Evidence map›Paper›PMID 42154325›Full record

ReviewActa neuropathologica2026

Future directions in the treatment of brain metastases: evaluating the role of cellular players in the tumour microenvironment.

Chris W Govaerts, J Marc C van Dijk, Anouk van der Hoorn, Frank A E Kruyt

Abstract readReview
In one paragraph

Review in Acta neuropathologica, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Chris W GovaertsDepartment of Medical Oncology, University Medical Center Groningen, University of Groningen, Hanzeplein 1, 9713 GZ, Groningen, The Netherlands.ORCID http://orcid.org/0000-0002-5478-7158
J Marc C van DijkDepartment of Neurosurgery, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.ORCID http://orcid.org/0000-0002-0814-5680
Anouk van der HoornDepartment of Radiology, Medical Imaging Center (MIC), University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.ORCID http://orcid.org/0000-0003-4649-327X
Frank A E KruytDepartment of Medical Oncology, University Medical Center Groningen, University of Groningen, Hanzeplein 1, 9713 GZ, Groningen, The Netherlands. f.a.e.kruyt@umcg.nl.ORCID http://orcid.org/0000-0002-2445-9380

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent clinical trials have demonstrated the efficacy of different modalities of systemic therapy in treating brain metastases, including immune checkpoint inhibitors and various types of targeted therapy. These findings expand treatment options for these intracranial tumours, which are linked to significant morbidity and poor outcomes. Despite these advances, important challenges remain. These include the difficulty of identifying predictors of intracranial response to such therapies. The intracranial activity of anti-tumour agents is dependent on the complex interplay between the cellular components of the tumour microenvironment, consisting of both brain-resident cell types and peripheral immune cells. A deeper understanding of these interactions is essential for identifying mechanisms that contribute to inter- and intratumoural heterogeneity in treatment sensitivity. This review provides a comprehensive overview of the mechanisms by which the constituent cell types of the tumour microenvironment of brain metastases contribute to tumour progression and therapy resistance. Herein, a conceptual model of the relevant biological pathways is outlined along with references to how specific vulnerabilities could be utilised to develop more effective therapeutic strategies.

Indexed as

Brain NeoplasmsTumor MicroenvironmentAnimalsHumansBrain metastasisCell–cell interactionImmune therapyTumour microenvironment

Identifiers

PMID42154325
PMCPMC13186852

What OpenQuestion holds

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Registered trials

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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.