Evidence map›Paper›PMID 39911397›Full record

ReviewFrontiers in immunology2025

Overcoming immune evasion with innovative multi-target approaches for glioblastoma.

Hai Su, Yin Peng, Yilong Wu, Xiaoli Zeng

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Targeting the COX-2/PGECancer immunology, immunotherapy : CII · 2026
    Review
  5. Article
  6. Review
  7. Article
  8. 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

4 authors.

Hai SuDepartment of Neurosurgery, Yongchuan Hospital of Chongqing Medical University, Chongqing, China.
Yin PengDepartment of Neurosurgery, Yongchuan Hospital of Chongqing Medical University, Chongqing, China.
Yilong WuDepartment of Neurosurgery, Yongchuan Hospital of Chongqing Medical University, Chongqing, China.
Xiaoli ZengDepartment of Oncology, The First Affiliated Hospital of Gannan Medical University, Ganzhou, Jiangxi, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma (GBM) cells leverage complex endogenous and environmental regulatory mechanisms to drive proliferation, invasion, and metastasis. Tumor immune evasion, facilitated by a multifactorial network, poses a significant challenge to effective therapy, as evidenced by the limited clinical benefits of monotherapies, highlighting the adaptive nature of immune evasion. This review explores glioblastoma's immune evasion mechanisms, the role of ICIs in the tumor microenvironment, and recent clinical advancements, offering theoretical insights and directions for monotherapy and combination therapy in glioblastoma management.

Indexed as

Brain NeoplasmsGlioblastomaImmune Checkpoint InhibitorsImmune EvasionTumor EscapeAnimalsHumansImmunotherapyTumor MicroenvironmentImmune Checkpoint Inhibitorsglioblastomaimmune checkpointimmune evasionimmunotherapyPD-1

Identifiers

PMID39911397
PMCPMC11794508

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.