Evidence map›Paper›PMID 41809120›Full record

ReviewImmunoTargets and therapy2026

Recurrent Glioblastoma and the Tumor Immune Landscape: Emerging Immunotherapeutic Strategies.

Zixuan Cao, Shurong Tong, Zihan Wang, Chenhui Ji, Chaoyong Zhang, Xingliang Dai, Bingshan Wu

Abstract readReview
In one paragraph

Review in ImmunoTargets and therapy, 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

7 authors.

Zixuan Cao *The First College of Clinical Medicine, Anhui Medical University, Hefei, People's Republic of China.ORCID 0009-0007-2917-3895
Shurong Tong *The First College of Clinical Medicine, Anhui Medical University, Hefei, People's Republic of China.ORCID 0009-0003-5144-7662
Zihan Wang *Department of Oncology, The First Affiliated Hospital of Anhui Medical University, Hefei, People's Republic of China.ORCID 0009-0001-5721-8508
Chenhui JiDepartment of Neurosurgery, The First Affiliated Hospital of Anhui Medical University, Hefei, People's Republic of China.ORCID 0009-0003-9078-6579
Chaoyong ZhangDepartment of Neurosurgery, The Taihe County People's Hospital, Fuyang, People's Republic of China.
Xingliang DaiDepartment of Neurosurgery, The First Affiliated Hospital of Anhui Medical University, Hefei, People's Republic of China.ORCID 0000-0002-0685-4766
Bingshan WuDepartment of Neurosurgery, The First Affiliated Hospital of Anhui Medical University, Hefei, People's Republic of China.ORCID 0000-0002-8881-0045

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma (GBM) is the most aggressive malignant tumor affecting the central nervous system. Current standard of care provides only modest clinical benefits, most patients eventually develop tumor recurrence, at which point therapeutic options become markedly restricted and the prognosis remains dismal. In recent years, immunotherapy has achieved significant clinical success in several solid tumors and has become a key strategy for advanced cancers owing to its specificity and potent antitumor activity. Nevertheless, the immunosuppressive tumor microenvironment of recurrent GBM (rGBM), along with its pronounced heterogeneity, and the presence of blood-brain barrier collectively undermine the efficacy of immunotherapy. With increasing insights into the tumor microenvironment and immune escape mechanisms, alongside refinements in immunotherapeutic strategies, immunotherapy may ultimately become one of the therapeutic options for patients with rGBM. Currently, principal immunotherapies under investigation for rGBM include immune checkpoint inhibitors, CAR-T cell therapy, oncolytic virotherapy, and cancer vaccines. In this review, we comprehensively summarize the clinical evidence for these approaches, highlight their mechanisms of action, and critically evaluate the key challenges that limit clinical translation. By integrating recent therapeutic progress and unresolved obstacles, we aim to provide a timely perspective on the optimization of immunotherapy in rGBM and to inform the rational design of future clinical trials.

Indexed as

cancer vaccinesCAR-T cell therapyimmune checkpoint inhibitorsimmunotherapyoncolytic virotherapyrecurrent glioblastomatumor microenvironment

Identifiers

PMID41809120
PMCPMC12970017

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.