Evidence map›Paper›PMID 42192798›Full record

ReviewBrain sciences2026

Evolving Landscape of Glioblastoma Research: Integrating Therapeutic Advances and Diagnostic Frontiers.

Nirupama A Sabnis, Luke C Cooksey, Hareesh Jayakumar, Mariana Moguel Mendez, Ezek Mathew, Roland Max Petty, Amalendu Ranjan, Luis Colon-Perez, Rob Dickerman, Porunelloor A Mathew and 1 more

Abstract readReview
In one paragraph

Review in Brain sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
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

11 authors.

Nirupama A SabnisDepartment of Microbiology, Immunology and Genetics, University of North Texas Health, Fort Worth, TX 76107, USA.ORCID 0000-0002-8686-1578
Luke C CookseyDepartment of Microbiology, Immunology and Genetics, University of North Texas Health, Fort Worth, TX 76107, USA.ORCID 0000-0003-3162-9744
Hareesh JayakumarBiology Department, Uppsala University, 753 10 Uppsala, Sweden.ORCID 0009-0004-5149-2735
Mariana Moguel MendezBurnette School of Medicine, Texas Christian University, Fort Worth, TX 76109, USA.
Ezek MathewDepartment of Microbiology, Immunology and Genetics, University of North Texas Health, Fort Worth, TX 76107, USA.ORCID 0000-0002-8957-9607
Roland Max PettyCollege of Science and Engineering, Texas Christian University, Fort Worth, TX 76109, USA.
Amalendu RanjanDepartment of Microbiology, Immunology and Genetics, University of North Texas Health, Fort Worth, TX 76107, USA.ORCID 0000-0002-3641-7751
Luis Colon-PerezDepartment of Pharmacology and Neuroscience, University of North Texas Health, Fort Worth, TX 76107, USA.ORCID 0000-0001-8918-2418
Rob DickermanSystems Science, University of North Texas Health, Fort Worth, TX 76107, USA.
Porunelloor A MathewDepartment of Microbiology, Immunology and Genetics, University of North Texas Health, Fort Worth, TX 76107, USA.ORCID 0000-0001-8137-0895
Bruce A BunnellDepartment of Microbiology, Immunology and Genetics, University of North Texas Health, Fort Worth, TX 76107, USA.ORCID 0000-0001-6196-3722

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma (GB) remains the most aggressive primary brain malignancy, with the Stupp regimen persisting as the standard of care for nearly two decades despite poor survival outcomes. This review was synthesized by extensively reviewing and analyzing the literature from PubMed, Scopus, and Web of Science to evaluate the emerging promising therapeutic and diagnostic strategies for combating GB. Results indicate significant progress in molecularly targeted therapies, biomimetic nanocarriers, and advanced radiotherapy. While immunotherapeutic approaches, such as checkpoint inhibitors and vaccines, show variable clinical success, the integration of bioinformatics and machine learning has significantly enhanced treatment response prediction. Furthermore, advances in radiomics and molecular imaging have improved the differentiation between true tumor progression and pseudoprogression, potentially reducing invasive diagnostic requirements. Additionally, other emerging and investigational adjuvant therapeutic approaches have shown promise. We conclude that, while multimodal strategies integrating molecular and computational approaches offer a path toward personalized GB management, significant barriers-namely tumor heterogeneity and the blood-brain barrier-persist. Future research must prioritize precision-based combinatorial models to successfully translate these preclinical advancements into improved clinical outcomes for patients.

Indexed as

biomimetic nanocarriersblood–brain barrierGBMglioblastoma (GB)immunotherapymachine learningmolecular imagingprecision medicinetargeted therapies

Identifiers

PMID42192798
PMCPMC13204486

What OpenQuestion holds

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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.