PMID 30524896›Full record

ArticleOncoimmunology

Responsiveness to anti-PD-1 and anti-CTLA-4 immune checkpoint blockade in SB28 and GL261 mouse glioma models.

Vassilis Genoud, Eliana Marinari, Sergey I Nikolaev, John C Castle, Valesca Bukur, Pierre-Yves Dietrich, Hideho Okada, Paul R Walker

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 119 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
119citing papers in PubMed, 1 pooled it
6.1field-weighted citation impact, top 2% of its field
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

119 citing papers in PubMed, 1 synthesis or guideline pooled it, 177 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Translational Theranostics in Glioblastoma: FAPI-46 as a Precision Medicine Tool.Journal of nuclear medicine : official publication, Society of Nuclear Medicine · 2026
    Article
  5. Review
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  7. Article
  8. Article
  9. Review
  10. Article
  11. Review
  12. Advances and challenges in glioblastoma immunotherapy: a meta-analysis of immune checkpoint inhibitors.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  13. Article
  14. Article
  15. Article
  16. Pharmacologic DPP-4 inhibition promotes CD8bioRxiv : the preprint server for biology · 2026
    Article
  17. Article
  18. Article
  19. Article
  20. Article

59 more citing papers are in PubMed but not listed here.

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

8 authors at 4 institutions in 3 countries.

Vassilis GenoudTranslational research center for hemato-oncology, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
Eliana MarinariTranslational research center for hemato-oncology, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
Sergey I NikolaevDepartment of Genetic Medicine and Development, University of Geneva, Geneva, Switzerland.
John C CastleBiomarker Development Center, Translational Oncology at the University Medical Center of Johannes Gutenberg University, Mainz, Germany.
Valesca BukurBiomarker Development Center, Translational Oncology at the University Medical Center of Johannes Gutenberg University, Mainz, Germany.
Pierre-Yves DietrichTranslational research center for hemato-oncology, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
Hideho OkadaDepartment of Neurological Surgery, University of California, San Francisco, California, USA.
Paul R WalkerTranslational research center for hemato-oncology, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
University of Geneva · CHUniversity Medical Center of the Johannes Gutenberg University Mainz · DEParker Institute for Cancer Immunotherapy · USUniversity Hospital of Geneva · CH

Funding

Preclinical development of breakthrough immunotherapy for brain tumorsR35NS105068 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI OKADA, HIDEHO · 2018 to 2025
$6.0M
NINDS NIH HHS R35 NS105068
6 · The paper itself

Abstract

Immune checkpoint blockade (ICB) is currently evaluated in patients with glioblastoma (GBM), based on encouraging clinical data in other cancers, and results from studies with the methylcholanthrene-induced GL261 mouse glioma. In this paper, we describe a novel model faithfully recapitulating some key human GBM characteristics, including low mutational load, a factor reported as a prognostic indicator of ICB response. Consistent with this observation, SB28 is completely resistant to ICB, contrasting with treatment sensitivity of the more highly mutated GL261. Moreover, SB28 shows features of a poorly immunogenic tumor, with low MHC-I expression and modest CD8

Indexed as

GL261GlioblastomaImmune checkpoint blockadeMutational loadSB28

Identifiers

PMID30524896
PMCPMC6279422
OpenAlexW2891184788

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.